FRG2B (FSHD region gene 2 family member B)

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Gene Gene information from NCBI Gene database.
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Entrez ID 441581
Gene name FSHD region gene 2 family member B
Gene symbol FRG2B
Synonyms (NCBI Gene)
-
Chromosome 10
Chromosome location 10q26.3
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
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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.
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MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
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UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96QU4
Protein name Protein FRG2-like-1 (FSHD region gene 2 protein family member B) (HSA10-FRG2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15315 FRG2 60 → 241 Facioscapulohumeral muscular dystrophy candidate 2 Family
Sequence 
MGKGNEDPDLHCSSIQCSTDQPPFQQISFTEKGSDEKKPFKEKGKTAFSHSSEKHIQRQG
SEPNPNKENSEETKLKAGNSTAGSEPESSSYRENCRKRKMSSKDSCQDTAGNCPEKECSL
SLNKKSRSSTPVHNSEIQETCDAHHRGRSRACTGRSKRHRSRALGVQTPSIRKSLVTSVR
AMSEAVYQDLAQVWAQQIHSPLTCEQLTLLTRLRGPLCAQVQTLYSMATQAAYVFPAESW
LVPATLPGPGESALDREAHPFPGQEITETVSGSDEAKL
Sequence length 278
Interactions View interactions

No strongly related genes found yet for FRG2B.

No additional diseases found yet through genes similar to FRG2B.