Cadherin-23 is a protein that in humans is encoded by the CDH23 gene. This gene is a member of the cadherin superfamily, genes encoding calcium dependent...
10 KB (1,364 words) - 16:01, 13 October 2024
CDH23 antisense RNA 1 is a protein that in humans is encoded by the CDH23-AS1 gene. GRCh38: Ensembl release 89: ENSG00000223817 – Ensembl, May 2017 "Human...
398 bytes (52 words) - 16:03, 13 October 2024
type I can be caused by mutations in any one of several different genes: CDH23, MYO7A, PCDH15, USH1C and USH1G. These genes function in the development...
34 KB (3,528 words) - 20:30, 29 October 2024
worldwide SMPD1 Usher syndrome 1:23000 in the U.S. 1:28000 in Norway 1:12500 in Germany CDH23, CLRN1, DFNB31, GPR98, MYO7A, PCDH15, USH1C, USH1G, USH2A...
99 KB (10,142 words) - 15:38, 13 October 2024
monosomy 1:2,000-2,500 live female births Usher syndrome MYO7A, USH1C, CDH23, PCDH15, USH1G, USH2A, GPR98, DFNB31, CLRN1 recessive 3-6:100,000 (type...
42 KB (983 words) - 18:14, 6 October 2024
Cyclin-Y CDC123: Cell division cycle protein 123 homolog CDH23: cadherin-like 23 CDH23-AS1: CDH23 antisense RNA 1 CDNF: cerebral dopamine neurotrophic factor...
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HGNC:1758 Q9H159 2639 CDH20 HGNC:1760 Q9HBT6 2640 CDH22 HGNC:13251 Q9UJ99 2641 CDH23 HGNC:13733 Q9H251 2642 CDH24 HGNC:14265 Q86UP0 2643 CDH26 HGNC:15902 Q8IXH8...
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Kachar, Bechara; Steel, Karen P.; Noben-Trauth, Konrad (2001). "Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer...
7 KB (533 words) - 13:27, 27 October 2024
localized and of these fifteen have been cloned. Mutations in the ACTG1, CABP2, CDH23, CLDN14, COCH, COL11A2, DFNA5, ESPN, EYA4, GJB2, GJB6, KCNQ4, MYO15A, MYO6...
20 KB (1,858 words) - 21:17, 11 October 2024
cadherin 18, type 2 CDH19 – cadherin 19, type 2 CDH20 – cadherin 20, type 2 CDH23 – cadherin 23 (neurosensory epithelium) CDH22, CDH24, CDH26, CDH28 CELSR1...
32 KB (3,594 words) - 21:23, 2 October 2024