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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YDL058W | USO1 | SGDID:S000002216 | MYH7 |
Myosin-7 (Myosin heavy chain 7) (Myosin heavy chain slow isoform) (MyHC-slow) (Myosin heavy chain, cardiac muscle beta isoform) (MyHC-beta) |
Bos taurus | 6fsa_b | Q9BE39 | 99.00 | 7.20E-14 | 7.70E-18 | 190.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | CTHT_0012280 |
CTHT_0012280 |
Chaetomium thermophilum | 4xri_a | G0S143 | 95.40 | 0.00015 | 1.80E-08 | 84.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | Ap2a2 Adtab |
AP-2 complex subunit alpha-2 (100 kDa coated vesicle protein C) (Adaptor protein complex AP-2 subunit alpha-2) (Adaptor-related protein complex 2 subunit alpha-2) (Alpha-adaptin C) (Alpha2-adaptin) (Clathrin assembly protein complex 2 alpha-C large chain) (Plasma membrane adaptor HA2/AP2 adaptin alpha C subunit) |
Rattus norvegicus | 2vgl_a | P18484 | 96.70 | 3.10E-06 | 3.70E-10 | 97.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | AP2B1 ADTB2 CLAPB1 |
AP-2 complex subunit beta (AP105B) (Adaptor protein complex AP-2 subunit beta) (Adaptor-related protein complex 2 subunit beta) (Beta-2-adaptin) (Beta-adaptin) (Clathrin assembly protein complex 2 beta large chain) (Plasma membrane adaptor HA2/AP2 adaptin beta subunit) |
Homo sapiens | Cerebellar Degeneration,Branchiooculofacial Syndrome,Char Syndrome,Rhabdomyosarcoma,Mental Retardation, Autosomal Dominant 56,Patent Ductus Arteriosus 1,Ataxia-Telangiectasia,Hypocalciuric Hypercalcemia, Familial, Type Iii |
2vgl_b | P63010 | ENSG00000006125 | AP2B1 | 97.00 | 7.20E-07 | 8.80E-11 | 100.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | KPNA6 IPOA7 |
Importin subunit alpha-7 (Karyopherin subunit alpha-6) |
Homo sapiens | 4uad_a | O60684 | ENSG00000025800 | KPNA6 | 98.80 | 3.40E-13 | 4.20E-17 | 149.80 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YDL058W | USO1 | SGDID:S000002216 | VAC8 YEB3 YEL013W |
Vacuolar protein 8 |
Saccharomyces cerevisiae | 5xjg_c | P39968 | 99.00 | 3.10E-14 | 3.90E-18 | 158.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | KPNB1 NTF97 |
Importin subunit beta-1 (Importin-90) (Karyopherin subunit beta-1) (Nuclear factor p97) (Pore targeting complex 97 kDa subunit) (PTAC97) |
Homo sapiens | Retinitis Pigmentosa,Venezuelan Equine Encephalitis,Influenza,Campomelic Dysplasia |
1qgr_a | Q14974 | ENSG00000108424 | KPNB1 | 96.50 | 6.10E-06 | 7.50E-10 | 97.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | SKLU-Cont10078 |
SKLU-Cont10078 |
Lachancea kluyveri | 6mzg_e | A0A493R6X8 | 95.90 | 4.30E-05 | 5.20E-09 | 85.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | YEF3 EFC1 TEF3 YEF3A YLR249W L9672.5 |
Elongation factor 3A (EF-3) (EF-3A) (EC 3.6.4.-) (Eukaryotic elongation factor 3) (eEF3) (Translation elongation factor 3A) (Yeast elongation factor 3) |
3.6.4.- | Saccharomyces cerevisiae | 2iw3_a | P16521 | 95.70 | 8.00E-05 | 9.10E-09 | 91.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDL058W | USO1 | SGDID:S000002216 | Ap1b1 Adtb1 |
AP-1 complex subunit beta-1 (Adaptor protein complex AP-1 subunit beta-1) (Adaptor-related protein complex 1 subunit beta-1) (Beta-1-adaptin) (Beta-adaptin 1) (Clathrin assembly protein complex 1 beta large chain) (Golgi adaptor HA1/AP1 adaptin beta subunit) |
Rattus norvegicus | 1w63_j | P52303 | 96.90 | 1.40E-06 | 1.80E-10 | 97.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | unc-45 Tom34 CG2708 |
unc-45 Tom34 CG2708 |
Drosophila melanogaster | 3now_a | Q960B1 | 98.80 | 5.30E-13 | 6.50E-17 | 159.20 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | sys-1 CELE_T23D8.9 T23D8.9 |
sys-1 CELE_T23D8.9 T23D8.9 |
Caenorhabditis elegans | 3c2g_a | Q9XVI2 | 96.50 | 9.50E-06 | 7.90E-10 | 99.00 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | KPNA5 |
Importin subunit alpha-6 (Karyopherin subunit alpha-5) |
Homo sapiens | Ebola Hemorrhagic Fever,Influenza,Bicipital Tenosynovitis |
4u2x_f | O15131 | ENSG00000196911 | KPNA5 | 97.00 | 8.90E-07 | 1.10E-10 | 83.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | TOR2 DRR2 TSC14 YKL203C |
Serine/threonine-protein kinase TOR2 (EC 2.7.1.67) (EC 2.7.11.1) (Dominant rapamycin resistance protein 2) (Phosphatidylinositol 4-kinase TOR2) (PI4-kinase TOR2) (PI4K TOR2) (PtdIns-4-kinase TOR2) (Target of rapamycin kinase 2) (Temperature-sensitive CSG2 suppressor protein 14) |
2.7.1.67,2.7.11.1, | Saccharomyces cerevisiae | 6emk_c | P32600 | 95.20 | 0.00025 | 2.90E-08 | 96.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDL058W | USO1 | SGDID:S000002216 | AP1B1 ADTB1 BAM22 CLAPB2 |
AP-1 complex subunit beta-1 (Adaptor protein complex AP-1 subunit beta-1) (Adaptor-related protein complex 1 subunit beta-1) (Beta-1-adaptin) (Beta-adaptin 1) (Clathrin assembly protein complex 1 beta large chain) (Golgi adaptor HA1/AP1 adaptin beta subunit) |
Homo sapiens | Ichthyosis,Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, And Keratoderma,Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Recessive,Meningioma, Familial,Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant |
6cri_i | Q10567 | ENSG00000100280 | AP1B1 | 96.70 | 2.50E-06 | 3.10E-10 | 94.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | Myosin 2 heavy chain striated muscle |
Myosin 2 heavy chain striated muscle |
Aphonopelma | 3jbh_g | A0A140UGH3 | 98.60 | 7.50E-12 | 8.10E-16 | 170.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | MYH7 MYHCB |
Myosin-7 (Myosin heavy chain 7) (Myosin heavy chain slow isoform) (MyHC-slow) (Myosin heavy chain, cardiac muscle beta isoform) (MyHC-beta) |
Homo sapiens | Ventricular Septal Defect,Muscular Disease,Heart Disease,Lymphopenia,Congenital Fiber-Type Disproportion,Mitral Valve Insufficiency,Severe Combined Immunodeficiency,Aortic Valve Disease 2,Congenital Structural Myopathy,Myopathy,Cardiomyopathy, Dilated, 1e,Myofibrillar Myopathy,Atrial Heart Septal Defect,Mitochondrial Dna Depletion Syndrome 12b,Muscle Tissue Disease,Neuromuscular Disease,Myopathy, Myosin Storage, Autosomal Dominant,Bethlem Myopathy 1,Hypertrophic Cardiomyopathy,Myosinopathies,Familial Isolated Dilated Cardiomyopathy,Rasopathy,Autosomal Dominant Distal Myopathy,Myocardial Infarction,Myopathy, Distal, 1,Muscular Dystrophy,Progressive Familial Heart Block,Tibial Muscular Dystrophy,Hyaline Body Myopathy,Atrial Standstill 1,Combined Immunodeficiency,Dilated Cardiomyopathy,Oculopharyngeal Muscular Dystrophy,Combined T And B Cell Immunodeficiency,Long Qt Syndrome,Malignant Hyperthermia,Heart Conduction Disease,Muscular Dystrophy, Congenital, Lmna-Related,Ebstein Anomaly,Cardiac Conduction Defect,Cardiomyopathy, Familial Hypertrophic, 4,Congestive Heart Failure,Endocardial Fibroelastosis,Rigid Spine Muscular Dystrophy 1,Camptocormism,Noonan Syndrome With Multiple Lentigines,Respiratory Failure,Mobitz Type Ii Atrioventricular Block,Myopathy, Myofibrillar, 9, With Early Respiratory Failure,Long Qt Syndrome 2,Danon Disease,Congenital Myasthenic Syndrome,Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy,Scapuloperoneal Myopathy, Myh7-Related,Restrictive Cardiomyopathy,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Stormorken Syndrome,Immune Deficiency Disease,Familial Atrial Fibrillation,Atrioventricular Block,First-Degree Atrioventricular Block,Tricuspid Valve Disease,Barth Syndrome,Holt-Oram Syndrome,Long Qt Syndrome 1,Cardiomyopathy, Familial Hypertrophic, 1,Wolff-Parkinson-White Syndrome,Intrinsic Cardiomyopathy,Peripartum Cardiomyopathy,Lipoprotein Quantitative Trait Locus,Atrial Fibrillation,Scapuloperoneal Myopathy,Cardiac Arrest,Left Ventricular Noncompaction,Myopathy, Myosin Storage, Autosomal Recessive,Catecholaminergic Polymorphic Ventricular Tachycardia,Batten-Turner Congenital Myopathy,Myopathy, Congenital, With Fiber-Type Disproportion,Miyoshi Muscular Dystrophy,Craniosynostosis 4,Cardiomyopathy, Dilated, 1b |
5tby_a | P12883 | ENSG00000092054 | MYH7 | 98.80 | 4.50E-13 | 4.80E-17 | 182.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | Kpna2 Rch1 |
Importin subunit alpha-1 (Importin alpha P1) (Karyopherin subunit alpha-2) (Pendulin) (Pore targeting complex 58 kDa subunit) (PTAC58) (RAG cohort protein 1) (SRP1-alpha) |
Mus musculus | 1ial_a | P52293 | 99.00 | 5.20E-14 | 6.30E-18 | 156.30 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | TNPO1 KPNB2 MIP1 TRN |
Transportin-1 (Importin beta-2) (Karyopherin beta-2) (M9 region interaction protein) (MIP) |
Homo sapiens | Retinitis Pigmentosa,Meningoencephalitis,Amyotrophic Lateral Sclerosis 20,Retinitis Pigmentosa 2 |
1qbk_b | Q92973 | ENSG00000083312 | TNPO1 | 96.60 | 4.00E-06 | 5.00E-10 | 98.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | Copb1 Copb |
Coatomer subunit beta (Beta-coat protein) (Beta-COP) |
Mus musculus | 5a1y_o | Q9JIF7 | 95.00 | 0.00037 | 4.00E-08 | 86.50 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | unc-45 CELE_F30H5.1 F30H5.1 |
unc-45 CELE_F30H5.1 F30H5.1 |
Caenorhabditis elegans | 4i2w_a | G5EG62 | 98.70 | 2.00E-12 | 1.90E-16 | 167.00 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | PPP2R1A |
Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform (Medium tumor antigen-associated 61 kDa protein) (PP2A subunit A isoform PR65-alpha) (PP2A subunit A isoform R1-alpha) |
Homo sapiens | Uterine Body Mixed Cancer,Uterine Carcinosarcoma,Lung Cancer Susceptibility 3,Carcinosarcoma,Suppression Of Tumorigenicity 12,Uterine Corpus Cancer,Clear Cell Adenofibroma,Female Reproductive Endometrioid Cancer,Breast Cancer,Squamous Cell Carcinoma, Head And Neck,Colorectal Cancer,Ovarian Serous Cystadenocarcinoma,Endometrial Serous Adenocarcinoma,Cystadenocarcinoma,Serous Cystadenocarcinoma,Endometrioid Ovary Carcinoma,Microcephaly,Breast Disease,Mixed Cell Type Cancer,Gastric Adenocarcinoma,Brachydactyly,Mental Retardation, Autosomal Dominant 36,Ovarian Clear Cell Carcinoma,Uterine Corpus Endometrial Carcinoma,Autism Spectrum Disorder,Lung Cancer |
1b3u_b | P30153 | 96.90 | 1.50E-06 | 1.90E-10 | 96.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDL058W | USO1 | SGDID:S000002216 | SRP1 KAP60 YNL189W N1606 |
Importin subunit alpha (Karyopherin subunit alpha) (Karyopherin-60) (Serine-rich RNA polymerase I suppressor protein) |
Saccharomyces cerevisiae | 1ee4_b | Q02821 | 99.00 | 7.20E-14 | 9.00E-18 | 151.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | CLASP2 KIAA0627 |
CLIP-associating protein 2 (Cytoplasmic linker-associated protein 2) (Protein Orbit homolog 2) (hOrbit2) |
Homo sapiens | Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome |
5nr4_a | O75122 | ENSG00000163539 | CLASP2 | 95.50 | 0.00013 | 1.60E-08 | 70.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | HGH1 YGR187C G7538 |
Protein HGH1 (HMG1/2 protein homolog) |
Saccharomyces cerevisiae | 6hb1_d | P48362 | 98.30 | 2.20E-10 | 2.30E-14 | 130.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | IPO4 IMP4B RANBP4 |
Importin-4 (Imp4) (Importin-4b) (Imp4b) (Ran-binding protein 4) (RanBP4) |
Homo sapiens | Anemia, Congenital Dyserythropoietic, Type Ia |
5xah_a | Q8TEX9 | ENSG00000196497 | IPO4 | 95.60 | 0.0001 | 1.30E-08 | 78.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | DOHH HLRC1 |
Deoxyhypusine hydroxylase (hDOHH) (EC 1.14.99.29) (Deoxyhypusine dioxygenase) (Deoxyhypusine monooxygenase) (HEAT-like repeat-containing protein 1) |
1.14.99.29 | Homo sapiens | Familial Expansile Osteolysis |
4d4z_a | Q9BU89 | 95.20 | 0.00021 | 2.50E-08 | 72.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YDL058W | USO1 | SGDID:S000002216 | CTHT_0033460 |
CTHT_0033460 |
Chaetomium thermophilum | 4gmo_a | G0S5S6 | 97.10 | 5.80E-07 | 5.60E-11 | 111.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | Ap1g1 Adtg Clapg1 |
AP-1 complex subunit gamma-1 (Adaptor protein complex AP-1 subunit gamma-1) (Adaptor-related protein complex 1 subunit gamma-1) (Clathrin assembly protein complex 1 gamma-1 large chain) (Gamma-adaptin) (Gamma1-adaptin) (Golgi adaptor HA1/AP1 adaptin subunit gamma-1) |
Mus musculus | 6cri_r | P22892 | 96.90 | 1.10E-06 | 1.30E-10 | 99.80 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | Kpnb1 Impnb |
Importin subunit beta-1 (Karyopherin subunit beta-1) (Nuclear factor p97) (Pore targeting complex 97 kDa subunit) (PTAC97) (SCG) |
Mus musculus | 1ukl_b | P70168 | 96.20 | 1.70E-05 | 2.10E-09 | 93.00 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | CTNND1 KIAA0384 |
Catenin delta-1 (Cadherin-associated Src substrate) (CAS) (p120 catenin) (p120(ctn)) (p120(cas)) |
Homo sapiens | Esophagus Carcinoma In Situ,Melanoma,Cleft Lip,Cleft Lip With Or Without Cleft Palate,Ectodermal Dysplasia,Colon Adenocarcinoma,Euryblepharon,Lobular Neoplasia,Breast Cancer,Colorectal Cancer,Pulmonary Sclerosing Hemangioma,Blepharocheilodontic Syndrome 2,Blepharocheilodontic Syndrome 1,Gastric Cancer,Prostate Cancer,Cri-Du-Chat Syndrome,Ectropion,Distichiasis,Tooth Agenesis,Gastric Cancer, Hereditary Diffuse,Lung Cancer,Pancreatic Cancer |
3l6x_a | O60716 | ENSG00000198561 | CTNND1 | 98.90 | 1.10E-13 | 1.20E-17 | 165.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | USO1 VDP |
General vesicular transport factor p115 (Protein USO1 homolog) (Transcytosis-associated protein) (TAP) (Vesicle-docking protein) |
Bos taurus | 3grl_a | P41541 | 100.00 | 3.10E-54 | 3.30E-58 | 536.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | KLLA0_E20769g |
KLLA0_E20769g |
Kluyveromyces lactis | 5vch_b | Q6CMF0 | 95.30 | 0.00018 | 2.20E-08 | 87.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | Bicdl1 Bicdr1 Ccdc64 |
BICD family-like cargo adapter 1 (Bicaudal D-related protein 1) (BICD-related protein 1) (BICDR-1) (Coiled-coil domain-containing protein 64A) |
Mus musculus | 6f1t_x | A0JNT9 | 95.10 | 0.00035 | 3.20E-08 | 80.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | Ap2a2 Adtab |
AP-2 complex subunit alpha-2 (100 kDa coated vesicle protein C) (Adaptor protein complex AP-2 subunit alpha-2) (Adaptor-related protein complex 2 subunit alpha-2) (Alpha-adaptin C) (Alpha2-adaptin) (Clathrin assembly protein complex 2 alpha-C large chain) (Plasma membrane adaptor HA2/AP2 adaptin alpha C subunit) |
Mus musculus | 2jkt_l | P17427 | 96.70 | 3.00E-06 | 3.50E-10 | 97.40 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | RAP1GDS1 |
Rap1 GTPase-GDP dissociation stimulator 1 (Exchange factor smgGDS) (SMG GDS protein) (SMG P21 stimulatory GDP/GTP exchange protein) |
Homo sapiens | Schwartz-Jampel Syndrome, Type 1 |
5xgc_a | P52306 | ENSG00000138698 | RAP1GDS1 | 99.00 | 5.10E-14 | 6.30E-18 | 156.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | PKP2 |
Plakophilin-2 |
Homo sapiens | Arrhythmogenic Right Ventricular Dysplasia, Familial, 2,Heart Disease,Cardiomyopathy, Dilated, 1e,Naxos Disease,Hypertrophic Cardiomyopathy,Familial Isolated Arrhythmogenic Right Ventricular Dysplasia,Arrhythmogenic Right Ventricular Dysplasia, Familial, 1,Familial Woolly Hair Syndrome,Atrial Standstill 1,Dilated Cardiomyopathy,Right Bundle Branch Block,Long Qt Syndrome,Arrhythmogenic Right Ventricular Dysplasia, Familial, 9,Left Bundle Branch Hemiblock,Heart Conduction Disease,Cardiac Sarcoidosis,Arrhythmogenic Right Ventricular Dysplasia, Familial, 3,Arrhythmogenic Right Ventricular Dysplasia, Familial, 4,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form,Cardiac Arrhythmia,Palmoplantar Keratosis,Arrhythmogenic Right Ventricular Dysplasia, Familial, 10,Arrhythmogenic Right Ventricular Dysplasia, Familial, 13,Long Qt Syndrome 2,Left Ventricular Noncompaction 1,Arrhythmogenic Right Ventricular Dysplasia, Familial, 11,Arrhythmogenic Right Ventricular Dysplasia, Familial, 5,Arrhythmogenic Right Ventricular Dysplasia, Familial, 6,Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy,Restrictive Cardiomyopathy,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Arrhythmogenic Right Ventricular Dysplasia, Familial, 12,Cardiomyopathy, Dilated, With Woolly Hair And Keratoderma,Familial Atrial Fibrillation,Long Qt Syndrome 1,Intrinsic Cardiomyopathy,Lipoprotein Quantitative Trait Locus,Arrhythmogenic Right Ventricular Dysplasia, Familial, 8,Left Ventricular Noncompaction,Anomalous Left Coronary Artery From The Pulmonary Artery,Catecholaminergic Polymorphic Ventricular Tachycardia,Palmoplantar Keratoderma, Nonepidermolytic |
3tt9_a | Q99959 | ENSG00000057294 | PKP2 | 97.80 | 8.80E-09 | 1.00E-12 | 103.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | PFAG_00718 |
PFAG_00718 |
Plasmodium falciparum | 5ewp_b | W7FPA1 | 97.70 | 1.70E-08 | 1.90E-12 | 104.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | hmp-2 K05C4.6 |
Beta-catenin-like protein hmp-2 (Protein humpback-2) |
Caenorhabditis elegans | 4r10_a | O44326 | 99.00 | 8.00E-14 | 9.70E-18 | 159.70 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | CTNNB1 CTNNB OK/SW-cl.35 PRO2286 |
Catenin beta-1 (Beta-catenin) |
Homo sapiens | Adult Hepatocellular Carcinoma,Pancreatic Adenocarcinoma,Mesothelioma, Malignant,Skin Melanoma,Bone Remodeling Disease,Heart Disease,Bone Resorption Disease,Uterine Body Mixed Cancer,Uterine Carcinosarcoma,Endometrial Cancer,Bile Duct Disease,Squamous Cell Carcinoma,Pfeiffer Syndrome,Retinitis Pigmentosa,Thyroid Gland Cancer,Hair Disease,Lung Cancer Susceptibility 3,Adenoid Cystic Carcinoma,Carcinosarcoma,Spasticity,Liver Benign Neoplasm,Cowden Syndrome,Polycystic Kidney Disease,Suppression Of Tumorigenicity 12,Melanoma,Endometrial Hyperplasia,Desmoid Tumor,Thyroid Gland Anaplastic Carcinoma,Diabetes Mellitus,Mullerian Aplasia And Hyperandrogenism,Adenoma,Parathyroid Carcinoma,Diffuse Idiopathic Skeletal Hyperostosis,Clubfoot,Cerebral Palsy,Rectum Adenocarcinoma,Peripheral Nervous System Neoplasm,Uterine Corpus Cancer,Bone Sarcoma,Pancreatoblastoma,Clear Cell Renal Cell Carcinoma,Alzheimer Disease,Hepatoblastoma,Rasopathy,Myocardial Infarction,Pleomorphic Adenoma,Mucoepidermoid Carcinoma,Intravascular Fasciitis,Atypical Teratoid Rhabdoid Tumor,Bile Duct Cancer,Intestinal Benign Neoplasm,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,Mammary Analogue Secretory Carcinoma,Amelogenesis Imperfecta,Retinal Cancer,Pseudosarcomatous Fibromatosis,Biliary Tract Disease,Embryonal Sarcoma,Infratentorial Cancer,Isolated Anorectal Malformation,Endocervical Carcinoma,Classic Pulmonary Blastoma,Cataract 30,Alopecia,Parathyroid Adenoma,Polymorphous Low-Grade Adenocarcinoma,Colon Adenocarcinoma,Neuroblastoma,Colonic Benign Neoplasm,Vulvar Intraepithelial Neoplasia,Fibromatosis,Bile Duct Adenocarcinoma,Small Intestine Adenocarcinoma,Intrahepatic Cholangiocarcinoma,Tubular Adenocarcinoma,Sclerosing Hemangioma,Leukemia, Acute Myeloid,Nephronophthisis,Bone Marrow Cancer,Basal Cell Carcinoma,Leber Plus Disease,Hemangioma,Atypical Polypoid Adenomyoma,Hemimegalencephaly,Fibrolamellar Carcinoma,Cataract,Vitreoretinopathy,Neurodevelopmental Disorder With Spastic Diplegia And Visual Defects,Liver Cirrhosis,Chondroma,Adenomyoma,Autonomic Nervous System Neoplasm,Carney Complex Variant,Dilated Cardiomyopathy,Basal Cell Nevus Syndrome,Ureteral Obstruction,Aortic Valve Disease 1,Bladder Cancer,Liver Adenomatosis,Simpson-Golabi-Behmel Syndrome,Focal Segmental Glomerulosclerosis,Small Intestine Cancer,Brain Cancer,Colonic Disease,Hair Follicle Neoplasm,Microcystic Stromal Tumor,Vaginal Adenoma,Endometrial Adenocarcinoma,Intrahepatic Bile Duct Adenoma,Oropharynx Cancer,Cervix Carcinoma,Ulcerative Colitis,Osteoporosis,Ovarian Cancer,Adenocarcinoma,In Situ Carcinoma,T-Cell Acute Lymphoblastic Leukemia,Female Reproductive Endometrioid Cancer,Breast Ductal Carcinoma,Lobular Neoplasia,Acinar Cell Carcinoma,Breast Carcinoma In Situ,Breast Cancer,Squamous Cell Carcinoma, Head And Neck,Actinic Keratosis,Microphthalmia,Malignant Astrocytoma,High Grade Glioma,Exudative Vitreoretinopathy 7,Colorectal Cancer,Peripheral Nervous System Disease,Pulmonary Sclerosing Hemangioma,Gallbladder Cancer,Hepatocellular Carcinoma,Endometrioid Ovary Carcinoma,Keratoacanthoma,Microcephaly,Frozen Shoulder,Rhabdomyosarcoma,Tongue Disease,Spastic Diplegia,Ovarian Disease,Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease,Teratoma,Bipolar Disorder,Alacrima, Achalasia, And Mental Retardation Syndrome,Gonadal Dysgenesis,Peutz-Jeghers Syndrome,Sarcoma,Cleft Palate, Isolated,Liposarcoma,Spondyloarthropathy,Hyaline Fibromatosis Syndrome,Skin Carcinoma,Gastric Cancer,Lymphangioma,Cone-Rod Dystrophy 2,Prostate Cancer,Disease Of Mental Health,Signet Ring Cell Adenocarcinoma,Pancreatic Ductal Adenocarcinoma,Brittle Bone Disorder,Cholangiocarcinoma,Conventional Fibrosarcoma,Pseudomyxoma Peritonei,Testicular Gonadoblastoma,Cervical Cancer,Ovarian Cystadenocarcinoma,Mixed Cell Type Cancer,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Central Nervous System Cancer,Pulmonary Fibrosis, Idiopathic,Congenital Myasthenic Syndrome,Adrenal Cortical Carcinoma,Retinal Detachment,Ovary Adenocarcinoma,Gastric Adenocarcinoma,Type 2 Diabetes Mellitus,Plasmacytoma,Cervical Squamous Cell Carcinoma,Craniopharyngioma,Adamantinous Craniopharyngioma,Papillary Craniopharyngioma,Childhood Medulloblastoma,Nodular Medulloblastoma,Lynch Syndrome,Lung Squamous Cell Carcinoma,Adrenal Carcinoma,Adrenal Cortex Disease,Thyroid Gland Follicular Carcinoma,Schizophrenia,Merkel Cell Carcinoma,Albinism, Ocular, With Late-Onset Sensorineural Deafness,Bladder Urothelial Carcinoma,Holzgreve Syndrome,Renal Cell Carcinoma, Papillary, 1,Beckwith-Wiedemann Syndrome,Malaria,Familial Adenomatous Polyposis,Arrhythmogenic Right Ventricular Cardiomyopathy,Sarcoma, Synovial,Neural Tube Defects,Pilomatrixoma,Van Buchem Disease,Exudative Vitreoretinopathy,Esophageal Cancer,Odontochondrodysplasia,Orofacial Cleft,Exudative Vitreoretinopathy 1,Strabismus,Birt-Hogg-Dube Syndrome,Desmoid Disease, Hereditary,Tooth Agenesis,Respiratory System Benign Neoplasm,Reproductive Organ Benign Neoplasm,Gastrointestinal System Benign Neoplasm,Barrett Esophagus,Gastric Cancer, Hereditary Diffuse,Alveolar Soft Part Sarcoma,Autosomal Genetic Disease,Mantle Cell Lymphoma,Renal Hypodysplasia/Aplasia 1,Androgenic Alopecia,Renal Fibrosis,Colorectal Adenoma,Colorectal Adenocarcinoma,Tongue Squamous Cell Carcinoma,Oral Squamous Cell Carcinoma,Hepatocellular Adenoma,Fibroma,Townes-Brocks Syndrome,Syndromic Intellectual Disability,Adrenal Cortical Adenoma,Gallbladder Adenoma,Ameloblastoma,Bone Squamous Cell Carcinoma,Brain Stem Medulloblastoma,Colon Adenoma,Large Intestine Adenocarcinoma,Nasopharyngeal Carcinoma,Wilms Tumor 1,Wolf-Hirschhorn Syndrome,Hypertension, Essential,Lipoprotein Quantitative Trait Locus,Pre-Malignant Neoplasm,Estrogen-Receptor Negative Breast Cancer,Cell Type Benign Neoplasm,Endocrine Organ Benign Neoplasm,Central Nervous System Benign Neoplasm,Cardiovascular Organ Benign Neoplasm,Uterine Benign Neoplasm,Osteoblastoma,Vaginal Benign Neoplasm,Connective Tissue Benign Neoplasm,Colitis,Wilson-Turner X-Linked Mental Retardation Syndrome,Sclerosteosis,Gallbladder Disease,Primary Pigmented Nodular Adrenocortical Disease,Amelogenesis Imperfecta, Type Ig,Li-Fraumeni Syndrome,Norrie Disease,Anus, Imperforate,Myeloma, Multiple,Medulloblastoma,Autism,Melanoma, Cutaneous Malignant 1,Melanoma, Uveal,Autosomal Dominant Non-Syndromic Intellectual Disability 19,Lung Cancer,Adenomyosis,Osteoporosis-Pseudoglioma Syndrome,Pancreatic Cancer |
3sl9_b | P35222 | ENSG00000168036 | CTNNB1 | 97.20 | 2.60E-07 | 3.10E-11 | 86.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | PKP1 |
Plakophilin-1 (Band 6 protein) (B6P) |
Homo sapiens | Pemphigus,Naxos Disease,Ectodermal Dysplasia,Epidermolysis Bullosa Simplex,Tooth Ankylosis,Familial Woolly Hair Syndrome,Epidermolysis Bullosa,Bullous Skin Disease,Squamous Cell Carcinoma, Head And Neck,Palmoplantar Keratosis,Ectodermal Dysplasia/Skin Fragility Syndrome,Epidermolysis Bullosa Simplex, Dowling-Meara Type,Epidermolysis Bullosa Simplex With Mottled Pigmentation,Cardiomyopathy, Dilated, With Woolly Hair And Keratoderma,Palmoplantar Keratoderma, Epidermolytic,Palmoplantar Keratoderma, Nonepidermolytic |
1xm9_a | Q13835 | ENSG00000081277 | PKP1 | 98.90 | 2.70E-13 | 3.20E-17 | 151.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | SKLU-Cont10078 |
SKLU-Cont10078 |
Lachancea kluyveri | 6mze_e | A0A493R6X7 | 96.00 | 3.90E-05 | 4.80E-09 | 84.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | JUP CTNNG DP3 |
Junction plakoglobin (Catenin gamma) (Desmoplakin III) (Desmoplakin-3) |
Homo sapiens | Heart Disease,Endometrial Cancer,Pemphigus,Naxos Disease,Hypertrophic Cardiomyopathy,Familial Woolly Hair Syndrome,Grover'S Disease,Atrial Standstill 1,Dilated Cardiomyopathy,Bladder Cancer,Conjunctival Degeneration,Arrhythmogenic Right Ventricular Dysplasia, Familial, 9,Arrhythmogenic Right Ventricular Dysplasia, Familial, 4,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form,Colorectal Cancer,Diffuse Palmoplantar Keratoderma,Pemphigus Vulgaris, Familial,Cardiac Arrhythmia,Keratoderma With Woolly Hair,Pinguecula,Epidermolysis Bullosa, Lethal Acantholytic,Palmoplantar Keratosis,Gastric Cancer,Arrhythmogenic Right Ventricular Dysplasia, Familial, 10,Left Ventricular Noncompaction 1,Arrhythmogenic Right Ventricular Dysplasia, Familial, 11,Arrhythmogenic Right Ventricular Dysplasia, Familial, 5,Arrhythmogenic Right Ventricular Dysplasia, Familial, 6,Ectodermal Dysplasia/Skin Fragility Syndrome,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Arrhythmogenic Right Ventricular Dysplasia, Familial, 12,Palmoplantar Keratoderma And Woolly Hair,Cardiomyopathy, Dilated, With Woolly Hair And Keratoderma,Wolff-Parkinson-White Syndrome,Arrhythmogenic Right Ventricular Dysplasia, Familial, 8,Left Ventricular Noncompaction,Lung Cancer,Palmoplantar Keratoderma, Nonepidermolytic |
3ifq_a | P14923 | 99.00 | 6.10E-14 | 7.60E-18 | 158.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDL058W | USO1 | SGDID:S000002216 | KPNA1 RCH2 |
Importin subunit alpha-5 (Karyopherin subunit alpha-1) (Nucleoprotein interactor 1) (NPI-1) (RAG cohort protein 2) (SRP1-beta) [Cleaved into: Importin subunit alpha-5, N-terminally processed] |
Homo sapiens | Retinitis Pigmentosa,Venezuelan Equine Encephalitis |
2jdq_a | P52294 | ENSG00000114030 | KPNA1 | 98.90 | 2.00E-13 | 2.40E-17 | 150.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | RAPTOR1 RAPTOR1B At3g08850 T16O11.22 |
Regulatory-associated protein of TOR 1 (Protein RAPTOR 1) (Protein RAPTOR 1B) (AtRaptor1b) |
Arabidopsis thaliana | 5wbj_a | Q93YQ1 | 96.80 | 3.10E-06 | 3.00E-10 | 111.30 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | HSPBP1 HSPBP PP1845 |
Hsp70-binding protein 1 (HspBP1) (Heat shock protein-binding protein 1) (Hsp70-binding protein 2) (HspBP2) (Hsp70-interacting protein 1) (Hsp70-interacting protein 2) |
Homo sapiens | Sjogren-Larsson Syndrome,Parkinson Disease, Late-Onset,Spinocerebellar Ataxia, Autosomal Recessive 16 |
1xqr_a | Q9NZL4 | ENSG00000133265 | HSPBP1 | 97.60 | 3.80E-08 | 4.30E-12 | 105.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | KPNA4 QIP1 |
Importin subunit alpha-3 (Importin alpha Q1) (Qip1) (Karyopherin subunit alpha-4) |
Homo sapiens | Chikungunya |
5xzx_a | O00629 | ENSG00000186432 | KPNA4 | 98.90 | 1.30E-13 | 1.60E-17 | 149.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | PSE1 KAP121 YMR308C YM9952.10C |
Importin subunit beta-3 (Karyopherin subunit beta-3) (Karyopherin-121) (Protein secretion enhancer 1) |
Saccharomyces cerevisiae | 3w3u_a | P32337 | 96.00 | 3.50E-05 | 4.40E-09 | 92.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | KAP95 YLR347C L8300.15 |
Importin subunit beta-1 (Importin-95) (Karyopherin subunit beta-1) (Karyopherin-95) |
Saccharomyces cerevisiae | 3nd2_a | Q06142 | 96.20 | 1.90E-05 | 2.30E-09 | 92.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | yibA b3594 JW3568 |
Protein YibA |
Escherichia coli | 1oyz_a | P0ADK6 | 95.30 | 0.00019 | 2.30E-08 | 72.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | ||||
YDL058W | USO1 | SGDID:S000002216 | SHE4 YOR035C OR26.26 |
SWI5-dependent HO expression protein 4 |
Saccharomyces cerevisiae | 3opb_a | P51534 | 98.50 | 1.40E-11 | 1.50E-15 | 153.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | CTNNBL1 C20orf33 PP8304 |
Beta-catenin-like protein 1 (Nuclear-associated protein) (NAP) (Testis development protein NYD-SP19) |
Homo sapiens | Niemann-Pick Disease, Type C1 |
4mfu_a | Q8WYA6 | ENSG00000132792 | CTNNBL1 | 98.30 | 2.50E-10 | 2.50E-14 | 136.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | 3H10.030 GE21DRAFT_7666 |
3H10.030 GE21DRAFT_7666 |
Neurospora crassa | 4rxh_b | Q9C2K9 | 98.80 | 3.70E-13 | 4.50E-17 | 151.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | CTHT_0034860 |
CTHT_0034860 |
Chaetomium thermophilum | 5mu7_a | G0S6G7 | 96.40 | 9.50E-06 | 1.20E-09 | 85.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | APC DP2.5 |
Adenomatous polyposis coli protein (Protein APC) (Deleted in polyposis 2.5) |
Homo sapiens | Adult Hepatocellular Carcinoma,Endocrine Gland Cancer,Endometrial Cancer,Duodenal Benign Neoplasm,Pseudohypoparathyroidism,Lung Cancer Susceptibility 3,Urinary System Disease,Cowden Syndrome,Desmoid Tumor,Adenoma,Parathyroid Carcinoma,Rectum Cancer,B-Lymphoblastic Leukemia/Lymphoma With Hyperdiploidy,B-Lymphoblastic Leukemia/Lymphoma With Hypodiploidy,Myh-Associated Polyposis,Hepatoblastoma,Bile Duct Cancer,Intestinal Benign Neoplasm,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,Ocular Cancer,Myeloid Leukemia Associated With Down Syndrome,Retinal Cancer,Infratentorial Cancer,Cervix Disease,Lymphatic System Disease,Female Reproductive System Disease,Small Intestine Benign Neoplasm,Familial Colorectal Cancer,Supratentorial Primitive Neuroectodermal Tumor,Male Reproductive System Disease,Colon Adenocarcinoma,Colonic Benign Neoplasm,Pilocytic Astrocytoma,Gastrointestinal System Disease,Fibromatosis,Serrated Polyposis Syndrome,Bile Duct Adenocarcinoma,Inherited Cancer-Predisposing Syndrome,Intrahepatic Cholangiocarcinoma,Apc-Associated Polyposis Conditions,Hematologic Cancer,Leukemia, Acute Lymphoblastic,B-Lymphoblastic Leukemia/Lymphoma With T,Liver Cirrhosis,Thoracic Cancer,Ampulla Of Vater Benign Neoplasm,Intestinal Disease,Brain Cancer,Endocrine System Disease,Colonic Disease,Oropharynx Cancer,Cervix Carcinoma,Gastric Adenocarcinoma And Proximal Polyposis Of The Stomach,Immune System Disease,Nervous System Disease,Anal Squamous Cell Carcinoma,Familial Adenomatous Polyposis Due To 5q22.2 Microdeletion,Ovarian Cancer,Adenocarcinoma,Eye Disease,Breast Cancer,Large Intestine Cancer,Colorectal Cancer,Nervous System Cancer,Gastrointestinal System Cancer,Hepatocellular Carcinoma,Fourth Cranial Nerve Palsy,Attenuated Familial Adenomatous Polyposis,Deficiency Anemia,Mccune-Albright Syndrome,Juvenile Polyposis Syndrome,Familial Adenomatous Polyposis 1,Peutz-Jeghers Syndrome,Gastric Cancer,Lymphangioma,Reproductive System Disease,Prostate Cancer,Disease Of Mental Health,Cholangiocarcinoma,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Central Nervous System Cancer,Respiratory System Disease,Gastric Adenocarcinoma,Cranial Nerve Palsy,Craniopharyngioma,Male Reproductive Organ Cancer,Lynch Syndrome,Sensory System Disease,Lymphoma, Non-Hodgkin, Familial,Familial Adenomatous Polyposis,Esophageal Cancer,Inflammatory Bowel Disease,Desmoid Disease, Hereditary,Gastrointestinal System Benign Neoplasm,Barrett Esophagus,Alveolar Soft Part Sarcoma,Tumor Predisposition Syndrome,Autosomal Genetic Disease,Colorectal Cancer, Hereditary Nonpolyposis, Type 5,Uterine Anomalies,Gastrointestinal Stromal Tumor,Periampullary Adenoma,Colorectal Adenoma,Colorectal Adenocarcinoma,Villous Adenoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Colon Adenoma,Duodenum Adenoma,Autism Spectrum Disorder,Lymphatic System Cancer,Cell Type Benign Neoplasm,Cardiovascular Organ Benign Neoplasm,Leukemia, Chronic Lymphocytic,Medulloblastoma,Lung Cancer,Cenani-Lenz Syndactyly Syndrome,Pancreatic Cancer |
5iz8_a | P25054 | ENSG00000134982 | APC | 98.60 | 4.50E-12 | 5.20E-16 | 138.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | Ctnnb1 Catnb |
Catenin beta-1 (Beta-catenin) |
Mus musculus | 3bct_a | Q02248 | 99.20 | 2.80E-15 | 3.50E-19 | 165.70 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | USO1 VDP |
General vesicular transport factor p115 (Protein USO1 homolog) (Transcytosis-associated protein) (TAP) (Vesicle-docking protein) |
Homo sapiens | Achondrogenesis,Streptococcal Meningitis,Cone-Rod Dystrophy 2,Hermansky-Pudlak Syndrome |
2w3c_a | O60763 | ENSG00000138768 | USO1 | 100.00 | 8.90E-45 | 9.50E-49 | 443.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL058W | USO1 | SGDID:S000002216 | VMA13 CLS11 YPR036W YP3085.02 |
V-type proton ATPase subunit H (V-ATPase subunit H) (V-ATPase 54 kDa subunit) (Vacuolar proton pump subunit H) |
Saccharomyces cerevisiae | 1ho8_a | P41807 | 98.30 | 2.30E-10 | 2.30E-14 | 136.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL058W | USO1 | SGDID:S000002216 | Os01g0253300 LOC_Os01g14950 |
Importin subunit alpha-1a |
Oryza sativa | 4b8j_a | Q71VM4 | 98.80 | 3.60E-13 | 4.30E-17 | 153.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |