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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YFL047W | RGD2 | SGDID:S000001847 | MYO9B MYR5 |
Unconventional myosin-IXb (Unconventional myosin-9b) |
Homo sapiens | Refractory Celiac Disease,Dermatitis Herpetiformis,Ulcerative Colitis,Celiac Disease 4,Inflammatory Bowel Disease,Inflammatory Bowel Disease 5,Inflammatory Bowel Disease 6,Colitis,Jejunoileitis,Celiac Disease 1 |
5c5s_a | Q13459 | ENSG00000099331 | MYO9B | 99.70 | 2.50E-22 | 1.70E-26 | 195.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | PACSIN2 |
Protein kinase C and casein kinase substrate in neurons protein 2 (Syndapin-2) (Syndapin-II) (SdpII) |
Homo sapiens | Thiopurines, Poor Metabolism Of, 1,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive |
3abh_b | Q9UNF0 | ENSG00000100266 | PACSIN2 | 99.90 | 1.60E-27 | 1.10E-31 | 243.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | CHN1 ARHGAP2 CHN |
N-chimaerin (A-chimaerin) (Alpha-chimerin) (N-chimerin) (NC) (Rho GTPase-activating protein 2) |
Homo sapiens | Exotropia,Anisometropia,Hypertropia,Accommodative Esotropia,Esotropia,Hypotropia,Duane Retraction Syndrome,Binocular Vision Disease,Abnormal Retinal Correspondence,Autosomal Dominant Robinow Syndrome,Ocular Motility Disease,Dandy-Walker Syndrome,Sensorineural Hearing Loss,Night Blindness,Suppression Amblyopia,Amblyopia,Ametropic Amblyopia,Diaphragmatic Eventration,Diaphragm Disease,Paralytic Squint,Partial Third-Nerve Palsy,Abducens Nerve Disease,Tukel Syndrome,Hydronephrosis,Cleft Palate, Isolated,Duane Retraction Syndrome 2,Duane Retraction Syndrome 1,Strabismus,Nonaka Myopathy,Robinow Syndrome, Autosomal Dominant 2,Marden-Walker Syndrome,Duane-Radial Ray Syndrome,Laryngomalacia,Robinow Syndrome,Congenital Ptosis |
2osa_a | P15882 | ENSG00000128656 | CHN1 | 99.70 | 4.40E-23 | 3.00E-27 | 195.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | ARAP3 CENTD3 |
Arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 3 (Centaurin-delta-3) (Cnt-d3) |
Homo sapiens | Gastrointestinal Anthrax,Oropharyngeal Anthrax |
5jd0_a | Q8WWN8 | ENSG00000120318 | ARAP3 | 99.70 | 5.30E-21 | 3.70E-25 | 182.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | FCHO2 |
F-BAR domain only protein 2 |
Homo sapiens | Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, And Acne,Developmental And Epileptic Encephalopathy 4 |
2v0o_a | Q0JRZ9 | ENSG00000157107 | FCHO2 | 99.80 | 6.30E-25 | 4.40E-29 | 219.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | GMIP |
GEM-interacting protein (GMIP) |
Homo sapiens | 3qwe_a | Q9P107 | ENSG00000089639 | GMIP | 99.80 | 1.20E-24 | 8.00E-29 | 218.10 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YFL047W | RGD2 | SGDID:S000001847 | SRGAP2 ARHGAP34 FNBP2 KIAA0456 SRGAP2A |
SLIT-ROBO Rho GTPase-activating protein 2 (srGAP2) (Formin-binding protein 2) (Rho GTPase-activating protein 34) |
Homo sapiens | Childhood Pilocytic Astrocytoma,Undetermined Early-Onset Epileptic Encephalopathy,Pilomyxoid Astrocytoma,West Syndrome,Disease Of Mental Health,Gestational Trophoblastic Neoplasm,Avoidant Personality Disorder,Chromosome 3pter-P25 Deletion Syndrome,Early Infantile Epileptic Encephalopathy |
5i6r_a | O75044 | ENSG00000266028 | SRGAP2 | 99.90 | 6.50E-29 | 4.40E-33 | 267.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | ARHGAP11A KIAA0013 |
Rho GTPase-activating protein 11A (Rho-type GTPase-activating protein 11A) |
Homo sapiens | Benign Epilepsy With Centrotemporal Spikes,Prader-Willi Syndrome,Chromosome 15q13.3 Deletion Syndrome |
3eap_a | Q6P4F7 | ENSG00000198826 | ARHGAP11A | 99.70 | 6.50E-23 | 4.50E-27 | 203.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | HOF1 CYK2 YMR032W YM9973.05 |
Cytokinesis protein 2 (Homolog of CDC15 protein 1) |
Saccharomyces cerevisiae | 4wpe_a | Q05080 | 99.80 | 2.70E-25 | 1.80E-29 | 225.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YFL047W | RGD2 | SGDID:S000001847 | RACGAP1 KIAA1478 MGCRACGAP |
Rac GTPase-activating protein 1 (Male germ cell RacGap) (MgcRacGAP) (Protein CYK4 homolog) (CYK4) (HsCYK-4) |
Homo sapiens | Uterine Body Mixed Cancer,Uterine Carcinosarcoma,Cataract 36 |
2ovj_a | Q9H0H5 | ENSG00000161800 | RACGAP1 | 99.60 | 1.80E-20 | 1.20E-24 | 177.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | ARHGAP32 GRIT KIAA0712 RICS |
Rho GTPase-activating protein 32 (Brain-specific Rho GTPase-activating protein) (GAB-associated Cdc42/Rac GTPase-activating protein) (GC-GAP) (GTPase regulator interacting with TrkA) (Rho-type GTPase-activating protein 32) (Rho/Cdc42/Rac GTPase-activating protein RICS) (RhoGAP involved in the beta-catenin-N-cadherin and NMDA receptor signaling) (p200RhoGAP) (p250GAP) |
Homo sapiens | Neuroblastoma,Borna Disease,Chromosome 17q23.1-Q23.2 Deletion Syndrome,Disease Of Mental Health,Bartter Syndrome, Type 2, Antenatal,Johanson-Blizzard Syndrome,Jacobsen Syndrome |
3iug_a | A7KAX9 | ENSG00000134909 | ARHGAP32 | 99.70 | 6.80E-23 | 4.70E-27 | 198.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | ARHGAP15 BM-024 BM-030 BM-046 |
Rho GTPase-activating protein 15 (ArhGAP15) (Rho-type GTPase-activating protein 15) |
Homo sapiens | Diverticulitis,Diverticulitis Of Colon,Meier-Gorlin Syndrome 2,Bladder Squamous Cell Carcinoma,Mowat-Wilson Syndrome,Epilepsy, Idiopathic Generalized 9 |
3byi_b | Q53QZ3 | ENSG00000075884 | ARHGAP15 | 99.70 | 4.10E-23 | 2.90E-27 | 198.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | RGD1 YBR260C YBR1728 |
RHO GTPase-activating protein RGD1 (RhoGAP) (Related GAP domain protein 1) |
Saccharomyces cerevisiae | 4wpc_a | P38339 | 99.80 | 1.80E-23 | 1.20E-27 | 213.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YFL047W | RGD2 | SGDID:S000001847 | Pacsin3 |
Protein kinase C and casein kinase II substrate protein 3 |
Mus musculus | 3qe6_a | Q99JB8 | 99.90 | 1.00E-28 | 7.00E-33 | 251.70 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YFL047W | RGD2 | SGDID:S000001847 | RALBP1 RLIP1 RLIP76 |
RalA-binding protein 1 (RalBP1) (76 kDa Ral-interacting protein) (Dinitrophenyl S-glutathione ATPase) (DNP-SG ATPase) (Ral-interacting protein 1) |
Homo sapiens | Lung Cancer |
2mbg_a | Q15311 | ENSG00000017797 | RALBP1 | 99.80 | 7.20E-25 | 4.90E-29 | 217.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | Synd CG15694 D-Synd Dmel\CG33094 synd syndapin CG33094 Dmel_CG33094 |
Synd CG15694 D-Synd Dmel\CG33094 synd syndapin CG33094 Dmel_CG33094 |
