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YMR161W HLJ1 / SGDID:S000004771

SGD CSV

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 Caenorhabditis elegans	Flag Escherichia coli
YMR161W	HLJ1	SGDID:S000004771	PAM16 TIM16 YJL104W J0822	Mitochondrial import inner membrane translocase subunit TIM16 (Presequence translocated-associated motor subunit PAM16)		Saccharomyces cerevisiae		2guz_b	P42949			98.10	1.00E-09	1.10E-13	70.10	0	0	0	0	0
YMR161W	HLJ1	SGDID:S000004771	DNAJB12	DnaJ homolog subfamily B member 12		Homo sapiens		2ctp_a	Q9NXW2	ENSG00000148719	DNAJB12	98.30	1.30E-10	1.50E-14	76.70	0	1	0	0	0
YMR161W	HLJ1	SGDID:S000004771	dnaJ groP b0015 JW0014	Chaperone protein DnaJ (HSP40) (Heat shock protein J)		Escherichia coli		1bqz_a	P08622			98.60	9.20E-12	1.00E-15	82.20	0	0	0	0	1
YMR161W	HLJ1	SGDID:S000004771	Dnajc16 Kiaa0962	DnaJ homolog subfamily C member 16		Mus musculus		2cug_a	Q80TN4			98.50	1.40E-11	1.50E-15	84.60	0	0	1	0	0
YMR161W	HLJ1	SGDID:S000004771	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			98.00	3.20E-09	2.80E-13	92.00	0	0	0	0	0
YMR161W	HLJ1	SGDID:S000004771	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	98.30	1.30E-10	1.40E-14	82.80	1	1	0	0	0
YMR161W	HLJ1	SGDID:S000004771	dnj-12 CELE_F39B2.10 F39B2.10	dnj-12 CELE_F39B2.10 F39B2.10		Caenorhabditis elegans		2och_a	O45502			98.20	5.20E-10	5.60E-14	73.10	0	0	0	1	0
YMR161W	HLJ1	SGDID:S000004771	dnaJ2 TTHA1489	Chaperone protein DnaJ 2		Thermus thermophilus		4j7z_b	Q56237			98.50	2.00E-11	2.10E-15	87.90	0	0	0	0	0
YMR161W	HLJ1	SGDID:S000004771	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	98.50	3.00E-11	3.10E-15	85.50	1	1	0	0	0
YMR161W	HLJ1	SGDID:S000004771	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	98.40	4.10E-11	4.20E-15	84.80	1	1	0	0	0
YMR161W	HLJ1	SGDID:S000004771	dnj-2 B0035.2	DnaJ homolog dnj-2 (DnaJ domain protein 2)		Caenorhabditis elegans		2qsa_a	Q17433			98.40	7.80E-11	8.10E-15	84.70	0	0	0	1	0
YMR161W	HLJ1	SGDID:S000004771	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	98.50	2.70E-11	2.80E-15	88.00	1	1	0	0	0
YMR161W	HLJ1	SGDID:S000004771	SIS1 YNL007C N2879	Protein SIS1		Saccharomyces cerevisiae		6d6x_a	P25294			98.20	3.40E-10	3.60E-14	76.30	0	0	0	0	0
YMR161W	HLJ1	SGDID:S000004771	DNAJB3 HCG3	DnaJ homolog subfamily B member 3		Homo sapiens		2ej7_a	Q8WWF6	ENSG00000227802	DNAJB3	98.10	8.60E-10	9.40E-14	73.30	0	1	0	0	0
YMR161W	HLJ1	SGDID:S000004771	JAC1 SEO2 YGL018C	J-type co-chaperone JAC1, mitochondrial (J-type accessory chaperone 1)		Saccharomyces cerevisiae		3uo3_b	P53193			97.80	8.80E-09	8.50E-13	81.90	0	0	0	0	0
YMR161W	HLJ1	SGDID:S000004771	DNAJC27 RABJS RBJ	DnaJ homolog subfamily C member 27 (Rab and DnaJ domain-containing protein)		Homo sapiens	Eyelid Benign Neoplasm,Desmoid Disease, Hereditary	2ys8_a	Q9NZQ0	ENSG00000115137	DNAJC27	98.00	2.20E-09	2.30E-13	73.30	1	1	0	0	0
YMR161W	HLJ1	SGDID:S000004771	hscB yfhE b2527 JW2511	Co-chaperone protein HscB (Hsc20)		Escherichia coli		1fpo_a	P0A6L9			97.90	4.50E-09	4.40E-13	82.50	0	0	0	0	1
YMR161W	HLJ1	SGDID:S000004771	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	97.80	7.40E-09	7.10E-13	84.20	1	1	0	0	0
YMR161W	HLJ1	SGDID:S000004771	cbpA b1000 JW0985	Curved DNA-binding protein		Escherichia coli		3ucs_c	P36659			98.50	3.30E-11	3.60E-15	78.80	0	0	0	0	1
YMR161W	HLJ1	SGDID:S000004771	hscB VC_0751	Co-chaperone protein HscB homolog		Vibrio cholerae		4it5_d	Q9KTX9			98.10	1.40E-09	1.40E-13	85.40	0	0	0	0	0
YMR161W	HLJ1	SGDID:S000004771	ST	Small t antigen (ST) (ST-AG)		Simian virus		2pf4_e	P03081			97.90	4.60E-09	4.30E-13	84.10	0	0	0	0	0
YMR161W	HLJ1	SGDID:S000004771	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	98.40	6.40E-11	6.40E-15	91.50	1	1	0	0	0
YMR161W	HLJ1	SGDID:S000004771	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	98.50	2.20E-11	2.40E-15	79.30	1	1	0	0	0
YMR161W	HLJ1	SGDID:S000004771	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			98.30	1.10E-10	1.30E-14	88.40	0	0	1	0	0
YMR161W	HLJ1	SGDID:S000004771	TbgDal_VI2240	TbgDal_VI2240		Trypanosoma brucei		6hix_bk	C9ZQR6			98.60	8.50E-12	7.90E-16	111.90	0	0	0	0	0
YMR161W	HLJ1	SGDID:S000004771	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			97.90	5.50E-09	5.80E-13	74.90	0	0	0	0	0
YMR161W	HLJ1	SGDID:S000004771	YDJ1 MAS5 YNL064C N2418 YNL2418C	Mitochondrial protein import protein MAS5 (Yeast dnaJ protein 1)		Saccharomyces cerevisiae		5vso_a	P25491			98.60	9.20E-12	1.00E-15	81.60	0	0	0	0	0
YMR161W	HLJ1	SGDID:S000004771	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	98.10	8.60E-10	9.50E-14	72.60	1	1	0	0	0
YMR161W	HLJ1	SGDID:S000004771	Dnajc5 Cspalpha	DnaJ homolog subfamily C member 5 (Cysteine string protein) (CSP) (Cysteine-string protein isoform alpha)		Mus musculus		2ctw_a	P60904			98.40	7.10E-11	7.40E-15	85.10	0	0	1	0	0
YMR161W	HLJ1	SGDID:S000004771	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	98.40	6.00E-11	6.40E-15	81.60	1	1	0	0	0
YMR161W	HLJ1	SGDID:S000004771	SEC63 NPL1 PTL1 YOR254C	Protein translocation protein SEC63 (Protein NPL1) (Sec62/63 complex 73 kDa subunit)		Saccharomyces cerevisiae		6n3q_d	P14906			97.80	9.80E-09	9.50E-13	96.20	0	0	0	0	0
YMR161W	HLJ1	SGDID:S000004771	DNAJB8	DnaJ homolog subfamily B member 8		Homo sapiens	Fatal Infantile Hypertonic Myofibrillar Myopathy	2dmx_a	Q8NHS0	ENSG00000179407	DNAJB8	98.70	1.90E-12	2.00E-16	89.90	1	1	0	0	0