Yeast Systematic Name | Yeast Symbol | SGDID | Analog Name | Analog Description | EC | Organism | Disease | Structure | Uniprot | Human ID | Human Symbol | HHsearch Probability | HHsearch E_value | HHsearch P_value | HHsearch Score | Flag Disease related | Flag Homo sapiens | Flag Mus musculus | Flag Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YER111C | SWI4 | SGDID:S000000913 | TRPV4 |
Transient receptor potential cation channel subfamily V member 4 (TrpV4) (Vanilloid receptor-related osmotically activated channel) (VR-OAC) |
Gallus gallus | 3jxj_a | A0A1D5PXA5 | 97.00 | 7.40E-07 | 9.80E-11 | 81.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | ALDOA |
Fructose-bisphosphate aldolase A (EC 4.1.2.13) (Muscle-type aldolase) |
4.1.2.13 | Oryctolagus cuniculus | 6mwq_d | P00883 | 97.90 | 4.60E-09 | 4.60E-13 | 117.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YER111C | SWI4 | SGDID:S000000913 | ILK ILK1 ILK2 |
Integrin-linked protein kinase (EC 2.7.11.1) (59 kDa serine/threonine-protein kinase) (Beta-integrin-linked kinase) (ILK-1) (ILK-2) (p59ILK) |
2.7.11.1 | Homo sapiens | Polycystic Kidney Disease,Thyroid Gland Anaplastic Carcinoma,Hypertrophic Cardiomyopathy,Dilated Cardiomyopathy,Hypermobile Ehlers-Danlos Syndrome,Focal Segmental Glomerulosclerosis,Brain Cancer,Ovarian Cancer,Colorectal Cancer,Prostate Cancer,Hyperphosphatemia,Exudative Vitreoretinopathy,Renal Fibrosis,Lung Cancer,Pancreatic Cancer |
2kbx_a | Q13418 | ENSG00000166333 | ILK | 97.30 | 1.50E-07 | 2.00E-11 | 79.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YER111C | SWI4 | SGDID:S000000913 | ZDHHC17 HIP14 HIP3 HYPH KIAA0946 HSPC294 |
Palmitoyltransferase ZDHHC17 (EC 2.3.1.225) (Acyltransferase ZDHHC17) (EC 2.3.1.-) (DHHC domain-containing cysteine-rich protein 17) (DHHC17) (Huntingtin yeast partner H) (Huntingtin-interacting protein 14) (HIP-14) (Huntingtin-interacting protein 3) (HIP-3) (Huntingtin-interacting protein H) (Putative MAPK-activating protein PM11) (Putative NF-kappa-B-activating protein 205) (Zinc finger DHHC domain-containing protein 17) |
2.3.1.225 | Homo sapiens | Huntington Disease,Hypoparathyroidism, X-Linked |
3eu9_a | Q8IUH5 | ENSG00000186908 | ZDHHC17 | 98.50 | 2.70E-11 | 3.60E-15 | 110.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YER111C | SWI4 | SGDID:S000000913 | Trpv5 Ecac1 |
Transient receptor potential cation channel subfamily V member 5 (TrpV5) (Epithelial calcium channel 1) (ECaC1) (Osm-9-like TRP channel 3) (OTRPC3) |
Oryctolagus cuniculus | 6o1u_d | Q9XSM3 | 97.30 | 1.60E-07 | 1.80E-11 | 107.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | trpv4 |
trpv4 |
Xenopus tropicalis | 6c8f_a | F7BWY7 | 97.10 | 4.00E-07 | 4.90E-11 | 99.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | CDKN2A CDKN2 MTS1 |
Cyclin-dependent kinase inhibitor 2A (Cyclin-dependent kinase 4 inhibitor A) (CDK4I) (Multiple tumor suppressor 1) (MTS-1) (p16-INK4a) (p16-INK4) (p16INK4A) |
Homo sapiens | Melanoma-Astrocytoma Syndrome,Spitzoid Melanoma,Melanoma In Congenital Melanocytic Nevus,Adult Hepatocellular Carcinoma,Breast Papillomatosis,Pancreatic Adenocarcinoma,Supratentorial Cancer,Mesothelioma, Malignant,Skin Melanoma,Cervical Intraepithelial Neoplasia,Gliomatosis Cerebri,Heart Disease,Uterine Carcinosarcoma,Endometrial Cancer,Tonsillar Fossa Cancer,Peritoneum Cancer,Cervix Uteri Carcinoma In Situ,Acanthoma,Squamous Cell Carcinoma,Follicular Dendritic Cell Sarcoma,Ocular Melanoma,Childhood Acute Lymphocytic Leukemia,Childhood B-Cell Acute Lymphoblastic Leukemia,Retinitis Pigmentosa,Peritoneal Mesothelioma,Malignant Exocrine Pancreas Neoplasm,Pancreas Sarcoma,Lung Cancer Susceptibility 3,Uterus Carcinoma In Situ,Penile Cancer,Acral Lentiginous Melanoma,Penile Benign Neoplasm,Adenoid Cystic Carcinoma,Carcinosarcoma,Coronary Restenosis,Chordoma,Bone Cancer,Vulva Basal Cell Carcinoma,Suppression Of Tumorigenicity 12,Melanoma,Desmoid Tumor,Epidermolytic Acanthoma,Osteogenesis Imperfecta, Type Xiii,Muir-Torre Syndrome,Diabetes Mellitus,Chondromyxoid Fibroma,Dedifferentiated Liposarcoma,Adenoma,Malignant Peritoneal Mesothelioma,Papillary Squamous Carcinoma,Cholecystitis,Leiomyosarcoma,Vaginal Cancer,Bilateral Breast Cancer,B-Lymphoblastic Leukemia/Lymphoma,Peripheral Nervous System Neoplasm,Uterine Corpus Cancer,Connective Tissue Cancer,B-Lymphoblastic Leukemia/Lymphoma, Bcr-Abl1-Like,Collecting Duct Carcinoma,Alzheimer Disease,Plasma Cell Leukemia,Ovarian Seromucinous Carcinoma,Primary Cutaneous B-Cell Lymphoma,Vulvar Disease,Sarcomatoid Mesothelioma,Urinary Bladder Inverted Papilloma,Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type,Vulvar Seborrheic Keratosis,Myocardial Infarction,Vulva Squamous Cell Carcinoma,Pleomorphic Adenoma,Mucoepidermoid Carcinoma,Ischemic Fasciitis,Borst-Jadassohn Intraepidermal Carcinoma,Cervical Basaloid Squamous Cell Carcinoma,Neurofibroma,B-Cell Lymphoma,Bile Duct Cancer,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,Oral Cancer,Laryngeal Small Cell Carcinoma,Plasmablastic Lymphoma,Ocular Cancer,Human Cytomegalovirus Infection,Inverted Transitional Papilloma,Intracranial Meningioma,Retinal Cancer,Familial Retinoblastoma,Anal Canal Carcinoma,Posterior Fossa Ependymoma,Male Urethral Cancer,Lymphohistiocytoid Mesothelioma,Cervix Disease,Malignant Pleural Mesothelioma,Retroperitoneum Carcinoma,Endocervical Carcinoma,Vulvar Eccrine Porocarcinoma,Neurofibromatosis, Type I,Leukemia,Cholangiolocellular Carcinoma,Vulva Cancer,Adenosquamous Carcinoma,Neuroblastoma,Vulvar Intraepithelial Neoplasia,Pilocytic Astrocytoma,Gliofibroma,Cervical Adenoid Cystic Carcinoma,Proliferative Verrucous Leukoplakia,Childhood Leukemia,Middle Ear Carcinoma,Glomus Tumor,Esophagus Adenocarcinoma,Laryngeal Disease,Inherited Cancer-Predisposing Syndrome,Nasal Cavity Adenocarcinoma,Barrett'S Adenocarcinoma,Adenocarcinoma In Situ,Malignant Spiradenoma,Large Congenital Melanocytic Nevus,Glioma,Supraglottis Neoplasm,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Noonan Syndrome 1,Vaginal Tubulovillous Adenoma,Anal Canal Paget'S Disease,Basal Cell Carcinoma,Penile Urethral Cancer,Atypical Polypoid Adenomyoma,Inflammatory Liposarcoma,Leukemia, Acute Lymphoblastic,Hereditary Melanoma,Cervicitis,Early Invasive Cervical Adenocarcinoma,Low-Grade Astrocytoma,Adult Malignant Schwannoma,Larynx Cancer,Laryngeal Benign Neoplasm,Rectal Disease,Adenomyoma,Papilloma,Bizarre Leiomyoma,Kidney Cancer,Ovarian Brenner Tumor,Plexiform Neurofibroma,Perivascular Epithelioid Cell Tumor,Atypical Neurofibroma,Benign Mesothelioma,Pleural Cancer,Cystic Teratoma,Transitional Cell Carcinoma,Thyroid Lymphoma,Phimosis,Dysplastic Nevus Syndrome,Nodular Malignant Melanoma,Bladder Cancer,Bladder Clear Cell Adenocarcinoma,Urethra Clear Cell Adenocarcinoma,Megaesophagus,Spitz Nevus,Precursor T-Cell Acute Lymphoblastic Leukemia,Hypopharynx Cancer,Bile Duct Adenoma,Lung Adenoma,Endometrial Adenocarcinoma,Laryngeal Squamous Cell Carcinoma,Prostate Squamous Cell Carcinoma,Oropharynx Cancer,Cervix Carcinoma,Soft Palate Cancer,Oral Cavity Cancer,Keratinizing Squamous Cell Carcinoma,Basaloid Squamous Cell Carcinoma,Anal Squamous Cell Carcinoma,Middle Ear Squamous Cell Carcinoma,Endometrial Squamous Cell Carcinoma,Fallopian Tube Squamous Cell Carcinoma,Lip And Oral Cavity Cancer,Ovarian Cancer,Supraglottis Cancer,Burkitt Lymphoma,Lung Giant Cell Carcinoma,Adenocarcinoma,In Situ Carcinoma,T-Cell Acute Lymphoblastic Leukemia,Eye Disease,Mucinous Adenocarcinoma,Maxillary Sinus Benign Neoplasm,Pancreatic Adenosquamous Carcinoma,Trachea Carcinoma In Situ,Breast Cancer,Glioblastoma,Tonsil Cancer,Squamous Cell Carcinoma, Head And Neck,Actinic Keratosis,Hereditary Breast Ovarian Cancer Syndrome,Well-Differentiated Liposarcoma,Malignant Astrocytoma,High Grade Glioma,Gliosarcoma,Pleomorphic Liposarcoma,Giant Cell Glioblastoma,Mediastinum Liposarcoma,Anaplastic Astrocytoma,Colorectal Cancer,Peripheral Nervous System Disease,Nervous System Cancer,Familial Hypercholesterolemia,Histiocytic Sarcoma,Epstein-Barr Virus-Associated Gastric Carcinoma,Gallbladder Cancer,Squamous Cell Papilloma,Hepatocellular Carcinoma,Anus Disease,Ameloblastic Carcinoma,Tenosynovial Giant Cell Tumor,Nasal Cavity Cancer,Nasal Cavity Lymphoma,Fallopian Tube Endometrioid Adenocarcinoma,Skin Squamous Cell Carcinoma,Malignant Spindle Cell Melanoma,Inverted Papilloma,Oligodendroglioma,Malignant Peripheral Nerve Sheath Tumor,Neurilemmomatosis,Anus Cancer,Pheochromocytoma,Central Nervous System Lymphoma,Rhabdomyosarcoma,Intracranial Aneurysm,Tongue Disease,Bowenoid Papulosis,Atrophic Vulva,Teratoma,Vulvar Dystrophy,Fibrosarcoma Of Bone,Localized Osteosarcoma,Anogenital Venereal Wart,Leukemia, Acute Lymphoblastic 3,Bone Osteosarcoma,Liposarcoma,Skin Carcinoma,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Pancreatic Ductal Adenocarcinoma,Neurofibrosarcoma,Pancreatic Ductal Carcinoma,Cervical Cancer,Chronic Cervicitis,Cecal Benign Neoplasm,Ovarian Cystadenocarcinoma,Penile Disease,Infiltrating Angiolipoma,Central Nervous System Cancer,Rhabdoid Cancer,Lung Benign Neoplasm,Integumentary System Disease,Keratosis,Retinoblastoma,Cervical Adenocarcinoma,Endometrial Mucinous Adenocarcinoma,Ovary Adenocarcinoma,Gastric Adenocarcinoma,Type 2 Diabetes Mellitus,Plasmacytoma,Verrucous Carcinoma,Bladder Squamous Cell Carcinoma,Cervical Squamous Cell Carcinoma,Esophagus Verrucous Carcinoma,Childhood Medulloblastoma,Lynch Syndrome,Lung Squamous Cell Carcinoma,Sensory System Disease,Merkel Cell Carcinoma,Endometrial Transitional Cell Carcinoma,Bladder Urothelial Carcinoma,Keratosis, Seborrheic,Renal Cell Carcinoma, Papillary, 1,Small Cell Cancer Of The Lung,Adult T-Cell Leukemia,Esophageal Cancer,Respiratory System Benign Neoplasm,Reproductive Organ Benign Neoplasm,Tetralogy Of Fallot,Barrett Esophagus,Myelodysplastic Syndrome,Small Cell Carcinoma,Tumor Predisposition Syndrome,Diffuse Large B-Cell Lymphoma,Ewing Sarcoma,Mantle Cell Lymphoma,Melanoma-Pancreatic Cancer Syndrome,Gastrointestinal Stromal Tumor,Colorectal Adenoma,Colorectal Adenocarcinoma,Tongue Squamous Cell Carcinoma,Oral Squamous Cell Carcinoma,Gallbladder Adenoma,Bone Squamous Cell Carcinoma,Salivary Gland Carcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Cecum Adenoma,Tonsil Squamous Cell Carcinoma,Mucosal Melanoma,Parotid Gland Adenoid Cystic Carcinoma,Endocervical Adenocarcinoma,Nasopharyngeal Carcinoma,Wolf-Hirschhorn Syndrome,Meningioma, Familial,Lymphoma,Lipoprotein Quantitative Trait Locus,Pre-Malignant Neoplasm,Ductal Carcinoma In Situ,Cell Type Benign Neoplasm,Male Reproductive Organ Benign Neoplasm,Pharynx Cancer,Persistent Hyperplastic Primary Vitreous,Li-Fraumeni Syndrome,Dermatofibrosarcoma Protuberans,Myeloma, Multiple,Medulloblastoma,Spinal Disease,Melanoma, Cutaneous Malignant 1,Recessive Dystrophic Epidermolysis Bullosa,Melanoma, Cutaneous Malignant 2,Melanoma, Uveal,Retinitis Pigmentosa 11,Lung Cancer,Osteogenic Sarcoma,Pancreatic Cancer |
1dc2_a | P42771 | 96.70 | 3.20E-06 | 4.20E-10 | 70.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YER111C | SWI4 | SGDID:S000000913 | legA12 lpg0483 |
legA12 lpg0483 |
Legionella pneumophila | 5vrq_a | Q5ZY89 | 96.90 | 1.30E-06 | 1.60E-10 | 90.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | TV1425 TVG1472127 |
Putative ankyrin repeat protein TV1425 |
Thermoplasma volcanium | 2rfm_b | Q978J0 | 98.00 | 1.50E-09 | 1.90E-13 | 96.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | PSMD10 |
26S proteasome non-ATPase regulatory subunit 10 (26S proteasome regulatory subunit p28) (Gankyrin) (p28(GANK)) |
Homo sapiens | Dedifferentiated Liposarcoma,Hepatocellular Carcinoma,Retinoblastoma |
1uoh_a | O75832 | ENSG00000101843 | PSMD10 | 98.50 | 1.90E-11 | 2.60E-15 | 110.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | AVO2 YMR068W YM9916.07 |
Target of rapamycin complex 2 subunit AVO2 (TORC2 subunit AVO2) (Adheres voraciously to TOR2 protein 2) |
Saccharomyces cerevisiae | 6emk_h | Q04749 | 97.90 | 4.70E-09 | 4.80E-13 | 115.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | Asap2 Ddef2 Gm1523 Gm592 |
Arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2 (Development and differentiation-enhancing factor 2) (Paxillin-associated protein with ARF GAP activity 3) (PAG3) (Pyk2 C-terminus-associated protein) (PAP) |
Mus musculus | 1dcq_a | Q7SIG6 | 96.90 | 1.40E-06 | 1.70E-10 | 83.00 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | Trpc4 Trrp4 |
Short transient receptor potential channel 4 (TrpC4) (Capacitative calcium entry channel Trp4) (Receptor-activated cation channel TRP4) |
Mus musculus | 5z96_a | Q9QUQ5 | 97.00 | 9.50E-07 | 1.10E-10 | 99.80 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | LMJF_29_1100 |
LMJF_29_1100 |
Leishmania major | 3ljn_a | E9ADW8 | 98.30 | 1.50E-10 | 2.00E-14 | 112.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | spa |
Immunoglobulin G-binding protein A (IgG-binding protein A) (Staphylococcal protein A) (SpA) |
Staphylococcus aureus | 5cbn_a | P38507 | 97.00 | 8.10E-07 | 1.00E-10 | 79.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | legA1 lpg2416 |
legA1 lpg2416 |
Legionella pneumophila | 2aja_b | Q5ZSV0 | 97.60 | 3.30E-08 | 4.00E-12 | 99.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | ASB9 |
Ankyrin repeat and SOCS box protein 9 (ASB-9) |
Homo sapiens | Uterine Corpus Endometrial Carcinoma |
3d9h_a | Q96DX5 | ENSG00000102048 | ASB9 | 98.10 | 5.20E-10 | 6.50E-14 | 107.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | Trpv1 Vr1 Vr1l |
Transient receptor potential cation channel subfamily V member 1 (TrpV1) (Capsaicin receptor) (Osm-9-like TRP channel 1) (OTRPC1) (Vanilloid receptor 1) (Vanilloid receptor type 1-like) |
Rattus norvegicus | 2pnn_a | O35433 | 97.20 | 2.80E-07 | 3.70E-11 | 84.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | NFKB2 LYT10 |
Nuclear factor NF-kappa-B p100 subunit (DNA-binding factor KBF2) (H2TF1) (Lymphocyte translocation chromosome 10 protein) (Nuclear factor of kappa light polypeptide gene enhancer in B-cells 2) (Oncogene Lyt-10) (Lyt10) [Cleaved into: Nuclear factor NF-kappa-B p52 subunit] |
Homo sapiens | Immunodeficiency 10,B Cell Deficiency,Ectodermal Dysplasia,B-Cell Non-Hodgkin Lymphoma,B-Cell Lymphoma,Common Variable Immunodeficiency,Asbestos-Related Lung Carcinoma,Combined Immunodeficiency,Legionellosis,Osteopetrosis,Neuroaspergillosis,Immunodeficiency, Common Variable, 10,Splenic Marginal Zone Lymphoma,Lymphoma,Acth Deficiency, Isolated,Incontinentia Pigmenti,Immunodeficiency, Common Variable, 1 |
4ot9_a | Q00653 | ENSG00000077150 | NFKB2 | 98.20 | 4.10E-10 | 5.30E-14 | 109.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | Bd3460 |
Bd3460 |
Bdellovibrio bacteriovorus | 5cec_b | Q6MHS9 | 98.30 | 1.70E-10 | 2.20E-14 | 105.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | ANKRA2 ANKRA |
Ankyrin repeat family A protein 2 (RFXANK-like protein 2) |
Homo sapiens | Donnai-Barrow Syndrome,Three M Syndrome 1,Branchiooculofacial Syndrome |
3so8_a | Q9H9E1 | ENSG00000164331 | ANKRA2 | 98.00 | 2.30E-09 | 3.00E-13 | 92.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | Lebu_0176 |
Lebu_0176 |
Leptotrichia buccalis | 3t8k_a | C7NDE2 | 97.70 | 1.80E-08 | 2.30E-12 | 88.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | NFKBIA IKBA MAD3 NFKBI |
NF-kappa-B inhibitor alpha (I-kappa-B-alpha) (IkB-alpha) (IkappaBalpha) (Major histocompatibility complex enhancer-binding protein MAD3) |
Homo sapiens | Vascular Disease,Stomach Carcinoma In Situ,Bone Cancer,Leukemia, Chronic Myeloid,Diabetes Mellitus,Hepatitis B,Mycobacterium Malmoense,Ectodermal Dysplasia,B-Cell Lymphoma,Osteomyelitis, Sterile Multifocal, With Periostitis And Pustulosis,T-Cell Lymphoblastic Leukemia/Lymphoma,Carbuncle,Shigellosis,Periostitis,Hypohidrotic Ectodermal Dysplasia With Immunodeficiency,Newcastle Disease,Legionellosis,Ovarian Cancer,Burkitt Lymphoma,T-Cell Acute Lymphoblastic Leukemia,Crohn'S Disease,Squamous Cell Carcinoma, Head And Neck,Malignant Astrocytoma,Gliosarcoma,Giant Cell Glioblastoma,Parkinson Disease, Late-Onset,Colorectal Cancer,Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive,Hepatocellular Carcinoma,Human Immunodeficiency Virus Type 1,Tropical Spastic Paraparesis,Chromosome 14q11-Q22 Deletion Syndrome,Cardiomyopathy, Dilated, 1gg,Breast Adenocarcinoma,Cone-Rod Dystrophy 2,Prostate Cancer,Disease Of Mental Health,Rheumatoid Arthritis,Adult T-Cell Leukemia,Inflammatory Bowel Disease,Immune Deficiency Disease,Myelodysplastic Syndrome,Intellectual Developmental Disorder, X-Linked 108,Ectodermal Dysplasia And Immunodeficiency 2,Mantle Cell Lymphoma,Nasopharyngeal Carcinoma,Psoriatic Arthritis,Leukemia, Chronic Lymphocytic,Systemic Lupus Erythematosus,Myeloma, Multiple,Lung Cancer,Helicobacter Pylori Infection,Asthma,Pancreatic Cancer |
1nfi_e | P25963 | ENSG00000100906 | NFKBIA | 98.30 | 8.70E-11 | 1.20E-14 | 103.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | ACAP2 CENTB2 KIAA0041 |
Arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2 (Centaurin-beta-2) (Cnt-b2) |
Homo sapiens | Tethered Spinal Cord Syndrome |
6if3_a | Q15057 | ENSG00000114331 | ACAP2 | 97.30 | 1.50E-07 | 1.70E-11 | 85.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | PPP1R12A MBS MYPT1 |
Protein phosphatase 1 regulatory subunit 12A (130 kDa myosin-binding subunit of smooth muscle myosin phosphatase) (Myosin phosphatase-targeting subunit 1) (Myosin phosphatase target subunit 1) (PP1M subunit M110) (Protein phosphatase myosin-binding subunit) |
Gallus gallus | 1s70_b | Q90623 | 98.30 | 9.00E-11 | 1.20E-14 | 112.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | trpc4b trpc4a |
trpc4b trpc4a |
Danio rerio | 6g1k_b | U3N7D8 | 97.20 | 4.00E-07 | 4.20E-11 | 107.40 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | RFXANK ANKRA1 RFXB |
DNA-binding protein RFXANK (Ankyrin repeat family A protein 1) (Regulatory factor X subunit B) (RFX-B) (Regulatory factor X-associated ankyrin-containing protein) |
Homo sapiens | Severe Combined Immunodeficiency,Tibial Neuropathy,Tarsal Tunnel Syndrome,Combined Immunodeficiency,Discharging Ear,Purine Nucleoside Phosphorylase Deficiency,Alcoholic Gastritis,Acquired Thrombocytopenia,Omenn Syndrome,Retinitis Pigmentosa 48,Bare Lymphocyte Syndrome, Type I,Immune Deficiency Disease,Bare Lymphocyte Syndrome, Type Ii,Tumoral Calcinosis, Hyperphosphatemic, Familial, 1,Bjornstad Syndrome |
3uxg_a | O14593 | ENSG00000064490 | RFXANK | 97.90 | 4.40E-09 | 5.90E-13 | 89.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | YAR1 YPL239W |
Ankyrin repeat-containing protein YAR1 |
Saccharomyces cerevisiae | 4bsz_b | P46683 | 96.90 | 1.30E-06 | 1.70E-10 | 75.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | KLLA0_C04147g |
KLLA0_C04147g |
Kluyveromyces lactis | 5h2a_a | Q6CUK7 | 98.40 | 5.50E-11 | 6.90E-15 | 113.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | TNKS2 PARP5B TANK2 TNKL |
Poly [ADP-ribose] polymerase tankyrase-2 (EC 2.4.2.30) (ADP-ribosyltransferase diphtheria toxin-like 6) (ARTD6) (Poly [ADP-ribose] polymerase 5B) (Protein poly-ADP-ribosyltransferase tankyrase-2) (EC 2.4.2.-) (TNKS-2) (TRF1-interacting ankyrin-related ADP-ribose polymerase 2) (Tankyrase II) (Tankyrase-2) (TANK2) (Tankyrase-like protein) (Tankyrase-related protein) |
2.4.2.30 | Homo sapiens | Familial Isolated Hypoparathyroidism,Arthrogryposis, Renal Dysfunction, And Cholestasis 2,Cherubism,Arthrogryposis, Renal Dysfunction, And Cholestasis 1 |
4z68_a | Q9H2K2 | ENSG00000107854 | TNKS2 | 97.40 | 8.80E-08 | 1.20E-11 | 81.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YER111C | SWI4 | SGDID:S000000913 | 85/88 kDa calcium-independent phospholipase A2 (CaI-PLA2) (EC 3.1.1.4) (2-lysophosphatidylcholine acylhydrolase) (EC 3.1.1.5) (Group VI phospholipase A2) (GVI PLA2) (Intracellular membrane-associated calcium-independent phospholipase A2 beta) (iPLA2-beta) (PLA2G6) (Palmitoyl-CoA hydrolase) (EC 3.1.2.2) (Patatin-like phospholipase domain-containing protein 9) (PNPLA9) |
Cricetulus griseus | 6aun_a | A0A384E119 | 97.90 | 3.40E-09 | 4.00E-13 | 119.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
YER111C | SWI4 | SGDID:S000000913 | SWI6 YLR182W L9470.8 |
Regulatory protein SWI6 (Cell-cycle box factor subunit SWI6) (MBF subunit P90) (Trans-acting activator of HO endonuclease gene) |
Saccharomyces cerevisiae | 1sw6_b | P09959 | 98.50 | 2.40E-11 | 2.90E-15 | 120.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | TRPC3 TRP3 |
Short transient receptor potential channel 3 (TrpC3) (Transient receptor protein 3) (TRP-3) (hTrp-3) (hTrp3) |
Homo sapiens | T Cell And Nk Cell Immunodeficiency,Immunodeficiency 10,Progressive Familial Heart Block,Familial Episodic Pain Syndrome,Cerebellar Ataxia Type 42,Cerebellar Ataxia Type 41,Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques,Malignant Hypertension,Spinocerebellar Ataxia 14,Spinocerebellar Ataxia 41,Williams-Beuren Syndrome,Hereditary Ataxia,Hypertension, Essential,Mucolipidosis Iv |
5zbg_b | Q13507 | ENSG00000138741 | TRPC3 | 96.90 | 1.70E-06 | 1.90E-10 | 99.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | PPP1R13L IASPP NKIP1 PPP1R13BL RAI |
RelA-associated inhibitor (Inhibitor of ASPP protein) (Protein iASPP) (NFkB-interacting protein 1) (PPP1R13B-like protein) |
Homo sapiens | Basal Cell Carcinoma,Dilated Cardiomyopathy,Noonan Syndrome With Multiple Lentigines |
2vge_a | Q8WUF5 | ENSG00000104881 | PPP1R13L | 97.70 | 1.20E-08 | 1.50E-12 | 94.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | TRPC6 TRP6 |
Short transient receptor potential channel 6 (TrpC6) (Transient receptor protein 6) (TRP-6) |
Homo sapiens | Nephrotic Syndrome,T Cell And Nk Cell Immunodeficiency,Progressive Familial Heart Block,End Stage Renal Disease,Hypertrophic Pyloric Stenosis,Pyloric Stenosis,Genetic Steroid-Resistant Nephrotic Syndrome,Glutamate-Cysteine Ligase Deficiency,Familial Episodic Pain Syndrome,Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques,Familial Nephrotic Syndrome,Focal Segmental Glomerulosclerosis,Kidney Disease,Malignant Hypertension,Lipoid Nephrosis,Alport Syndrome,Focal Segmental Glomerulosclerosis 1,Pulmonary Hypertension,Focal Segmental Glomerulosclerosis 2,Hypothalamic Neoplasm,Diencephalic Neoplasm,Frasier Syndrome,Denys-Drash Syndrome,Hypertension, Essential,Membranous Nephropathy,Mucolipidosis Iv |
5yx9_b | Q9Y210 | ENSG00000137672 | TRPC6 | 97.60 | 2.80E-08 | 3.00E-12 | 117.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | ASPG |
ASPG |
3.5.1.1 | Cavia porcellus | 5dnc_b | H0W0T5 | 97.40 | 1.40E-07 | 1.30E-11 | 107.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YER111C | SWI4 | SGDID:S000000913 | CDKN2C CDKN6 |
Cyclin-dependent kinase 4 inhibitor C (Cyclin-dependent kinase 6 inhibitor) (p18-INK4c) (p18-INK6) |
Homo sapiens | Plasma Cell Neoplasm,Retinal Cancer,Parathyroid Adenoma,Leukemia, Acute Lymphoblastic,Ovarian Cancer,Breast Cancer,Multiple Endocrine Neoplasia,Oligodendroglioma,Pheochromocytoma,Retinoblastoma,Chromophobe Adenoma,Multiple Endocrine Neoplasia, Type Iv,Lymphoma, Non-Hodgkin, Familial,Multiple Endocrine Neoplasia, Type I,Meningioma, Familial,Lymphoma,Myeloma, Multiple,Medulloblastoma,Melanoma, Cutaneous Malignant 1,Lung Cancer |
1bu9_a | P42773 | 97.40 | 9.80E-08 | 1.30E-11 | 80.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YER111C | SWI4 | SGDID:S000000913 | Nfkbib Ikbb |
NF-kappa-B inhibitor beta (NF-kappa-BIB) (I-kappa-B-beta) (IkB-B) (IkB-beta) (IkappaBbeta) |
Mus musculus | 1k3z_d | Q60778 | 98.80 | 6.50E-13 | 8.60E-17 | 124.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | Espn |
Espin (Ectoplasmic specialization protein) |
Mus musculus | 5et1_b | Q9ET47 | 98.00 | 1.90E-09 | 2.40E-13 | 104.80 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | CDKN2A CDKN2 MTS1 |
Cyclin-dependent kinase inhibitor 2A (Cyclin-dependent kinase 4 inhibitor A) (CDK4I) (Multiple tumor suppressor 1) (MTS-1) (p16-INK4a) (p16-INK4) (p16INK4A) |
Homo sapiens | Melanoma-Astrocytoma Syndrome,Spitzoid Melanoma,Melanoma In Congenital Melanocytic Nevus,Adult Hepatocellular Carcinoma,Breast Papillomatosis,Pancreatic Adenocarcinoma,Supratentorial Cancer,Mesothelioma, Malignant,Skin Melanoma,Cervical Intraepithelial Neoplasia,Gliomatosis Cerebri,Heart Disease,Uterine Carcinosarcoma,Endometrial Cancer,Tonsillar Fossa Cancer,Peritoneum Cancer,Cervix Uteri Carcinoma In Situ,Acanthoma,Squamous Cell Carcinoma,Follicular Dendritic Cell Sarcoma,Ocular Melanoma,Childhood Acute Lymphocytic Leukemia,Childhood B-Cell Acute Lymphoblastic Leukemia,Retinitis Pigmentosa,Peritoneal Mesothelioma,Malignant Exocrine Pancreas Neoplasm,Pancreas Sarcoma,Lung Cancer Susceptibility 3,Uterus Carcinoma In Situ,Penile Cancer,Acral Lentiginous Melanoma,Penile Benign Neoplasm,Adenoid Cystic Carcinoma,Carcinosarcoma,Coronary Restenosis,Chordoma,Bone Cancer,Vulva Basal Cell Carcinoma,Suppression Of Tumorigenicity 12,Melanoma,Desmoid Tumor,Epidermolytic Acanthoma,Osteogenesis Imperfecta, Type Xiii,Muir-Torre Syndrome,Diabetes Mellitus,Chondromyxoid Fibroma,Dedifferentiated Liposarcoma,Adenoma,Malignant Peritoneal Mesothelioma,Papillary Squamous Carcinoma,Cholecystitis,Leiomyosarcoma,Vaginal Cancer,Bilateral Breast Cancer,B-Lymphoblastic Leukemia/Lymphoma,Peripheral Nervous System Neoplasm,Uterine Corpus Cancer,Connective Tissue Cancer,B-Lymphoblastic Leukemia/Lymphoma, Bcr-Abl1-Like,Collecting Duct Carcinoma,Alzheimer Disease,Plasma Cell Leukemia,Ovarian Seromucinous Carcinoma,Primary Cutaneous B-Cell Lymphoma,Vulvar Disease,Sarcomatoid Mesothelioma,Urinary Bladder Inverted Papilloma,Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type,Vulvar Seborrheic Keratosis,Myocardial Infarction,Vulva Squamous Cell Carcinoma,Pleomorphic Adenoma,Mucoepidermoid Carcinoma,Ischemic Fasciitis,Borst-Jadassohn Intraepidermal Carcinoma,Cervical Basaloid Squamous Cell Carcinoma,Neurofibroma,B-Cell Lymphoma,Bile Duct Cancer,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,Oral Cancer,Laryngeal Small Cell Carcinoma,Plasmablastic Lymphoma,Ocular Cancer,Human Cytomegalovirus Infection,Inverted Transitional Papilloma,Intracranial Meningioma,Retinal Cancer,Familial Retinoblastoma,Anal Canal Carcinoma,Posterior Fossa Ependymoma,Male Urethral Cancer,Lymphohistiocytoid Mesothelioma,Cervix Disease,Malignant Pleural Mesothelioma,Retroperitoneum Carcinoma,Endocervical Carcinoma,Vulvar Eccrine Porocarcinoma,Neurofibromatosis, Type I,Leukemia,Cholangiolocellular Carcinoma,Vulva Cancer,Adenosquamous Carcinoma,Neuroblastoma,Vulvar Intraepithelial Neoplasia,Pilocytic Astrocytoma,Gliofibroma,Cervical Adenoid Cystic Carcinoma,Proliferative Verrucous Leukoplakia,Childhood Leukemia,Middle Ear Carcinoma,Glomus Tumor,Esophagus Adenocarcinoma,Laryngeal Disease,Inherited Cancer-Predisposing Syndrome,Nasal Cavity Adenocarcinoma,Barrett'S Adenocarcinoma,Adenocarcinoma In Situ,Malignant Spiradenoma,Large Congenital Melanocytic Nevus,Glioma,Supraglottis Neoplasm,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Noonan Syndrome 1,Vaginal Tubulovillous Adenoma,Anal Canal Paget'S Disease,Basal Cell Carcinoma,Penile Urethral Cancer,Atypical Polypoid Adenomyoma,Inflammatory Liposarcoma,Leukemia, Acute Lymphoblastic,Hereditary Melanoma,Cervicitis,Early Invasive Cervical Adenocarcinoma,Low-Grade Astrocytoma,Adult Malignant Schwannoma,Larynx Cancer,Laryngeal Benign Neoplasm,Rectal Disease,Adenomyoma,Papilloma,Bizarre Leiomyoma,Kidney Cancer,Ovarian Brenner Tumor,Plexiform Neurofibroma,Perivascular Epithelioid Cell Tumor,Atypical Neurofibroma,Benign Mesothelioma,Pleural Cancer,Cystic Teratoma,Transitional Cell Carcinoma,Thyroid Lymphoma,Phimosis,Dysplastic Nevus Syndrome,Nodular Malignant Melanoma,Bladder Cancer,Bladder Clear Cell Adenocarcinoma,Urethra Clear Cell Adenocarcinoma,Megaesophagus,Spitz Nevus,Precursor T-Cell Acute Lymphoblastic Leukemia,Hypopharynx Cancer,Bile Duct Adenoma,Lung Adenoma,Endometrial Adenocarcinoma,Laryngeal Squamous Cell Carcinoma,Prostate Squamous Cell Carcinoma,Oropharynx Cancer,Cervix Carcinoma,Soft Palate Cancer,Oral Cavity Cancer,Keratinizing Squamous Cell Carcinoma,Basaloid Squamous Cell Carcinoma,Anal Squamous Cell Carcinoma,Middle Ear Squamous Cell Carcinoma,Endometrial Squamous Cell Carcinoma,Fallopian Tube Squamous Cell Carcinoma,Lip And Oral Cavity Cancer,Ovarian Cancer,Supraglottis Cancer,Burkitt Lymphoma,Lung Giant Cell Carcinoma,Adenocarcinoma,In Situ Carcinoma,T-Cell Acute Lymphoblastic Leukemia,Eye Disease,Mucinous Adenocarcinoma,Maxillary Sinus Benign Neoplasm,Pancreatic Adenosquamous Carcinoma,Trachea Carcinoma In Situ,Breast Cancer,Glioblastoma,Tonsil Cancer,Squamous Cell Carcinoma, Head And Neck,Actinic Keratosis,Hereditary Breast Ovarian Cancer Syndrome,Well-Differentiated Liposarcoma,Malignant Astrocytoma,High Grade Glioma,Gliosarcoma,Pleomorphic Liposarcoma,Giant Cell Glioblastoma,Mediastinum Liposarcoma,Anaplastic Astrocytoma,Colorectal Cancer,Peripheral Nervous System Disease,Nervous System Cancer,Familial Hypercholesterolemia,Histiocytic Sarcoma,Epstein-Barr Virus-Associated Gastric Carcinoma,Gallbladder Cancer,Squamous Cell Papilloma,Hepatocellular Carcinoma,Anus Disease,Ameloblastic Carcinoma,Tenosynovial Giant Cell Tumor,Nasal Cavity Cancer,Nasal Cavity Lymphoma,Fallopian Tube Endometrioid Adenocarcinoma,Skin Squamous Cell Carcinoma,Malignant Spindle Cell Melanoma,Inverted Papilloma,Oligodendroglioma,Malignant Peripheral Nerve Sheath Tumor,Neurilemmomatosis,Anus Cancer,Pheochromocytoma,Central Nervous System Lymphoma,Rhabdomyosarcoma,Intracranial Aneurysm,Tongue Disease,Bowenoid Papulosis,Atrophic Vulva,Teratoma,Vulvar Dystrophy,Fibrosarcoma Of Bone,Localized Osteosarcoma,Anogenital Venereal Wart,Leukemia, Acute Lymphoblastic 3,Bone Osteosarcoma,Liposarcoma,Skin Carcinoma,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Pancreatic Ductal Adenocarcinoma,Neurofibrosarcoma,Pancreatic Ductal Carcinoma,Cervical Cancer,Chronic Cervicitis,Cecal Benign Neoplasm,Ovarian Cystadenocarcinoma,Penile Disease,Infiltrating Angiolipoma,Central Nervous System Cancer,Rhabdoid Cancer,Lung Benign Neoplasm,Integumentary System Disease,Keratosis,Retinoblastoma,Cervical Adenocarcinoma,Endometrial Mucinous Adenocarcinoma,Ovary Adenocarcinoma,Gastric Adenocarcinoma,Type 2 Diabetes Mellitus,Plasmacytoma,Verrucous Carcinoma,Bladder Squamous Cell Carcinoma,Cervical Squamous Cell Carcinoma,Esophagus Verrucous Carcinoma,Childhood Medulloblastoma,Lynch Syndrome,Lung Squamous Cell Carcinoma,Sensory System Disease,Merkel Cell Carcinoma,Endometrial Transitional Cell Carcinoma,Bladder Urothelial Carcinoma,Keratosis, Seborrheic,Renal Cell Carcinoma, Papillary, 1,Small Cell Cancer Of The Lung,Adult T-Cell Leukemia,Esophageal Cancer,Respiratory System Benign Neoplasm,Reproductive Organ Benign Neoplasm,Tetralogy Of Fallot,Barrett Esophagus,Myelodysplastic Syndrome,Small Cell Carcinoma,Tumor Predisposition Syndrome,Diffuse Large B-Cell Lymphoma,Ewing Sarcoma,Mantle Cell Lymphoma,Melanoma-Pancreatic Cancer Syndrome,Gastrointestinal Stromal Tumor,Colorectal Adenoma,Colorectal Adenocarcinoma,Tongue Squamous Cell Carcinoma,Oral Squamous Cell Carcinoma,Gallbladder Adenoma,Bone Squamous Cell Carcinoma,Salivary Gland Carcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Cecum Adenoma,Tonsil Squamous Cell Carcinoma,Mucosal Melanoma,Parotid Gland Adenoid Cystic Carcinoma,Endocervical Adenocarcinoma,Nasopharyngeal Carcinoma,Wolf-Hirschhorn Syndrome,Meningioma, Familial,Lymphoma,Lipoprotein Quantitative Trait Locus,Pre-Malignant Neoplasm,Ductal Carcinoma In Situ,Cell Type Benign Neoplasm,Male Reproductive Organ Benign Neoplasm,Pharynx Cancer,Persistent Hyperplastic Primary Vitreous,Li-Fraumeni Syndrome,Dermatofibrosarcoma Protuberans,Myeloma, Multiple,Medulloblastoma,Spinal Disease,Melanoma, Cutaneous Malignant 1,Recessive Dystrophic Epidermolysis Bullosa,Melanoma, Cutaneous Malignant 2,Melanoma, Uveal,Retinitis Pigmentosa 11,Lung Cancer,Osteogenic Sarcoma,Pancreatic Cancer |
1bi7_b | P42771 | 98.60 | 1.00E-11 | 1.10E-15 | 113.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YER111C | SWI4 | SGDID:S000000913 | TNKS PARP5A PARPL TIN1 TINF1 TNKS1 |
Poly [ADP-ribose] polymerase tankyrase-1 (EC 2.4.2.30) (ADP-ribosyltransferase diphtheria toxin-like 5) (ARTD5) (Poly [ADP-ribose] polymerase 5A) (Protein poly-ADP-ribosyltransferase tankyrase-1) (EC 2.4.2.-) (TNKS-1) (TRF1-interacting ankyrin-related ADP-ribose polymerase) (Tankyrase I) (Tankyrase-1) (TANK1) |
2.4.2.30 | Homo sapiens | Cornelia De Lange Syndrome,Lung Acinar Adenocarcinoma,Amyotrophic Lateral Sclerosis 1,Arthrogryposis, Renal Dysfunction, And Cholestasis 2,Cherubism,Meningioma, Familial,Arthrogryposis, Renal Dysfunction, And Cholestasis 1 |
5gp7_a | O95271 | ENSG00000173273 | TNKS | 97.90 | 4.70E-09 | 6.00E-13 | 91.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YER111C | SWI4 | SGDID:S000000913 | RNASEL RNS4 |
2-5A-dependent ribonuclease (2-5A-dependent RNase) (EC 3.1.26.-) (Ribonuclease 4) (Ribonuclease L) (RNase L) |
3.1.26.- | Homo sapiens | Viral Infectious Disease,Myalgic Encephalomyelitis/Chronic Fatigue Syndrome,Rasopathy,Dengue Disease,Prostate Cancer, Hereditary, 1,West Nile Encephalitis,West Nile Fever,Noonan Syndrome 1,Chronic Fatigue Syndrome,Herpes Simplex,West Nile Virus Infection,Vaccinia,Prostate Cancer,Lynch Syndrome,La Crosse Encephalitis,Noonan Syndrome 2,Paralytic Poliomyelitis,Aicardi-Goutieres Syndrome,Immune Deficiency Disease,Microphthalmia With Limb Anomalies |
1wdy_a | Q05823 | ENSG00000135828 | RNASEL | 98.40 | 5.40E-11 | 7.30E-15 | 109.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YER111C | SWI4 | SGDID:S000000913 | EF_0377 |
EF_0377 |
Enterococcus faecalis | 3hra_a | Q838Q8 | 98.40 | 4.80E-11 | 6.50E-15 | 104.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | Trpv2 Sac2b Vrl1 |
Transient receptor potential cation channel subfamily V member 2 (TrpV2) (Osm-9-like TRP channel 2) (OTRPC2) (Stretch-activated channel 2B) (Vanilloid receptor-like protein 1) (VRL-1) |
Rattus norvegicus | 2etb_a | Q9WUD2 | 97.20 | 2.60E-07 | 3.40E-11 | 83.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | Kank1 |
Kank1 |
Mus musculus | 5yay_a | E9Q238 | 97.80 | 9.00E-09 | 1.10E-12 | 97.40 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | MBP1 YDL056W |
Transcription factor MBP1 (MBF subunit p120) |
Saccharomyces cerevisiae | 1bm8_a | P39678 | 99.70 | 3.00E-21 | 3.00E-25 | 174.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | legAS4 lpg1718 |
legAS4 lpg1718 |
Legionella pneumophila | 5czy_a | Q5ZUS4 | 97.50 | 5.50E-08 | 6.20E-12 | 104.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | ANKRD27 PP12899 |
Ankyrin repeat domain-containing protein 27 (VPS9 domain-containing protein) |
Homo sapiens | Parastremmatic Dwarfism,Hermansky-Pudlak Syndrome,Pontiac Fever |
4b93_b | Q96NW4 | ENSG00000105186 | ANKRD27 | 98.60 | 6.30E-12 | 7.90E-16 | 120.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | bqt4 SPBC19C7.10 |
Bouquet formation protein 4 |
Schizosaccharomyces pombe | 5yca_a | O60158 | 99.30 | 4.80E-16 | 4.80E-20 | 156.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | ANK2 ANKB |
Ankyrin-2 (ANK-2) (Ankyrin-B) (Brain ankyrin) (Non-erythroid ankyrin) |
Homo sapiens | Timothy Syndrome,Heart Disease,Hypertrophic Cardiomyopathy,Familial Long Qt Syndrome,Legionnaire Disease,Long Qt Syndrome 12,Dilated Cardiomyopathy,Jervell And Lange-Nielsen Syndrome 1,Hereditary Spherocytosis,Long Qt Syndrome,Heart Conduction Disease,Progressive Familial Heart Block, Type Ia,Sick Sinus Syndrome,Andersen Cardiodysrhythmic Periodic Paralysis,Cardiac Arrhythmia,Developmental And Epileptic Encephalopathy 5,Long Qt Syndrome 13,Disease Of Mental Health,Long Qt Syndrome 3,Long Qt Syndrome 2,Long Qt Syndrome 6,Long Qt Syndrome 5,Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Long Qt Syndrome 9,Long Qt Syndrome 10,Long Qt Syndrome 11,Coffin-Siris Syndrome 1,Brugada Syndrome 3,Familial Atrial Fibrillation,Sinoatrial Node Disease,Long Qt Syndrome 1,Intrinsic Cardiomyopathy,Autism Spectrum Disorder,Atrial Fibrillation,Cardiac Arrest,Autism,Catecholaminergic Polymorphic Ventricular Tachycardia,Spinocerebellar Ataxia 5,Cardiac Arrhythmia, Ankyrin-B-Related |
5y4d_a | Q01484 | ENSG00000145362 | ANK2 | 97.90 | 4.70E-09 | 6.00E-13 | 113.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | Tnks Tnks1 |
Poly [ADP-ribose] polymerase tankyrase-1 (EC 2.4.2.30) (ADP-ribosyltransferase diphtheria toxin-like 5) (ARTD5) (Protein poly-ADP-ribosyltransferase tankyrase-1) (EC 2.4.2.-) (TRF1-interacting ankyrin-related ADP-ribose polymerase 1) (Tankyrase I) (Tankyrase-1) (TANK1) |
2.4.2.30 | Mus musculus | 6cf6_a | Q6PFX9 | 98.40 | 4.90E-11 | 6.50E-15 | 114.90 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YER111C | SWI4 | SGDID:S000000913 | Shank3 Prosap2 |
SH3 and multiple ankyrin repeat domains protein 3 (Shank3) (Proline-rich synapse-associated protein 2) (ProSAP2) (SPANK-2) |
Rattus norvegicus | 5g4x_a | Q9JLU4 | 98.30 | 1.80E-10 | 2.20E-14 | 113.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | nompC CG17468 CT30855 Dmel\CG11020 DmNompC jf24 l(2)25Dc l(2)jf24 nomp NOMPC NompC ORE-13 TRPN TRPN1 CG11020 Dmel_CG11020 |
nompC CG17468 CT30855 Dmel\CG11020 DmNompC jf24 l(2)25Dc l(2)jf24 nomp NOMPC NompC ORE-13 TRPN TRPN1 CG11020 Dmel_CG11020 |
Drosophila melanogaster | 5vkq_d | E0A9E1 | 98.00 | 1.70E-09 | 2.00E-13 | 133.50 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | SWH1 OSH1 YAR042W YAR044W |
Oxysterol-binding protein homolog 1 |
Saccharomyces cerevisiae | 5h28_a | P35845 | 98.30 | 9.10E-11 | 1.20E-14 | 109.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | AKT1 At2g26650 F18A8.2 |
Potassium channel AKT1 |
Arabidopsis thaliana | 5aar_a | Q38998 | 98.40 | 5.00E-11 | 6.80E-15 | 102.60 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | Trpv6 |
Transient receptor potential cation channel subfamily V member 6 (TrpV6) (Calcium transport protein 1) (CaT1) (Epithelial calcium channel 2) (ECaC2) |
Mus musculus | 2rfa_a | Q91WD2 | 98.30 | 2.00E-10 | 2.60E-14 | 104.00 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | CAO CPSRP43 At2g47450 T30B22.25 |
Signal recognition particle 43 kDa protein, chloroplastic (Chromo protein SRP43) (CpSRP43) |
Arabidopsis thaliana | 3deo_a | O22265 | 96.80 | 1.80E-06 | 2.40E-10 | 74.20 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | NAS6 YGR232W G8564 |
Probable 26S proteasome regulatory subunit p28 (Proteasome non-ATPase subunit 6) |
Saccharomyces cerevisiae | 1wg0_a | P50086 | 98.20 | 3.70E-10 | 4.90E-14 | 102.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | K1L |
K1L |
Vaccinia virus | 3kea_b | Q6IV60 | 97.90 | 4.50E-09 | 5.90E-13 | 98.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | EHMT1 EUHMTASE1 GLP KIAA1876 KMT1D |
Histone-lysine N-methyltransferase EHMT1 (EC 2.1.1.-) (Euchromatic histone-lysine N-methyltransferase 1) (Eu-HMTase1) (G9a-like protein 1) (GLP) (GLP1) (Histone H3-K9 methyltransferase 5) (H3-K9-HMTase 5) (Lysine N-methyltransferase 1D) |
2.1.1.- | Homo sapiens | Kleefstra Syndrome,Deafness, Autosomal Dominant 47,Hypoplastic Left Heart Syndrome,Polymicrogyria,Kleefstra Syndrome Due To A Point Mutation,Pontocerebellar Hypoplasia, Type 2a,Weaver Syndrome,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Kleefstra Syndrome 1,Chromosome 16p13.3 Deletion Syndrome, Proximal,Pitt-Hopkins Syndrome,Schizophrenia,Ogden Syndrome,Autism Spectrum Disorder,Kabuki Syndrome 1,Autosomal Dominant Non-Syndromic Intellectual Disability,Chromosomal Deletion Syndrome,Autism,Christianson Syndrome |
3b7b_a | Q9H9B1 | ENSG00000181090 | EHMT1 | 98.40 | 3.50E-11 | 4.70E-15 | 109.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YER111C | SWI4 | SGDID:S000000913 | ABAYE2397 |
ABAYE2397 |
Acinetobacter baumannii | 5d66_a | B0VB33 | 98.70 | 2.10E-12 | 2.80E-16 | 114.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | lin-12 R107.8 |
Protein lin-12 (Abnormal cell lineage protein 12) (Notch-like protein lin-12) |
Caenorhabditis elegans | 2fo1_e | P14585 | 98.20 | 2.50E-10 | 3.30E-14 | 112.00 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | KANK1 ANKRD15 KANK KIAA0172 |
KN motif and ankyrin repeat domain-containing protein 1 (Ankyrin repeat domain-containing protein 15) (Kidney ankyrin repeat-containing protein) |
Homo sapiens | Metanephric Adenoma,Chromosome 9p Deletion Syndrome,Nephrotic Syndrome,Cerebral Palsy,Inherited Congenital Spastic Tetraplegia,Cerebral Palsy, Spastic Quadriplegic, 2,Myeloproliferative Neoplasm,Quadriplegia,Renal Adenoma,Tukel Syndrome,Spastic Quadriplegia,Spastic Cerebral Palsy,Brain Glioma,Autosomal Dominant Non-Syndromic Intellectual Disability |
5ybu_a | Q14678 | ENSG00000107104 | KANK1 | 97.60 | 2.70E-08 | 3.50E-12 | 91.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | ASB11 |
Ankyrin repeat and SOCS box protein 11 (ASB-11) |
Homo sapiens | Lacrimal Duct Obstruction |
4uuc_a | Q8WXH4 | ENSG00000165192 | ASB11 | 98.50 | 2.00E-11 | 2.70E-15 | 109.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | TRPV2 VRL |
