FAM47E-STBD1: Difference between revisions

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{{Underlinked|date=August 2014}}
{{Infobox_gene}}
{{Infobox_gene}}
'''FAM47E-STBD1 readthrough''' is a [[protein]] that in humans is encoded by the FAM47E-STBD1 [[gene]].<ref name="entrez">
{{cite web | title = Entrez Gene: FAM47E-STBD1 readthrough | url = https://www.ncbi.nlm.nih.gov/gene/100631383 }}</ref>


'''FAM47E-STBD1 readthrough''' is a [[protein]] that in humans is encoded by the FAM47E-STBD1 [[gene]].
== Function ==
<ref name="entrez">
{{cite web
| title = Entrez Gene: FAM47E-STBD1 readthrough
| url = https://www.ncbi.nlm.nih.gov/gene/100631383
| accessdate = 2014-08-01 <!-- T07:39:39.583052-08:00 -->
}}</ref>


==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.<ref name="entrez" />
 
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].


== References ==
== References ==
{{reflist}}
{{reflist}}


== Further reading ==
== Further reading ==
{{refbegin | 2}}
{{refbegin | 2}}
*{{Cite journal
* {{cite journal | vauthors = Simón-Sánchez J, Schulte C, Bras JM, Sharma M, Gibbs JR, Berg D, Paisan-Ruiz C, Lichtner P, Scholz SW, Hernandez DG, Krüger R, Federoff M, Klein C, Goate A, Perlmutter J, Bonin M, Nalls MA, Illig T, Gieger C, Houlden H, Steffens M, Okun MS, Racette BA, Cookson MR, Foote KD, Fernandez HH, Traynor BJ, Schreiber S, Arepalli S, Zonozi R, Gwinn K, van der Brug M, Lopez G, Chanock SJ, Schatzkin A, Park Y, Hollenbeck A, Gao J, Huang X, Wood NW, Lorenz D, Deuschl G, Chen H, Riess O, Hardy JA, Singleton AB, Gasser T | display-authors = 6 | title = Genome-wide association study reveals genetic risk underlying Parkinson's disease | journal = Nature Genetics | volume = 41 | issue = 12 | pages = 1308–12 | date = December 2009 | pmid = 19915575 | pmc = 2787725 | doi = 10.1038/ng.487 }}
| pmid = 19915575
* {{cite journal | vauthors = Do CB, Tung JY, Dorfman E, Kiefer AK, Drabant EM, Francke U, Mountain JL, Goldman SM, Tanner CM, Langston JW, Wojcicki A, Eriksson N | title = Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease | journal = PLoS Genetics | volume = 7 | issue = 6 | pages = e1002141 | date = June 2011 | pmid = 21738487 | pmc = 3121750 | doi = 10.1371/journal.pgen.1002141 }}
| pmc = 2787725
| year = 2009
| author1 = Simón-Sánchez
| first1 = J
| title = Genome-wide association study reveals genetic risk underlying Parkinson's disease
| journal = Nature Genetics
| volume = 41
| issue = 12
| pages = 1308–12
| last2 = Schulte
| first2 = C
| last3 = Bras
| first3 = J. M.
| last4 = Sharma
| first4 = M
| last5 = Gibbs
| first5 = J. R.
| last6 = Berg
| first6 = D
| last7 = Paisan-Ruiz
| first7 = C
| last8 = Lichtner
| first8 = P
| last9 = Scholz
| first9 = S. W.
| last10 = Hernandez
| first10 = D. G.
| last11 = Krüger
| first11 = R
| last12 = Federoff
| first12 = M
| last13 = Klein
| first13 = C
| last14 = Goate
| first14 = A
| last15 = Perlmutter
| first15 = J
| last16 = Bonin
| first16 = M
| last17 = Nalls
| first17 = M. A.
| last18 = Illig
| first18 = T
| last19 = Gieger
| first19 = C
| last20 = Houlden
| first20 = H
| last21 = Steffens
| first21 = M
| last22 = Okun
| first22 = M. S.
| last23 = Racette
| first23 = B. A.
| last24 = Cookson
| first24 = M. R.
| last25 = Foote
| first25 = K. D.
| last26 = Fernandez
| first26 = H. H.
| last27 = Traynor
| first27 = B. J.
| last28 = Schreiber
| first28 = S
| last29 = Arepalli
| first29 = S
| last30 = Zonozi
| first30 = R
| display-authors = 29
| doi = 10.1038/ng.487
}}
*{{Cite journal
| pmid = 21738487
| pmc = 3121750
| year = 2011
| author1 = Do
| first1 = C. B.
| title = Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease
| journal = PLOS Genetics
| volume = 7
| issue = 6
| pages = e1002141
| last2 = Tung
| first2 = J. Y.
| last3 = Dorfman
| first3 = E
| last4 = Kiefer
| first4 = A. K.
| last5 = Drabant
| first5 = E. M.
| last6 = Francke
| first6 = U
| last7 = Mountain
| first7 = J. L.
| last8 = Goldman
| first8 = S. M.
| last9 = Tanner
| first9 = C. M.
| last10 = Langston
| first10 = J. W.
| last11 = Wojcicki
| first11 = A
| last12 = Eriksson
| first12 = N
| doi = 10.1371/journal.pgen.1002141
}}
 
{{refend}}
{{refend}}


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[[Category:Genes on human chromosome 4]]
[[Category:Genes on human chromosome 4]]


{{gene-4-stub}}
{{gene-4-stub}}

Revision as of 21:19, 29 January 2018

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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Ensembl

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UniProt

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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

FAM47E-STBD1 readthrough is a protein that in humans is encoded by the FAM47E-STBD1 gene.[1]

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.[1]

References

  1. ↑ 1.0 1.1 "Entrez Gene: FAM47E-STBD1 readthrough".

Further reading

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

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