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3238 HOXD12

3238

HOXD12

homeobox D12

protein-coding

Homo sapiens

基因描述

Type Description
Definition homeobox D12

研究结论

Date Results Publications
2010-06-28 11:26:00 data show no significant difference in HOXD11, HOXD12 & HOXD13 genotype frequencies between the autism spectrum disorder & healthy controls, but one SNP in promoter region of HOXD11 was observed in only 4 patients with ASD 19540081
2010-02-08 11:43:00 In human embryonic stem cell (hESCs)differentiation, a 1.8kb region between HOXD11 and HOXD12 (D11.12) that is associated with PcG proteins was discovered, it shows alteration in nuclease sensitivity as hESCs differentiate. 20085705
2010-01-21 00:00:00 Data show that HOXD12 are important susceptible genes of idiopathic congenital talipes equinovarus. 16331564
2010-01-20 21:35:00 Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) 19938081
2009-08-12 21:34:00 Observational study of gene-disease association. (HuGE Navigator) 19540081

名称对应

Type IDs
Synonymous HOX4H
Gene
UniProtKB-ID: HXD12_HUMAN
UniprotKB: P35452
UniParc: UPI0000DBDD98, UPI0000EE2EA3
EMBL: CH471058, AF154915, AC009336, BC121103, BC121104
Ensembl: ENSG00000170178
KO: hsa:3238
Nucleutide sequences
EMBL-CDS: AAF79044.1, AAI21105.1, AAI21104.1, EAX11094.1
Ensembl_TRS: ENST00000406506
Protein sequencees
Ensembl_PRO: ENSP00000385586
RefSeq: NP_067016.3
Others
UniRef100: UniRef100_P35452
UniRef90: UniRef90_P35452
UniRef50: UniRef50_P35452
UniGene: Hs.450028
CCDS: CCDS46456.1

全选

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研究热度

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