|
Symbol Name ID |
Rai1
retinoic acid induced 1 MGI:103291 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Ventriculomegaly |
Aplasia/Hypoplasia of the corpus callosum |
Corticospinal tract hypoplasia |
EEG abnormality |
Abnormal nerve conduction velocity |
Abnormality of speech or vocalization |
Delayed speech and language development |
Anxiety |
Atypical behavior |
Onychotillomania |
Hyperactivity |
Attention deficit hyperactivity disorder |
Motor stereotypy |
Self hugging |
Head-banging |
Self-injurious behavior |
Self-mutilation |
Hyperacusis |
Polyembolokoilamania |
Intellectual disability |
Sleep abnormality |
Sleep-wake inversion |
Areflexia |
Hyporeflexia |
Gait disturbance |
Global developmental delay |
Peripheral neuropathy |
Seizure |
Impaired pain sensation |
Pain insensitivity |
| Disease(s) Associated with RAI1 | |||||||||||||||||||||||||||||||
| Smith-Magenis syndrome |
| Mouse Phenotypes | seizures |
tonic-clonic seizures |
abnormal brain wave pattern |
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| Availability | Mouse Genotype | |||
| Rai1tm1Jrl/Rai1tm1Jrl | ||||
| Rai1tm1Jrl/Rai1+ | ||||
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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