Symbol Name ID |
Aipl1
aryl hydrocarbon receptor-interacting protein-like 1 MGI:2148800 |
Darker colors indicate more annotations |
Human Phenotypes | Encephalocele |
Photophobia |
Aplasia/Hypoplasia of the cerebellar vermis |
Abnormality of neuronal migration |
Hemiplegia/hemiparesis |
Intellectual disability |
Hyperreflexia |
Global developmental delay |
Seizure |
Disease(s) Associated with AIPL1 | |||||||||
Leber congenital amaurosis | |||||||||
retinitis pigmentosa |
Mouse Phenotypes | abnormal Muller cell morphology |
decreased retina photoreceptor cell number |
decreased retina cone cell number |
abnormal retina bipolar cell morphology |
abnormal retina photoreceptor morphology |
abnormal photoreceptor inner segment morphology |
abnormal photoreceptor outer segment morphology |
abnormal retina cone cell morphology |
retina rod cell degeneration |
retina photoreceptor degeneration |
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Availability | Mouse Genotype | ||||||||||
Aipl1tm1Mad/Aipl1tm1Mad | |||||||||||
Aipl1tm1Visu/Aipl1tm1Visu | |||||||||||
Aipl1tvrm119/Aipl1tvrm119 | |||||||||||
Aipl1tvrm127/Aipl1tvrm127 | |||||||||||
Aipl1tm1Mad/Aipl1+ | |||||||||||
Aipl1tvrm119/Aipl1tvrm127 |
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 08/02/2024 MGI 6.24 |
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