Symbol Name ID |
Foxp2
forkhead box P2 MGI:2148705 |
Darker colors indicate more annotations |
Human Phenotypes | Drooling |
Feeding difficulties |
Negativism |
Lack of spontaneous play |
Delayed early-childhood social milestone development |
Impaired ability to form peer relationships |
Autistic behavior |
Autism |
Hyperactivity |
Attention deficit hyperactivity disorder |
Inflexible adherence to routines |
Abnormal repetitive mannerisms |
Restrictive behavior |
Disease(s) Associated with FOXP2 | |||||||||||||
attention deficit hyperactivity disorder | |||||||||||||
autistic disorder | |||||||||||||
schizophrenia | |||||||||||||
speech-language disorder-1 |
Mouse Phenotypes | abnormal motor learning |
decreased exploration in new environment |
abnormal eating behavior |
abnormal response to novel object |
abnormal motor capabilities/coordination/movement |
abnormal reflex |
abnormal righting response |
impaired righting response |
decreased startle reflex |
impaired coordination |
decreased locomotor activity |
positive geotaxis |
bradykinesia |
abnormal vocalization |
decreased vocalization |
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Availability | Mouse Genotype | |||||||||||||||
Foxp2N549K/Foxp2N549K | ||||||||||||||||
Foxp2R552H/Foxp2R552H | ||||||||||||||||
Foxp2S321X/Foxp2S321X | ||||||||||||||||
Foxp2tm1Bux/Foxp2tm1Bux | ||||||||||||||||
Foxp2tm1Momo/Foxp2tm1Momo | ||||||||||||||||
Foxp2tm2.1Woen/Foxp2tm2.1Woen | ||||||||||||||||
Foxp2R552H/Foxp2+ | ||||||||||||||||
Foxp2tm1Bux/Foxp2+ | ||||||||||||||||
Foxp2tm1Momo/Foxp2+ | ||||||||||||||||
Foxp2tm2.2Woen/Foxp2+ | ||||||||||||||||
Foxp2tm1Sfis/Foxp2tm1.2Sfis Edil3Tg(Sox2-cre)1Amc/? (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 03/12/2024 MGI 6.23 |
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