FAM47E-STBD1

FAM47E-STBD1
Identifiers
AliasesFAM47E-STBD1, FAM47E-STBD1 readthrough
External IDsGeneCards: FAM47E-STBD1
Gene location (Human)
Chr.Chromosome 4 (human)[1]
Band4q21.1Start76,251,721 bp[1]
End76,311,129 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

100631383

n/a

Ensembl

ENSG00000272414

n/a

UniProt

Q6ZV65

n/a

RefSeq (mRNA)

NM_001242939

n/a

RefSeq (protein)

NP_001130042
NP_001229865

n/a

Location (UCSC)Chr 4: 76.25 – 76.31 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

FAM47E-STBD1 readthrough is a protein that in humans is encoded by the FAM47E-STBD1 gene.[3]

Function

This locus represents naturally occurring read-through transcription between the neighboring FAM47E (family with sequence similarity 47, member E) and STBD1 (starch binding domain 1) genes on chromosome 4. The read-through transcript encodes a protein that shares sequence identity with the upstream gene product but its C-terminal region is distinct due to frameshifts relative to the downstream gene.[3]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000272414 - Ensembl, May 2017
  2. ↑ "Human PubMed Reference:".
  3. 1 2 "Entrez Gene: FAM47E-STBD1 readthrough".

Further reading

  • Simón-Sánchez J, Schulte C, Bras JM, Sharma M, Gibbs JR, Berg D, et al. (December 2009). "Genome-wide association study reveals genetic risk underlying Parkinson's disease". Nature Genetics. 41 (12): 1308–12. doi:10.1038/ng.487. PMC 2787725. PMID 19915575.
  • Do CB, Tung JY, Dorfman E, Kiefer AK, Drabant EM, Francke U, Mountain JL, Goldman SM, Tanner CM, Langston JW, Wojcicki A, Eriksson N (June 2011). "Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease". PLoS Genetics. 7 (6): e1002141. doi:10.1371/journal.pgen.1002141. PMC 3121750. PMID 21738487.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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