ANKRD31 (ankyrin repeat domain 31)

2014-11-01  

Identity

HGNC
LOCATION
5q13.3
LOCUSID
ALIAS
-
FUSION GENES

Other Information

Locus ID:

NCBI: 256006
MIM: 618423
HGNC: 26853
Ensembl: ENSG00000145700

Variants:

dbSNP: 256006
ClinVar: 256006
TCGA: ENSG00000145700
COSMIC: ANKRD31

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000145700ENST00000274361Q8N7Z5
ENSG00000145700ENST00000506364D6RJB7

Expression (GTEx)

0
1
2
3
4
5
6
7
8

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
342574192021Pathogenic variants of meiotic double strand break (DSB) formation genes PRDM9 and ANKRD31 in premature ovarian insufficiency.6
342574192021Pathogenic variants of meiotic double strand break (DSB) formation genes PRDM9 and ANKRD31 in premature ovarian insufficiency.6
275416422016Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype.31
275416422016Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype.31

Citation

Dessen P

ANKRD31 (ankyrin repeat domain 31)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/60336/favicon/favicon-16x16.png