Symbol Name ID |
Ptchd1
patched domain containing 1 MGI:2685233 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Lack of spontaneous play |
Impaired ability to form peer relationships |
Autism |
Inflexible adherence to routines |
Motor stereotypy |
Restrictive behavior |
Disease(s) Associated with PTCHD1 | ||||||
autistic disorder |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal cognition |
impaired avoidance learning behavior |
abnormal contextual conditioning behavior |
impaired contextual conditioning behavior |
abnormal cued conditioning behavior |
impaired cued conditioning behavior |
increased exploration in new environment |
increased aggression |
abnormal locomotor behavior |
abnormal gait |
increased vertical activity |
hyperactivity |
abnormal sleep pattern |
fragmentation of sleep/wake states |
abnormal vocalization |
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Availability | Mouse Genotype | ||||||||||||||||
Ptchd1tm1b(KOMP)IcsOrl/Ptchd1tm1b(KOMP)IcsOrl | |||||||||||||||||
Ptchd1tm1b(KOMP)IcsOrl/Y | |||||||||||||||||
Ptchd1tm2.2Gfng/Y | * | ||||||||||||||||
Ptchd1tm2.1Gfng/Y Ssttm2.1(cre)Zjh/Sst+ (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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