| Entrez gene ID | | 3998 |
| Official gene symbol | | LMAN1 |
| Full name | | lectin, mannose-binding, 1 |
| Aliases | | ,ERGIC-53,ERGIC53,F5F8D,FMFD1,MCFD1,MR60,gp58, |
| Gene summary | | The protein encoded by this gene is a type I integral membrane protein localized in the intermediate region between the endoplasmic reticulum and the Golgi, presumably recycling between the two compartments. The protein is a mannose-specific lectin and is a member of a novel family of plant lectin homologs in the secretory pathway of animal cells. Mutations in the gene are associated with a coagulation defect. Using positional cloning, the gene was identified as the disease gene leading to combined factor V-factor VIII deficiency, a rare, autosomal recessive disorder in which both coagulation factors V and VIII are diminished. [provided by RefSeq] |
| Location | | Chromosome: 18 Locus: 18q21.3-q22 |
| Gene position | | 57026508 - 56995055 Map Viewer |
| Gene orientation | | minus |
| Gene size | | 31454 bp |
| Gene sequence |
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| OMIM ID | | 601567 |
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