'''Guanylyl cyclase-activating protein 1''' is an [[enzyme]] that in humans is encoded by the ''GUCA1A'' [[gene]].<ref name="pmid9425234">{{cite journal |vauthors=Payne AM, Downes SM, Bessant DA, Taylor R, Holder GE, Warren MJ, Bird AC, Bhattacharya SS | title = A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1 | journal = Hum Mol Genet | volume = 7 | issue = 2 | pages = 273–7 |date=Mar 1998 | pmid = 9425234 | pmc = | doi =10.1093/hmg/7.2.273 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: GUCA1A guanylate cyclase activator 1A (retina)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2978| accessdate = }}</ref>
'''Guanylyl cyclase-activating protein 1''' is an [[enzyme]] that in humans is encoded by the ''GUCA1A'' [[gene]].<ref name="pmid9425234">{{cite journal |vauthors=Payne AM, Downes SM, Bessant DA, Taylor R, Holder GE, Warren MJ, Bird AC, Bhattacharya SS | title = A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1 | journal = Hum Mol Genet | volume = 7 | issue = 2 | pages = 273–7 |date=Mar 1998 | pmid = 9425234 | pmc = | doi =10.1093/hmg/7.2.273 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: GUCA1A guanylate cyclase activator 1A (retina)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2978| accessdate = }}</ref>
Guanylyl cyclase-activating protein 1 is an enzyme that in humans is encoded by the GUCA1Agene.[1][2]
References
↑Payne AM, Downes SM, Bessant DA, Taylor R, Holder GE, Warren MJ, Bird AC, Bhattacharya SS (Mar 1998). "A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1". Hum Mol Genet. 7 (2): 273–7. doi:10.1093/hmg/7.2.273. PMID9425234.
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Downes SM, Holder GE, Fitzke FW, et al. (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. PMID11146732.
Mungall AJ, Palmer SA, Sims SK, et al. (2003). "The DNA sequence and analysis of human chromosome 6". Nature. 425 (6960): 805–11. doi:10.1038/nature02055. PMID14574404.
Peshenko IV, Moiseyev GP, Olshevskaya EV, Dizhoor AM (2004). "Factors that determine Ca2+ sensitivity of photoreceptor guanylyl cyclase. Kinetic analysis of the interaction between the Ca2+-bound and the Ca2+-free guanylyl cyclase activating proteins (GCAPs) and recombinant photoreceptor guanylyl cyclase 1 (RetGC-1)". Biochemistry. 43 (43): 13796–804. doi:10.1021/bi048943m. PMID15504042.
Jiang L, Katz BJ, Yang Z, et al. (2005). "Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A)". Mol. Vis. 11: 143–51. PMID15735604.
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. PMID15953638.
