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

FAM47E-STBD1
Identifiers
AliasesFAM47E-STBD1, FAM47E-STBD1 readthrough, FAM47E
External IDsGeneCards: FAM47E-STBD1; OMA:FAM47E-STBD1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001242939

n/a

RefSeq (protein)

NP_001130042
NP_001229865
NP_001229868

n/a

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

Function

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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

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000272414Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ a b "Entrez Gene: FAM47E-STBD1 readthrough".

Further reading

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