DISP1 (dispatched RND transporter family member 1)

2013-08-01  

Identity

HGNC
DISP1
LOCATION
1q41
LOCUSID
84976
ALIAS
DISPA
FUSION GENES
Show Gene Fusions

Other Information

Locus ID:

NCBI: 84976
MIM: 607502
HGNC: 19711
Ensembl: ENSG00000228106

Variants:

dbSNP: 84976
ClinVar: 84976
TCGA: ENSG00000228106
COSMIC: DISP1

RNA/Proteins

References

Pubmed IDYearTitleCitations
203796142010Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.62
191841102009Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans.25
227331342013The hedgehog processing pathway is required for NSCLC growth and survival.23
207993232010Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH.17
209518452011New cases and refinement of the critical region in the 1q41q42 microdeletion syndrome.10
258243022016Whole-genome association analysis of treatment response in obsessive-compulsive disorder.8
299536822018Pharmacogenetic evaluation of a DISP1 gene variant in antidepressant treatment of obsessive-compulsive disorder.1

Citation

Dessen P

DISP1 (dispatched RND transporter family member 1)

Atlas Genet Cytogenet Oncol Haematol. 2013-08-01

Online version: http://atlasgeneticsoncology.org/gene/53490/disp1