SMARCA2

Source: Wikipedia, the free encyclopedia.
SMARCA2
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_011416
NM_026003
NM_001347439

RefSeq (protein)
Location (UCSC)Chr 9: 1.98 – 2.19 MbChr 19: 26.58 – 26.76 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Probable global transcription activator SNF2L2 is a protein that in humans is encoded by the SMARCA2 gene.[5][6]

Function

The protein encoded by this gene is a member of the

polymorphism.[6]

Interactions

SMARCA2 has been shown to

interact
with:

- Nicolaides Baraitser Syndrome (NCBRS)

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000080503Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000024921Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. S2CID 43436716
    .
  6. ^ a b "Entrez Gene: SMARCA2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2".
  7. ^
    PMID 8895581
    .
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Further reading