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AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

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YER155C BEM2 / SGDID:S000000957
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
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
YER155C BEM2 SGDID:S000000957
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 99.70 7.90E-23 8.60E-27 225.80 1 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
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 1.10E-23 1.20E-27 231.20 0 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
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 1.60E-21 1.80E-25 210.10 1 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
RASGRP4
RAS guanyl-releasing protein 4
Homo sapiens
Mast-Cell Leukemia,Mastocytosis,Bleeding Disorder, Platelet-Type, 18,Asthma
6axg_a Q8TDF6 ENSG00000171777 RASGRP4 100.00 2.20E-38 2.40E-42 374.00 1 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
Arhgap12
Rho GTPase-activating protein 12 (Rho-type GTPase-activating protein 12)
Mus musculus
6gvc_q Q8C0D4 99.80 1.00E-23 1.20E-27 226.20 0 0 1 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
RASGRP2 CDC25L MCG7
RAS guanyl-releasing protein 2 (Calcium and DAG-regulated guanine nucleotide exchange factor I) (CalDAG-GEFI) (Cdc25-like protein) (hCDC25L) (F25B3.3 kinase-like protein)
Homo sapiens
Leukocyte Adhesion Deficiency, Type Iii,Hemorrhagic Disease,Combined Immunodeficiency,Glanzmann Thrombasthenia,Leukocyte Adhesion Deficiency, Type I,Thrombocytopenia,Bleeding Disorder, Platelet-Type, 18,Stormorken Syndrome
6axf_g Q7LDG7 ENSG00000068831 RASGRP2 99.90 7.00E-34 7.70E-38 331.10 1 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
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 5.90E-22 6.30E-26 220.00 1 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
Rgl2 Rab2l Rlf
Ral guanine nucleotide dissociation stimulator-like 2 (RalGDS-like 2) (RalGDS-like factor) (Ras-associated protein RAB2L)
Mus musculus
4jgw_a Q61193 99.90 3.50E-30 3.70E-34 308.50 0 0 1 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
RALGPS1 KIAA0351 RALGEF2
Ras-specific guanine nucleotide-releasing factor RalGPS1 (Ral GEF with PH domain and SH3-binding motif 1) (Ral guanine nucleotide exchange factor 2) (RalGEF 2) (RalA exchange factor RalGPS1)
Homo sapiens
Developmental And Epileptic Encephalopathy 4
3qxl_a Q5JS13 ENSG00000136828 RALGPS1 99.70 6.50E-23 7.00E-27 227.80 1 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
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 6.50E-23 7.50E-27 216.20 1 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
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
1nvu_s Q07889 100.00 3.10E-38 3.20E-42 380.90 1 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
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 1.40E-21 1.50E-25 209.20 1 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
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 3.10E-22 3.60E-26 207.30 1 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
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
4nyi_s Q07889 ENSG00000115904 SOS1 100.00 2.80E-35 3.00E-39 352.60 1 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
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 3.40E-23 3.90E-27 215.50 0 0 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
RGD1 YBR260C YBR1728
RHO GTPase-activating protein RGD1 (RhoGAP) (Related GAP domain protein 1)
Saccharomyces cerevisiae
5my3_a P38339 99.70 3.20E-22 3.60E-26 214.20 0 0 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
Rasgrf1 Cdc25 Grf1
Ras-specific guanine nucleotide-releasing factor 1 (Ras-GRF1) (CDC25Mm) (Guanine nucleotide-releasing protein) (GNRP) (Ras-specific nucleotide exchange factor CDC25)
Mus musculus
2ije_s P27671 99.80 7.00E-24 7.70E-28 229.60 0 0 1 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
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 7.40E-23 8.80E-27 211.50 1 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
RASGRP1 RASGRP
RAS guanyl-releasing protein 1 (Calcium and DAG-regulated guanine nucleotide exchange factor II) (CalDAG-GEFII) (Ras guanyl-releasing protein)
Homo sapiens
Leukocyte Adhesion Deficiency, Type Iii,Combined Immunodeficiency,Autoimmune Lymphoproliferative Syndrome,Fibrosclerosis Of Breast,Lupus Erythematosus,Leukocyte Adhesion Deficiency, Type I,Bleeding Disorder, Platelet-Type, 18,Immunodeficiency 64,Systemic Lupus Erythematosus,Lymphoproliferative Syndrome
4l9m_a O95267 ENSG00000172575 RASGRP1 99.90 1.10E-33 1.20E-37 342.10 1 1 0 0 0 0 0 0
YER155C BEM2 SGDID:S000000957
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 4.90E-22 5.50E-26 212.80 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab