DNAJC30, DnaJ heat shock protein family (Hsp40) member C30

DNAJC30, DnaJ heat shock protein family (Hsp40) member C30

• 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 Synonyms (dnaJ homolog subfamily C member 30, mitochondrial, DnaJ (Hsp40) homolog, subfamily C, member 30, Williams Beuren syndrome chromosome region 18, dnaJ homolog subfamily C member 30, williams-Beuren syndrome chromosomal region 18 protein, WBSCR18,)
• NCBI Gene ID: 84277
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q96LL9
  UNIPROT ID#>>B3KSU4
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

DnaJ heat shock protein family (Hsp40) member C30 interacts with:

• exosome component 6
  family with sequence similarity 209 member A
  fetal and adult testis expressed 1
  glutathione peroxidase 8 (putative)
  jagunal homolog 1
  KASH domain containing 5
  leucine rich repeat containing 25
  major facilitator superfamily domain containing 14B
  sialic acid binding Ig like lectin 12
  solute carrier family 10 member 4
  solute carrier family 51 subunit alpha
  transmembrane protein 31
  transmembrane protein 52B
  transmembrane protein 86B

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.