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

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YMR232W FUS2 / SGDID:S000004845
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
YMR232W FUS2 SGDID:S000004845
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 99.30 3.60E-16 4.30E-20 155.50 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
Itsn1 Ese1 Itsn
Intersectin-1 (EH and SH3 domains protein 1)
Mus musculus
3jv3_a Q9Z0R4 99.30 1.30E-16 1.60E-20 149.40 0 0 1 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
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 99.10 7.70E-15 9.50E-19 146.40 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
Arhgef9
Rho guanine nucleotide exchange factor 9 (Collybistin) (Rac/Cdc42 guanine nucleotide exchange factor 9)
Rattus norvegicus
2dfk_a Q9QX73 99.00 5.10E-14 5.80E-18 140.00 0 0 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
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 99.10 3.20E-15 3.80E-19 146.90 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
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 99.00 3.70E-14 4.40E-18 143.30 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
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 99.10 3.40E-15 4.00E-19 149.70 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
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 99.20 1.80E-15 2.10E-19 148.30 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
Arhgef3
Rho guanine nucleotide exchange factor 3
Mus musculus
2z0q_a Q91X46 99.10 6.30E-15 7.60E-19 141.50 0 0 1 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
Farp2 Kiaa0793
FERM, ARHGEF and pleckstrin domain-containing protein 2 (FERM domain including RhoGEF) (FIR) (FERM, RhoGEF and pleckstrin domain-containing protein 2)
Mus musculus
4gyv_f Q91VS8 99.20 5.30E-16 6.40E-20 138.50 0 0 1 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
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 99.00 6.40E-14 7.80E-18 135.10 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
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
3eo2_a Q7Z628 ENSG00000173848 NET1 99.20 2.00E-15 2.30E-19 138.60 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
EHI_010670
EHI_010670
Entamoeba histolytica
4gou_a C4LYV4 99.30 7.10E-17 7.50E-21 170.70 0 0 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
Mcf2l Dbs
Guanine nucleotide exchange factor DBS (DBL's big sister) (MCF2-transforming sequence-like protein)
Mus musculus
1kz7_c Q64096 99.00 4.60E-14 5.40E-18 136.90 0 0 1 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
Tiam1 Tiam-1
T-lymphoma invasion and metastasis-inducing protein 1 (TIAM-1)
Mus musculus
1foe_a Q60610 99.10 1.30E-14 1.60E-18 140.90 0 0 1 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
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 99.10 1.60E-14 1.90E-18 137.50 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
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 99.20 2.10E-15 2.50E-19 146.50 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
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 99.00 6.90E-14 8.00E-18 136.70 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
Vav1 Vav
Proto-oncogene vav (p95vav)
Mus musculus
2vrw_b P27870 99.30 2.40E-16 2.90E-20 154.60 0 0 1 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
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 99.20 2.30E-15 2.80E-19 145.20 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
BCR BCR1 D22S11
Breakpoint cluster region protein (EC 2.7.11.1) (Renal carcinoma antigen NY-REN-26)
2.7.11.1 Homo sapiens
Childhood Acute Lymphocytic Leukemia,Leukemia, Chronic Myeloid,Denture Stomatitis,B-Lymphoblastic Leukemia/Lymphoma,B-Cell Lymphoma,Amyotrophic Lateral Sclerosis 1,Essential Thrombocythemia,Myeloproliferative Neoplasm,Philadelphia-Negative Chronic Myeloid Leukemia,Leukemia,Childhood Leukemia,Acute Leukemia,Leukemia, Acute Myeloid,Hematologic Cancer,Leukemia, Acute Lymphoblastic,Precursor T-Cell Acute Lymphoblastic Leukemia,Chronic Monocytic Leukemia,Chronic Leukemia,Myeloid Leukemia,Burkitt Lymphoma,8p11 Myeloproliferative Syndrome,Chromosome 8p11 Myeloproliferative Syndrome,Leukemia, Acute Lymphoblastic 3,Lymphoma, Non-Hodgkin, Familial,Chromosome 22q11.2 Deletion Syndrome, Distal,Amyotrophic Lateral Sclerosis 9,Amyotrophic Lateral Sclerosis 3,Leukemia, Chronic Lymphocytic,B-Cell Adult Acute Lymphocytic Leukemia
5n6r_a P11274 ENSG00000186716 BCR 99.20 7.70E-16 9.40E-20 137.40 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
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 99.00 4.30E-14 5.20E-18 133.60 1 1 0 0 0 0 0 0
YMR232W FUS2 SGDID:S000004845
ARHGEF11 KIAA0380
Rho guanine nucleotide exchange factor 11 (PDZ-RhoGEF)
Homo sapiens
Fetal Macrosomia
1xcg_e O15085 ENSG00000132694 ARHGEF11 99.20 2.30E-15 2.70E-19 145.90 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab