DNAJC30 Products

Description

DNAJC30 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]

Bioinformatics

Entrez	84277 Human
Uniprot	AAH05056 Human NM_032317 Human
Product By Gene ID	84277
Alternate Names	dnaJ homolog subfamily C member 30 MGC12943 WBSCR18 Williams-Beuren syndrome chromosomal region 18 protein Williams Beuren syndrome chromosome region 18 DnaJ (Hsp40) homolog, subfamily C, member 30

Bioinformatics Tool for DNAJC30

Discover related pathways, diseases and genes to DNAJC30. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.