Version 5.4
| Bos taurus Gene: WBSCR27 | |||||
|---|---|---|---|---|---|
| Summary | |||||
| InnateDB Gene | IDBG-640018.3 | ||||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||
| Gene Symbol | WBSCR27 | ||||
| Gene Name | Uncharacterized protein | ||||
| Synonyms | |||||
| Species | Bos taurus | ||||
| Ensembl Gene | ENSBTAG00000001374 | ||||
| Encoded Proteins |
Williams Beuren syndrome chromosome region 27
|
||||
| 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 ENSG00000165171:
This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008] |
||||
| Gene Information | |||||
| Type | Protein coding | ||||
| Genomic Location | Chromosome 25:33983208-33987224 | ||||
| Strand | Forward strand | ||||
| Band | |||||
| Transcripts |
|
||||
| Interactions | |||||
| Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
|
||||
| Gene Ontology | |||||
Molecular Function |
|
||||
| Biological Process |
|
||||
| Cellular Component |
|
||||
| Orthologs | |||||
|
Species
Homo sapiens
Mus musculus
|
Gene ID
Gene Order
|
||||
| Cross-References | |||||
| SwissProt | |||||
| TrEMBL | F1N1B0 | ||||
| UniProt Splice Variant | |||||
| Entrez Gene | 509616 | ||||
| UniGene | Bt.16810 | ||||
| RefSeq | XM_003584049 XM_003587837 | ||||
| HUGO | HGNC:19068 | ||||
| OMIM | |||||
| CCDS | |||||
| HPRD | |||||
| IMGT | |||||
| EMBL | DAAA02058197 | ||||
| GenPept | |||||
| RNA Seq Atlas | 509616 | ||||