Type | Description |
---|---|
Definition | tolloid like 1 |
Date | Results | Publications |
---|---|---|
2021-02-02 13:29:00 | Genetic variation in the TLL1 gene is not associated with fibrosis in patients with metabolic associated fatty liver disease. | 33306709 |
2020-07-18 12:11:00 | The incidence of hepatocellular carcinoma was not influenced by TLL1 genotypes even when considering an additional group of 348 noncirrhotic patients, being 2% in AA vs 1% AT/TT patients (P = 0.58). In a large cohort of Caucasian hepatitis C cirrhotics treated with direct-acting antiviral, TLL1 variants do not predict hepatocellular carcinoma development. | 31177595 |
2020-05-23 11:07:00 | The TLL1 variant was independently associated with hepatocellular carcinoma after hepatitis C virus eradication by interferon-free regimen; it might be involved in hepatic fibrogenesis and thereby carcinogenesis | 30382363 |
2019-10-26 12:39:00 | TLL-1 genetic variants determined fibrotic improvement in chronic hepatitis C with curative antivirals, particularly in patients with mild liver disease. | 30305682 |
2019-10-05 13:10:00 | The results of this large-scale cohort study imply that the combination of the PNPLA3 and TLL1 genotype may be associated with an increased risk of advanced fibrosis among patients with nonalcoholic fatty liver disease. | 28744823 |
Type | IDs |
---|---|
Synonymous | ASD6, TLL |
Gene |
UniProtKB-ID:
TLL1_HUMAN,
B7ZLW3_HUMAN
UniprotKB:
O43897,
B7ZLW3
UniParc:
UPI0000072EED,
UPI000189A88A,
UPI000006F809
EMBL:
BC136429,
AF282732,
CH471056,
U91963,
BC016922,
BC136430,
BC144085
Ensembl:
ENSG00000038295
KO:
hsa:7092
|
Nucleutide sequences |
EMBL-CDS:
AAI36430.1,
AAI36431.1,
AAB93878.1,
AAH16922.1,
EAX04813.1,
AAF86287.1,
AAI44086.1
Ensembl_TRS:
ENST00000061240,
ENST00000513213
|
Protein sequencees |
Ensembl_PRO:
ENSP00000061240,
ENSP00000422937
RefSeq:
XP_024309962.1,
XP_024309963.1,
XP_016864059.1,
XP_011530516.1,
NP_036596.3,
NP_001191689.1
|
Others |
UniRef100:
UniRef100_O43897,
UniRef100_B7ZLW3
UniRef90:
UniRef90_O43897
UniRef50:
UniRef50_O43897
UniGene:
Hs.106513
CCDS:
CCDS56342.1,
CCDS3811.1
|
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Refseq |
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