GNAT2
المظهر
GNAT2 (G protein subunit alpha transducin 2) هوَ بروتين يُشَفر بواسطة جين GNAT2 في الإنسان.[1][2]
الوظيفة
[عدل]هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
الأهمية السريرية
[عدل]هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
المراجع
[عدل]- ^ Morris TA، Fong SL (أكتوبر 1993). "Characterization of the gene encoding human cone transducin alpha-subunit (GNAT2)". Genomics. ج. 17 ع. 2: 442–8. DOI:10.1006/geno.1993.1345. PMID:8406495.
- ^ "Entrez Gene: GNAT2 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2". مؤرشف من الأصل في 2010-12-05.
قراءة متعمقة
[عدل]- Wilkie TM، Gilbert DJ، Olsen AS، وآخرون (1993). "Evolution of the mammalian G protein alpha subunit multigene family". Nat. Genet. ج. 1 ع. 2: 85–91. DOI:10.1038/ng0592-85. PMID:1302014.
- Arshavsky VYu؛ Gray-Keller MP؛ Bownds MD (1991). "cGMP suppresses GTPase activity of a portion of transducin equimolar to phosphodiesterase in frog rod outer segments. Light-induced cGMP decreases as a putative feedback mechanism of the photoresponse". J. Biol. Chem. ج. 266 ع. 28: 18530–7. PMID:1655754.
- Mazzoni MR، Malinski JA، Hamm HE (1991). "Structural analysis of rod GTP-binding protein, Gt. Limited proteolytic digestion pattern of Gt with four proteases defines monoclonal antibody epitope". J. Biol. Chem. ج. 266 ع. 21: 14072–81. PMID:1713215.
- Fawzi AB، Fay DS، Murphy EA، وآخرون (1991). "Rhodopsin and the retinal G-protein distinguish among G-protein beta gamma subunit forms". J. Biol. Chem. ج. 266 ع. 19: 12194–200. PMID:1905716.
- Kubo M، Hirano T، Kakinuma M (1991). "Molecular cloning and sequence analysis of cDNA and genomic DNA for the human cone transducin alpha subunit". FEBS Lett. ج. 291 ع. 2: 245–8. DOI:10.1016/0014-5793(91)81294-I. PMID:1936270.
- Lerea CL، Bunt-Milam AH، Hurley JB (1990). "Alpha transducin is present in blue-, green-, and red-sensitive cone photoreceptors in the human retina". Neuron. ج. 3 ع. 3: 367–76. DOI:10.1016/0896-6273(89)90261-4. PMID:2534964.
- Blatt C، Eversole-Cire P، Cohn VH، وآخرون (1988). "Chromosomal localization of genes encoding guanine nucleotide-binding protein subunits in mouse and human". Proc. Natl. Acad. Sci. U.S.A. ج. 85 ع. 20: 7642–6. DOI:10.1073/pnas.85.20.7642. PMC:282248. PMID:2902634.
- Buss JE، Mumby SM، Casey PJ، وآخرون (1987). "Myristoylated alpha subunits of guanine nucleotide-binding regulatory proteins". Proc. Natl. Acad. Sci. U.S.A. ج. 84 ع. 21: 7493–7. DOI:10.1073/pnas.84.21.7493. PMC:299322. PMID:3118369.
- Hirano T (1994). "[Analysis of cell specific transcription of the human cone transducin alpha subunit gene]". Hokkaido Igaku Zasshi. ج. 68 ع. 6: 885–93. PMID:8112713.
- Morris TA، Fong WB، Ward MJ، وآخرون (1997). "Localization of upstream silencer elements involved in the expression of cone transducin alpha-subunit (GNAT2)". Invest. Ophthalmol. Vis. Sci. ج. 38 ع. 1: 196–206. PMID:9008644.
- Kohl S، Baumann B، Rosenberg T، وآخرون (2002). "Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia". Am. J. Hum. Genet. ج. 71 ع. 2: 422–5. DOI:10.1086/341835. PMC:379175. PMID:12077706.
- Aligianis IA، Forshew T، Johnson S، وآخرون (2002). "Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2)". J. Med. Genet. ج. 39 ع. 9: 656–60. DOI:10.1136/jmg.39.9.656. PMC:1735242. PMID:12205108.
- Strausberg RL، Feingold EA، Grouse LH، وآخرون (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. ج. 99 ع. 26: 16899–903. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
- Piña AL، Baumert U، Loyer M، Koenekoop RK (2004). "A three base pair deletion encoding the amino acid (lysine-270) in the alpha-cone transducin gene". Mol. Vis. ج. 10: 265–71. PMID:15094710.
- Gerhard DS، Wagner L، Feingold EA، وآخرون (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. ج. 14 ع. 10B: 2121–7. DOI:10.1101/gr.2596504. PMC:528928. PMID:15489334.
- Rosenberg T، Baumann B، Kohl S، وآخرون (2005). "Variant phenotypes of incomplete achromatopsia in two cousins with GNAT2 gene mutations". Invest. Ophthalmol. Vis. Sci. ج. 45 ع. 12: 4256–62. DOI:10.1167/iovs.04-0317. PMID:15557429.