Meniere Disease(Meniere's disease)
An Autosomal dominant mode(s) within the Ear disorders category
Candidate Gene Information
An Autosomal dominant mode(s) within the Ear disorders category
Reported Pathogenic variants
S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
1 | FAM136A/84908 | family with sequence similarity 136 member A | 2p13.3 | Chr2, NC_000002.12 (70295976..70302067, complement) |
6092 nt | 4 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
2 | DTNA/1837 | dystrobrevin alpha | 18q12.1 | Chr18, NC_000018.10 (34493312..34891844) |
398533 nt | 33 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
3 | MYO7A/4647 | myosin VIIA | 11q13.5 | Chr11, NC_000011.10 (77128246..77215241) |
86996 nt | 56 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
4 | CDH23/64072 | cadherin related 23 | 10q22.1 | Chr10, NC_000010.11 (71396920..71815947) |
419028 nt | 71 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
5 | SHROOM2/357 | shroom family member 2 | Xp22.2 | ChrX, NC_000023.11 (9786429..9949443) |
163015 nt | 12 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
6 | TECTA/7007 | tectorin alpha | 11q23.3 | Chr11, NC_000011.10 (121101243..121191490) |
90248 nt | 24 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
Variant Information | ||||||||
Disorder Cross-References: OMIM GTR MedGen MalaCards EMBL-EBI OLS Monarch Initiative NORD |
Patient care services
Clinical Symptoms & Disabilities
Prevalence
Under development |