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Symbol
Name
ID
Aipl1
aryl hydrocarbon receptor-interacting protein-like 1
MGI:2148800
Phenotype annotations related to nervous system
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
Availability Mouse Genotype
Aipl1tm1Mad/Aipl1tm1Mad
Aipl1tm1Visu/Aipl1tm1Visu
Aipl1tvrm119/Aipl1tvrm119
Aipl1tvrm127/Aipl1tvrm127
Aipl1tm1Mad/Aipl1+
Aipl1tvrm119/Aipl1tvrm127

Contributing Projects:
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
The Jackson Laboratory