Gene: Cdh23 (cadherin 23 (otocadherin)) Mus musculus
Analyze
Symbol:
Cdh23
Name:
cadherin 23 (otocadherin)
Description:
ENCODES a protein that exhibits protein N-terminus binding (ortholog); INVOLVED IN adult locomotory behavior; auditory receptor cell stereocilium organization; inner ear auditory receptor cell differentiation; PARTICIPATES IN auditory mechanotransduction pathway; retinitis pigmentosa pathway; ASSOCIATED WITH abnormal auditory brainstem response; abnormal cochlea morphology; abnormal cochlear ganglion morphology; ASSOCIATED WITH Presbycusis; retinal disease; Usher syndrome type 1D; FOUND IN centrosome; cochlear hair cell ribbon synapse; kinocilium; INTERACTS WITH 17alpha-ethynylestradiol; 2,2',4,4',5,5'-hexachlorobiphenyl; 2,2',5,5'-tetrachlorobiphenyl
Type:
protein-coding
RefSeq Status:
VALIDATED
Also known as:
4930542A03Rik; age related hearing loss 1; ahl; ahl1; bob; bobby; bus; bustling; cadherin-23; mdfw; modifier of deaf waddler; nmf112; nmf181; nmf252; otocadherin; sals; USH1D; v; waltzer
Orthologs:
Species
Gene symbol and name
Data Source
Assertion derived from
less info ...
Orthologs 1
Homo sapiens (human):
CDH23 (cadherin related 23) HGNC
EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OrthoDB, OrthoMCL, Panther
Rattus norvegicus (Norway rat):
Cdh23 (cadherin-related 23) HGNC
NCBI, HomoloGene, Inparanoid, Panther, OrthoDB, Ensembl
Chinchilla lanigera (long-tailed chinchilla):
Cdh23 (cadherin related 23) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Pan paniscus (bonobo/pygmy chimpanzee):
CDH23 (cadherin related 23) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Canis lupus familiaris (dog):
CDH23 (cadherin related 23) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):
Cdh23 (cadherin related 23) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Sus scrofa (pig):
CDH23 (cadherin related 23) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Other homologs 2
Homo sapiens (human):
FAT2 (FAT atypical cadherin 2) HGNC
OrthoMCL
Homo sapiens (human):
FAT4 (FAT atypical cadherin 4) HGNC
OrthoMCL
Homo sapiens (human):
DCHS1 (dachsous cadherin-related 1) HGNC
OrthoMCL
Homo sapiens (human):
DCHS2 (dachsous cadherin-related 2) HGNC
OrthoMCL
Alliance orthologs 3
Rattus norvegicus (Norway rat):
Cdh23 (cadherin-related 23)
Alliance
DIOPT (Hieranoid, InParanoid, OrthoFinder, OrthoInspector, PhylomeDB)
Homo sapiens (human):
CDH23 (cadherin related 23)
Alliance
DIOPT (Ensembl Compara, HGNC, Hieranoid, InParanoid, OrthoFinder, OrthoInspector, PANTHER, PhylomeDB, Roundup)
Danio rerio (zebrafish):
cdh23 (cadherin-related 23)
Alliance
DIOPT (Ensembl Compara, Hieranoid, OMA, OrthoFinder, PANTHER, PhylomeDB, TreeFam)
Caenorhabditis elegans (roundworm):
cdh-3
Alliance
DIOPT (OMA, TreeFam)
Latest Assembly:
GRCm38 - Mouse Genome Assembly GRCm38
Position:
Mouse Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl GRCm38 10 60,302,748 - 60,696,513 (-) NCBI GRCm38 GRCm38 mm10 GRCm38 MGSCv37 10 59,766,022 - 60,159,238 (-) NCBI GRCm37 mm9 NCBIm37 MGSCv36 10 59,698,731 - 60,052,690 (-) NCBI mm8 Celera 10 61,399,607 - 61,796,629 (-) NCBI Celera Cytogenetic Map 10 B4 NCBI cM Map 10 30.11 NCBI
JBrowse:
View Region in Genome Browser (JBrowse)
Model
Disease Annotations
Imported Annotations - ClinVar
autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:12075507 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:11090341 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:11138009 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:12075507 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:17850630 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:22899989 autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:25279224 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:18429043 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:24033266 , PMID:26969326 autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:21940737 autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:11090341 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:16679490 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:17850630 , PMID:22899989 autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:25741868 autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:24033266 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:11857743 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:24033266 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:24033266 , PMID:25741868 autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:23804846 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:16679490 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:20146813 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness, autosomal recessive 12 ClinVar PMID:25963016 autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601386 ClinVar PMID:19888295 more ... autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601386 ClinVar PMID:12522556 autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601386 ClinVar PMID:11090341 autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601386 ClinVar PMID:12910270 , PMID:15829536 autosomal recessive nonsyndromic deafness 12 ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601386 ClinVar PMID:24033266 combined saposin deficiency ISO RGD:733851 8554872 ClinVar Annotator: match by term: PROSAPOSIN DEFICIENCY ClinVar PMID:25741868 combined saposin deficiency ISO RGD:733851 8554872 ClinVar Annotator: match by term: Combined saposin deficiency ClinVar PMID:24033266 , PMID:25741868 combined saposin deficiency ISO RGD:733851 8554872 ClinVar Annotator: match by term: Combined saposin deficiency ClinVar PMID:18429043 , PMID:24033266 combined saposin deficiency ISO RGD:733851 8554872 ClinVar Annotator: match by term: Combined saposin deficiency ClinVar PMID:24033266 combined saposin