| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YNL148C | ALF1 | SGDID:S000005092 | DCTN1 |
Dynactin subunit 1 (150 kDa dynein-associated polypeptide) (DAP-150) (DP-150) (p135) (p150-glued) |
Homo sapiens | Supranuclear Palsy, Progressive, 1,Retinitis Pigmentosa,Bardet-Biedl Syndrome,Neuromuscular Disease,Amyotrophic Lateral Sclerosis 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Lateral Sclerosis,Motor Neuron Disease,Muscular Atrophy,Distal Hereditary Motor Neuropathies,Distal Hereditary Motor Neuropathy Type 7,Autosomal Dominant Distal Hereditary Motor Neuronopathy,Distal Hereditary Motor Neuronopathy Type 7,Motor Peripheral Neuropathy,Genetic Motor Neuron Disease,Dystonia,Charcot-Marie-Tooth Disease,Parkinson Disease, Late-Onset,Perry Syndrome,Charcot-Marie-Tooth Disease And Deafness,Respiratory Failure,Neuronal Ceroid Lipofuscinosis,Neuropathy, Hereditary Sensory And Autonomic, Type Ic,Disease Of Mental Health,Mental Depression,Hemochromatosis, Type 1,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Lissencephaly,Oculogyric Crisis,Huntington Disease,Neuropathy, Hereditary Sensory And Autonomic, Type Iia,Neuronopathy, Distal Hereditary Motor, Type Viib,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Neuronopathy, Distal Hereditary Motor, Type Va |
2hqh_d | Q14203 | ENSG00000204843 | DCTN1 | 99.50 | 3.60E-18 | 3.10E-22 | 126.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YNL148C | ALF1 | SGDID:S000005092 | Dctn1 |
Dynactin subunit 1 (150 kDa dynein-associated polypeptide) (DAP-150) (DP-150) (p150-glued) |
Rattus norvegicus | 2m02_a | P28023 | 99.50 | 2.50E-18 | 2.10E-22 | 126.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YNL148C | ALF1 | SGDID:S000005092 | KIF13B GAKIN KIAA0639 |
Kinesin-like protein KIF13B (Kinesin-like protein GAKIN) |
Homo sapiens | Hereditary Spastic Paraplegia,Muscular Dystrophy, Congenital, With Cataracts And Intellectual Disability,Spastic Paraplegia 37, Autosomal Dominant |
2cow_a | Q9NQT8 | ENSG00000197892 | KIF13B | 99.50 | 1.30E-18 | 1.10E-22 | 131.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YNL148C | ALF1 | SGDID:S000005092 | TbgDal_X17140 |
TbgDal_X17140 |
Trypanosoma brucei | 4b6m_a | D0A053 | 99.30 | 1.50E-16 | 1.30E-20 | 115.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YNL148C | ALF1 | SGDID:S000005092 | CLIP4 RSNL2 |
CAP-Gly domain-containing linker protein 4 (Restin-like protein 2) |
Homo sapiens | 2z0w_a | Q8N3C7 | ENSG00000115295 | CLIP4 | 99.40 | 1.90E-17 | 1.60E-21 | 123.70 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YNL148C | ALF1 | SGDID:S000005092 | tbcb-1 F53F4.3 |
Tubulin-specific chaperone B (Tubulin-folding cofactor B) (CoB) |
Caenorhabditis elegans | 1lpl_a | Q20728 | 99.30 | 1.30E-16 | 1.10E-20 | 118.50 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
| YNL148C | ALF1 | SGDID:S000005092 | CLIP1 CYLN1 RSN |
CAP-Gly domain-containing linker protein 1 (Cytoplasmic linker protein 1) (Cytoplasmic linker protein 170 alpha-2) (CLIP-170) (Reed-Sternberg intermediate filament-associated protein) (Restin) |
Homo sapiens | Distal Hereditary Motor Neuronopathy Type 7,Perry Syndrome,Lissencephaly,Neuronopathy, Distal Hereditary Motor, Type Viib,Autosomal Recessive Non-Syndromic Intellectual Disability |
2cp6_a | P30622 | ENSG00000130779 | CLIP1 | 99.40 | 9.20E-18 | 7.20E-22 | 138.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YNL148C | ALF1 | SGDID:S000005092 | CLIP2 CYLN2 KIAA0291 WBSCR3 WBSCR4 WSCR4 |
CAP-Gly domain-containing linker protein 2 (Cytoplasmic linker protein 115) (CLIP-115) (Cytoplasmic linker protein 2) (Williams-Beuren syndrome chromosomal region 3 protein) (Williams-Beuren syndrome chromosomal region 4 protein) |
Homo sapiens | Charcot-Marie-Tooth Disease,Tukel Syndrome,Supravalvular Aortic Stenosis,Williams-Beuren Syndrome,Autosomal Recessive Non-Syndromic Intellectual Disability |
2cp2_a | Q9UDT6 | ENSG00000106665 | CLIP2 | 99.50 | 1.90E-18 | 1.60E-22 | 128.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YNL148C | ALF1 | SGDID:S000005092 | BIK1 YCL029C YCL29C |
Nuclear fusion protein BIK1 |
Saccharomyces cerevisiae | 6fc5_a | P11709 | 99.40 | 2.50E-17 | 2.10E-21 | 124.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YNL148C | ALF1 | SGDID:S000005092 | CLIP3 CLIPR59 |
CAP-Gly domain-containing linker protein 3 (Cytoplasmic linker protein 170-related 59 kDa protein) (CLIP-170-related 59 kDa protein) (CLIPR-59) |
Homo sapiens | 2cp0_a | Q96DZ5 | ENSG00000105270 | CLIP3 | 99.40 | 2.60E-17 | 2.20E-21 | 122.70 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YNL148C | ALF1 | SGDID:S000005092 | CEP350 CAP350 KIAA0480 GM133 |
Centrosome-associated protein 350 (Cep350) (Centrosome-associated protein of 350 kDa) |
Homo sapiens | Seckel Syndrome 7,Epidermal Appendage Tumor,Epiphyseal Dysplasia, Multiple, 4,Cone-Rod Dystrophy 2,Cone-Rod Dystrophy 20,Orofaciodigital Syndrome Ix,Joubert Syndrome 1 |
2coz_a | Q5VT06 | ENSG00000135837 | CEP350 | 99.40 | 2.10E-17 | 1.70E-21 | 129.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |