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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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