- NFATC2IP-AS1 [Search on AGR]
Homo sapiens ASSOCIATED WITH chromosome 16p11.2 deletion syndrome, 220-kb; Schizophrenia; schizophrenia
- NPIPB9 [Search on AGR]
Homo sapiens ASSOCIATED WITH chromosome 16p11.2 deletion syndrome, 220-kb; Schizophrenia; schizophrenia; INTERACTS WITH acrylamide; aristolochic acid A; ethylparaben
- DUX1 [Search on AGR]
Homo sapiens The human genome contains hundreds of repeats of the 3.3-kb family in regions associated with heterochromatin. The DUX gene family, including DUX1, resides within these 3.3-kb repeated elements (Beckers et al., 2001 [PubMed 11245978]). See DUX4 (MIM 606009).[supplied by OMIM, Mar 2008]
- DUX5 [Search on AGR]
Homo sapiens The human genome contains hundreds of repeats of the 3.3-kb family in regions associated with heterochromatin. The DUX gene family, including DUX5, resides within these 3.3-kb repeated elements (Beckers et al., 2001 [PubMed 11245978]). See DUX4 (MIM 606009).[supplied by OMIM, Mar 2008]
- DUX3 [Search on AGR]
Homo sapiens The human genome contains hundreds of repeats of the 3.3-kb family in regions associated with heterochromatin. The DUX gene family, including DUX3, resides within these 3.3-kb repeated elements (Beckers et al., 2001 [PubMed 11245978]). See DUX4 (MIM 606009).[supplied by OMIM, Mar 2008]
- NPIPB8 [Search on AGR]
Homo sapiens ASSOCIATED WITH chromosome 16p11.2 deletion syndrome, 220-kb; Schizophrenia; schizophrenia; INTERACTS WITH 2-palmitoylglycerol; cadmium atom; cadmium dichloride
- ATP2A1-AS1 [Search on AGR]
Homo sapiens ASSOCIATED WITH Brody myopathy; chromosome 16p11.2 deletion syndrome, 220-kb; genetic disease; INTERACTS WITH 2,2',5,5'-tetrachlorobiphenyl; acrylamide; aflatoxin B1
- Dpys [Search on AGR]
Homo sapiens Dihydropyrimidinase catalyzes the conversion of 5,6-dihydrouracil to 3-ureidopropionate in pyrimidine metabolism. Dihydropyrimidinase is expressed at a high level in liver and kidney as a major 2.5-kb transcript and a minor 3.8-kb transcript. Defects in the DPYS gene are linked to dihydropyrimidinuria. [provided by RefSeq, Jul 2008]