Gene Gene information from NCBI Gene database.
Entrez ID 25822
Gene name DnaJ heat shock protein family (Hsp40) member B5
Gene symbol DNAJB5
Synonyms (NCBI Gene)
Hsc40
Chromosome 9
Chromosome location 9p13.3
Summary This gene encodes a member of the DNAJ heat shock protein 40 family of co-chaperone proteins. The encoded protein contains an N-terminal DNAJ domain and a C-terminal substrate binding domain but lacks the cysteine-rich domain found in other DNAJ family me
miRNA miRNA information provided by mirtarbase database.
163
miRTarBase ID miRNA Experiments Reference
MIRT024402 hsa-miR-215-5p Microarray 19074876
MIRT026797 hsa-miR-192-5p Microarray 19074876
MIRT044713 hsa-miR-320a CLASH 23622248
MIRT658979 hsa-miR-129-1-3p HITS-CLIP 19536157
MIRT658978 hsa-miR-129-2-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
15
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IEA
GO:0005515 Function Protein binding IPI 18457437, 21078624, 22810586, 23414517
GO:0005634 Component Nucleus IEA
GO:0005829 Component Cytosol IBA
GO:0005829 Component Cytosol IDA 21231916
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611328 14887 ENSG00000137094
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O75953
Protein name DnaJ homolog subfamily B member 5 (Heat shock protein Hsp40-2) (Heat shock protein Hsp40-3) (Heat shock protein cognate 40) (Hsc40)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00226 DnaJ 4 65 DnaJ domain Domain
PF01556 DnaJ_C 171 330 DnaJ C terminal domain Domain
Sequence
Sequence length 348
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
2
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Peripheral neuropathy Conflicting classifications of pathogenicity rs774909609 RCV000235050
Skeletal myopathy Conflicting classifications of pathogenicity rs774909609 RCV000235050