GenTIGSA Gene Database on Rare Genetic Disorders
  Beta Version

Lists of Rare Genetic Disorders  

Spinocerebellar Ataxia Type 27(Cerebellar ataxia autosomal dominant FGF14-related)      Explore Disorder's Alias
An Autosomal dominant mode(s) within the Neurodegenerative 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 FGF14/2259 fibroblast growth factor 14 13q33.1 Chr13, NC_000013.11
(101710804..102402443, complement)
691640 nt 16 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

Variant Information
Disorder Cross-References:      GARD          GTR          MalaCards          NORD     

Patient care services
Clinical Symptoms & Disabilities

Prevalence
Under development