Symbol: Name: ID: |
DNAJC30 DnaJ (Hsp40) homolog, subfamily C, member 30 GFS:5526 |
Gene name: | DNAJC30 |
Chromosome: | 7q11.23 |
Previous Symbols: | WBSCR18 |
Previous Names: | Williams Beuren syndrome chromosome region 18 |
Aliases: | |
Name Aliases: | |
Locus Type: | gene with protein product |
Mouse Genome Database ID: | MGI:1913364 | Rat Genome Database ID: | RGD:1595783 |
HGNC ID: | HGNC:16410 | RefSeq IDs: | NM_032317 |
Entrez Gene ID: | 84277 | Ensembl Gene ID: | ENSG00000176410 |
VEGA IDs: | OTTHUMG00000023290 | UniProt ID: | Q96LL9 |
UCSC ID: | uc003tys.1 | OMIM ID: | |
Pubmed: | PMID12073013 | ||
CCDS IDs: | CCDSCCDS5556.1 |
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].
Products for DNAJC30 gene
Catalog | Product Name | Application | Company |
GFS:E05526 | DnaJ (Hsp40) homolog, subfamily C, member 30; ELISA kit | ELISA | n/a |
GFS:A05526 | DnaJ (Hsp40) homolog, subfamily C, member 30; Anti | ANTIBODIES | n/a |
GFS:P05526 | DnaJ (Hsp40) homolog, subfamily C, member 30; Protien | Protien | n/a |