Symbol Name ID |
Kmt2d
lysine (K)-specific methyltransferase 2D MGI:2682319 |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties |
Feeding difficulties in infancy |
Atypical behavior |
Weak cry |
Disease(s) Associated with KMT2D | ||||
Kabuki syndrome |
Mouse Phenotypes | impaired contextual conditioning behavior |
abnormal object recognition memory |
impaired spatial learning |
decreased coping response |
increased grooming behavior |
abnormal motor capabilities/coordination/movement |
abnormal pinna reflex |
impaired righting response |
hyporesponsive to tactile stimuli |
limb grasping |
impaired coordination |
abnormal gait |
short stride length |
increased vertical activity |
increased locomotor activity |
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Availability | Mouse Genotype | |||||||||||||||
Kmt2dbapa/Kmt2dbapa | ||||||||||||||||
Kmt2dGt(RRT024)Byg/Kmt2d+ |
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 05/14/2024 MGI 6.23 |
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