Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
93145
Gene name Gene Name - the full gene name approved by the HGNC.
Olfactomedin 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
OLFM2
Synonyms (NCBI Gene) Gene synonyms aliases
NOE2, NOELIN2, NOELIN2_V1, OlfC
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1203090 hsa-miR-1827 CLIP-seq
MIRT1203091 hsa-miR-3126-5p CLIP-seq
MIRT1203092 hsa-miR-3620 CLIP-seq
MIRT1203093 hsa-miR-4419a CLIP-seq
MIRT1203094 hsa-miR-4510 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25298399, 32296183
GO:0005576 Component Extracellular region IDA 21228389
GO:0005634 Component Nucleus IDA 25298399
GO:0005654 Component Nucleoplasm IDA
GO:0005737 Component Cytoplasm IDA 25298399
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
617492 17189 ENSG00000105088
Protein
UniProt ID O95897
Protein name Noelin-2 (Olfactomedin-2)
Protein function Involved in transforming growth factor beta (TGF-beta)-induced smooth muscle differentiation. TGF-beta induces expression and translocation of OLFM2 to the nucleus where it binds to SRF, causing its dissociation from the transcriptional represso
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12308 Noelin-1 25 121 Neurogenesis glycoprotein Family
PF02191 OLF 198 444 Olfactomedin-like domain Family
Tissue specificity TISSUE SPECIFICITY: Expressed in aortic smooth muscle (at protein level) (PubMed:25298399). In the fetus, expressed in the brain and ocular tissues including lens vesicle and optic cup (PubMed:27844144). {ECO:0000269|PubMed:25298399, ECO:0000269|PubMed:27
Sequence
Sequence length 454
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Colorectal cancer Colorectal Carcinoma rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 31545220
Fatty Liver Stimulate 35806447, 36982296
Hypoxia Associate 35711425
Inflammation Stimulate 35806447
Liver Failure Associate 36982296
Neoplasm Invasiveness Associate 31545220
Non alcoholic Fatty Liver Disease Stimulate 35806447
Non alcoholic Fatty Liver Disease Associate 36982296
Obesity Morbid Stimulate 36982296
Pneumonia Lipid Associate 36982296