Spinocerebellar Ataxia, X-Linked 5 (SCAX5)

Alias:
X-Linked Non Progressive Cerebellar Ataxia
X-Linked Spinocerebellar Ataxia 5
Scax5
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Spinocerebellar Ataxia, X-Linked 5, also known as x-linked non progressive cerebellar ataxia, is related to spinocerebellar ataxia, x-linked 4 and spinocerebellar ataxia, x-linked 3, and has symptoms including ataxia and action tremor. An important gene associated with Spinocerebellar Ataxia, X-Linked 5 is ATP2B3 (ATPase Plasma Membrane Ca2+ Transporting 3). Affiliated tissues include eye and brain, and related phenotypes are nonprogressive cerebellar ataxia and strabismus
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XL
XLD
Newborn
<1/1000000
12
82
3

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top