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Symbol Name ID |
2700049A03Rik
RIKEN cDNA 2700049A03 gene MGI:1924217 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypoplasia of the brainstem |
Hydrocephalus |
Ventriculomegaly |
Polymicrogyria |
Dysplastic corpus callosum |
Hypoplasia of the corpus callosum |
Anencephaly |
Aplasia of the olfactory bulb |
Cerebellar vermis hypoplasia |
Cerebellar dysplasia |
Molar tooth sign on MRI |
Occipital meningocele |
Hyporeflexia |
Global developmental delay |
| Disease(s) Associated with KIAA0586 | ||||||||||||||
| Joubert syndrome 23 | ||||||||||||||
| short-rib thoracic dysplasia 14 with polydactyly |
| Mouse Phenotypes | abnormal neural tube morphology |
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| Availability | Mouse Genotype | |
| 2700049A03Riktm1.2Arte/2700049A03Riktm1.2Arte | ||
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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