Symbol Name ID |
Ebf3
early B cell factor 3 MGI:894289 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Dysphagia |
Cerebellar vermis hypoplasia |
Cerebellar atrophy |
Ataxia |
Dysmetria |
Gait ataxia |
Truncal ataxia |
Speech apraxia |
Delayed speech and language development |
Dysarthria |
Motor stereotypy |
Intellectual disability |
Broad-based gait |
Global developmental delay |
Motor delay |
Delayed fine motor development |
Delayed ability to walk |
Seizure |
Pain insensitivity |
Disease(s) Associated with EBF3 | ||||||||||||||||||||
hypotonia, ataxia, and delayed development syndrome |
Mouse Phenotypes | small olfactory bulb |
abnormal sensory neuron innervation pattern |
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Availability | Mouse Genotype | ||
Ebf3tm1Reed/Ebf3tm1Reed |
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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