Symbol Name ID |
Kcna10
potassium voltage-gated channel, shaker-related subfamily, member 10 MGI:3037820 |
Age | E7 | E11 | E14.5 | E15 | E16.5 | E17 | E18.5 | P |
Immunohistochemistry (section) | 1 | 1 | 1 | 2 | ||||
In situ reporter (knock in) | 1 | 1 | ||||||
RT-PCR | 1 | 1 | 1 | 1 | 1 |
Kcna10 potassium voltage-gated channel, shaker-related subfamily, member 10 (Synonyms: Kcna8, Kv1.8) | |
Results | Reference |
4* | J:183945 Carlisle FA, Steel KP, Lewis MA, Specific expression of Kcna10, Pxn and Odf2 in the organ of Corti. Gene Expr Patterns. 2012 May;12(5-6):172-9 |
1 | J:332398 Khan MN, Cherukuri P, Negro F, Rajput A, Fabrowski P, Bansal V, Lancelin C, Lee TI, Bian Y, Mayer WP, Akay T, Muller D, Bonn S, Farina D, Marquardt T, ERR2 and ERR3 promote the development of gamma motor neuron functional properties required for proprioceptive movement control. PLoS Biol. 2022 Dec;20(12):e3001923 |
7* | J:210785 Lee SI, Conrad T, Jones SM, Lagziel A, Starost MF, Belyantseva IA, Friedman TB, Morell RJ, A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction. Hear Res. 2013 Jun;300:1-9 |
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 12/10/2024 MGI 6.24 |
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