Gene Gene information from NCBI Gene database.
Entrez ID 56944
Gene name Olfactomedin like 3
Gene symbol OLFML3
Synonyms (NCBI Gene)
HNOEL-isoOLF44
Chromosome 1
Chromosome location 1p13.2
Summary This gene encodes a member of the olfactomedin-like gene family which also includes genes encoding noelin, tiarin, myocilin, amassin, optimedin, photomedin, and latrophilin. The encoded protein is a secreted extracellular matrix glycoprotein with a C-term
miRNA miRNA information provided by mirtarbase database.
37
miRTarBase ID miRNA Experiments Reference
MIRT017928 hsa-miR-335-5p Microarray 18185580
MIRT1203277 hsa-miR-193a-3p CLIP-seq
MIRT1203278 hsa-miR-193b CLIP-seq
MIRT1203279 hsa-miR-3125 CLIP-seq
MIRT1203280 hsa-miR-3136-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IBA
GO:0007165 Process Signal transduction IBA
GO:1903561 Component Extracellular vesicle HDA 24769233
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610088 24956 ENSG00000116774
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NRN5
Protein name Olfactomedin-like protein 3 (HNOEL-iso) (hOLF44)
Protein function Secreted scaffold protein that plays an essential role in dorsoventral patterning during early development. Stabilizes axial formation by restricting chordin (CHRD) activity on the dorsal side. Acts by facilitating the association between the to
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02191 OLF 139 399 Olfactomedin-like domain Family
Tissue specificity TISSUE SPECIFICITY: Abundant in placenta, moderate in liver and heart, whereas fairly weak in other tissues examined. On term placenta, mainly localized extracellularly surrounding the syncytiotrophoblastic cells and very rarely expressed in the maternal
Sequence
Sequence length 406
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
8
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
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
EBV-positive nodal T- and NK-cell lymphoma Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPOTHYROIDISM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LIVER CIRRHOSIS, EXPERIMENTAL CTD
★★☆☆☆
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, 39380021
★☆☆☆☆
Found in Text Mining only
Fetal Growth Retardation Associate 40285515
★☆☆☆☆
Found in Text Mining only
Pre Eclampsia Inhibit 40285515
★☆☆☆☆
Found in Text Mining only