FAM47E-STBD1

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Identifiers
Aliases
External IDs	GeneCards: [1]
Orthologs
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a
Wikidata
View/Edit Human

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

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. [provided by RefSeq, Jul 2011].

Further reading

• Simón-Sánchez, J; Schulte, C; Bras, J. M.; Sharma, M; Gibbs, J. R.; Berg, D; Paisan-Ruiz, C; Lichtner, P; Scholz, S. W.; Hernandez, D. G.; Krüger, R; Federoff, M; Klein, C; Goate, A; Perlmutter, J; Bonin, M; Nalls, M. A.; Illig, T; Gieger, C; Houlden, H; Steffens, M; Okun, M. S.; Racette, B. A.; Cookson, M. R.; Foote, K. D.; Fernandez, H. H.; Traynor, B. J.; Schreiber, S; Arepalli, S; et al. (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, C. B.; Tung, J. Y.; Dorfman, E; Kiefer, A. K.; Drabant, E. M.; Francke, U; Mountain, J. L.; Goldman, S. M.; Tanner, C. M.; Langston, J. W.; Wojcicki, A; Eriksson, N (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.