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Gene Gene information from NCBI Gene database.
Entrez ID 448831
Gene name FSHD region gene 2
Gene symbol FRG2
Synonyms (NCBI Gene)
FRG2A
Chromosome 4
Chromosome location 4q35.2
miRNA miRNA information provided by mirtarbase database.
111 Show/Hide all (111)
miRTarBase ID miRNA Experiments Reference
MIRT1004381 hsa-miR-1253 CLIP-seq
MIRT1004382 hsa-miR-1299 CLIP-seq
MIRT1004383 hsa-miR-1827 CLIP-seq
MIRT1004384 hsa-miR-2114 CLIP-seq
MIRT1004385 hsa-miR-219-2-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005634 Component Nucleus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609032 19136 ENSG00000205097
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q64ET8
Protein name Protein FRG2 (FSHD region gene 2 protein)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15315 FRG2 60 → 241 Facioscapulohumeral muscular dystrophy candidate 2 Family
Tissue specificity 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 chromosom
Sequence
Sequence length 278
Interactions View interactions