Protein-coding gene in the species Homo sapiens
LOC118142757 Identifiers Aliases GUCA1A External IDs OMIM : 600364 ; MGI : 1922712 ; HomoloGene : 129540 ; GeneCards : GUCA1A ; OMA :GUCA1A - orthologs Wikidata
Guanylyl cyclase-activating protein 1 is an enzyme that in humans is encoded by the GUCA1A gene .[ 4] [ 5]
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(2001). "Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1" . Arch. Ophthalmol . 119 (1): 96–105. doi :10.1001/archopht.119.11.1667 PMID 11146732 . Wilkie SE, Li Y, Deery EC, et al. (2001). "Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy" . Am. J. Hum. Genet . 69 (3): 471–80. doi :10.1086/323265 . PMC 1235478 PMID 11484154 . Hwang JY, Koch KW (2002). "Calcium- and myristoyl-dependent properties of guanylate cyclase-activating protein-1 and protein-2". Biochemistry . 41 (43): 13021–8. doi :10.1021/bi026618y . PMID 12390029 . Hwang JY, Koch KW (2002). "The myristoylation of the neuronal Ca2+ -sensors guanylate cyclase-activating protein 1 and 2". Biochim. Biophys. Acta . 1600 (1–2): 111–7. doi :10.1016/S1570-9639(02)00451-X . PMID 12445466 . Strausberg RL, Feingold EA, Grouse LH, et al. (2003). 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"A novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD)" . Invest. Ophthalmol. Vis. Sci . 46 (4): 1124–32. doi :10.1167/iovs.04-1431 . PMC 1352313 PMID 15790869 . Michaelides M, Wilkie SE, Jenkins S, et al. (2005). "Mutation in the gene GUCA1A, encoding guanylate cyclase-activating protein 1, causes cone, cone-rod, and macular dystrophy". Ophthalmology . 112 (8): 1442–7. doi :10.1016/j.ophtha.2005.02.024 . PMID 15953638 .
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