Symbol Name ID |
Morc2a
microrchidia 2A MGI:1921772 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Urinary incontinence |
Fatigue |
Disease(s) Associated with MORC2 | ||
Charcot-Marie-Tooth disease axonal type 2Z |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal cognition |
enhanced contextual conditioning behavior |
limb grasping |
ataxia |
impaired coordination |
decreased grip strength |
abnormal gait |
decreased locomotor activity |
paraparesis |
|
Availability | Mouse Genotype | ||||||||||
Morc2aem1Snupy/Morc2a+ | |||||||||||
Morc2atm1b(KOMP)Wtsi/Morc2a+ | |||||||||||
Morc2atm1.1Pngr/Morc2atm1.1Pngr Tg(Nes-cre)1Kln/0 (conditional) |
* |
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 04/16/2024 MGI 6.23 |
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