Symbol Name ID |
Myt1l
myelin transcription factor 1-like MGI:1100511 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Autistic behavior |
Polyphagia |
Aggressive behavior |
Self-mutilation |
Disease(s) Associated with MYT1L | ||||
autosomal dominant intellectual developmental disorder 39 |
Mouse Phenotypes | behavior/neurological phenotype |
impaired contextual conditioning behavior |
impaired cued conditioning behavior |
abnormal habituation to a new environment |
decreased aggression towards mice |
decreased anxiety-related response |
hyporesponsive to tactile stimuli |
increased startle reflex |
impaired coordination |
decreased grip strength |
weakness |
abnormal limb posture |
increased vertical activity |
increased locomotor activity |
hyperactivity |
abnormal social/conspecific interaction behavior |
abnormal nest building behavior |
decreased social investigation |
excessive vocalization |
|
Availability | Mouse Genotype | |||||||||||||||||||
Myt1lem1Jdd/Myt1l+ | * | |||||||||||||||||||
Myt1lem1Mwer/Myt1l+ | * |
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 04/30/2024 MGI 6.23 |
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