TLE6 (TLE family member 6, subcortical maternal complex member)

2008-08-01  

Identity

HGNC
LOCATION
19p13.3
LOCUSID
ALIAS
GRG6,PREMBL
FUSION GENES

Other Information

Locus ID:

NCBI: 79816
MIM: 612399
HGNC: 30788
Ensembl: ENSG00000104953

Variants:

dbSNP: 79816
ClinVar: 79816
TCGA: ENSG00000104953
COSMIC: TLE6

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000104953ENST00000246112Q9H808
ENSG00000104953ENST00000452088Q9H808
ENSG00000104953ENST00000453329C9J532
ENSG00000104953ENST00000482627K7ENW8

Expression (GTEx)

0
5
10
15

References

Pubmed IDYearTitleCitations
265372482015TLE6 mutation causes the earliest known human embryonic lethality.26
243564392013Transcription factors FOXG1 and Groucho/TLE promote glioblastoma growth.20
185511792008Novel roles for MLH3 deficiency and TLE6-like amplification in DNA mismatch repair-deficient gastrointestinal tumorigenesis and progression.15

Citation

Dessen P

TLE6 (TLE family member 6, subcortical maternal complex member)

Atlas Genet Cytogenet Oncol Haematol. 2008-08-01

Online version: http://atlasgeneticsoncology.org/gene/50289/tle6