spastic paraplegia 38 (autosomal dominant, Silver syndrome) Gene Detail


Symbol:
Name:
ID:
SPG38
spastic paraplegia 38 (autosomal dominant, Silver syndrome)
GC:06936
Aliases & Descriptions for SPG38 gene
Gene name: SPG38
Chromosome: 4p16-p15
Previous Symbols:
Previous Names:
Aliases:
Name Aliases:
product Type: gene with protein/antibody/ELISA product

spastic paraplegia 38 (autosomal dominant, Silver syndrome) database Links


Mouse Genome Database ID: Rat Genome Database ID:
According to HGNC, Entrez Gene, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL, OMIM, GeneLoc , and/or Ensembl, miRBase
HGNC ID: HGNC:33485 RefSeq IDs:
Entrez Gene ID: 100049707 Ensembl Gene ID:
VEGA IDs: UniProt ID:
UCSC ID: OMIM ID: 612335
Pubmed: PMID18401025
CCDS IDs:

Products for SPG38 gene

(SPECIES:Human;Rat;Mouse and other species fluids)

Catalog Product Name Application Brand Products with us for SPG38 gene
GCE06936 spastic paraplegia 38 (autosomal dominant, Silver syndrome) ELISA kit ELISA n/a
GCPA06936 spastic paraplegia 38 (autosomal dominant, Silver syndrome) Polyconal Antibody Polyconal Antibody n/a
GCMA06936 spastic paraplegia 38 (autosomal dominant, Silver syndrome) Monaconal Antibody Monaconal Antibody n/a
GCP06936 spastic paraplegia 38 (autosomal dominant, Silver syndrome) Protein Protein n/a
ASPGSPG9SPG7SPG5BSPG46SPG45SPG43SPG41SPG3BSPG38SPG37SPG36SPG34SPG32SPG30SPG29SPG28SPG27SPG26SPG25 SPG38 - related Gene