OLFM2 (olfactomedin 2)

2014-11-01  

Identity

HGNC
LOCATION
19p13.2
LOCUSID
ALIAS
NOE2,NOELIN2,NOELIN2_V1,OlfC
FUSION GENES

Other Information

Locus ID:

NCBI: 93145
MIM: 617492
HGNC: 17189
Ensembl: ENSG00000105088

Variants:

dbSNP: 93145
ClinVar: 93145
TCGA: ENSG00000105088
COSMIC: OLFM2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000105088ENST00000264833O95897
ENSG00000105088ENST00000590841K7EIS8
ENSG00000105088ENST00000592448K7ELC6
ENSG00000105088ENST00000593091K7EKW2

Expression (GTEx)

0
50
100
150

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
171221262006SNPs and interaction analyses of noelin 2, myocilin, and optineurin genes in Japanese patients with open-angle glaucoma.22
171221262006SNPs and interaction analyses of noelin 2, myocilin, and optineurin genes in Japanese patients with open-angle glaucoma.22
252983992014Olfactomedin 2, a novel regulator for transforming growth factor-β-induced smooth muscle differentiation of human embryonic stem cell-derived mesenchymal cells.9
278441442017Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders.3
295538612018Increased plasma olfactomedin 2 after interventional therapy is a predictor for restenosis in lower extremity arteriosclerosis obliterans patients.0

Citation

Dessen P

OLFM2 (olfactomedin 2)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/71113/olfm2