| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YMR032W | HOF1 | SGDID:S000004635 | imp2 SPBC11C11.02 |
Septation protein imp2 |
Schizosaccharomyces pombe | 5c1f_b | Q10199 | 99.80 | 1.40E-23 | 1.30E-27 | 214.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR032W | HOF1 | SGDID:S000004635 | 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 | 99.80 | 1.70E-24 | 1.70E-28 | 218.50 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
| YMR032W | HOF1 | SGDID:S000004635 | 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 | 99.80 | 1.30E-23 | 1.20E-27 | 215.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR032W | HOF1 | SGDID:S000004635 | GMIP |
GEM-interacting protein (GMIP) |
Homo sapiens | 3qwe_a | Q9P107 | ENSG00000089639 | GMIP | 99.70 | 5.20E-23 | 4.80E-27 | 209.10 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YMR032W | HOF1 | SGDID:S000004635 | 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 | 99.80 | 1.50E-24 | 1.40E-28 | 220.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR032W | HOF1 | SGDID:S000004635 | Pacsin3 |
Protein kinase C and casein kinase II substrate protein 3 |
Mus musculus | 3qe6_a | Q99JB8 | 99.80 | 9.80E-25 | 9.30E-29 | 223.10 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR032W | HOF1 | SGDID:S000004635 | 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 | 99.80 | 4.60E-24 | 4.40E-28 | 216.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR032W | HOF1 | SGDID:S000004635 | Pacsin1 Pacsin |
Protein kinase C and casein kinase substrate in neurons protein 1 (Syndapin-1) |
Mus musculus | 2x3v_a | Q61644 | 99.80 | 2.00E-24 | 1.80E-28 | 225.80 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR032W | HOF1 | SGDID:S000004635 | 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 | 99.70 | 3.60E-23 | 3.50E-27 | 210.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR032W | HOF1 | SGDID:S000004635 | NEB |
Nebulin |
Homo sapiens | Muscular Disease,Childhood-Onset Nemaline Myopathy,Congenital Fiber-Type Disproportion,Congenital Structural Myopathy,Myopathy,Myofibrillar Myopathy,Congenital Nemaline Myopathy,Muscle Tissue Disease,Neuromuscular Disease,Bethlem Myopathy 1,Distal Nebulin Myopathy,Myositis,Myopathy, Myofibrillar, 1,Nemaline Myopathy 3,Muscular Dystrophy,Tibial Muscular Dystrophy,Hyaline Body Myopathy,Reducing Body Myopathy,Severe Congenital Nemaline Myopathy,Intermediate Congenital Nemaline Myopathy,Typical Congenital Nemaline Myopathy,Nemaline Myopathy,Myopathy, Myofibrillar, 4,Endocardial Fibroelastosis,Dysphagia,Foot Drop,Centronuclear Myopathy,Myopathy, Myofibrillar, 9, With Early Respiratory Failure,Central Core Myopathy,Myopathy, Spheroid Body,Strabismus,Primary Cutaneous Amyloidosis,Distal Arthrogryposis,Cardioneuromyopathy With Hyaline Masses And Nemaline Rods,Cardiomyopathy, Familial Hypertrophic, 1,Multiple Pterygium Syndrome, Lethal Type,Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome,Left Ventricular Noncompaction,Batten-Turner Congenital Myopathy,Nemaline Myopathy 2,Multiple Pterygium Syndrome, Escobar Variant |
1ark_a | P20929 | 99.10 | 7.50E-15 | 6.10E-19 | 115.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR032W | HOF1 | SGDID:S000004635 | 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 | 99.70 | 5.00E-22 | 4.80E-26 | 197.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR032W | HOF1 | SGDID:S000004635 | HOF1 CYK2 YMR032W YM9973.05 |
Cytokinesis protein 2 (Homolog of CDC15 protein 1) |
Saccharomyces cerevisiae | 4wpe_a | Q05080 | 100.00 | 2.90E-35 | 2.70E-39 | 305.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR032W | HOF1 | SGDID:S000004635 | RGD1 YBR260C YBR1728 |
RHO GTPase-activating protein RGD1 (RhoGAP) (Related GAP domain protein 1) |
Saccharomyces cerevisiae | 4wpc_a | P38339 | 99.60 | 1.80E-20 | 1.70E-24 | 193.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR032W | HOF1 | SGDID:S000004635 | SYP1 YCR030C YCR30C/YCR29C |
Suppressor of yeast profilin deletion |
Saccharomyces cerevisiae | 3g9g_a | P25623 | 99.70 | 8.40E-22 | 7.40E-26 | 202.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR032W | HOF1 | SGDID:S000004635 | 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 | 99.80 | 1.50E-24 | 1.40E-28 | 230.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR032W | HOF1 | SGDID:S000004635 | 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 | 99.80 | 8.80E-24 | 7.70E-28 | 232.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR032W | HOF1 | SGDID:S000004635 | FYB1 FYB SLAP130 |
FYN-binding protein 1 (Adhesion and degranulation promoting adaptor protein) (ADAP) (FYB-120/130) (p120/p130) (FYN-T-binding protein) (SLAP-130) (SLP-76-associated phosphoprotein) |
Homo sapiens | Rh Isoimmunization,Blood Group Incompatibility,Otopalatodigital Syndrome Spectrum Disorder,Congenital Autosomal Recessive Small-Platelet Thrombocytopenia,Glucosephosphate Dehydrogenase Deficiency,Thrombocytopenia 3,Hereditary Thrombocytopenia With Normal Platelets,Thrombocytopenia,Melnick-Needles Syndrome |
2gtj_a | O15117 | ENSG00000082074 | FYB1 | 98.30 | 1.90E-10 | 1.50E-14 | 98.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |