TM4SF20 (transmembrane 4 L six family member 20)

2016-08-01  

Identity

HGNC
LOCATION
2q36.3
LOCUSID
ALIAS
PRO994,SLI5,TCCE518

Other Information

Locus ID:

NCBI: 79853
MIM: 615404
HGNC: 26230
Ensembl: ENSG00000168955

Variants:

dbSNP: 79853
ClinVar: 79853
TCGA: ENSG00000168955
COSMIC: TM4SF20

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000168955ENST00000304568Q53R12
ENSG00000168955ENST00000449706C9JES4

Expression (GTEx)

0
5
10
15
20
25
30
35
40
45
50

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
204797602011Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.100
238103812013TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.14
274992932016Inverting the Topology of a Transmembrane Protein by Regulating the Translocation of the First Transmembrane Helix.9
274992932016Inverting the Topology of a Transmembrane Protein by Regulating the Translocation of the First Transmembrane Helix.9
308087122019Identification of residues critical for topology inversion of the transmembrane protein TM4SF20 through regulated alternative translocation.1

Citation

Dessen P

TM4SF20 (transmembrane 4 L six family member 20)

Atlas Genet Cytogenet Oncol Haematol. 2016-08-01

Online version: http://atlasgeneticsoncology.org/gene/55911/tm4sf20