DnaJ (Hsp40) homolog, subfamily C, member 30
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]
DNAJC30 Gene Set
interacting proteins for DNAJC30 from the Pathway Commons Protein-Protein Interactions dataset.