Type | Description |
---|---|
Definition | ladybird homeobox 1 |
Date | Results | Publications |
---|---|---|
2020-02-08 12:51:00 | A LBX1 single nucleotide polymorphism, rs11190870, was associated with a strong susceptibility for adult spinal deformity. | 31365516 |
2019-08-24 12:27:00 | The pooled results showed a statistically significant association between LBX1 gene polymorphisms and adolescent idiopathic scoliosis (for rs11190870, T vs C, OR = 1.54, 95% CI = 1.48-1.61, P < .00001; for rs625039, G vs A, OR = 1.50, 95% CI: 1.38-1.62; P < .00001; for rs678741, G vs A, OR = 0.74, 95% CI: 0.63-0.86; P < .0001; for rs11598564, G vs A, OR = 1.41, 95% CI: 1.31-1.51; P < .0001) Meta-Analysis) | 31277174 |
2019-06-08 10:14:00 | We have replicated the association of the LBX1 locus with AIS in French-Canadian population, a novel European descent cohort, which is known for its unique genetic architecture. | 28604496 |
2019-04-06 11:51:00 | Genome-wide association study on the etiology of adolescent idiopathic scoliosis using samples from more than 5 000 patients and 6 000 normal controls showed two genes: LBX1-AS1 on 10q24.32 and TNIK on 3q26.2 highly related to AIS initiation and progression [review] | 30107698 |
2019-02-23 12:19:00 | Homozygous LBX1 Frameshift Mutation Causes Recessive Congenital Central Hypoventilation Syndrome. | 30487221 |
Type | IDs |
---|---|
Synonymous | HPX-6, HPX6, LBX1H, homeobox |
Gene |
UniProtKB-ID:
LBX1_HUMAN
UniprotKB:
P52954
UniParc:
UPI00001F95A1
EMBL:
BC069156,
BC136321,
CH471066,
X90828,
AL135794
Ensembl:
ENSG00000138136
KO:
hsa:10660
|
Nucleutide sequences |
EMBL-CDS:
CAA62342.1,
EAW49777.1,
AAI36322.1,
AAH69156.1
Ensembl_TRS:
ENST00000370193
|
Protein sequencees |
Ensembl_PRO:
ENSP00000359212
RefSeq:
NP_006553.2
|
Others |
UniRef100:
UniRef100_P52954
UniRef90:
UniRef90_P52954
UniRef50:
UniRef50_P52954
UniGene:
Hs.37128
CCDS:
CCDS31270.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
---|---|---|---|---|---|---|---|---|
Refseq |
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