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Symbol Name ID |
Foxp1
forkhead box P1 MGI:1914004 |
| Darker colors indicate more annotations |
| Human Phenotypes | Feeding difficulties |
Feeding difficulties in infancy |
Aggressive behavior |
Attention deficit hyperactivity disorder |
Inflexible adherence to routines |
Speech articulation difficulties |
Atypical behavior |
Autistic behavior |
Schizophrenia |
Compulsive behaviors |
Motor stereotypy |
Repetitive compulsive behavior |
Self-injurious behavior |
| Disease(s) Associated with FOXP1 | |||||||||||||
| intellectual disability-severe speech delay-mild dysmorphism syndrome | |||||||||||||
| schizophrenia |
| Mouse Phenotypes | hyperactivity |
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| Availability | Mouse Genotype | |
| Foxp1tm1b(KOMP)Wtsi/Foxp1+ | ||
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 03/25/2025 MGI 6.24 |
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