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 |
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YJL073W | JEM1 | SGDID:S000003609 | YDJ1 MAS5 YNL064C N2418 YNL2418C |
Mitochondrial protein import protein MAS5 (Yeast dnaJ protein 1) |
Saccharomyces cerevisiae | 5vso_a | P25491 | 98.10 | 6.60E-10 | 9.10E-14 | 77.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YJL073W | JEM1 | SGDID:S000003609 | DNAJA3 HCA57 TID1 |
DnaJ homolog subfamily A member 3, mitochondrial (DnaJ protein Tid-1) (hTid-1) (Hepatocellular carcinoma-associated antigen 57) (Tumorous imaginal discs protein Tid56 homolog) |
Homo sapiens | Alternating Esotropia,Hepatocellular Carcinoma,Congenital Myasthenic Syndrome,Myasthenic Syndrome, Congenital, 12,Codas Syndrome |
2dn9_a | Q96EY1 | ENSG00000103423 | DNAJA3 | 97.70 | 1.30E-08 | 1.70E-12 | 71.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJL073W | JEM1 | SGDID:S000003609 | Dnajc5 Cspalpha |
DnaJ homolog subfamily C member 5 (Cysteine string protein) (CSP) (Cysteine-string protein isoform alpha) |
Mus musculus | 2ctw_a | P60904 | 98.00 | 2.10E-09 | 2.70E-13 | 83.40 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YJL073W | JEM1 | SGDID:S000003609 | DNAJC12 JDP1 |
DnaJ homolog subfamily C member 12 (J domain-containing protein 1) |
Homo sapiens | Hyperphenylalaninemia,Hyperphenylalaninemia, Mild, Non-Bh4-Deficient,Dystonia,Non-Proliferative Fibrocystic Change Of The Breast,Proliferative Type Fibrocystic Change Of Breast,Mild Hyperphenylalaninemia |
2ctq_a | Q9UKB3 | ENSG00000108176 | DNAJC12 | 98.00 | 1.80E-09 | 2.20E-13 | 84.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJL073W | JEM1 | SGDID:S000003609 | SEC63 NPL1 PTL1 YOR254C |
Protein translocation protein SEC63 (Protein NPL1) (Sec62/63 complex 73 kDa subunit) |
Saccharomyces cerevisiae | 6n3q_d | P14906 | 97.60 | 3.10E-08 | 3.60E-12 | 100.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YJL073W | JEM1 | SGDID:S000003609 | DNAJB8 |
DnaJ homolog subfamily B member 8 |
Homo sapiens | Fatal Infantile Hypertonic Myofibrillar Myopathy |
2dmx_a | Q8NHS0 | ENSG00000179407 | DNAJB8 | 98.20 | 2.90E-10 | 3.80E-14 | 84.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJL073W | JEM1 | SGDID:S000003609 | PAM16 TIM16 YJL104W J0822 |
Mitochondrial import inner membrane translocase subunit TIM16 (Presequence translocated-associated motor subunit PAM16) |
Saccharomyces cerevisiae | 2guz_b | P42949 | 97.60 | 3.30E-08 | 4.40E-12 | 67.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YJL073W | JEM1 | SGDID:S000003609 | DNAJB12 |
DnaJ homolog subfamily B member 12 |
Homo sapiens | 2ctp_a | Q9NXW2 | ENSG00000148719 | DNAJB12 | 97.80 | 6.70E-09 | 9.10E-13 | 73.40 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YJL073W | JEM1 | SGDID:S000003609 | dnaJ groP b0015 JW0014 |
Chaperone protein DnaJ (HSP40) (Heat shock protein J) |
Escherichia coli | 1bqz_a | P08622 | 98.20 | 2.00E-10 | 2.70E-14 | 81.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | ||||
YJL073W | JEM1 | SGDID:S000003609 | Dnajc16 Kiaa0962 |
DnaJ homolog subfamily C member 16 |
Mus musculus | 2cug_a | Q80TN4 | 98.00 | 1.30E-09 | 1.80E-13 | 80.20 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YJL073W | JEM1 | SGDID:S000003609 | PRP19 PSO4 YLL036C |
Pre-mRNA-processing factor 19 (EC 2.3.2.27) (RING-type E3 ubiquitin transferase PRP19) |
2.3.2.27 | Saccharomyces cerevisiae | 5y88_t | P32523 | 97.40 | 9.20E-08 | 9.30E-12 | 90.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YJL073W | JEM1 | SGDID:S000003609 | DNAJC5 CLN4 |
DnaJ homolog subfamily C member 5 (Ceroid-lipofuscinosis neuronal protein 4) (Cysteine string protein) (CSP) |
Homo sapiens | Retinitis Pigmentosa,Visual Epilepsy,Ceroid Lipofuscinosis, Neuronal, 4b, Autosomal Dominant,Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 1,Cystic Fibrosis,Mucopolysaccharidosis Iii,Mucopolysaccharidosis-Plus Syndrome,Syphilitic Meningitis,Dementia,Ceroid Lipofuscinosis, Neuronal, 9,Prostate Carcinoma In Situ,Spinocerebellar Ataxia, Autosomal Recessive 7,Adult Neuronal Ceroid Lipofuscinosis,Ceroid Lipofuscinosis, Neuronal, 13,Plasmodium Malariae Malaria,Neuronal Ceroid Lipofuscinosis,Ceroid Lipofuscinosis, Neuronal, 8, Northern Epilepsy Variant,Neuronal Ceroid-Lipofuscinoses,Ceroid Lipofuscinosis, Neuronal, 10,Disease Of Mental Health,Ceroid Lipofuscinosis, Neuronal, 7,Malaria,Retinitis Pigmentosa 72,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,Ceroid Lipofuscinosis, Neuronal, 11,Ceroid Lipofuscinosis, Neuronal, 3,Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive,Ceroid Lipofuscinosis, Neuronal, 2,Mucopolysaccharidosis, Type Iiia,Ceroid Lipofuscinosis, Neuronal, 1 |
2n04_a | Q9H3Z4 | ENSG00000101152 | DNAJC5 | 98.10 | 1.00E-09 | 1.30E-13 | 84.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJL073W | JEM1 | SGDID:S000003609 | dnj-12 CELE_F39B2.10 F39B2.10 |
dnj-12 CELE_F39B2.10 F39B2.10 |
Caenorhabditis elegans | 2och_a | O45502 | 97.80 | 8.10E-09 | 1.10E-12 | 72.40 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
YJL073W | JEM1 | SGDID:S000003609 | dnaJ2 TTHA1489 |
Chaperone protein DnaJ 2 |
Thermus thermophilus | 4j7z_b | Q56237 | 97.90 | 2.70E-09 | 3.40E-13 | 82.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YJL073W | JEM1 | SGDID:S000003609 | DNAJB2 HSJ1 HSPF3 |
DnaJ homolog subfamily B member 2 (Heat shock 40 kDa protein 3) (Heat shock protein J1) (HSJ-1) |
Homo sapiens | Fatal Infantile Hypertonic Myofibrillar Myopathy,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 5,Dnajb2-Related Charcot-Marie-Tooth Disease Type 2,Spinal Muscular Atrophy,Charcot-Marie-Tooth Disease Type 2a2a,Muscular Atrophy,Spastic Paraplegia 55, Autosomal Recessive,Motor Peripheral Neuropathy,Charcot-Marie-Tooth Disease,Hereditary Neuropathies,Charcot-Marie-Tooth Disease, Axonal, Type 2r,Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 1,Charcot-Marie-Tooth Disease, Recessive Intermediate D,Charcot-Marie-Tooth Disease, Axonal, Type 2b2,Charcot-Marie-Tooth Disease Intermediate Type,Charcot-Marie-Tooth Disease, Axonal, Type 2p,Huntington Disease,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Charcot-Marie-Tooth Disease, Axonal, Type 2h,Charcot-Marie-Tooth Disease, Axonal, Type 2k,Charcot-Marie-Tooth Disease, Axonal, Type 2t,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Neuronopathy, Distal Hereditary Motor, Type Va |
2lgw_a | P25686 | ENSG00000135924 | DNAJB2 | 98.10 | 9.70E-10 | 1.20E-13 | 83.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJL073W | JEM1 | SGDID:S000003609 | DNAJC30 WBSCR18 |
DnaJ homolog subfamily C member 30, mitochondrial (Williams-Beuren syndrome chromosomal region 18 protein) |
Homo sapiens | Spinocerebellar Ataxia 15,Williams-Beuren Syndrome,Leber Hereditary Optic Neuropathy, Modifier Of |
2yua_a | Q96LL9 | ENSG00000176410 | DNAJC30 | 97.90 | 3.00E-09 | 3.80E-13 | 81.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJL073W | JEM1 | SGDID:S000003609 | dnj-2 B0035.2 |
DnaJ homolog dnj-2 (DnaJ domain protein 2) |
Caenorhabditis elegans | 2qsa_a | Q17433 | 98.00 | 1.60E-09 | 2.00E-13 | 83.90 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
YJL073W | JEM1 | SGDID:S000003609 | SIS1 YNL007C N2879 |
Protein SIS1 |
Saccharomyces cerevisiae | 6d6x_a | P25294 | 97.70 | 1.60E-08 | 2.00E-12 | 73.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YJL073W | JEM1 | SGDID:S000003609 | DNAJB3 HCG3 |
DnaJ homolog subfamily B member 3 |
Homo sapiens | 2ej7_a | Q8WWF6 | ENSG00000227802 | DNAJB3 | 97.80 | 8.70E-09 | 1.20E-12 | 73.40 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YJL073W | JEM1 | SGDID:S000003609 | JAC1 SEO2 YGL018C |
J-type co-chaperone JAC1, mitochondrial (J-type accessory chaperone 1) |
Saccharomyces cerevisiae | 3uo3_a | P53193 | 97.40 | 1.10E-07 | 1.20E-11 | 82.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YJL073W | JEM1 | SGDID:S000003609 | DNAJB9 MDG1 UNQ743/PRO1471 |
DnaJ homolog subfamily B member 9 (Endoplasmic reticulum DNA J domain-containing protein 4) (ER-resident protein ERdj4) (ERdj4) (Microvascular endothelial differentiation gene 1 protein) (Mdg-1) |
Homo sapiens | Non-Gestational Choriocarcinoma,Fibrillary Glomerulonephritis,Retinitis Pigmentosa 49,Tungiasis |
2ctr_a | Q9UBS3 | ENSG00000128590 | DNAJB9 | 97.70 | 1.80E-08 | 2.30E-12 | 74.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJL073W | JEM1 | SGDID:S000003609 | hscB yfhE b2527 JW2511 |
Co-chaperone protein HscB (Hsc20) |
Escherichia coli | 1fpo_a | P0A6L9 | 97.70 | 2.00E-08 | 2.40E-12 | 85.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | ||||
YJL073W | JEM1 | SGDID:S000003609 | HSCB DNAJC20 HSC20 |
Iron-sulfur cluster co-chaperone protein HscB (DnaJ homolog subfamily C member 20) [Cleaved into: Iron-sulfur cluster co-chaperone protein HscB, cytoplasmic (C-HSC20); Iron-sulfur cluster co-chaperone protein HscB, mitochondrial] |
Homo sapiens | Bardet-Biedl Syndrome,Mitochondrial Myopathy,Combined Oxidative Phosphorylation Deficiency 19,Hypercholesterolemia, Familial, 4,Anemia, Sideroblastic, 1,Multiple Mitochondrial Dysfunctions Syndrome 1,Anemia, Sideroblastic, And Spinocerebellar Ataxia,Myopathy, Lactic Acidosis, And Sideroblastic Anemia 1 |
3bvo_a | Q8IWL3 | ENSG00000100209 | HSCB | 97.60 | 4.10E-08 | 4.60E-12 | 86.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJL073W | JEM1 | SGDID:S000003609 | cbpA b1000 JW0985 |
Curved DNA-binding protein |
Escherichia coli | 3ucs_c | P36659 | 98.00 | 2.10E-09 | 2.80E-13 | 75.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | ||||
YJL073W | JEM1 | SGDID:S000003609 | hscB VC_0751 |
Co-chaperone protein HscB homolog |
Vibrio cholerae | 4it5_d | Q9KTX9 | 97.80 | 6.70E-09 | 7.90E-13 | 88.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YJL073W | JEM1 | SGDID:S000003609 | ST |
Small t antigen (ST) (ST-AG) |
Simian virus | 2pf4_e | P03081 | 97.40 | 1.40E-07 | 1.50E-11 | 82.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YJL073W | JEM1 | SGDID:S000003609 | DNAJC24 DPH4 ZCSL3 |
DnaJ homolog subfamily C member 24 (CSL-type zinc finger-containing protein 3) (Diphthamide biosynthesis protein 4) |
Homo sapiens | Diphtheria,Aniridia 1,Iris Disease,Benign Epilepsy With Centrotemporal Spikes,Coloboma Of Optic Nerve,Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome,Gillespie Syndrome |
2l6l_a | Q6P3W2 | ENSG00000170946 | DNAJC24 | 97.90 | 3.30E-09 | 4.00E-13 | 88.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJL073W | JEM1 | SGDID:S000003609 | DNAJA1 DNAJ2 HDJ2 HSJ2 HSPF4 |
DnaJ homolog subfamily A member 1 (DnaJ protein homolog 2) (HSDJ) (Heat shock 40 kDa protein 4) (Heat shock protein J2) (HSJ-2) (Human DnaJ protein 2) (hDj-2) |
Homo sapiens | Oculopharyngeal Muscular Dystrophy |
2lo1_a | P31689 | ENSG00000086061 | DNAJA1 | 98.10 | 4.90E-10 | 6.60E-14 | 78.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YJL073W | JEM1 | SGDID:S000003609 | Dnajc10 Erdj5 Jpdi |
DnaJ homolog subfamily C member 10 (EC 1.8.4.-) (Endoplasmic reticulum DNA J domain-containing protein 5) (ER-resident protein ERdj5) (ERdj5) (Endoplasmic reticulum DnaJ-PDI fusion protein 1) (J domain-containing protein disulfide isomerase-like protein) (J domain-containing PDI-like protein) (JPDI) |
1.8.4.- | Mus musculus | 3apq_a | Q9DC23 | 98.00 | 1.30E-09 | 1.80E-13 | 87.50 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YJL073W | JEM1 | SGDID:S000003609 | TbgDal_VI2240 |
TbgDal_VI2240 |
Trypanosoma brucei | 6hix_bk | C9ZQR6 | 98.00 | 1.70E-09 | 1.80E-13 | 105.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YJL073W | JEM1 | SGDID:S000003609 | DNAJC6 |
Putative tyrosine-protein phosphatase auxilin (EC 3.1.3.48) (DnaJ homolog subfamily C member 6) |
3.1.3.48 | Bos taurus | 1xi5_m | Q27974 | 97.30 | 1.90E-07 | 2.50E-11 | 71.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |