|Mus musculus Gene: Dnajc30|
|Last Modified||2014-10-13 [Report errors or provide feedback]|
|Gene Name||DnaJ (Hsp40) homolog, subfamily C, member 30|
DnaJ (Hsp40) homolog, subfamily C, member 30
|Useful resources||Stemformatics EHFPI ImmGen|
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000176410:
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]
|Genomic Location||Chromosome 5:135064202-135065862|
|Number of Interactions||
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
|UniProt Splice Variant|
|RNA Seq Atlas|