Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10439
Gene name Gene Name - the full gene name approved by the HGNC.
Olfactomedin 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
OLFM1
Synonyms (NCBI Gene) Gene synonyms aliases
AMY, NOE1, NOELIN1, OlfA
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q34.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene product shares extensive sequence similarity with the rat neuronal olfactomedin-related ER localized protein. While the exact function of the encoded protein is not known, its abundant expression in brain suggests that it may have an essential r
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT733175 hsa-miR-200a-3p RNA-seq, qRT-PCR 33968190
MIRT1203020 hsa-miR-1206 CLIP-seq
MIRT1203021 hsa-miR-1224-5p CLIP-seq
MIRT1203022 hsa-miR-1271 CLIP-seq
MIRT1203023 hsa-miR-1289 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003190 Process Atrioventricular valve formation ISS
GO:0005515 Function Protein binding IPI 17043677, 31413325
GO:0005615 Component Extracellular space ISS
GO:0005783 Component Endoplasmic reticulum ISS
GO:0007399 Process Nervous system development IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605366 17187 ENSG00000130558
Protein
UniProt ID Q99784
Protein name Noelin (Neuronal olfactomedin-related ER localized protein) (Olfactomedin-1)
Protein function Contributes to the regulation of axonal growth in the embryonic and adult central nervous system by inhibiting interactions between RTN4R and LINGO1. Inhibits RTN4R-mediated axon growth cone collapse (By similarity). May play an important role i
PDB 4XAT , 6QHJ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12308 Noelin-1 54 153 Neurogenesis glycoprotein Family
PF02191 OLF 230 476 Olfactomedin-like domain Family
Sequence
Sequence length 485
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Prostate cancer Malignant neoplasm of prostate rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 19208208
Unknown
Disease term Disease name Evidence References Source
Colorectal Cancer Colorectal Cancer In summary, our data strongly demonstrated that upregulation of GRB7 conferred MEKi resistance in CRC cells with KRAS mutations by mediating RTK signaling through the recruitment of PLK1. GWAS, CBGDA
Metabolic Syndrome Metabolic Syndrome GWAS
Oligodendroglioma Oligodendroglioma GWAS
Insomnia Insomnia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Leukoplakia Associate 36444596
Neuroblastoma Associate 35538114
Renal Insufficiency Stimulate 38195505
Sarcoma Ewing Associate 25025207
Smoke Inhalation Injury Associate 32564237