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89884 LHX4

89884

LHX4

LIM homeobox 4

protein-coding

Homo sapiens

基因描述

Type Description
Definition LIM homeobox 4

研究结论

Date Results Publications
2017-06-24 12:36:00 LHX4 Mutation is associated with Pituitary Deficits. 27820671
2016-02-06 11:45:00 The study identified 4 new LHX4 heterozygous allelic variants in patients with congenital hypopituitarism: W204X, delK242, N271S and Q346R. 25955177
2015-08-29 10:47:00 A novel homozygous mutation in LHX4 associated with a lethal phenotype, implying that recessive mutations in LHX4 may be incompatible with life. 25871839
2015-01-10 10:19:00 we found that LHX4 upregulated beta-catenin levels in human colorectal cancer cell lines 25034524
2014-01-11 10:29:00 Data indicate that HESX1, LHX4 and SOX3 polymorphisms may be associated with pituitary stalk interruption syndrome (PSIS). 23199197

名称对应

Type IDs
Synonymous CPHD4
Gene
UniProtKB-ID: LHX4_HUMAN, A0A0S2Z5S4_HUMAN
UniprotKB: Q969G2, A0A0S2Z5S4
UniParc: UPI000007340D
EMBL: AF405427, AH011598, AB037683, AF282899, AF405428, AL139141, AF405425, AB055703, BC011759, AY053457, AF405430, AF405426, AF179849, KU178818, AF405429
Ensembl: ENSG00000121454
KO: hsa:89884
Nucleutide sequences
EMBL-CDS: AAL07260.1, BAC01272.1, AAK69169.1, AAH11759.1, AAM19349.1, AAK70923.1, AAM91896.1, BAB62817.1, ALQ34276.1
Ensembl_TRS: ENST00000263726
Protein sequencees
Ensembl_PRO: ENSP00000263726
RefSeq: XP_011508410.1, XP_016858244.1, XP_011508407.1, NP_203129.1, XP_011508408.1
Others
UniRef100: UniRef100_Q969G2
UniRef90: UniRef90_Q969G2
UniRef50: UniRef50_Q969G2
UniGene: Hs.658487
CCDS: CCDS1338.1

全选

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