Results for "friedreich ataxia 2": 25 genes

Name

FRDA2 Gene

Friedreich ataxia 2

SCAR2 Gene

spinocerebellar ataxia, autosomal recessive 2

SCAR3 Gene

spinocerebellar ataxia, autosomal recessive 3

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]

SCASI Gene

spinocerebellar ataxia with saccadic intrusions

CLA3 Gene

cerebellar ataxia 3 (cerebellar parenchyma disorder 1)

SCA20 Gene

spinocerebellar ataxia 20

SCA21 Gene

spinocerebellar ataxia 21

SCA25 Gene

spinocerebellar ataxia 25

SCA26 Gene

spinocerebellar ataxia 26

EA7 Gene

Episodic ataxia, type 7

SPAX3 Gene

Ataxia, spastic, 3, autosomal recessive

SAX1 Gene

spastic ataxia 1 (autosomal dominant)

SCA18 Gene

spinocerebellar ataxia 18 (sensory with neurogenic muscular atrophy)

EA8 Gene

Episodic ataxia, type 8

EA3 Gene

Episodic ataxia, type 3

SCAX2 Gene

spinocerebellar ataxia, X-linked 2

SCAX3 Gene

spinocerebellar ataxia, X-linked 3

SCAX4 Gene

spinocerebellar ataxia, X-linked 4

SCAX5 Gene

Spinocerebellar ataxia, X-linked 5

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]

SCA9 Gene

spinocerebellar ataxia 9

SCA37 Gene

spinocerebellar ataxia 37

SCA32 Gene

spinocerebellar ataxia 32

SCA30 Gene

spinocerebellar ataxia 30