GenTIGSA Gene Database on Rare Genetic Disorders
  Beta Version

Lists of Rare Genetic Disorders  

Meniere Disease(Meniere's disease) 
An Autosomal dominant mode(s) within the Ear disorders category
Reported Pathogenic variants
Candidate Gene Information
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