OLFM4
protein-coding gene in the species Homo sapiens
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Summary
OLFM4 is a gene[1]. OLFM4 ranks in the top 2% of gene entities by monthly Wikipedia readership (44 views/month).[2]
Key Facts
- Subclass of: protein-coding gene[3]
- HomoloGene ID: 4684[4]
- Genomic start: 53602894[5], 53028813[6]
- Genomic end: 53052057[7], 53626192[8]
- Ortholog: Olfm4[9], olfm4.1[10], olfm4.2[11]
- Encodes: Olfactomedin 4[12]
- Found in taxon: Homo sapiens[13]
- Chromosome: human chromosome 13[14]
- Genetic association: amyotrophic lateral sclerosis[15]
- Strand orientation: forward strand[16]
- Exact match: http://identifiers.org/ncbigene/10562[17]
- Cytogenetic location: 13q14.3[18]
- Expressed in: urethra[19], jejunal mucosa[20], duodenum[21], mucosa of ileum[22], beta cell[23], rectum[24], cecum[25], appendix[26], mucosa of transverse colon[27], bone marrow[28]
Why It Matters
OLFM4 is known by 10 alternative names across languages and contexts.[29]