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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 |
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YLR425W | TUS1 | SGDID:S000004417 | VAV1 VAV |
Proto-oncogene vav |
Homo sapiens | Common Variable Immunodeficiency,T-Cell Lymphoblastic Leukemia/Lymphoma,Angioimmunoblastic T-Cell Lymphoma,Leukemia, Acute Myeloid,Burkitt Lymphoma,T-Cell Acute Lymphoblastic Leukemia,Leukocyte Adhesion Deficiency, Type I,Neuropathy, Hereditary Sensory, Type Id,Wiskott-Aldrich Syndrome,Acute Promyelocytic Leukemia,Cd45 Deficiency,Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema |
3bji_a | P15498 | ENSG00000141968 | VAV1 | 99.80 | 1.90E-25 | 2.00E-29 | 250.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR425W | TUS1 | SGDID:S000004417 | ARHGEF12 KIAA0382 LARG |
Rho guanine nucleotide exchange factor 12 (Leukemia-associated RhoGEF) |
Homo sapiens | Leukemia,Open-Angle Glaucoma,Glaucoma, Primary Open Angle |
1txd_a | Q9NZN5 | ENSG00000196914 | ARHGEF12 | 99.80 | 6.20E-26 | 6.20E-30 | 257.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR425W | TUS1 | SGDID:S000004417 | Mcf2l Dbs |
Guanine nucleotide exchange factor DBS (DBL's big sister) (MCF2-transforming sequence-like protein) |
Mus musculus | 1kz7_c | Q64096 | 99.70 | 6.00E-22 | 6.10E-26 | 221.50 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YLR425W | TUS1 | SGDID:S000004417 | ARHGEF11 KIAA0380 |
Rho guanine nucleotide exchange factor 11 (PDZ-RhoGEF) |
Homo sapiens | Fetal Macrosomia |
1xcg_e | O15085 | ENSG00000132694 | ARHGEF11 | 99.80 | 2.50E-25 | 2.60E-29 | 249.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR425W | TUS1 | SGDID:S000004417 | ARHGEF4 KIAA1112 |
Rho guanine nucleotide exchange factor 4 (APC-stimulated guanine nucleotide exchange factor 1) (Asef) (Asef1) |
Homo sapiens | Locked-In Syndrome,Epidermolysis Bullosa Simplex, Dowling-Meara Type |
2pz1_a | Q9NR80 | ENSG00000136002 | ARHGEF4 | 99.90 | 1.40E-27 | 1.50E-31 | 277.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR425W | TUS1 | SGDID:S000004417 | AFUA_5G08550 |
AFUA_5G08550 |
Neosartorya fumigata | 5o51_a | Q4WUI2 | 99.90 | 7.80E-33 | 7.40E-37 | 314.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YLR425W | TUS1 | SGDID:S000004417 | Arhgef3 |
Rho guanine nucleotide exchange factor 3 |
Mus musculus | 2z0q_a | Q91X46 | 99.80 | 2.80E-25 | 2.90E-29 | 247.20 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YLR425W | TUS1 | SGDID:S000004417 | AKAP13 BRX HT31 LBC |
A-kinase anchor protein 13 (AKAP-13) (AKAP-Lbc) (Breast cancer nuclear receptor-binding auxiliary protein) (Guanine nucleotide exchange factor Lbc) (Human thyroid-anchoring protein 31) (Lymphoid blast crisis oncogene) (LBC oncogene) (Non-oncogenic Rho GTPase-specific GTP exchange factor) (Protein kinase A-anchoring protein 13) (PRKA13) (p47) |
Homo sapiens | Corneal Dystrophy,Long Qt Syndrome,Breast Cancer,Crouzon Syndrome With Acanthosis Nigricans,Long Qt Syndrome 1 |
4d0n_b | Q12802 | ENSG00000170776 | AKAP13 | 99.90 | 7.90E-27 | 8.10E-31 | 262.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR425W | TUS1 | SGDID:S000004417 | ARHGEF25 GEFT |
Rho guanine nucleotide exchange factor 25 (Guanine nucleotide exchange factor GEFT) (Rac/Cdc42/Rho exchange factor GEFT) (RhoA/Rac/Cdc42 guanine nucleotide exchange factor GEFT) (p63RhoGEF) |
Homo sapiens | Atrophic Rhinitis,Moyamoya Angiopathy,Rhabdomyosarcoma |
2rgn_b | Q86VW2 | ENSG00000240771 | ARHGEF25 | 99.80 | 4.80E-25 | 4.90E-29 | 246.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR425W | TUS1 | SGDID:S000004417 | Vav1 Vav |
Proto-oncogene vav (p95vav) |
Mus musculus | 2vrw_b | P27870 | 99.80 | 2.40E-25 | 2.50E-29 | 252.70 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YLR425W | TUS1 | SGDID:S000004417 | Arhgef9 |
Rho guanine nucleotide exchange factor 9 (Collybistin) (Rac/Cdc42 guanine nucleotide exchange factor 9) |
Rattus norvegicus | 2dfk_a | Q9QX73 | 99.80 | 1.10E-25 | 1.10E-29 | 257.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YLR425W | TUS1 | SGDID:S000004417 | FGD5 ZFYVE23 |
FYVE, RhoGEF and PH domain-containing protein 5 (Zinc finger FYVE domain-containing protein 23) |
Homo sapiens | Gastroduodenitis,Aarskog-Scott Syndrome |
3mpx_a | Q6ZNL6 | ENSG00000154783 | FGD5 | 99.90 | 1.80E-28 | 1.80E-32 | 282.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR425W | TUS1 | SGDID:S000004417 | TRIO |
Triple functional domain protein (EC 2.7.11.1) (PTPRF-interacting protein) |
2.7.11.1 | Homo sapiens | Intellectual Developmental Disorder, Autosomal Dominant 44, With Microcephaly,Trio-Related Intellectual Disability,Microcephaly,Clark-Baraitser Syndrome,Deafness, Autosomal Recessive 28,Disease Of Mental Health,Hermansky-Pudlak Syndrome 7,Intellectual Developmental Disorder, Autosomal Dominant 63, With Macrocephaly |
1nty_a | O75962 | ENSG00000038382 | TRIO | 99.70 | 2.90E-22 | 3.00E-26 | 219.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR425W | TUS1 | SGDID:S000004417 | ITSN2 KIAA1256 SH3D1B SWAP |
Intersectin-2 (SH3 domain-containing protein 1B) (SH3P18) (SH3P18-like WASP-associated protein) |
Homo sapiens | Speech Disorder,Epilepsy, Focal, With Speech Disorder And With Or Without Mental Retardation |
3jzy_a | Q9NZM3 | ENSG00000198399 | ITSN2 | 99.80 | 2.90E-25 | 3.00E-29 | 260.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR425W | TUS1 | SGDID:S000004417 | Tiam1 Tiam-1 |
T-lymphoma invasion and metastasis-inducing protein 1 (TIAM-1) |
Mus musculus | 1foe_a | Q60610 | 99.80 | 1.50E-23 | 1.50E-27 | 235.80 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YLR425W | TUS1 | SGDID:S000004417 | EHI_010670 |
EHI_010670 |
Entamoeba histolytica | 4gou_a | C4LYV4 | 99.70 | 3.10E-22 | 2.90E-26 | 239.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YLR425W | TUS1 | SGDID:S000004417 | ARHGEF1 |
Rho guanine nucleotide exchange factor 1 (115 kDa guanine nucleotide exchange factor) (p115-RhoGEF) (p115RhoGEF) (Sub1.5) |
Homo sapiens | Atrophic Rhinitis,Giant Axonal Neuropathy,Megaesophagus,Skin Lipoma,Immunodeficiency 62 |
3odo_a | Q92888 | ENSG00000076928 | ARHGEF1 | 99.80 | 3.20E-26 | 3.30E-30 | 258.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR425W | TUS1 | SGDID:S000004417 | ITSN1 ITSN SH3D1A |
Intersectin-1 (SH3 domain-containing protein 1A) (SH3P17) |
Homo sapiens | Vaccinia,Schizophrenia 1,Down Syndrome,Autism Spectrum Disorder,Chromosomal Duplication Syndrome |
1ki1_b | Q15811 | ENSG00000205726 | ITSN1 | 99.80 | 8.00E-25 | 8.30E-29 | 242.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR425W | TUS1 | SGDID:S000004417 | PREX1 KIAA1415 |
Phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 1 protein (P-Rex1) (PtdIns(3,4,5)-dependent Rac exchanger 1) |
Homo sapiens | Gastric Tubular Adenocarcinoma |
5fi0_g | Q8TCU6 | ENSG00000124126 | PREX1 | 99.80 | 1.10E-24 | 1.10E-28 | 244.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR425W | TUS1 | SGDID:S000004417 | SOS1 |
Son of sevenless homolog 1 (SOS-1) |
Homo sapiens | Heart Septal Defect,Heart Disease,Lung Cancer Susceptibility 3,Pulmonary Valve Stenosis,Atrial Heart Septal Defect,Neurofibromatosis-Noonan Syndrome,Neuroma,Hypertrophic Cardiomyopathy,Rasopathy,Noonan Syndrome-Like Disorder With Loose Anagen Hair,Keratosis Pilaris Atrophicans Faciei,Costello Syndrome,Joubert Syndrome 3,Neurofibromatosis, Type I,Villonodular Synovitis,Pilocytic Astrocytoma,Fibromatosis,Cryptorchidism, Unilateral Or Bilateral,Skin Granular Cell Tumor,Pseudo-Turner Syndrome,Noonan Syndrome 1,Noonan Syndrome And Noonan-Related Syndrome,Dilated Cardiomyopathy,Aortic Valve Disease 1,Gingival Hypertrophy,Noonan Syndrome-Like Disorder With Loose Anagen Hair 2,Adenocarcinoma,Neurofibromatosis,Breast Cancer,Patent Foramen Ovale,Colorectal Cancer,Gingival Overgrowth,Pulmonary Valve Disease,Hepatocellular Carcinoma,Cardiofaciocutaneous Syndrome 1,Embryonal Rhabdomyosarcoma,Rhabdomyosarcoma,Noonan Syndrome With Multiple Lentigines,Noonan Syndrome 3,Gingival Disease,Prostate Cancer,Keratosis Pilaris Atrophicans,Noonan Syndrome 4,Prostate Transitional Cell Carcinoma,Fibromatosis, Gingival, 1,Tetralogy Of Fallot,Epilepsy, Familial Temporal Lobe, 8,Patent Ductus Arteriosus 1,Ptosis,Juvenile Myelomonocytic Leukemia,Gingival Fibromatosis,Lung Cancer,Pulmonic Stenosis |
1dbh_a | Q07889 | ENSG00000115904 | SOS1 | 99.80 | 1.70E-23 | 1.70E-27 | 235.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR425W | TUS1 | SGDID:S000004417 | FARP1 CDEP PLEKHC2 |
FERM, ARHGEF and pleckstrin domain-containing protein 1 (Chondrocyte-derived ezrin-like protein) (FERM, RhoGEF and pleckstrin domain-containing protein 1) (Pleckstrin homology domain-containing family C member 2) (PH domain-containing family C member 2) |
Homo sapiens | Nystagmus 7, Congenital, Autosomal Dominant,Nystagmus 3, Congenital, Autosomal Dominant,Congenital Nystagmus,Pathologic Nystagmus,Nystagmus 2, Congenital, Autosomal Dominant,Nystagmus 4, Congenital, Autosomal Dominant |
4h6y_b | Q9Y4F1 | ENSG00000152767 | FARP1 | 99.80 | 4.50E-24 | 4.70E-28 | 247.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR425W | TUS1 | SGDID:S000004417 | NET1 ARHGEF8 |
Neuroepithelial cell-transforming gene 1 protein (Proto-oncogene p65 Net1) (Rho guanine nucleotide exchange factor 8) |
Homo sapiens | Breast Cancer,Skin Squamous Cell Carcinoma,Oppositional Defiant Disorder |
4xh9_d | Q7Z628 | ENSG00000173848 | NET1 | 99.90 | 6.20E-28 | 6.20E-32 | 272.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |