Symbol
Name
ID

Myt1l
myelin transcription factor 1-like
MGI:1100511

Phenotype annotations related to behavior/neurological

*	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

Myt1l^em1Jdd/Myt1l⁺

Myt1l^em1Mwer/Myt1l⁺

Contributing Projects: 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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