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1496 CTNNA2

1496

CTNNA2

catenin alpha 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition catenin alpha 2

研究结论

Date Results Publications
2019-02-16 11:15:00 Novel-miR-4885 can bind to 3' untranslated region of CTNNA2 to reduce cell adhesion. 30526004
2017-10-14 12:38:00 Single nucleotide polymorphisms in CTNNA2 show associations in Schizophrenia and general cognitive function. 28746715
2017-05-20 14:24:00 One association in the CTNNA2 gene on chromosome 2p12 [rs1567532, hazard ratio (HR) = 1.75, 95% confidence interval (CI) 1.19-2.58, P = 0.005 for homozygotes for the minor allele] and one in the last intron of the RUNX2 gene on chromosome 6p21 (rs12209785, HR = 0.88, 95% CI 0.80-0.98, P = 0.014 for heterozygotes) are of particular relevance. These loci do not coincide with those that showed the strongest associations in t 27497070
2017-05-20 12:27:00 SNP 50-kb upstream from CTNNA2 was associated with impulsivity in Native American sample. 27167163
2016-01-16 11:12:00 Single nucleotide polymorphism in CTNNA2 is associated with breast cancer susceptibility. 25824743

名称对应

Type IDs
Synonymous CAP-R, CAPR, CDCBM9, CT114, CTNR
Gene
UniProtKB-ID: CTNA2_HUMAN, F6KRI5_HUMAN, Q49AD3_HUMAN
UniprotKB: P26232, F6KRI5, Q49AD3
UniParc: UPI00001AE85A, UPI00001A9CD8, UPI00001A3E86, UPI000056F1A6, UPI0001B30105, UPI0000D9D4EC, UPI0001915222
EMBL: AK303035, AC011741, AK127226, BX537769, CH471053, AC008067, AC016670, BC040458, AC011746, FJ695201, AK295181, M94151, AC093322, AC010975, HQ589336, AK295493, BC052996, AC096573, AC016716, AC096753, AC104780
Ensembl: ENSG00000066032
KO: hsa:1496
Nucleutide sequences
EMBL-CDS: BAG54457.1, BAH12003.1, AAY14763.1, AAY14758.1, AAH52996.1, EAW99564.1, CAD97832.1, AAX93241.1, AAY15008.1, BAH12088.1, EAW99565.1, BAH13884.1, AAX88946.1, AAA58407.2, AAY15073.1, AEF32484.1, AAH40458.1
Ensembl_TRS: ENST00000629316, ENST00000343114, ENST00000541047, ENST00000466387, ENST00000496558, ENST00000402739
Protein sequencees
Ensembl_PRO: ENSP00000384638, ENSP00000418191, ENSP00000341500, ENSP00000419295, ENSP00000444675, ENSP00000486160
RefSeq: NP_001307739.1, XP_016858894.1, XP_024308484.1, NP_001158355.1, XP_016858893.1, NP_001269528.1, NP_001269527.1, XP_024308482.1, XP_024308483.1, XP_011530858.1, NP_001269526.1, XP_016858895.1, XP_016858892.1, XP_011530859.1, NP_004380.2, NP_001269529.1, XP_011530857.1
Others
UniRef100: UniRef100_Q49AD3, UniRef100_F6KRI5, UniRef100_P26232
UniRef90: UniRef90_Q49AD3, UniRef90_P26232
UniRef50: UniRef50_A0A2K6FJ73, UniRef50_Q61301
UniGene: Hs.167368
CCDS: CCDS54371.1, CCDS42703.2, CCDS62944.1, CCDS74531.1, CCDS62945.1

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