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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YGL195W | GCN1 | SGDID:S000003163 | TNPO1 KPNB2 MIP1 TRN |
Transportin-1 (Importin beta-2) (Karyopherin beta-2) (M9 region interaction protein) (MIP) |
Homo sapiens | Retinitis Pigmentosa,Meningoencephalitis,Amyotrophic Lateral Sclerosis 20,Retinitis Pigmentosa 2 |
1qbk_b | Q92973 | ENSG00000083312 | TNPO1 | 99.40 | 3.00E-17 | 3.30E-21 | 217.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL195W | GCN1 | SGDID:S000003163 | AP2B1 ADTB2 CLAPB1 |
AP-2 complex subunit beta (AP105B) (Adaptor protein complex AP-2 subunit beta) (Adaptor-related protein complex 2 subunit beta) (Beta-2-adaptin) (Beta-adaptin) (Clathrin assembly protein complex 2 beta large chain) (Plasma membrane adaptor HA2/AP2 adaptin beta subunit) |
Homo sapiens | Cerebellar Degeneration,Branchiooculofacial Syndrome,Char Syndrome,Rhabdomyosarcoma,Mental Retardation, Autosomal Dominant 56,Patent Ductus Arteriosus 1,Ataxia-Telangiectasia,Hypocalciuric Hypercalcemia, Familial, Type Iii |
2vgl_b | P63010 | ENSG00000006125 | AP2B1 | 99.60 | 1.80E-19 | 1.90E-23 | 228.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL195W | GCN1 | SGDID:S000003163 | PSE1 KAP121 YMR308C YM9952.10C |
Importin subunit beta-3 (Karyopherin subunit beta-3) (Karyopherin-121) (Protein secretion enhancer 1) |
Saccharomyces cerevisiae | 3w3u_a | P32337 | 99.50 | 4.20E-19 | 4.60E-23 | 241.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGL195W | GCN1 | SGDID:S000003163 | AP1B1 ADTB1 BAM22 CLAPB2 |
AP-1 complex subunit beta-1 (Adaptor protein complex AP-1 subunit beta-1) (Adaptor-related protein complex 1 subunit beta-1) (Beta-1-adaptin) (Beta-adaptin 1) (Clathrin assembly protein complex 1 beta large chain) (Golgi adaptor HA1/AP1 adaptin beta subunit) |
Homo sapiens | Ichthyosis,Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, And Keratoderma,Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Recessive,Meningioma, Familial,Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant |
6cri_i | Q10567 | ENSG00000100280 | AP1B1 | 99.50 | 6.00E-19 | 6.50E-23 | 221.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL195W | GCN1 | SGDID:S000003163 | Ap1b1 Adtb1 |
AP-1 complex subunit beta-1 (Adaptor protein complex AP-1 subunit beta-1) (Adaptor-related protein complex 1 subunit beta-1) (Beta-1-adaptin) (Beta-adaptin 1) (Clathrin assembly protein complex 1 beta large chain) (Golgi adaptor HA1/AP1 adaptin beta subunit) |
Rattus norvegicus | 1w63_j | P52303 | 99.60 | 1.40E-19 | 1.50E-23 | 228.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGL195W | GCN1 | SGDID:S000003163 | CAND1 KIAA0829 TIP120 TIP120A |
Cullin-associated NEDD8-dissociated protein 1 (Cullin-associated and neddylation-dissociated protein 1) (TBP-interacting protein of 120 kDa A) (TBP-interacting protein 120A) (p120 CAND1) |
Homo sapiens | Familial Hypertension,Cockayne Syndrome |
1u6g_c | Q86VP6 | 99.40 | 5.80E-18 | 5.80E-22 | 238.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |