Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
56944
Gene name Gene Name - the full gene name approved by the HGNC.
Olfactomedin like 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
OLFML3
Synonyms (NCBI Gene) Gene synonyms aliases
HNOEL-iso, OLF44
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p13.2
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0007275 Process Multicellular organism development IEA
GO:1903561 Component Extracellular vesicle HDA 24769233
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610088 24956 ENSG00000116774
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Epilepsy Epilepsy rs113994140, rs28937874, rs1589762127, rs104894166, rs28939075, rs2134001459, rs104894167, rs119488099, rs119488100, rs387906420, rs121917752, rs121918622, rs281865564, rs387907313, rs397514670
View all (165 more)
30868120
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 32711556, 39380021
Fetal Growth Retardation Associate 40285515
Pre Eclampsia Inhibit 40285515