BTBD9: Difference between revisions
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'''BTBD9''' is a human gene. | '''BTBD9''' is a human [[gene]]. | ||
There is some evidence that it may be associated with [[restless legs syndrome]].<ref name="pmid17637780">{{cite journal |vauthors=Winkelmann J, Schormair B, Lichtner P |title=Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions |journal=Nat. Genet. |volume=39 |issue=8 |pages=1000–6 |year=2007 |pmid=17637780 |doi=10.1038/ng2099|display-authors=etal}}</ref> | There is some evidence that it may be associated with [[restless legs syndrome]].<ref name="pmid17637780">{{cite journal |vauthors=Winkelmann J, Schormair B, Lichtner P |title=Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions |journal=Nat. Genet. |volume=39 |issue=8 |pages=1000–6 |year=2007 |pmid=17637780 |doi=10.1038/ng2099|display-authors=etal}}</ref> |
Latest revision as of 20:25, 23 July 2018
BTB (POZ) domain containing 9 | |
---|---|
Identifiers | |
Symbol | BTBD9 |
Entrez | 114781 |
HUGO | 21228 |
OMIM | 611237 |
RefSeq | NM_152733 |
Other data | |
Locus | Chr. 6 p21 |
BTBD9 is a human gene.
There is some evidence that it may be associated with restless legs syndrome.[1]
Synaptic Plasticity
Recent evidence using Btbd9 knockout mice argue that BTBD9 is involved in synaptic plasticity, learning and memory, and protein alterations associated with vesicle recycling and endocytosis.[2]
References
- ↑ Winkelmann J, Schormair B, Lichtner P, et al. (2007). "Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions". Nat. Genet. 39 (8): 1000–6. doi:10.1038/ng2099. PMID 17637780.
- ↑ DeAndrade, Mark P.; Zhang, Li; Doroodchi, Atbin; Yokoi, Fumiaki; Cheetham, Chad C.; Chen, Huan-Xin; Roper, Steven N.; Sweatt, J. David; Li, Yuqing (2012). Di Cunto, Ferdinando, ed. "Enhanced Hippocampal Long-Term Potentiation and Fear Memory in Btbd9 Mutant Mice". PLoS ONE. 7 (4): e35518. Bibcode:2012PLoSO...7E5518D. doi:10.1371/journal.pone.0035518. PMC 3334925. PMID 22536397.
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