Version 5.4
| Homo sapiens Protein: FRG2 | |||
|---|---|---|---|
| Summary | |||
| InnateDB Protein | IDBP-48125.5 | ||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||
| Gene Symbol | FRG2 | ||
| Protein Name | FSHD region gene 2 | ||
| Synonyms | |||
| Species | Homo sapiens | ||
| Ensembl Protein | ENSP00000368039 | ||
| InnateDB Gene | IDBG-48123 (FRG2) | ||
| Protein Structure |
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| UniProt Annotation | |||
| Function | |||
| Subcellular Localization | Nucleus {ECO:0000269PubMed:15520407}. | ||
| Disease Associations | |||
| Tissue Specificity | Expression is undetectable in all tissues tested except for differentiating myoblasts of FSHD patients, which display low, yet distinct levels of expression, partly from FRG2, but predominantly originating from its homolog on chromosome 10. {ECO:0000269PubMed:15520407}. | ||
| Comments | |||
| 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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| Gene Ontology | |||
Molecular Function |
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| Biological Process |
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| Cellular Component |
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| Protein Structure and Domains | |||
| PDB ID | |||
| InterPro | |||
| PFAM | |||
| PRINTS | |||
| PIRSF | |||
| SMART | |||
| TIGRFAMs | |||
| Post-translational Modifications | |||
| Modification | |||
| Cross-References | |||
| SwissProt | Q64ET8 | ||
| PhosphoSite | PhosphoSite-Q64ET8 | ||
| TrEMBL | |||
| UniProt Splice Variant | |||
| Entrez Gene | 448831 | ||
| UniGene | Hs.730594 | ||
| RefSeq | NP_001005217 | ||
| HUGO | HGNC:19136 | ||
| OMIM | 609032 | ||
| CCDS | CCDS34123 | ||
| HPRD | 16418 | ||
| IMGT | |||
| EMBL | AF146191 AY714545 BC144572 | ||
| GenPept | AAI44573 AAU14220 | ||