| Type | Description |
|---|---|
| Definition | xin actin binding repeat containing 2 |
| Date | Results | Publications |
|---|---|---|
| 2019-09-28 12:37:00 | Report pathogenic XIRP1/2 rare variants in arrhythmogenic disorders such as sudden unexplained nocturnal death syndrome and Brugada syndrome. | 29306897 |
| 2016-08-27 12:11:00 | Genetic information from this patient implies that genes involved in development and maintenance of extraocular muscles can cause congenital ocular motility disorders as well. | 24475916 |
| 2015-11-28 11:22:00 | A genome-wide association study reveals 2 new susceptibility loci for atopic dermatitis, XIRP2 and DMRTA1. | 25865352 |
| 2010-06-30 22:06:00 | Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) | 20520587 |
| 2010-06-30 22:06:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
| Type | IDs |
|---|---|
| Synonymous | CMYA3 |
| Gene |
UniProtKB-ID:
XIRP2_HUMAN
UniprotKB:
A4UGR9
UniParc:
UPI000049B156,
UPI000163AC97,
UPI000171BE69,
UPI0000E9BBED,
UPI0000E9BBEC,
UPI000185D585,
UPI0000F72B65,
UPI000171BEAD
EMBL:
AJ626901,
AL832382,
EF119717,
AL832331,
EF119719,
AL832336,
AC093684,
AC108494,
AK122889,
AY820969,
AK096430,
CH471058,
AL831970,
EF119711,
BC018673,
AL832360,
AL832452,
AC092601,
EF119718,
EF119722,
AC133782,
AL833291,
AL831985,
AL832011,
EF119721,
EF119720,
BC022888
Ensembl:
ENSG00000163092
KO:
hsa:129446
|
| Nucleutide sequences |
EMBL-CDS:
ABO69246.1,
ABO69247.1,
CAD91137.1,
CAD91146.1,
CAD89919.1,
CAD38624.1,
ABO69249.1,
EAX11311.1,
CAF25193.1,
ABO69245.1,
BAG53782.1,
CAD89958.1,
CAD91139.1,
AAH18673.1,
ABO69250.1,
CAD91156.1,
AAY24138.1,
CAD91141.2,
ABO69251.1,
CAD91154.1,
AAV87913.1,
ABO69248.1
Ensembl_TRS:
ENST00000409728,
ENST00000628543,
ENST00000409273,
ENST00000409043,
ENST00000409195,
ENST00000409605
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000386840,
ENSP00000386981,
ENSP00000486198,
ENSP00000387255,
ENSP00000386619,
ENSP00000386454
RefSeq:
XP_016858798.1,
NP_001073278.1,
NP_001186072.1,
NP_001186074.1,
NP_001186073.1,
NP_689594.4
|
| Others |
UniRef100:
UniRef100_A4UGR9
UniRef90:
UniRef90_A4UGR9
UniRef50:
UniRef50_A4UGR9
UniGene:
Hs.73680
CCDS:
CCDS42769.1,
CCDS42768.1,
CCDS56144.1,
CCDS56145.1,
CCDS56143.1
|
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|---|---|---|---|---|---|---|---|---|
| Refseq |
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