Atxn8os
Gene Detail

Symbol Name ID

Atxn8os ATXN8 opposite strand MGI:1891412

Synonyms

Klhl1as, Sca8

Feature Type

unclassified non-coding RNA gene

Genetic Map

Chromosome 14
Syntenic

Sequence Map

Chr14:96556570-96557009 bp From MGI annotation of GRCm38   440 bp   ±  kb flank VEGA Genome Browser | Ensembl Genome Browser | UCSC Browser | NCBI Map Viewer

Mouse Genome Browser

Alleles and phenotypes

All alleles(2) : Targeted(2)
 

Mice both homozygous and heterozygous for disruption of this gene develop abnormalities in gait and defects in motor coordination with time. Dendritic atrophy of Purkinje cells is also seen.

 

Gene Ontology (GO) classifications

All GO classifications: (1 annotations)

Component

cytoplasm

Other database links

Entrez Gene	108639
DFCI	TC1668151
DoTS	DT.101357266

Sequences

Length	Strain/Species
transcript	TC1668151	DFCI | MGI Sequence Detail	450	Not Applicable

All sequences(3)

References

(Earliest) J:62929 Nemes JP, et al., The SCA8 transcript is an antisense RNA to a brain-specific transcript encoding a novel actin-binding protein (KLHL1). Hum Mol Genet. 2000 Jun 12;9(10):1543-51
(Latest) J:112937 He Y, et al., Targeted deletion of a single Sca8 ataxia locus allele in mice causes abnormal gait, progressive loss of motor coordination, and Purkinje cell dendritic deficits. J Neurosci. 2006 Sep 27;26(39):9975-82
All references(9)