N syndrome (mental retardation, malformations, chromosome breakage) | NSX ELISA | NSX Antibody | NSX Protein

N syndrome (mental retardation, malformations, chromosome breakage) Gene Detail

Symbol: Name: ID:	NSX N syndrome (mental retardation, malformations, chromosome breakage) GFS:28477
Gene name:	NSX
Chromosome:	X
Previous Symbols:
Previous Names:
Aliases:
Name Aliases:
Locus Type:	phenotype only

N syndrome (mental retardation, malformations, chromosome breakage) External Links

Mouse Genome Database ID:		Rat Genome Database ID:
HGNC ID:	HGNC:8019	RefSeq IDs:
Entrez Gene ID:	4906	Ensembl Gene ID:
VEGA IDs:		UniProt ID:
UCSC ID:		OMIM ID:	310465
Pubmed:
CCDS IDs:

Aliases & Descriptions for NSX gene

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

Products for NSX gene

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

Catalog	Product Name	Application	Company
GFS:E28477	N syndrome (mental retardation, malformations, chromosome breakage); ELISA kit	ELISA	n/a
GFS:A28477	N syndrome (mental retardation, malformations, chromosome breakage); Anti	ANTIBODIES	n/a
GFS:P28477	N syndrome (mental retardation, malformations, chromosome breakage); Protien	Protien	n/a

Products
with us for NSX gene

N syndrome (mental retardation, malformations, chromosome breakage) Gene Detail

N syndrome (mental retardation, malformations, chromosome breakage) External Links

Summary for NSX