|
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 | Aggressive behavior |
Attention deficit hyperactivity disorder |
Autistic behavior |
Polyphagia |
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 |
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| 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 05/19/2026 MGI 6.24 |
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