Biology:WDR72
From HandWiki
Short description: Protein-coding gene in the species Homo sapiens
 Generic protein structure example |
WD repeat-containing protein 72 is a protein that in humans is encoded by the WDR72 gene.[1] WDR72 contains 7 WD40 repeats, which are predicted to form the blades of a 7 beta propeller structure.
Clinical significance
Mutations in this gene cause autosomal-recessive hypomaturation amelogenesis imperfecta.[2]
References
- ↑ "Entrez Gene: WD repeat domain 72". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=256764.
- ↑ "Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta". Am. J. Hum. Genet. 85 (5): 699–705. November 2009. doi:10.1016/j.ajhg.2009.09.014. PMID 19853237.
Further reading
- "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score". Mol. Med. 16 (7–8): 247–53. 2010. doi:10.2119/molmed.2009.00159. PMID 20379614.
- "Genome-wide association study of hematological and biochemical traits in a Japanese population". Nat. Genet. 42 (3): 210–5. 2010. doi:10.1038/ng.531. PMID 20139978.
- "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. 2004. doi:10.1101/gr.2596504. PMID 15489334.
- "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. 2004. doi:10.1038/ng1285. PMID 14702039.
- "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. 1996. doi:10.1101/gr.6.9.791. PMID 8889548.
- "A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose". Diabetes 59 (2): 539–49. 2010. doi:10.2337/db09-0653. PMID 19875614.
- "New loci associated with kidney function and chronic kidney disease". Nat. Genet. 42 (5): 376–84. 2010. doi:10.1038/ng.568. PMID 20383146.
- "Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta". Am. J. Hum. Genet. 85 (5): 699–705. 2009. doi:10.1016/j.ajhg.2009.09.014. PMID 19853237.
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