Mus musculus Gene: Dnajc30 | |||||||
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Summary | |||||||
InnateDB Gene | IDBG-144880.6 | ||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||
Gene Symbol | Dnajc30 | ||||||
Gene Name | DnaJ (Hsp40) homolog, subfamily C, member 30 | ||||||
Synonyms | 1300007M11Rik; Wbscr18 | ||||||
Species | Mus musculus | ||||||
Ensembl Gene | ENSMUSG00000061118 | ||||||
Encoded Proteins |
DnaJ (Hsp40) homolog, subfamily C, member 30
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Protein Structure |
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Useful resources | Stemformatics EHFPI ImmGen | ||||||
Entrez Gene | |||||||
Summary |
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] |
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Gene Information | |||||||
Type | Protein coding | ||||||
Genomic Location | Chromosome 5:135064202-135065862 | ||||||
Strand | Forward strand | ||||||
Band | G2 | ||||||
Transcripts |
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Interactions | |||||||
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.
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Gene Ontology | |||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||
Species
Homo sapiens
Bos taurus
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Gene ID
Gene Order
Not yet available
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Cross-References | |||||||
SwissProt | P59041 | ||||||
TrEMBL | Q6IS32 | ||||||
UniProt Splice Variant | |||||||
Entrez Gene | 66114 | ||||||
UniGene | |||||||
RefSeq | NM_025362 | ||||||
OMIM | |||||||
CCDS | CCDS39315 | ||||||
HPRD | |||||||
IMGT | |||||||
MGI ID | MGI:1913364 | ||||||
MGI Symbol | Dnajc30 | ||||||
EMBL | AF412026 BC069966 | ||||||
GenPept | AAH69966 AAM62308 | ||||||
RNA Seq Atlas | 66114 | ||||||