Version 5.4
| Homo sapiens Gene: FAM47C | |||
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| Summary | |||
| InnateDB Gene | IDBG-55563.5 | ||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||
| Gene Symbol | FAM47C | ||
| Gene Name | family with sequence similarity 47, member C | ||
| Synonyms | |||
| Species | Homo sapiens | ||
| Ensembl Gene | ENSG00000198173 | ||
| Encoded Proteins |
family with sequence similarity 47, member C
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| Protein Structure |
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| Useful resources | Stemformatics EHFPI ImmGen | ||
| Entrez Gene | |||
| Summary |
This gene encodes a product belonging to a family of proteins with unknown function. The coding sequence of this family member includes several tandemly repeated regions. [provided by RefSeq, Sep 2011] |
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| Gene Information | |||
| Type | Protein coding | ||
| Genomic Location | Chromosome X:37008397-37011666 | ||
| Strand | Forward strand | ||
| Band | p21.1 | ||
| 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.
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| Orthologs | |||
| No orthologs found for this gene | |||
| Cross-References | |||
| SwissProt | Q5HY64 | ||
| TrEMBL | |||
| UniProt Splice Variant | |||
| Entrez Gene | 442444 | ||
| UniGene | Hs.535216 | ||
| RefSeq | NM_001013736 | ||
| HUGO | HGNC:25301 | ||
| OMIM | |||
| CCDS | CCDS35227 | ||
| HPRD | |||
| IMGT | |||
| EMBL | AK125992 BX842568 | ||
| GenPept | BAC86381 CAI40150 | ||
| RNA Seq Atlas | 442444 | ||