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Symbol Name ID |
Bhlhe22
basic helix-loop-helix family, member e22 MGI:1930001 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Mouse Phenotypes | nervous system phenotype |
abnormal axon guidance |
decreased brain size |
absent corpus callosum |
absent hippocampal commissure |
absent anterior commissure |
abnormal pyramidal decussation morphology |
abnormal cerebral cortex morphology |
abnormal somatosensory cortex morphology |
disorganized barrel cortex |
abnormal nervous system tract morphology |
abnormal anterior corticospinal tract morphology |
abnormal corticospinal tract morphology |
abnormal motor neuron morphology |
decreased amacrine cell number |
abnormal retina cone bipolar cell morphology |
abnormal nervous system physiology |
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| Availability | Mouse Genotype | |||||||||||||||||
| Bhlhe22tm1Gan/Bhlhe22tm1Gan | ||||||||||||||||||
| Bhlhe22tm1Meg/Bhlhe22tm1Meg | * | |||||||||||||||||
| Bhlhe22tm2.1Meg/Bhlhe22tm2.1Meg Emx1tm1(cre)Krj/Emx1+ (conditional) |
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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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