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Aliases for SCA18 Gene

Aliases for SCA18 Gene

  • Spinocerebellar Ataxia 18 (Sensory With Neurogenic Muscular Atrophy) 2 3
  • SMNA 3

External Ids for SCA18 Gene

Summaries for SCA18 Gene

GeneCards Summary for SCA18 Gene

SCA18 (Spinocerebellar Ataxia 18 (Sensory With Neurogenic Muscular Atrophy)) is a Genetic Locus. Diseases associated with SCA18 include Spinocerebellar Ataxia 18.

No data available for Entrez Gene Summary , UniProtKB/Swiss-Prot , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for SCA18 Gene

Genomics for SCA18 Gene

Genomic Location for SCA18 Gene

Unknown strand

Genomic View for SCA18 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for Regulatory Elements and RefSeq DNA sequence for SCA18 Gene

Proteins for SCA18 Gene

Post-translational modifications for SCA18 Gene

No Post-translational modifications

No data available for DME Specific Peptides for SCA18 Gene

Domains & Families for SCA18 Gene

Graphical View of Domain Structure for InterPro Entry

No data available for Gene Families , Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for SCA18 Gene

Function for SCA18 Gene

Animal Model Products

No data available for Molecular function , Enzyme Numbers (IUBMB) , Gene Ontology (GO) - Molecular Function , Phenotypes , Human Phenotype Ontology , Animal Models , miRNA , Transcription Factor Targets and HOMER Transcription for SCA18 Gene

Localization for SCA18 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS and Gene Ontology (GO) - Cellular Components for SCA18 Gene

Pathways & Interactions for SCA18 Gene

SuperPathways for SCA18 Gene

No Data Available

Interacting Proteins for SCA18 Gene

Gene Ontology (GO) - Biological Process for SCA18 Gene


No data available for Pathways by source and SIGNOR curated interactions for SCA18 Gene

Transcripts for SCA18 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for SCA18 Gene

No ASD Table

Relevant External Links for SCA18 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for SCA18 Gene

Expression for SCA18 Gene

NURSA nuclear receptor signaling pathways regulating expression of SCA18 Gene:

No Expression Related Data Available

No data available for mRNA expression in normal human tissues , mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , mRNA differential expression in normal tissues , Protein differential expression in normal tissues , Protein expression , Protein tissue co-expression partners and mRNA Expression by UniProt/SwissProt for SCA18 Gene

Orthologs for SCA18 Gene

No data available for Orthologs and Evolution for SCA18 Gene

Paralogs for SCA18 Gene

No data available for Paralogs for SCA18 Gene

Variants for SCA18 Gene

Relevant External Links for SCA18 Gene

SNPedia medical, phenotypic, and genealogical associations of SNPs for

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot , Sequence variations from dbSNP and Humsavar , Structural Variations from Database of Genomic Variants (DGV) and Variation tolerance for SCA18 Gene

Disorders for SCA18 Gene

MalaCards: The human disease database

(1) MalaCards diseases for SCA18 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
spinocerebellar ataxia 18
  • spinocerebellar ataxia type 18
- elite association - COSMIC cancer census association via MalaCards
Search SCA18 in MalaCards View complete list of genes associated with diseases

Relevant External Links for SCA18

Genetic Association Database (GAD)
Human Genome Epidemiology (HuGE) Navigator
genes like me logo Genes that share disorders with SCA18: view

No data available for UniProtKB/Swiss-Prot and Genatlas for SCA18 Gene

Publications for SCA18 Gene

  1. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families. (PMID: 15148151) Brusco A. … Taroni F. (Arch. Neurol. 2004) 3 46 64
  2. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32. (PMID: 11992570) Brkanac Z. … Raskind W.H. (Am. J. Med. Genet. 2002) 2 3 64

Products for SCA18 Gene

Sources for SCA18 Gene

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