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Symbol Name ID |
Pex2
peroxisomal biogenesis factor 2 MGI:107486 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Feeding difficulties in infancy |
Poor suck |
Lethargy |
| Disease(s) Associated with PEX2 | |||
| peroxisome biogenesis disorder 5A |
| Mouse Phenotypes | behavior/neurological phenotype |
aphagia |
abnormal motor capabilities/coordination/movement |
limb grasping |
impaired balance |
trunk curl |
abnormal head movements |
abnormal gait |
decreased locomotor activity |
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| Availability | Mouse Genotype | |||||||||
| Pex2tm1Plf/Pex2tm1Plf | * | |||||||||
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 04/30/2024 MGI 6.23 |
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