| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YOL112W | MSB4 | SGDID:S000005472 | GYP1 YOR070C YOR29-21 |
GTPase-activating protein GYP1 (GAP for YPT1) |
Saccharomyces cerevisiae | 1fkm_a | Q08484 | 99.90 | 2.60E-30 | 2.00E-34 | 265.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YOL112W | MSB4 | SGDID:S000005472 | sky CG9339 |
GTPase-activating protein skywalker |
Drosophila melanogaster | 5hjn_a | Q9VIH7 | 99.90 | 9.50E-31 | 8.00E-35 | 267.00 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
| YOL112W | MSB4 | SGDID:S000005472 | TBC1D15 |
TBC1D15 |
Sus scrofa | 5tuc_a | F1SH24 | 99.90 | 2.40E-32 | 2.00E-36 | 275.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YOL112W | MSB4 | SGDID:S000005472 | TBC1D7 TBC7 HSPC239 |
TBC1 domain family member 7 (Cell migration-inducing protein 23) |
Homo sapiens | Subependymal Glioma,Benign Ependymoma,Kidney Angiomyolipoma,Tuberous Sclerosis,Isolated Megalencephaly,Kidney Benign Neoplasm,Megalencephaly,Astigmatism,Scalp-Ear-Nipple Syndrome,Macrocephaly/Megalencephaly Syndrome, Autosomal Recessive |
3qwl_a | Q9P0N9 | ENSG00000145979 | TBC1D7-LOC100130357 | 99.80 | 4.10E-26 | 3.60E-30 | 222.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YOL112W | MSB4 | SGDID:S000005472 | Shark TBC1D15 GTPase-activating Protein |
Shark TBC1D15 GTPase-activating Protein |
Squalomorphii | 5tub_a | A0A1U7Q1Z6 | 99.90 | 5.00E-32 | 4.30E-36 | 272.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YOL112W | MSB4 | SGDID:S000005472 | TBC1D22A C22orf4 |
TBC1 domain family member 22A |
Homo sapiens | Febrile Seizures, Familial, 6,Febrile Seizures, Familial, 5,Generalized Epilepsy With Febrile Seizures Plus, Type 4,Febrile Seizures, Familial, 1,Febrile Seizures, Familial, 4,Generalized Epilepsy With Febrile Seizures Plus, Type 2,Generalized Epilepsy With Febrile Seizures Plus, Type 7,Epilepsy, Familial Temporal Lobe, 5,Febrile Seizures, Familial, 11,Febrile Seizures, Familial, 8 |
2qfz_a | Q8WUA7 | ENSG00000054611 | TBC1D22A | 99.90 | 1.60E-30 | 1.30E-34 | 261.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YOL112W | MSB4 | SGDID:S000005472 | RABGAP1L HHL KIAA0471 |
Rab GTPase-activating protein 1-like |
Homo sapiens | 3hzj_c | Q5R372 | ENSG00000152061 | RABGAP1L | 99.90 | 5.40E-31 | 4.60E-35 | 260.80 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YOL112W | MSB4 | SGDID:S000005472 | RABGAP1 HSPC094 |
Rab GTPase-activating protein 1 (GAP and centrosome-associated protein) (Rab6 GTPase-activating protein GAPCenA) |
Homo sapiens | Charcot-Marie-Tooth Disease, Type 4h,Warburg Micro Syndrome,Warburg Micro Syndrome 1,Martsolf Syndrome |
4nc6_a | Q9Y3P9 | ENSG00000011454 | RABGAP1 | 99.90 | 5.60E-31 | 4.80E-35 | 260.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YOL112W | MSB4 | SGDID:S000005472 | TBC1D4 AS160 KIAA0603 |
TBC1 domain family member 4 (Akt substrate of 160 kDa) (AS160) |
Homo sapiens | Acanthosis Nigricans,Diabetes Mellitus,Hyperinsulinism,Type 2 Diabetes Mellitus,Type 2 Diabetes 5 |
3qyb_a | O60343 | ENSG00000136111 | TBC1D4 | 99.90 | 2.30E-30 | 2.00E-34 | 254.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YOL112W | MSB4 | SGDID:S000005472 | TBC1D14 KIAA1322 |
TBC1 domain family member 14 |
Homo sapiens | 2qq8_a | Q9P2M4 | ENSG00000132405 | TBC1D14 | 99.90 | 5.00E-30 | 4.30E-34 | 257.00 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YOL112W | MSB4 | SGDID:S000005472 | CHLREDRAFT_195581 |
CHLREDRAFT_195581 |
Chlamydomonas reinhardtii | 4p17_b | A8JCA4 | 100.00 | 1.50E-38 | 1.30E-42 | 316.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YOL112W | MSB4 | SGDID:S000005472 | TBC1D20 C20orf140 |
TBC1 domain family member 20 |
Homo sapiens | Rab18 Deficiency,Microphthalmia,Microcephaly,Hepatitis C Virus,Spastic Diplegia,Spastic Quadriplegia,Lens Disease,Warburg Micro Syndrome 4,Warburg Micro Syndrome 3,Warburg Micro Syndrome 2,Spastic Cerebral Palsy,Warburg Micro Syndrome,Warburg Micro Syndrome 1,Martsolf Syndrome |
4hl4_a | Q96BZ9 | ENSG00000125875 | TBC1D20 | 99.90 | 6.10E-30 | 5.30E-34 | 250.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YOL112W | MSB4 | SGDID:S000005472 | SBE2 |
SBE2, cell-wall formation |
pfam Family | PF17076 | 99.80 | 7.70E-25 | 5.80E-29 | 241.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
| YOL112W | MSB4 | SGDID:S000005472 | TBC1D1 KIAA1108 |
TBC1 domain family member 1 |
Homo sapiens | Cakut,Colloid Adenoma,Generalized Epilepsy With Febrile Seizures Plus, Type 7,Warburg Micro Syndrome 3,Warburg Micro Syndrome 2,Epilepsy, Familial Temporal Lobe, 5 |
3qye_b | Q86TI0 | ENSG00000065882 | TBC1D1 | 99.90 | 2.00E-30 | 1.70E-34 | 259.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |