Bos taurus Gene: DNAJC30 | |||||||
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Summary | |||||||
InnateDB Gene | IDBG-648722.3 | ||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||
Gene Symbol | DNAJC30 | ||||||
Gene Name | dnaJ homolog subfamily C member 30 | ||||||
Synonyms | WBSCR18 | ||||||
Species | Bos taurus | ||||||
Ensembl Gene | ENSBTAG00000009022 | ||||||
Encoded Proteins |
dnaJ homolog subfamily C member 30
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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] |
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Gene Information | |||||||
Type | Protein coding | ||||||
Genomic Location | Chromosome 25:34084148-34085617 | ||||||
Strand | Forward strand | ||||||
Band | |||||||
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
Mus musculus
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Gene ID
Gene Order
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Cross-References | |||||||
SwissProt | |||||||
TrEMBL | Q3SZ23 | ||||||
UniProt Splice Variant | |||||||
Entrez Gene | 617118 | ||||||
UniGene | Bt.48961 | ||||||
RefSeq | NM_001080917 | ||||||
HUGO | |||||||
OMIM | |||||||
CCDS | |||||||
HPRD | |||||||
IMGT | |||||||
EMBL | BC103226 DAAA02058197 | ||||||
GenPept | AAI03227 | ||||||
RNA Seq Atlas | 617118 | ||||||