Drosophila melanogaster | 3i2w_b | Q9VDI1 | 99.90 | 1.10E-27 | 7.40E-32 | 242.30 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YFL047W | RGD2 | SGDID:S000001847 | PIK3R1 |
Phosphatidylinositol 3-kinase regulatory subunit alpha (PI3-kinase regulatory subunit alpha) (PI3K regulatory subunit alpha) (PtdIns-3-kinase regulatory subunit alpha) (Phosphatidylinositol 3-kinase 85 kDa regulatory subunit alpha) (PI3-kinase subunit p85-alpha) (PtdIns-3-kinase regulatory subunit p85-alpha) |
Bos taurus | 6d85_a | P23727 | 99.60 | 5.40E-20 | 3.70E-24 | 172.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YFL047W | RGD2 | SGDID:S000001847 | DLC1 ARHGAP7 KIAA1723 STARD12 |
Rho GTPase-activating protein 7 (Deleted in liver cancer 1 protein) (DLC-1) (HP protein) (Rho-type GTPase-activating protein 7) (START domain-containing protein 12) (StARD12) (StAR-related lipid transfer protein 12) |
Homo sapiens | Neural Tube Closure Defect,Colorectal Cancer,Hepatocellular Carcinoma,Neural Tube Defects,Hyperoxaluria, Primary, Type Ii |
3kuq_a | Q96QB1 | ENSG00000164741 | DLC1 | 99.70 | 3.00E-22 | 2.10E-26 | 193.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | imp2 SPBC11C11.02 |
Septation protein imp2 |
Schizosaccharomyces pombe | 5c1f_b | Q10199 | 99.90 | 5.40E-28 | 3.80E-32 | 247.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YFL047W | RGD2 | SGDID:S000001847 | ARHGAP20 KIAA1391 |
Rho GTPase-activating protein 20 (Rho-type GTPase-activating protein 20) |
Homo sapiens | 3msx_b | Q9P2F6 | ENSG00000137727 | ARHGAP20 | 99.70 | 3.00E-22 | 2.10E-26 | 189.90 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YFL047W | RGD2 | SGDID:S000001847 | FES FPS |
Tyrosine-protein kinase Fes/Fps (EC 2.7.10.2) (Feline sarcoma/Fujinami avian sarcoma oncogene homolog) (Proto-oncogene c-Fes) (Proto-oncogene c-Fps) (p93c-fes) |
2.7.10.2 | Homo sapiens | Melanoma,Leukemia, Chronic Myeloid,Latent Syphilis,Sjogren-Larsson Syndrome,Leukemia,Myeloid Leukemia,Sarcoma,Ewing Sarcoma Of Bone,Neurofibrosarcoma,Acute Promyelocytic Leukemia,Miller-Dieker Lissencephaly Syndrome,Myopathy, Centronuclear, 2 |
4dyl_a | P07332 | ENSG00000182511 | FES | 99.90 | 1.40E-29 | 9.80E-34 | 269.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YFL047W | RGD2 | SGDID:S000001847 | Arhgap12 |
Rho GTPase-activating protein 12 (Rho-type GTPase-activating protein 12) |
Mus musculus | 6gvc_q | Q8C0D4 | 99.80 | 8.20E-24 | 5.70E-28 | 205.50 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YFL047W | RGD2 | SGDID:S000001847 | ARHGAP1 CDC42GAP RHOGAP1 |
Rho GTPase-activating protein 1 (CDC42 GTPase-activating protein) (GTPase-activating protein rhoGAP) (Rho-related small GTPase protein activator) (Rho-type GTPase-activating protein 1) (p50-RhoGAP) |
Homo sapiens | Noma,Microphthalmia,Dent Disease 1,Non-Syndromic X-Linked Intellectual Disability,Lowe Oculocerebrorenal Syndrome |
1am4_b | Q07960 | ENSG00000175220 | ARHGAP1 | 99.70 | 1.40E-22 | 9.80E-27 | 191.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | ARHGAP35 GRF1 GRLF1 KIAA1722 P190A p190ARHOGAP |
Rho GTPase-activating protein 35 (Glucocorticoid receptor DNA-binding factor 1) (Glucocorticoid receptor repression factor 1) (GRF-1) (Rho GAP p190A) (p190-A) |
Homo sapiens | 3fk2_a | Q9NRY4 | ENSG00000160007 | ARHGAP35 | 99.80 | 2.10E-24 | 1.40E-28 | 211.20 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YFL047W | RGD2 | SGDID:S000001847 | PIK3R2 |
Phosphatidylinositol 3-kinase regulatory subunit beta (PI3-kinase regulatory subunit beta) (PI3K regulatory subunit beta) (PtdIns-3-kinase regulatory subunit beta) (Phosphatidylinositol 3-kinase 85 kDa regulatory subunit beta) (PI3-kinase subunit p85-beta) (PtdIns-3-kinase regulatory subunit p85-beta) |
Homo sapiens | Endometrial Cancer,Cowden Syndrome,Plasma Cell Neoplasm,Cowden Syndrome 1,Congenital Lipomatous Overgrowth, Vascular Malformations, And Epidermal Nevi,Nevus, Epidermal,Polymicrogyria,Endometrial Adenocarcinoma,Breast Cancer,Colorectal Cancer,Hepatocellular Carcinoma,Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome,Hydrocephalus,Megalencephaly,Immunodeficiency 14,Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1,Polydactyly,Prostate Cancer,Proteus Syndrome,Erythrocytosis, Familial, 1,Myeloma, Multiple,Lung Cancer |
2xs6_a | O00459 | ENSG00000105647 | PIK3R2 | 99.70 | 1.60E-21 | 1.10E-25 | 186.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | Pacsin1 Pacsin |
Protein kinase C and casein kinase substrate in neurons protein 1 (Syndapin-1) |
Mus musculus | 2x3v_a | Q61644 | 99.90 | 9.80E-28 | 6.80E-32 | 247.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YFL047W | RGD2 | SGDID:S000001847 | Arhgap35 Grlf1 P190A p190ARHOGAP |
Rho GTPase-activating protein 35 (GAP-associated protein p190) (Glucocorticoid receptor DNA-binding factor 1) |
Rattus norvegicus | 5irc_a | P81128 | 99.70 | 7.80E-23 | 5.50E-27 | 194.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YFL047W | RGD2 | SGDID:S000001847 | PACSIN1 KIAA1379 |
Protein kinase C and casein kinase substrate in neurons protein 1 (Syndapin-1) |
Homo sapiens | Autosomal Recessive Non-Syndromic Intellectual Disability |
3q84_h | Q9BY11 | ENSG00000124507 | PACSIN1 | 99.90 | 8.80E-29 | 6.10E-33 | 251.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | TRIP10 CIP4 STOT STP |
Cdc42-interacting protein 4 (Protein Felic) (Salt tolerant protein) (hSTP) (Thyroid receptor-interacting protein 10) (TR-interacting protein 10) (TRIP-10) |
Homo sapiens | Myopathy, Centronuclear, 1,Wiskott-Aldrich Syndrome,Pontocerebellar Hypoplasia,Myopathy, Centronuclear, 2,Familial Hypocalciuric Hypercalcemia |
2efk_a | Q15642 | ENSG00000125733 | TRIP10 | 99.90 | 1.20E-27 | 8.40E-32 | 243.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFL047W | RGD2 | SGDID:S000001847 | SYP1 YCR030C YCR30C/YCR29C |
Suppressor of yeast profilin deletion |
Saccharomyces cerevisiae | 3g9g_a | P25623 | 99.70 | 4.50E-22 | 3.10E-26 | 198.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YFL047W | RGD2 | SGDID:S000001847 | FNBP1 FBP17 KIAA0554 |
Formin-binding protein 1 (Formin-binding protein 17) (hFBP17) |
Homo sapiens | Eccrine Adenocarcinoma,Pontocerebellar Hypoplasia,Persistent Hyperplastic Primary Vitreous,Familial Hypocalciuric Hypercalcemia |
2efl_a | Q96RU3 | ENSG00000187239 | FNBP1 | 99.90 | 8.00E-29 | 5.60E-33 | 252.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |