| 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 | |||||||
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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 | ||||||