RNF212B (ring finger protein 212B)

2014-11-01  

Identity

HGNC
LOCATION
14q11.2
LOCUSID
ALIAS
C14orf164

Other Information

Locus ID:

NCBI: 100507650
HGNC: 20438
Ensembl: ENSG00000215277

Variants:

dbSNP: 100507650
ClinVar: 100507650
TCGA: ENSG00000215277
COSMIC: RNF212B

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000215277ENST00000399905A8MVE6
ENSG00000215277ENST00000399910A8MTL3
ENSG00000215277ENST00000430154A8MTL3
ENSG00000215277ENST00000470456H0YJB3
ENSG00000215277ENST00000492621G3V2N7

Expression (GTEx)

0
1
2
3
4
5
6
7

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
371241372023A pathogenic variant in the uncharacterized RNF212B gene results in severe aneuploidy male infertility and repeated IVF failure.2
371241372023A pathogenic variant in the uncharacterized RNF212B gene results in severe aneuploidy male infertility and repeated IVF failure.2

Citation

Dessen P

RNF212B (ring finger protein 212B)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/72703/css/lib/gene-explorer/