|
Symbol Name ID |
Tecpr2
tectonin beta-propeller repeat containing 2 MGI:2144865 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Spastic paraplegia |
Spastic gait |
Hypoplasia of the corpus callosum |
Cerebral atrophy |
Cerebellar atrophy |
Dysmetria |
Gait ataxia |
Dysarthria |
Intellectual disability |
Areflexia |
Global developmental delay |
Seizure |
Bilateral tonic-clonic seizure |
| Disease(s) Associated with TECPR2 | ||||||||||||||
| hereditary spastic paraplegia 49 |
| Mouse Phenotypes | neurodegeneration |
axonal dystrophy |
axonal spheroids |
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| Availability | Mouse Genotype | |||
| Tecpr2em1Wei/Tecpr2em1Wei | ||||
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 04/23/2024 MGI 6.23 |
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