KOMP Knock Out Knockout Mouse Mice
Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 Synonyms: KQT2, Nmf134 Gene nomenclature, locus information, and GO, OMIM, and PMID associations
are updated daily from MGI
MGI: MGI:1309503 ( Current, 103.57cM, Gene) Ensembl: ENSMUSG16346 ( Kcnq2), ENSMUSG89747, ENSMUSG89863 NCBI: 16536, 16558 Vega: OTTMUSG16558 ( Kcnq2, "potassium voltage-gated channel, subfamily Q, member 2") CCDS: 17193, 17193.1, 17194, 17194.1, 17195, 17195.1, 17196, 17196.1, 17197, 17197.1, 17198, 17198.1, 17199, 17199.1, 17200, 17200.1, 50845, 50846, 50847, 50848 OMIM:
, EPILEPSY, BENIGN NEONATAL, 1; EBN1
, POTASSIUM CHANNEL, VOLTAGE-GATED, KQT-LIKE SUBFAMILY, MEMBER 2; KCNQ2
, MYOKYMIA WITH NEONATAL EPILEPSY
613720 Gene Ontology: Kcnq2
Mouse Phenome DB: Kcnq2
UCSC: Chr.2:181,075,579-181,135,300(-) IMPC: Kcnq2
Non-KOMP projects associated with this gene exist at: EUCOMM, TIGM. You can view the status of all IKMC projects for Kcnq2. Researchers interested in Kcnq2 are also interested* in
* Based on co-mentions in published literature. For more gene-gene associations visit genecloud.org.
The KOMP Repository Collection is located at the MMRRC at the University of California, Davis and Children’s Hospital Oakland Research Institute. Question? Comments? For Mice, Cells, and germplasm please contact us at firstname.lastname@example.org, US 1-888-KOMP-MICE or International +1-530-752-KOMP, or for vectors email@example.com or +1-510-450-7917.