| 释义 |
- Function
- References
- Further reading
{{Infobox_gene}}AUTS2, activator of transcription and developmental regulator is a protein that in humans is encoded by the AUTS2 gene. [1]FunctionThis gene has been implicated in neurodevelopment and as a candidate gene for numerous neurological disorders, including autism spectrum disorders, intellectual disability, and developmental delay. Mutations in this gene have also been associated with non-neurological disorders, such as acute lymphoblastic leukemia, aging of the skin, early-onset androgenetic alopecia, and certain cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. References 1. ^{{cite web| title = Entrez Gene: AUTS2, activator of transcription and developmental regulator| url = https://www.ncbi.nlm.nih.gov/gene/26053| accessdate = 2017-09-12}}
Further reading {{refbegin | 2}}- {{cite journal |vauthors=Gratacòs M, Costas J, de Cid R, Bayés M, González JR, Baca-García E, de Diego Y, Fernández-Aranda F, Fernández-Piqueras J, Guitart M, Martín-Santos R, Martorell L, Menchón JM, Roca M, Sáiz-Ruiz J, Sanjuán J, Torrens M, Urretavizcaya M, Valero J, Vilella E, Estivill X, Carracedo A |title=Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment |journal=Am. J. Med. Genet. B Neuropsychiatr. Genet. |volume=150B |issue=6 |pages=808–16 |year=2009 |pmid=19086053 |doi=10.1002/ajmg.b.30902 |url=}}
- {{cite journal |vauthors=Trynka G, Zhernakova A, Romanos J, Franke L, Hunt KA, Turner G, Bruinenberg M, Heap GA, Platteel M, Ryan AW, de Kovel C, Holmes GK, Howdle PD, Walters JR, Sanders DS, Mulder CJ, Mearin ML, Verbeek WH, Trimble V, Stevens FM, Kelleher D, Barisani D, Bardella MT, McManus R, van Heel DA, Wijmenga C |title=Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling |journal=Gut |volume=58 |issue=8 |pages=1078–83 |year=2009 |pmid=19240061 |doi=10.1136/gut.2008.169052 |url=}}
- {{cite journal |vauthors=Elia J, Gai X, Xie HM, Perin JC, Geiger E, Glessner JT, D'arcy M, deBerardinis R, Frackelton E, Kim C, Lantieri F, Muganga BM, Wang L, Takeda T, Rappaport EF, Grant SF, Berrettini W, Devoto M, Shaikh TH, Hakonarson H, White PS |title=Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes |journal=Mol. Psychiatry |volume=15 |issue=6 |pages=637–46 |year=2010 |pmid=19546859 |pmc=2877197 |doi=10.1038/mp.2009.57 |url=}}
- {{cite journal |vauthors=Hamshere ML, Green EK, Jones IR, Jones L, Moskvina V, Kirov G, Grozeva D, Nikolov I, Vukcevic D, Caesar S, Gordon-Smith K, Fraser C, Russell E, Breen G, St Clair D, Collier DA, Young AH, Ferrier IN, Farmer A, McGuffin P, Holmans PA, Owen MJ, O'Donovan MC, Craddock N |title=Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept |journal=Br J Psychiatry |volume=195 |issue=1 |pages=23–9 |year=2009 |pmid=19567891 |pmc=2802523 |doi=10.1192/bjp.bp.108.061424 |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 |year=2009 |pmid=19913121 |pmc=2775832 |doi=10.1016/j.ajhg.2009.10.014 |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 |year=2010 |pmid=20379614 |pmc=2896464 |doi=10.2119/molmed.2009.00159 |url=}}
- {{cite journal |vauthors=Saus E, Brunet A, Armengol L, Alonso P, Crespo JM, Fernández-Aranda F, Guitart M, Martín-Santos R, Menchón JM, Navinés R, Soria V, Torrens M, Urretavizcaya M, Vallès V, Gratacòs M, Estivill X |title=Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients |journal=J Psychiatr Res |volume=44 |issue=14 |pages=971–8 |year=2010 |pmid=20398908 |doi=10.1016/j.jpsychires.2010.03.007 |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 |year=2010 |pmid=20628086 |pmc=2945168 |doi=10.2337/dc10-0452 |url=}}
- {{cite journal |vauthors=Huang XL, Zou YS, Maher TA, Newton S, Milunsky JM |title=A de novo balanced translocation breakpoint truncating the autism susceptibility candidate 2 (AUTS2) gene in a patient with autism |journal=Am. J. Med. Genet. A |volume=152A |issue=8 |pages=2112–4 |year=2010 |pmid=20635338 |doi=10.1002/ajmg.a.33497 |url=}}
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