DNAJC30 抗体
(DnaJ (Hsp40) Homolog, Subfamily C, Member 30 (DNAJC30))
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].
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Latest Publications for our DNAJC30 抗体
: "The 7q11.23 Protein DNAJC30 Interacts with ATP Synthase and Links Mitochondria to Brain Development. ..." in: Cell, Vol. 175, Issue 4, pp. 1088-1104.e23, (2018) (PubMed).Aliases for DNAJC30 抗体
DnaJ heat shock protein family (Hsp40) member C30 (DNAJC30) 抗体DnaJ heat shock protein family (Hsp40) member C30 (Dnajc30) 抗体
1300007M11Rik 抗体
WBSCR18 抗体
Wbscr18 抗体
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