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Aliases for SPG38 Gene

Aliases for SPG38 Gene

  • Spastic Paraplegia 38 (Autosomal Dominant, Silver Syndrome) 2 3

External Ids for SPG38 Gene

Previous GeneCards Identifiers for SPG38 Gene

  • GC00U922300

Summaries for SPG38 Gene

GeneCards Summary for SPG38 Gene

SPG38 (Spastic Paraplegia 38 (Autosomal Dominant, Silver Syndrome)) is a Genetic Locus. Diseases associated with SPG38 include Spastic Paraplegia 38, Autosomal Dominant.

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 SPG38 Gene

Genomics for SPG38 Gene

Genomic Location for SPG38 Gene

Unknown strand

Genomic View for SPG38 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for Regulatory Elements and RefSeq DNA sequence for SPG38 Gene

Proteins for SPG38 Gene

Post-translational modifications for SPG38 Gene

No Post-translational modifications

No data available for DME Specific Peptides for SPG38 Gene

Domains & Families for SPG38 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 SPG38 Gene

Function for SPG38 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 SPG38 Gene

Localization for SPG38 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS and Gene Ontology (GO) - Cellular Components for SPG38 Gene

Pathways & Interactions for SPG38 Gene

SuperPathways for SPG38 Gene

No Data Available

Interacting Proteins for SPG38 Gene

Gene Ontology (GO) - Biological Process for SPG38 Gene


No data available for Pathways by source and SIGNOR curated interactions for SPG38 Gene

Transcripts for SPG38 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for SPG38 Gene

No ASD Table

Relevant External Links for SPG38 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for SPG38 Gene

Expression for SPG38 Gene

NURSA nuclear receptor signaling pathways regulating expression of SPG38 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 SPG38 Gene

Orthologs for SPG38 Gene

No data available for Orthologs and Evolution for SPG38 Gene

Paralogs for SPG38 Gene

No data available for Paralogs for SPG38 Gene

Variants for SPG38 Gene

Relevant External Links for SPG38 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 SPG38 Gene

Disorders for SPG38 Gene

MalaCards: The human disease database

(1) MalaCards diseases for SPG38 Gene - From: OMIM, Orphanet, and GeneCards

Disorder Aliases PubMed IDs
spastic paraplegia 38, autosomal dominant
  • autosomal dominant spastic paraplegia type 38
- elite association - COSMIC cancer census association via MalaCards
Search SPG38 in MalaCards View complete list of genes associated with diseases
genes like me logo Genes that share disorders with SPG38: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for SPG38 Gene

Publications for SPG38 Gene

  1. Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4. (PMID: 18401025) Orlacchio A. … Kawarai T. (Neurology 2008) 2 3 64

Products for SPG38 Gene

Sources for SPG38 Gene

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