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Symbol Name ID |
Ddhd2
DDHD domain containing 2 MGI:1919358 |
| Darker colors indicate more annotations |
| Human Phenotypes | Dysphagia |
Optic nerve hypoplasia |
Spastic paraplegia |
Upper limb spasticity |
Spastic gait |
Hypoplasia of the corpus callosum |
Periventricular leukomalacia |
Periventricular white matter hyperintensities |
Syringomyelia |
Babinski sign |
Dysarthria |
Intellectual disability |
Hyperreflexia |
Gait disturbance |
Tip-toe gait |
Global developmental delay |
| Disease(s) Associated with DDHD2 | ||||||||||||||||
| hereditary spastic paraplegia 54 |
| Mouse Phenotypes | abnormal brain morphology |
abnormal neuron morphology |
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| Availability | Mouse Genotype | ||
| Ddhd2tm1Crv/Ddhd2tm1Crv | |||
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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