Symbol: Name: ID: |
KCNQ1DN KCNQ1 downstream neighbor GFS:2955 |
Gene name: | KCNQ1DN |
Chromosome: | 11p15.5 |
Previous Symbols: | |
Previous Names: | |
Aliases: | BWRT, HSA404617 |
Name Aliases: | |
Locus Type: | gene with protein product |
Mouse Genome Database ID: | Rat Genome Database ID: | ||
HGNC ID: | HGNC:13335 | RefSeq IDs: | NR_024627 |
Entrez Gene ID: | 55539 | Ensembl Gene ID: | ENSG00000237941 |
VEGA IDs: | OTTHUMG00000009942 | UniProt ID: | Q9H478 |
UCSC ID: | uc009ydq.2 | OMIM ID: | 610980 |
Pubmed: | PMID11056398 PMID 11063728 | ||
CCDS IDs: |
Imprinting is a phenomenon in which epigenetic modifications lead to expression or suppression of alleles of some genes based on their parental origin. Wilms tumor-2 (WT2; MIM 194071) is defined by maternal-specific loss of heterozygosity of a critical region on chromosome 11p15.5 that includes several imprinted genes. KCNQ1DN is an imprinted gene located within the WT2 critical region that is expressed from the maternal allele (Xin et al., 2000 [PubMed 11056398]).[supplied by OMIM, Mar 2008].
Products for KCNQ1DN gene
Catalog | Product Name | Application | Company |
GFS:E02955 | KCNQ1 downstream neighbor; ELISA kit | ELISA | n/a |
GFS:A02955 | KCNQ1 downstream neighbor; Anti | ANTIBODIES | n/a |
GFS:P02955 | KCNQ1 downstream neighbor; Protien | Protien | n/a |