Gene Gene information from NCBI Gene database.
Entrez ID 118427
Gene name Olfactomedin 3
Gene symbol OLFM3
Synonyms (NCBI Gene)
NOE3NOELIN3OPTIMEDIN
Chromosome 1
Chromosome location 1p21.1
miRNA miRNA information provided by mirtarbase database.
18
miRTarBase ID miRNA Experiments Reference
MIRT439119 hsa-miR-10b-5p 3'LIFE 25074381
MIRT439119 hsa-miR-10b-5p 3'LIFE 25074381
MIRT1203100 hsa-miR-4662a-5p CLIP-seq
MIRT2058633 hsa-miR-1208 CLIP-seq
MIRT2058634 hsa-miR-3127-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 12019210, 25416956, 31515488, 32296183
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IBA
GO:0005615 Component Extracellular space IEA
GO:0005794 Component Golgi apparatus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607567 17990 ENSG00000118733
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96PB7
Protein name Noelin-3 (Olfactomedin-3) (Optimedin)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12308 Noelin-1 46 145 Neurogenesis glycoprotein Family
PF02191 OLF 222 468 Olfactomedin-like domain Family
Tissue specificity TISSUE SPECIFICITY: In the eye, expressed in trabecular meshwork and neural retina; in non-ocular tissues, expressed in brain and lung. {ECO:0000269|PubMed:12019210}.
Sequence
Sequence length 478
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
12
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARPAL TUNNEL SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DISEASE OF PERITONEUM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alzheimer Disease Associate 32711556
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Multiple Sclerosis Associate 24511991
★☆☆☆☆
Found in Text Mining only
Obesity Associate 37800791
★☆☆☆☆
Found in Text Mining only
Parkinson Disease Associate 24511991
★☆☆☆☆
Found in Text Mining only
Urinary Bladder Neoplasms Associate 37800791
★☆☆☆☆
Found in Text Mining only