| Gene Symbol | FRG2 |
|---|---|
| Entrez Gene | 448831 |
| Alt Symbol | FRG2A |
| Species | Human |
| Gene Type | protein-coding |
| Description | FSHD region gene 2 |
| Other Description | FSHD region gene 2 protein|protein FRG2 |
| Swissprots | E7EN36 B7ZMJ1 Q64ET8 |
| Accessions | Q64ET8 AY714545 AAU14220 BC144572 AAI44573 XM_011532001 XP_011530303 XM_011547343 XP_011545645 NM_001005217 NP_001005217 NM_001286820 NP_001273749 |
| Subcellular Location | Nucleus {ECO:0000269|PubMed:15520407}. |
| 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:0000269|PubMed:15520407}. |
Human FRG2 ORF clone (NM_001005217.1) - CDCL109477 from Creative biogene
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Human FRG2 cDNA Clone(NM_001005217.1) - CDFH007110 from Creative biogene
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