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79816 TLE6

79816

TLE6

TLE family member 6, subcortical maternal complex member

protein-coding

Homo sapiens

基因描述

Type Description
Definition TLE family member 6, subcortical maternal complex member

研究结论

Date Results Publications
2020-12-05 13:03:00 Expanding the genetic and phenotypic spectrum of female infertility caused by TLE6 mutations. 31897846
2016-07-16 11:13:00 In this first report of a human defect in a member of the subcortical maternal subcritical maternal complex, we show that the TLE6 mutation is gender-specific and leads to the earliest known human embryonic lethality phenotype 26537248
2014-07-12 10:52:00 transcriptional programmes regulated by FOXG1 and Groucho/TLE are important for BTIC-initiated brain tumour growth, implicating FOXG1 and Groucho/TLE in GBM tumourigenesis 24356439
2010-01-21 00:00:00 Expression of Tle6-like in colon cancer cells increased cell proliferation, colony-formation, cell migration, and xenograft tumorgenicity. 18551179

名称对应

Type IDs
Synonymous GRG6, PREMBL
Gene
UniProtKB-ID: TLE6_HUMAN, Q6PJM9_HUMAN
UniprotKB: Q9H808, Q6PJM9
UniParc: UPI00001BDA02, UPI000007242D, UPI000059D62B
EMBL: BC013986, BC020206, AC006277, AK024071, BC007215, AC007766
Ensembl: ENSG00000104953
KO: hsa:79816
Nucleutide sequences
EMBL-CDS: BAB14815.1, AAH07215.1, AAH20206.1, AAH13986.1
Ensembl_TRS: ENST00000246112, ENST00000452088
Protein sequencees
Ensembl_PRO: ENSP00000246112, ENSP00000406893
RefSeq: XP_024307490.1, XP_024307491.1, XP_024307492.1, NP_079036.1, XP_011526603.1, XP_011526602.1, XP_005259702.1, NP_001137458.1
Others
UniRef100: UniRef100_Q9H808, UniRef100_Q6PJM9
UniRef90: UniRef90_A0A2R9A736, UniRef90_Q9H808
UniRef50: UniRef50_Q9H808, UniRef50_A0A2R9A736
UniGene: Hs.334507
CCDS: CCDS12100.1, CCDS45910.1

全选

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