deficiency ISO RGD:733851 8554872 ClinVar Annotator: match by term: PROSAPOSIN DEFICIENCY ClinVar PMID:18429043 more ... combined saposin deficiency ISO RGD:733851 8554872 ClinVar Annotator: match by term: Combined saposin deficiency ClinVar PMID:25991456 combined saposin deficiency ISO RGD:733851 8554872 ClinVar Annotator: match by term: PROSAPOSIN DEFICIENCY ClinVar Deafness ISO RGD:733851 8554872 ClinVar Annotator: match by term: Deafness ClinVar fundus dystrophy ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinal dystrophy ClinVar fundus dystrophy ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinal dystrophy ClinVar PMID:30718709 genetic disease ISO RGD:733851 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:12075507 more ... genetic disease ISO RGD:733851 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:11090341 more ... genetic disease ISO RGD:733851 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:24033266 more ... genetic disease ISO RGD:733851 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:11090341 , PMID:11138009 growth hormone secreting pituitary adenoma ISO RGD:733851 8554872 ClinVar Annotator: match by term: Somatotroph adenoma ClinVar PMID:28413019 Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:12075507 more ... Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:22135276 , PMID:24033266 Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:12075507 more ... Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:12075507 more ... Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:24033266 , PMID:26467025 Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:18429043 more ... Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:17850630 more ... Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:12075507 more ... Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:12075507 more ... Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:16679490 , PMID:24033266 Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:12075507 , PMID:24033266 Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:22899989 Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:18429043 , PMID:24033266 Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:12075507 more ... Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:25741868 Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:21436283 more ... Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:24033266 , PMID:25741868 Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:23804846 , PMID:24033266 Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:24033266 Hearing Loss ISO RGD:733851 8554872 ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive ClinVar PMID:18429043 more ... Krabbe disease ISO RGD:733851 8554872 ClinVar Annotator: match by term: Leukodystrophy, Globoid Cell ClinVar PMID:25741868 Krabbe disease ISO RGD:733851 8554872 ClinVar Annotator: match by term: Galactosylceramide beta-galactosidase deficiency ClinVar PMID:24033266 , PMID:25741868 Krabbe disease ISO RGD:733851 8554872 ClinVar Annotator: match by term: Galactosylceramide beta-galactosidase deficiency ClinVar PMID:18429043 , PMID:24033266 Krabbe disease ISO RGD:733851 8554872 ClinVar Annotator: match by term: Galactosylceramide beta-galactosidase deficiency ClinVar PMID:24033266 Krabbe disease ISO RGD:733851 8554872 ClinVar Annotator: match by term: Leukodystrophy, Globoid Cell ClinVar PMID:18429043 more ... Krabbe disease ISO RGD:733851 8554872 ClinVar Annotator: match by term: Galactosylceramide beta-galactosidase deficiency ClinVar PMID:25991456 Krabbe disease ISO RGD:733851 8554872 ClinVar Annotator: match by term: Leukodystrophy, Globoid Cell ClinVar melanoma ISO RGD:733851 8554872 ClinVar Annotator: match by term: Malignant melanoma ClinVar PMID:12075507 more ... metachromatic leukodystrophy ISO RGD:733851 8554872 ClinVar Annotator: match by term: Arylsulfatase A Deficiency ClinVar PMID:25741868 metachromatic leukodystrophy ISO RGD:733851 8554872 ClinVar Annotator: match by term: Metachromatic leukodystrophy ClinVar PMID:24033266 , PMID:25741868 metachromatic leukodystrophy ISO RGD:733851 8554872 ClinVar Annotator: match by term: Metachromatic leukodystrophy ClinVar PMID:18429043 , PMID:24033266 metachromatic leukodystrophy ISO RGD:733851 8554872 ClinVar Annotator: match by term: Metachromatic leukodystrophy ClinVar PMID:24033266 metachromatic leukodystrophy ISO RGD:733851 8554872 ClinVar Annotator: match by term: Arylsulfatase A Deficiency ClinVar PMID:18429043 more ... metachromatic leukodystrophy ISO RGD:733851 8554872 ClinVar Annotator: match by term: Metachromatic leukodystrophy ClinVar PMID:25991456 metachromatic leukodystrophy ISO RGD:733851 8554872 ClinVar Annotator: match by term: Arylsulfatase A Deficiency ClinVar pituitary adenoma ISO RGD:733851 8554872 ClinVar Annotator: match by term: PITUITARY ADENOMA, MULTIPLE TYPES ClinVar PMID:28413019 PITUITARY ADENOMA 5, MULTIPLE TYPES ISO RGD:733851 8554872 ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES ClinVar PMID:28413019 PITUITARY ADENOMA 5, MULTIPLE TYPES ISO RGD:733851 8554872 ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES ClinVar PMID:11857743 more ... PITUITARY ADENOMA 5, MULTIPLE TYPES ISO RGD:733851 8554872 ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES ClinVar PMID:16679490 more ... PITUITARY ADENOMA 5, MULTIPLE TYPES ISO RGD:733851 8554872 ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES ClinVar PMID:11138009 more ... PITUITARY ADENOMA 5, MULTIPLE TYPES ISO RGD:733851 8554872 ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES ClinVar PMID:16679490 more ... PITUITARY ADENOMA 5, MULTIPLE TYPES ISO RGD:733851 8554872 ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES ClinVar PMID:24033266 more ... PITUITARY ADENOMA 5, MULTIPLE TYPES ISO RGD:733851 8554872 ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES ClinVar PMID:24033266 , PMID:25741868 retinitis pigmentosa ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa ClinVar PMID:18429043 more ... retinitis pigmentosa ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa ClinVar PMID:24033266 more ... retinitis pigmentosa ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive ClinVar PMID:30718709 retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:24033266 , PMID:25741868 retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:12075507 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:11138009 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:12075507 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:16679490 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:12075507 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:24033266 , PMID:26467025 retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:18429043 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:11857743 , PMID:21738395 retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:16679490 retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:17850630 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:12075507 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:18429043 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:25741868 retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:12075507 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:12075507 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:11090341 , PMID:24033266 retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:11857743 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:16679490 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:23804846 , PMID:24033266 retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:12075507 , PMID:24033266 retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:22135276 , PMID:24033266 retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:18429043 , PMID:24033266 retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:21436283 more ... retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:16679490 , PMID:24033266 retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:22899989 retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar retinitis pigmentosa-deafness syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome ClinVar PMID:24033266 Usher syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome ClinVar PMID:12075507 more ... Usher syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome ClinVar PMID:24033266 more ... Usher syndrome ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome ClinVar PMID:24033266 Usher syndrome type 1 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1 ClinVar PMID:12075507 more ... Usher syndrome type 1 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1 ClinVar PMID:12075507 more ... Usher syndrome type 1 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1 ClinVar PMID:12075507 , PMID:15537665 Usher syndrome type 1 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1 ClinVar PMID:21569298 Usher syndrome type 1 ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1 ClinVar PMID:15537665 more ... Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601067 ClinVar Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1D ClinVar PMID:11138009 more ... Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1D ClinVar PMID:12075507 more ... Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID ClinVar PMID:24033266 more ... Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1D ClinVar PMID:16679490 more ... Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1D ClinVar PMID:12075507 more ... Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1D ClinVar PMID:12075507 more ... Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1D ClinVar PMID:15537665 more ... Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1D ClinVar PMID:25741868 Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1D ClinVar PMID:11857743 , PMID:21738395 Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1D ClinVar PMID:16679490 Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID ClinVar PMID:24033266 , PMID:25741868 Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1D ClinVar PMID:11857743 more ... Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by term: Usher syndrome, type 1D ClinVar PMID:16679490 more ... Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by null ClinVar PMID:12075507 , PMID:15537665 Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601067 ClinVar PMID:16963483 , PMID:24033266 Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601067 ClinVar PMID:25991456 Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601067 ClinVar PMID:11138009 Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601067 ClinVar PMID:11090341 Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601067 ClinVar PMID:11090341 , PMID:24033266 Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601067 ClinVar PMID:11138009 more ... Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601067 ClinVar PMID:22135276 , PMID:24033266 Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601067 ClinVar PMID:12075507 , PMID:24033266 Usher syndrome type 1D ISO RGD:733851 8554872 ClinVar Annotator: match by OMIM:601067 ClinVar PMID:24033266 Usher syndrome type 2A ISO RGD:733851 8554872 ClinVar Annotator: match by term: USHER SYNDROME, TYPE IIA ClinVar PMID:12075507 more ... Usher Syndrome, Type ID/F ISO RGD:733851 8554872 ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID/F, DIGENIC ClinVar PMID:15537665 more ... Usher Syndrome, Type ID/F ISO RGD:733851 8554872 ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID/F, DIGENIC ClinVar PMID:12075507 , PMID:15537665
Gene-Chemical Interaction Annotations
