spastic paraplegia 38 (autosomal dominant, Silver syndrome) | SPG38 ELISA | SPG38 Antibody | SPG38 Protein

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

Symbol: Name: ID:	SPG38 spastic paraplegia 38 (autosomal dominant, Silver syndrome) GFS:19076
Gene name:	SPG38
Chromosome:	4p16-p15
Previous Symbols:
Previous Names:
Aliases:
Name Aliases:
Locus Type:	phenotype only

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

Mouse Genome Database ID:		Rat Genome Database ID:
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:

Aliases & Descriptions for SPG38 gene

(According to HGNC, Entrez Gene, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL, OMIM, GeneLoc , and/or Ensembl, miRBase) About This Section

Products for SPG38 gene

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

Catalog	Product Name	Application	Company
GFS:E19076	spastic paraplegia 38 (autosomal dominant, Silver syndrome); ELISA kit	ELISA	n/a
GFS:A19076	spastic paraplegia 38 (autosomal dominant, Silver syndrome); Anti	ANTIBODIES	n/a
GFS:P19076	spastic paraplegia 38 (autosomal dominant, Silver syndrome); Protien	Protien	n/a

Products
with us for SPG38 gene

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

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

Summary for SPG38