Type | Description |
---|---|
Definition | cysteinyl-tRNA synthetase |
Date | Results | Publications |
---|---|---|
2021-03-20 13:30:00 | Endogenous TLR2 ligand embedded in the catalytic region of human cysteinyl-tRNA synthetase 1. | 32461342 |
2019-12-21 11:09:00 | Cysteinyl-tRNA Synthetase Mutations Cause a Multi-System, Recessive Disease That Includes Microcephaly, Developmental Delay, and Brittle Hair and Nails. | 30824121 |
2018-06-16 11:58:00 | Four single nucleotide polymorphisms (SNPs) of CARS were significantly associated with gastric cancer risk in both the discovery stage and the validation stage | 28409418 |
2016-11-12 11:53:00 | The risk (G and C) and non-risk (C and T) allele frequencies of the SNPs at the rs1888747 and rs739401 loci of FRMD3 and CARS, respectively, did not differ significantly between the diabetics with (case) and without (control) nephropathy (P > 0.05). | 26909942 |
2016-10-22 10:23:00 | Loss of CARS, the cysteinyl-tRNA synthetase, suppresses ferroptosis induced by erastin, which inhibits the cystine-glutamate antiporter known as system xc(-). | 26184909 |
Type | IDs |
---|---|
Synonymous | CARS1, CYSRS, MGC:11246 |
Gene |
UniProtKB-ID:
SYCC_HUMAN,
B4DPV7_HUMAN,
A0A024RCG3_HUMAN
UniprotKB:
P49589,
B4DPV7,
A0A024RCG3
UniParc:
UPI000002B485,
UPI0000136359,
UPI00004C4152,
UPI00017A77B3
EMBL:
BC002880,
AC108448,
BT009913,
AC131971,
L06845,
AK298514,
AF288206,
BX647906,
CH471158,
AF288207,
AK302644
Ensembl:
ENSG00000278191,
ENSG00000110619
KO:
hsa:833
|
Nucleutide sequences |
EMBL-CDS:
CAI46108.1,
EAX02541.1,
AAP88915.1,
AAA73901.1,
AAG00579.1,
AAG00578.1,
AAH02880.1,
BAG63885.1,
BAG60719.1,
EAX02540.1,
EAX02536.1
Gene_ORFName:
hCG_16441
Ensembl_TRS:
ENST00000397111,
ENST00000278224,
ENST00000612826,
ENST00000633248,
ENST00000380525,
ENST00000632612
|
Protein sequencees |
Ensembl_PRO:
ENSP00000278224,
ENSP00000380300,
ENSP00000487923,
ENSP00000369897,
ENSP00000488657,
ENSP00000482336
RefSeq:
XP_024304471.1,
XP_024304469.1,
NP_001742.1,
XP_024304470.1,
NP_001181926.1,
NP_001365066.1,
NP_001014437.1,
NP_001365069.1,
XP_024304472.1,
NP_001365065.1,
NP_001365067.1,
XP_024304473.1,
NP_644802.1,
NP_001365068.1
|
Others |
UniRef100:
UniRef100_B4DPV7,
UniRef100_P49589
UniRef90:
UniRef90_P49589
UniRef50:
UniRef50_P49589
UniGene:
Hs.274873
CCDS:
CCDS7742.1,
CCDS41602.1,
CCDS41600.1
|
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Refseq |
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