GBAS (gene)

Source: Wikipedia, the free encyclopedia.
NIPSNAP2
Identifiers
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_001483
NM_001202469

NM_008095

RefSeq (protein)

NP_001189398
NP_001474

n/a

Location (UCSC)Chr 7: 55.95 – 56 MbChr 5: 129.8 – 129.84 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Protein NipSnap homolog 2 is a protein that in humans is encoded by the GBAS gene.[5][6][7]

Chromosomal region 7p12, which contains GBAS, is amplified in approximately 40% of glioblastomas, the most common and malignant form of central nervous system tumor. The predicted 286-amino acid protein contains a signal peptide, a transmembrane domain, and 2 tyrosine phosphorylation sites. The GBAS transcript is expressed most abundantly in heart and skeletal muscle. GBAS protein might be involved in vesicular transport.[7]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000146729Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000029432Ensembl, 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. PMID 9615231
    .
  6. .
  7. ^ a b "Entrez Gene: GBAS glioblastoma amplified sequence".

Further reading