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Aliases for SPG41 Gene

Aliases for SPG41 Gene

  • Spastic Paraplegia 41 (Autosomal Dominant) 2 3

External Ids for SPG41 Gene

Previous GeneCards Identifiers for SPG41 Gene

  • GC00U922794

Summaries for SPG41 Gene

Entrez Gene Summary for SPG41 Gene

  • This locus was defined in a Chinese family. Nineteen individuals were genotyped and the interval was defined between D11S1324 and D11S1933. [provided by RefSeq, Feb 2010]

GeneCards Summary for SPG41 Gene

SPG41 (Spastic Paraplegia 41 (Autosomal Dominant)) is a Genetic Locus. Diseases associated with SPG41 include Spastic Paraplegia 41, Autosomal Dominant and Spastic Paraplegia 10.

Additional gene information for SPG41 Gene

No data available for CIViC summary , UniProtKB/Swiss-Prot , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for SPG41 Gene

Genomics for SPG41 Gene

Genomic Locations for SPG41 Gene

Genomic Locations for SPG41 Gene
Unknown strand

Genomic View for SPG41 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for SPG41 Gene

Proteins for SPG41 Gene

Post-translational modifications for SPG41 Gene

No Post-translational modifications

No data available for DME Specific Peptides for SPG41 Gene

Domains & Families for SPG41 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 SPG41 Gene

Function for SPG41 Gene

Animal Model Products

Clone Products

No data available for Molecular function , Enzyme Numbers (IUBMB) , Phenotypes From GWAS Catalog , Gene Ontology (GO) - Molecular Function , Phenotypes , Human Phenotype Ontology , Animal Models , miRNA , Transcription Factor Targets and HOMER Transcription for SPG41 Gene

Localization for SPG41 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS , Subcellular locations from the Human Protein Atlas (HPA) and Gene Ontology (GO) - Cellular Components for SPG41 Gene

Pathways & Interactions for SPG41 Gene

SuperPathways for SPG41 Gene

No Data Available

Interacting Proteins for SPG41 Gene

Gene Ontology (GO) - Biological Process for SPG41 Gene


No data available for Pathways by source and SIGNOR curated interactions for SPG41 Gene

Drugs & Compounds for SPG41 Gene

No Compound Related Data Available

Transcripts for SPG41 Gene

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for SPG41 Gene

No ASD Table

Relevant External Links for SPG41 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for SPG41 Gene

Expression for SPG41 Gene

NURSA nuclear receptor signaling pathways regulating expression of SPG41 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 , mRNA Expression by UniProt/SwissProt , Evidence on tissue expression from TISSUES and Phenotype-based relationships between genes and organs from Gene ORGANizer for SPG41 Gene

Orthologs for SPG41 Gene

No data available for Orthologs and Evolution for SPG41 Gene

Paralogs for SPG41 Gene

No data available for Paralogs for SPG41 Gene

Variants for SPG41 Gene

Additional Variant Information for SPG41 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 SPG41 Gene

Disorders for SPG41 Gene

MalaCards: The human disease database

(2) MalaCards diseases for SPG41 Gene - From: OMIM, Orphanet, and GeneCards

Disorder Aliases PubMed IDs
spastic paraplegia 41, autosomal dominant
  • spg41
spastic paraplegia 10
  • spastic paraplegia 10, autosomal dominant
- elite association - COSMIC cancer census association via MalaCards
Search SPG41 in MalaCards View complete list of genes associated with diseases

Additional Disease Information for SPG41

Genetic Association Database
Human Genome Epidemiology Navigator
genes like me logo Genes that share disorders with SPG41: view

No data available for UniProtKB/Swiss-Prot and Genatlas for SPG41 Gene

Publications for SPG41 Gene

  1. Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia. (PMID: 20932283) Alvarez V … Group for the Study of the Genetics of Spastic Paraplegia (BMC neurology 2010) 3 44 58
  2. A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia. (PMID: 18364116) Zhao GH … Tang BS (Chinese medical journal 2008) 2 3 58

Products for SPG41 Gene

Sources for SPG41 Gene

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