| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YLR347C | KAP95 | SGDID:S000004339 | PPP2R1A |
Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform (Medium tumor antigen-associated 61 kDa protein) (PP2A subunit A isoform PR65-alpha) (PP2A subunit A isoform R1-alpha) |
Homo sapiens | Uterine Body Mixed Cancer,Uterine Carcinosarcoma,Lung Cancer Susceptibility 3,Carcinosarcoma,Suppression Of Tumorigenicity 12,Uterine Corpus Cancer,Clear Cell Adenofibroma,Female Reproductive Endometrioid Cancer,Breast Cancer,Squamous Cell Carcinoma, Head And Neck,Colorectal Cancer,Ovarian Serous Cystadenocarcinoma,Endometrial Serous Adenocarcinoma,Cystadenocarcinoma,Serous Cystadenocarcinoma,Endometrioid Ovary Carcinoma,Microcephaly,Breast Disease,Mixed Cell Type Cancer,Gastric Adenocarcinoma,Brachydactyly,Mental Retardation, Autosomal Dominant 36,Ovarian Clear Cell Carcinoma,Uterine Corpus Endometrial Carcinoma,Autism Spectrum Disorder,Lung Cancer |
1b3u_a | P30153 | 99.30 | 2.20E-16 | 1.60E-20 | 182.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YLR347C | KAP95 | SGDID:S000004339 | CTHT_0012280 |
CTHT_0012280 |
Chaetomium thermophilum | 4xri_a | G0S143 | 99.70 | 1.90E-22 | 1.40E-26 | 242.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR347C | KAP95 | SGDID:S000004339 | ipo7.L ipo7 MGC52556 |
ipo7.L ipo7 MGC52556 |
Xenopus laevis | 6n88_a | O42480 | 98.90 | 4.20E-13 | 3.10E-17 | 165.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR347C | KAP95 | SGDID:S000004339 | JUP CTNNG DP3 |
Junction plakoglobin (Catenin gamma) (Desmoplakin III) (Desmoplakin-3) |
Homo sapiens | Heart Disease,Endometrial Cancer,Pemphigus,Naxos Disease,Hypertrophic Cardiomyopathy,Familial Woolly Hair Syndrome,Grover'S Disease,Atrial Standstill 1,Dilated Cardiomyopathy,Bladder Cancer,Conjunctival Degeneration,Arrhythmogenic Right Ventricular Dysplasia, Familial, 9,Arrhythmogenic Right Ventricular Dysplasia, Familial, 4,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form,Colorectal Cancer,Diffuse Palmoplantar Keratoderma,Pemphigus Vulgaris, Familial,Cardiac Arrhythmia,Keratoderma With Woolly Hair,Pinguecula,Epidermolysis Bullosa, Lethal Acantholytic,Palmoplantar Keratosis,Gastric Cancer,Arrhythmogenic Right Ventricular Dysplasia, Familial, 10,Left Ventricular Noncompaction 1,Arrhythmogenic Right Ventricular Dysplasia, Familial, 11,Arrhythmogenic Right Ventricular Dysplasia, Familial, 5,Arrhythmogenic Right Ventricular Dysplasia, Familial, 6,Ectodermal Dysplasia/Skin Fragility Syndrome,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Arrhythmogenic Right Ventricular Dysplasia, Familial, 12,Palmoplantar Keratoderma And Woolly Hair,Cardiomyopathy, Dilated, With Woolly Hair And Keratoderma,Wolff-Parkinson-White Syndrome,Arrhythmogenic Right Ventricular Dysplasia, Familial, 8,Left Ventricular Noncompaction,Lung Cancer,Palmoplantar Keratoderma, Nonepidermolytic |
3ifq_a | P14923 | 98.90 | 1.80E-13 | 1.40E-17 | 153.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YLR347C | KAP95 | SGDID:S000004339 | PSE1 KAP121 YMR308C YM9952.10C |
Importin subunit beta-3 (Karyopherin subunit beta-3) (Karyopherin-121) (Protein secretion enhancer 1) |
Saccharomyces cerevisiae | 3w3u_a | P32337 | 99.20 | 2.30E-15 | 1.80E-19 | 184.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR347C | KAP95 | SGDID:S000004339 | VAC8 YEB3 YEL013W |
Vacuolar protein 8 |
Saccharomyces cerevisiae | 5xjg_c | P39968 | 98.90 | 1.70E-13 | 1.30E-17 | 152.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR347C | KAP95 | SGDID:S000004339 | 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 | 98.90 | 2.90E-13 | 2.20E-17 | 153.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR347C | KAP95 | SGDID:S000004339 | 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 | 99.00 | 4.40E-14 | 3.30E-18 | 160.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YLR347C | KAP95 | SGDID:S000004339 | Kpnb1 Impnb |
Importin subunit beta-1 (Karyopherin subunit beta-1) (Nuclear factor p97) (Pore targeting complex 97 kDa subunit) (PTAC97) (SCG) |
Mus musculus | 1ukl_b | P70168 | 99.70 | 3.80E-21 | 2.90E-25 | 231.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR347C | KAP95 | SGDID:S000004339 | KAP95 YLR347C L8300.15 |
Importin subunit beta-1 (Importin-95) (Karyopherin subunit beta-1) (Karyopherin-95) |
Saccharomyces cerevisiae | 3nd2_a | Q06142 | 99.90 | 6.70E-29 | 5.10E-33 | 299.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR347C | KAP95 | SGDID:S000004339 | 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 | 98.90 | 2.90E-13 | 2.20E-17 | 152.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YLR347C | KAP95 | SGDID:S000004339 | KPNB1 NTF97 |
Importin subunit beta-1 (Importin-90) (Karyopherin subunit beta-1) (Nuclear factor p97) (Pore targeting complex 97 kDa subunit) (PTAC97) |
Homo sapiens | Retinitis Pigmentosa,Venezuelan Equine Encephalitis,Influenza,Campomelic Dysplasia |
1qgr_a | Q14974 | ENSG00000108424 | KPNB1 | 99.70 | 2.30E-22 | 1.80E-26 | 242.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YLR347C | KAP95 | SGDID:S000004339 | KLLA0_E20769g |
KLLA0_E20769g |
Kluyveromyces lactis | 5vch_b | Q6CMF0 | 99.10 | 6.20E-15 | 4.70E-19 | 181.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR347C | KAP95 | SGDID:S000004339 | 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 | 9.40E-18 | 7.10E-22 | 201.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YLR347C | KAP95 | SGDID:S000004339 | IPO9 IMP9 KIAA1192 RANBP9 HSPC273 |
Importin-9 (Imp9) (Ran-binding protein 9) (RanBP9) |
Homo sapiens | 6n1z_a | Q96P70 | ENSG00000198700 | IPO9 | 99.10 | 8.80E-15 | 6.50E-19 | 180.50 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |