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DNAJC30

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.

Gene Name:	DnaJ (Hsp40) homolog, subfamily C, member 30
Synonyms:	DNAJC30, WBSCR18
Target Sequences:	NM_032317 NP_115693.2 Q96LL9

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For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).

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