WDR37 (WD repeat domain 37)

2014-11-01  

Identity

HGNC
LOCATION
10p15.3
LOCUSID
ALIAS
NOCGUS
FUSION GENES

Other Information

Locus ID:

NCBI: 22884
MIM: 618586
HGNC: 31406
Ensembl: ENSG00000047056

Variants:

dbSNP: 22884
ClinVar: 22884
TCGA: ENSG00000047056
COSMIC: WDR37

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000047056ENST00000263150Q9Y2I8
ENSG00000047056ENST00000358220Q9Y2I8
ENSG00000047056ENST00000381329E7EQ49
ENSG00000047056ENST00000436154C9JGR9
ENSG00000047056ENST00000620998A0A087WTQ2
ENSG00000047056ENST00000650072A0A3B3IT47

Expression (GTEx)

0
5
10
15
20
25
30
35

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
203831462010New loci associated with kidney function and chronic kidney disease.337
203796142010Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.62
206770142010An approach based on a genome-wide association study reveals candidate loci for narcolepsy.16
201983152010Association of genetic variants with hemorrhagic stroke in Japanese individuals.11
197248952009Association of gene polymorphisms with chronic kidney disease in Japanese individuals.7
198512962010Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals.3
313275082019De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia.3
313275102019De Novo Missense Variants in WDR37 Cause a Severe Multisystemic Syndrome.3

Citation

Dessen P

WDR37 (WD repeat domain 37)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/75710/wdr37