SNTB1

Source: Wikipedia, the free encyclopedia.
SNTB1
Identifiers
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_021021

NM_016667

RefSeq (protein)

NP_066301

NP_057876

Location (UCSC)n/aChr 15: 55.5 – 55.77 Mb
PubMed search[2][3]
Wikidata
View/Edit HumanView/Edit Mouse

Beta-1-syntrophin is a protein that in humans is encoded by the SNTB1 gene.[4][5][6]

Function

Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally related genes.[6]

Interactions

SNTB1 has been shown to

interact with Dystrophin.[7]

References

  1. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000060429Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. PMID 8183929
    .
  5. .
  6. ^ a b "Entrez Gene: SNTB1 syntrophin, beta 1 (dystrophin-associated protein A1, 59kDa, basic component 1)".
  7. PMID 7844150
    .

Further reading


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