Symbol: Name: ID: |
WRB tryptophan rich basic protein GFS:2549 |
Gene name: | WRB |
Chromosome: | 21q22.3 |
Previous Symbols: | |
Previous Names: | |
Aliases: | CHD5 |
Name Aliases: | |
Locus Type: | gene with protein product |
Mouse Genome Database ID: | MGI:2136882 | Rat Genome Database ID: | RGD:735104 |
HGNC ID: | HGNC:12790 | RefSeq IDs: | NM_001146218 |
Entrez Gene ID: | 7485 | Ensembl Gene ID: | ENSG00000182093 |
VEGA IDs: | OTTHUMG00000066250 | UniProt ID: | O00258 |
UCSC ID: | uc002yxs.2 | OMIM ID: | 602915 |
Pubmed: | PMID9544840 | ||
CCDS IDs: | CCDSCCDS13664.1 |
This gene encodes a basic nuclear protein of unknown function. The gene is widely expressed in adult and fetal tissues. Since the region proposed to contain the gene(s) for congenital heart disease (CHD) in Down syndrome (DS) patients has been restricted to 21q22.2-22.3, this gene, which maps to 21q22.3, has a potential role in the pathogenesis of Down syndrome congenital heart disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq].
Products for WRB gene
Catalog | Product Name | Application | Company |
GFS:E02549 | tryptophan rich basic protein; ELISA kit | ELISA | n/a |
GFS:A02549 | tryptophan rich basic protein; Anti | ANTIBODIES | n/a |
GFS:P02549 | tryptophan rich basic protein; Protien | Protien | n/a |