Gene Symbol | FAM20A |
Entrez Gene ID | 54757 |
Full Name | FAM20A, golgi associated secretory pathway pseudokinase |
Synonyms | AI1G,AIGFS,FP2747 |
General protein information |
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Gene Type | protein-coding |
Organism | Homo sapiens(human) |
Genome | |
Summary | This locus encodes a protein that is likely secreted and may function in hematopoiesis. A mutation at this locus has been associated with amelogenesis imperfecta and gingival hyperplasia syndrome. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Aug 2011]. |
Disorder MIM: | |
Disorder Html: | Amelogenesis imperfecta, type IG (enamel-renal syndrome), 204690 (3) |