Mus musculus Gene: Dnajc30
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
Protein Structure
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]
Gene Information
Type Protein coding
Genomic Location Chromosome 5:135064202-135065862
Strand Forward strand
Band G2
Transcripts
ENSMUST00000071263 ENSMUSP00000094318
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.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0008150 biological_process
Cellular Component
GO:0005739 mitochondrion
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene
RefSeq NM_025362
OMIM
CCDS CCDS39315
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas