Version 5.4
| Mus musculus Gene: Wbscr16 | |||||||||
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| Summary | |||||||||
| InnateDB Gene | IDBG-202542.6 | ||||||||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||
| Gene Symbol | Wbscr16 | ||||||||
| Gene Name | Williams-Beuren syndrome chromosome region 16 homolog (human) | ||||||||
| Synonyms | 5730496C04Rik; AU019812 | ||||||||
| Species | Mus musculus | ||||||||
| Ensembl Gene | ENSMUSG00000061979 | ||||||||
| Encoded Proteins |
Williams-Beuren syndrome chromosome region 16 homolog (human)
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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 null:
This gene encodes an RCC1-like G-exchanging factor. It 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 5:134148054-134176774 | ||||||||
| Strand | Reverse 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 8 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
Bos taurus
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Gene ID
Gene Order
Not yet available
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| Cross-References | |||||||||
| SwissProt | |||||||||
| TrEMBL | |||||||||
| UniProt Splice Variant | |||||||||
| Entrez Gene | |||||||||
| UniGene | Mm.29508 | ||||||||
| RefSeq | NM_033572 XM_006504539 | ||||||||
| OMIM | |||||||||
| CCDS | CCDS19718 | ||||||||
| HPRD | |||||||||
| IMGT | |||||||||
| MGI ID | |||||||||
| MGI Symbol | |||||||||
| EMBL | |||||||||
| GenPept | |||||||||
| RNA Seq Atlas | |||||||||