|
Symbol Name ID Chromosome |
Kcnj12
potassium inwardly-rectifying channel, subfamily J, member 12 MGI:108495 11 |
| Experiment Type | Details | Chromosome | Reference |
|---|---|---|---|
| CROSS |
Cross Type: Backcross Mapping Panel: Copeland-Jenkins |
11 | J:36014 Takumi T, et al., Assignment of the murine inward rectifier potassium channel Irk2 (Kir2.2) gene to the central region of mouse chromosome 11. Genomics. 1996 15;37(2):270-2 |
| TEXT | 11 | J:125240 Yan J, et al., Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike. Am J Hum Genet. 2007 Mar;80(3):518-25 | |
| TEXT-Genetic Cross | 11 | J:47116 Liang Y, et al., Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2. Am J Hum Genet. 1998 Apr;62(4):904-15 | |
| TEXT-Physical Mapping | 11 | J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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