Type | Description |
---|---|
Definition | autophagy related 16 like 2 |
Date | Results | Publications |
---|---|---|
2020-06-20 10:49:00 | Results found ATG16L2 rs10898880 was significantly associated with the occurrence of grade 3-4 oral mucositis and myelosuppression in nasopharyngeal carcinoma (NPC) patients treated with radiotherapy. | 31692259 |
2019-04-20 10:46:00 | Patients with the ATG16L2 rs10898880 CC variant genotype had a better LRFS, PFS, and OS (adjusted hazard ratio = 0.59, 0.64, and 0.64; 95% confidence interval: 0.45-0.79, 0.48-0.84, and 0.48-0.86; p = 0.0004, 0.002, and 0.003, respectively), but a greater risk for development of severe RP (adjusted hazard ratio = 1.80, 95% confidence interval: 1.04-3.12, p = 0.037) than did patients with AA/AC genotypes. | 29454863 |
2017-07-22 11:27:00 | ATG16L2 is a susceptibility gene for Crohn's disease in the Chinese population. The rs11235604 single nucleotide polymorphism is remarkably associated with downregulation of the expression of ATG16L2. | 27611316 |
2017-07-08 10:15:00 | A novel SNP-systemic lupus erythematosus association was identified between FCHSD2 and P2RY2, peaking at rs11235667 on a 33-kb haplotype upstream of ATG16L2. | 26663301 |
2014-11-22 10:18:00 | Atg16L2 may play an important role in autophagy of T cells and serve as a potential biomarker to predict clinical relapse of Multiple sclerosis | 24406150 |
Type | IDs |
---|---|
Synonymous | ATG16B, WDR80 |
Gene |
UniProtKB-ID:
A16L2_HUMAN,
Q9H7Q5_HUMAN
UniprotKB:
Q8NAA4,
Q9H7Q5
UniParc:
UPI0000070258,
UPI0000140B06,
UPI0000EE46F3,
UPI000004D248
EMBL:
CH471076,
AK024423,
AL832974,
BC142718,
BC137489,
BC146660,
AK093017,
BC137490,
AK090597,
BC036713
Ensembl:
ENSG00000168010
KO:
hsa:89849
|
Nucleutide sequences |
EMBL-CDS:
CAH56355.1,
EAW74876.1,
AAI46661.1,
AAI42719.1,
BAC03485.1,
AAH36713.1,
AAI37490.1,
BAC04021.1,
AAI37491.1,
EAW74874.1,
BAB15713.1
Ensembl_TRS:
ENST00000321297
|
Protein sequencees |
Ensembl_PRO:
ENSP00000326340
RefSeq:
XP_006718796.1,
NP_203746.1,
XP_005274433.1,
NP_001305695.1,
XP_006718797.1,
XP_006718795.1,
XP_011543634.1,
XP_011543636.1,
XP_011543635.1
|
Others |
UniRef100:
UniRef100_Q9H7Q5,
UniRef100_Q8NAA4
UniRef90:
UniRef90_Q8NAA4,
UniRef90_Q9H7Q5
UniRef50:
UniRef50_Q8NAA4,
UniRef50_Q9H7Q5
UniGene:
Hs.653186
CCDS:
CCDS31634.1
|
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Refseq |
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