N syndrome (mental retardation, malformations, chromosome breakage) Gene Detail
| Symbol: Name: ID: |
NSX N syndrome (mental retardation, malformations, chromosome breakage) GC:15716 |
Aliases & Descriptions for NSX gene |
| Gene name: | NSX | |
| Chromosome: | X | |
| Previous Symbols: | ||
| Previous Names: | ||
| Aliases: | ||
| Name Aliases: | ||
| product Type: | gene with protein/antibody/ELISA product |
N syndrome (mental retardation, malformations, chromosome breakage) 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 |
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| 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: | ||||
Products for NSX gene
(SPECIES:Human;Rat;Mouse and other species fluids)
| Catalog | Product Name | Application | Brand | Products with us for NSX gene |
| GCE15716 | N syndrome (mental retardation, malformations, chromosome breakage) ELISA kit | ELISA | n/a | |
| GCPA15716 | N syndrome (mental retardation, malformations, chromosome breakage) Polyconal Antibody | Polyconal Antibody | n/a | |
| GCMA15716 | N syndrome (mental retardation, malformations, chromosome breakage) Monaconal Antibody | Monaconal Antibody | n/a | |
| GCP15716 | N syndrome (mental retardation, malformations, chromosome breakage) Protein | Protein | n/a |
| NSX | NSX - related Gene |