Transient receptor potential cation channel subfamily V member 2 (TrpV2) (Osm-9-like TRP channel 2) (OTRPC2) (Vanilloid receptor-like protein 1) (VRL-1) |
Homo sapiens | Dentin Sensitivity,Inflammatory Bowel Disease 28,Familial Episodic Pain Syndrome,Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques,Dilated Cardiomyopathy,Facial Dermatosis,Scapuloperoneal Spinal Muscular Atrophy,Brachyolmia |
2f37_b | Q9Y5S1 | ENSG00000187688 | TRPV2 | 97.90 | 2.60E-09 | 3.50E-13 | 96.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | OOU_Y34scaffold00628g4 |
OOU_Y34scaffold00628g4 |
Magnaporthe oryzae | 4ux5_b | L7I1M8 | 99.80 | 4.70E-25 | 4.30E-29 | 213.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER111C | SWI4 | SGDID:S000000913 | NOTCH1 TAN1 |
Neurogenic locus notch homolog protein 1 (Notch 1) (hN1) (Translocation-associated notch protein TAN-1) [Cleaved into: Notch 1 extracellular truncation (NEXT); Notch 1 intracellular domain (NICD)] |
Homo sapiens | Ventricular Septal Defect,Heart Septal Defect,Heart Disease,Richter'S Syndrome,Squamous Cell Carcinoma,Severe Combined Immunodeficiency,Lymphoblastic Lymphoma,Retinitis Pigmentosa,Myeloid And Lymphoid Neoplasms Associated With Fgfr1 Abnormalities,Ossifying Fibroma,Adenoid Cystic Carcinoma,Double Outlet Right Ventricle,Hajdu-Cheney Syndrome,Bone Cancer,Atrial Heart Septal Defect,Invasive Bladder Transitional Cell Carcinoma,Prion Disease,Connective Tissue Disease,Uterine Adnexa Cancer,Kleefstra Syndrome,Tongue Carcinoma,Orofacial Cleft 4,Clear Cell Renal Cell Carcinoma,Aortic Dissection,Alzheimer Disease,Rasopathy,Nodular Regenerative Hyperplasia,Mucoepidermoid Carcinoma,T-Cell Non-Hodgkin Lymphoma,Holoprosencephaly,Plasmablastic Lymphoma,T-Cell Lymphoblastic Leukemia/Lymphoma,Biliary Tract Disease,Infratentorial Cancer,Familial Thoracic Aortic Aneurysm And Aortic Dissection,Leukemia,Colon Adenocarcinoma,Neuroblastoma,Hypoplastic Left Heart Syndrome,Lacrimal Gland Adenoid Cystic Carcinoma,Shone Complex,Acute Leukemia,Intrahepatic Cholangiocarcinoma,Leukemia, Acute Myeloid,Bone Marrow Cancer,Basal Cell Carcinoma,Hematologic Cancer,Hemangioma,Leukemia, Acute Lymphoblastic,Combined Immunodeficiency,Basal Cell Nevus Syndrome,Aortic Disease,Aortic Valve Disease 1,Focal Segmental Glomerulosclerosis,Brain Cancer,Precursor T-Cell Acute Lymphoblastic Leukemia,Lung Adenoma,Oropharynx Cancer,Aplastic Anemia,Ovarian Cancer,T-Cell Acute Lymphoblastic Leukemia,Breast Cancer,Tonsil Cancer,Exudative Vitreoretinopathy 5,Microphthalmia,Malignant Astrocytoma,Adult Liposarcoma,Breast Liposarcoma,Anaplastic Astrocytoma,Colorectal Cancer,Peripheral Nervous System Disease,Hepatocellular Carcinoma,Splenic Diffuse Red Pulp Small B-Cell Lymphoma,Pheochromocytoma,Aneurysm,Hydrocephalus,Tongue Disease,Cerebral Degeneration,Spondylocostal Dysostosis 3, Autosomal Recessive,Alagille Syndrome 1,Skin Carcinoma,Hemophagocytic Lymphohistiocytosis, Familial, 2,Gastric Cancer,Friedreich Ataxia,Prostate Cancer,Disease Of Mental Health,Cervical Cancer,Aortic Aneurysm,Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, Type 1,Orofacial Cleft 8,Scalp-Ear-Nipple Syndrome,Lung Squamous Cell Carcinoma,Adenoiditis,Merkel Cell Carcinoma,Lymphoma, Non-Hodgkin, Familial,Mouth Disease,Adams-Oliver Syndrome 5,Loeys-Dietz Syndrome,Hypoplastic Left Heart Syndrome 1,Tetralogy Of Fallot,Myelodysplastic Syndrome,Mantle Cell Lymphoma,Peripheral T-Cell Lymphoma,Heart, Malformation Of,Tongue Squamous Cell Carcinoma,Acute Promyelocytic Leukemia,Bone Squamous Cell Carcinoma,Aortic Aneurysm, Familial Thoracic 1,Endosteal Hyperostosis, Autosomal Dominant,Wilms Tumor 1,Mental Retardation, Autosomal Dominant 40,Lipoprotein Quantitative Trait Locus,Cardiovascular Organ Benign Neoplasm,Brain Glioma,Patent Ductus Arteriosus 1,Adams-Oliver Syndrome,Wilson-Turner X-Linked Mental Retardation Syndrome,Dowling-Degos Disease,Leukemia, Chronic Lymphocytic,Marfan Syndrome,Left Ventricular Noncompaction,Myeloma, Multiple,Medulloblastoma,Lung Cancer,Oliver Syndrome,Pancreatic Cancer |
2f8y_a | P46531 | ENSG00000148400 | NOTCH1 | 98.40 | 6.40E-11 | 8.70E-15 | 105.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | KANK2 ANKRD25 KIAA1518 MXRA3 SIP |
KN motif and ankyrin repeat domain-containing protein 2 (Ankyrin repeat domain-containing protein 25) (Matrix-remodeling-associated protein 3) (SRC-1-interacting protein) (SIP) (SRC-interacting protein) (SRC1-interacting protein) |
Homo sapiens | Nephrotic Syndrome,Pseudoainhum,Familial Woolly Hair Syndrome,Succinic Semialdehyde Dehydrogenase Deficiency,Focal Segmental Glomerulosclerosis,Ectodermal Dysplasia 4, Hair/Nail Type,Striate Palmoplantar Keratoderma,Nephrotic Syndrome, Type 16,Palmoplantar Keratoderma And Woolly Hair,Woolly Hair, Autosomal Dominant,Gamma-Amino Butyric Acid Metabolism Disorder,Multiple Pterygium Syndrome, Escobar Variant |
4hbd_a | Q63ZY3 | ENSG00000197256 | KANK2 | 97.60 | 2.60E-08 | 3.20E-12 | 94.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER111C | SWI4 | SGDID:S000000913 | TRPV6 ECAC2 |
Transient receptor potential cation channel subfamily V member 6 (TrpV6) (CaT-like) (CaT-L) (Calcium transport protein 1) (CaT1) (Epithelial calcium channel 2) (ECaC2) |
Homo sapiens | Metatropic Dysplasia,Pseudohypoaldosteronism,Hypervitaminosis D,Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques,Pendred Syndrome,Hyperparathyroidism,Bone Mineral Density Quantitative Trait Locus 15,Aromatase Deficiency,Prostate Cancer,Hyperparathyroidism, Transient Neonatal,Scapuloperoneal Spinal Muscular Atrophy,Hyperparathyroidism, Neonatal Severe,Spondyloepiphyseal Dysplasia, Maroteaux Type,Spondylometaphyseal Dysplasia, Kozlowski Type,Brachyolmia,Autosomal Recessive Disease,Estrogen-Receptor Negative Breast Cancer,Mucolipidosis Iv |
6e2f_c | Q9H1D0 | ENSG00000165125 | TRPV6 | 97.60 | 3.60E-08 | 3.80E-12 | 113.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |