LRIT3 (leucine rich repeat, Ig-like and transmembrane domains 3)

2014-11-01  

Identity

HGNC
LOCATION
4q25
LOCUSID
ALIAS
CSNB1F,FIGLER4

Other Information

Locus ID:

NCBI: 345193
MIM: 615004
HGNC: 24783
Ensembl: ENSG00000183423

Variants:

dbSNP: 345193
ClinVar: 345193
TCGA: ENSG00000183423
COSMIC: LRIT3

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000183423ENST00000327908A0A0A0MR64
ENSG00000183423ENST00000594814Q3SXY7

Expression (GTEx)

0
1
2

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
203320992010A systematic gene-based screen of chr4q22-q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom counts.8
232462932013Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.0
274285142017Mutation screening of the LRIT3, CABP4, and GPR179 genes in Chinese patients with Schubert-Bornschein congenital stationary night blindness.0
283343772017LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells.0

Citation

Dessen P

LRIT3 (leucine rich repeat, Ig-like and transmembrane domains 3)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/68585/lrit3