Type | Description |
---|---|
Definition | catenin alpha 2 |
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 |
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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Refseq |
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