Results for "Spinocerebellar ataxia, X-linked, 3": 21 genes

Name

SCAR2 Gene

spinocerebellar ataxia, autosomal recessive 2

SCAR3 Gene

spinocerebellar ataxia, autosomal recessive 3

SCASI Gene

spinocerebellar ataxia with saccadic intrusions

SCA20 Gene

spinocerebellar ataxia 20

SCA21 Gene

spinocerebellar ataxia 21

SCA25 Gene

spinocerebellar ataxia 25

SCA26 Gene

spinocerebellar ataxia 26

SCA18 Gene

spinocerebellar ataxia 18 (sensory with neurogenic muscular atrophy)

SCA9 Gene

spinocerebellar ataxia 9

SCA37 Gene

spinocerebellar ataxia 37

SCA32 Gene

spinocerebellar ataxia 32

SCA30 Gene

spinocerebellar ataxia 30

NPAT Gene

nuclear protein, ataxia-telangiectasia locus

Enables transcription coactivator activity and transcription corepressor activity. Involved in cell cycle G1/S phase transition and positive regulation of transcription by RNA polymerase II. Located in Cajal body; Gemini of coiled bodies; and cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]

FRDA2 Gene

Friedreich ataxia 2

CLA3 Gene

cerebellar ataxia 3 (cerebellar parenchyma disorder 1)

EA7 Gene

Episodic ataxia, type 7

SPAX3 Gene

Ataxia, spastic, 3, autosomal recessive

SAX1 Gene

spastic ataxia 1 (autosomal dominant)

EA8 Gene

Episodic ataxia, type 8

EA3 Gene

Episodic ataxia, type 3

ATCAY Gene

ataxia, cerebellar, Cayman type

This gene encodes a neuron-restricted protein that contains a CRAL-TRIO motif common to proteins that bind small lipophilic molecules. Mutations in this gene are associated with cerebellar ataxia, Cayman type. [provided by RefSeq, Jul 2008]