| 释义 |
- Function
- References
- Further reading
{{Infobox_gene}}Disco interacting protein 2 homolog C is a protein that in humans is encoded by the DIP2C gene. [1]FunctionThis gene encodes a member of the disco-interacting protein homolog 2 family. The protein shares strong similarity with a Drosophila protein which interacts with the transcription factor disco and is expressed in the nervous system. [provided by RefSeq, Oct 2008]. References 1. ^{{cite web| title = Entrez Gene: Disco interacting protein 2 homolog C| url = https://www.ncbi.nlm.nih.gov/gene/22982| accessdate = 2018-07-26}}
Further reading {{refbegin | 2}}- {{cite journal |vauthors=Mukhopadhyay M, Pelka P, DeSousa D, Kablar B, Schindler A, Rudnicki MA, Campos AR |title=Cloning, genomic organization and expression pattern of a novel Drosophila gene, the disco-interacting protein 2 (dip2), and its murine homolog |journal=Gene |volume=293 |issue=1-2 |pages=59–65 |date=June 2002 |pmid=12137943 |doi= |url=}}
- {{cite journal |vauthors=Oguri M, Kato K, Yokoi K, Yoshida T, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y |title=Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals |journal=Am. J. Hypertens. |volume=23 |issue=1 |pages=70–7 |date=January 2010 |pmid=19851296 |doi=10.1038/ajh.2009.190 |url=}}
- {{cite journal |vauthors=Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M, Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ, Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S, Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE, Hingorani AD |title=Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip |journal=Am. J. Hum. Genet. |volume=85 |issue=5 |pages=628–42 |date=November 2009 |pmid=19913121 |pmc=2775832 |doi=10.1016/j.ajhg.2009.10.014 |url=}}
- {{cite journal |vauthors=Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y |title=Association of genetic variants with hemorrhagic stroke in Japanese individuals |journal=Int. J. Mol. Med. |volume=25 |issue=4 |pages=649–56 |date=April 2010 |pmid=20198315 |doi= |url=}}
- {{cite journal |vauthors=Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR |title=Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score |journal=Mol. Med. |volume=16 |issue=7-8 |pages=247–53 |date=2010 |pmid=20379614 |pmc=2896464 |doi=10.2119/molmed.2009.00159 |url=}}
- {{cite journal |vauthors=Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S |title=Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study |journal=Diabetes Care |volume=33 |issue=10 |pages=2250–3 |date=October 2010 |pmid=20628086 |pmc=2945168 |doi=10.2337/dc10-0452 |url=}}
- {{cite journal |vauthors=Li WD, Jiao H, Wang K, Zhang CK, Glessner JT, Grant SF, Zhao H, Hakonarson H, Arlen Price R |title=A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls |journal=Obesity (Silver Spring) |volume=21 |issue=9 |pages=E490–4 |date=September 2013 |pmid=23703922 |pmc=3762924 |doi=10.1002/oby.20303 |url=}}
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