Homo sapiens Gene: DNAJC30
Summary
InnateDB Gene IDBG-20247.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DNAJC30
Gene Name DnaJ (Hsp40) homolog, subfamily C, member 30
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000176410
Encoded Proteins
DnaJ (Hsp40) homolog, subfamily C, member 30
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This intronless gene encodes a member of the DNAJ molecular chaperone homology domain-containing protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 7:73680969-73683453
Strand Reverse strand
Band q11.23
Transcripts
ENST00000395176 ENSP00000378605
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
Experimentally validated
Total 3 [view]
Protein-Protein 2 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
Cellular Component
GO:0005739 mitochondrion
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt Q96LL9
TrEMBL
UniProt Splice Variant
Entrez Gene 84277
UniGene Hs.647046
RefSeq NM_032317
HUGO HGNC:16410
OMIM
CCDS CCDS5556
HPRD 10303
IMGT
EMBL AC073846 AF412025 AK058113 BC005056
GenPept AAH05056 AAM62307 AAS07471 BAB71671
RNA Seq Atlas 84277