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Symbol
Name
ID
Cdkn2a
cyclin dependent kinase inhibitor 2A
MGI:104738
Phenotype annotations related to vision/eye
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Proptosis
Horner syndrome
Opsoclonus
Disease(s) Associated with CDKN2A
neuroblastoma

Mouse Phenotypes
vision/eye phenotype
abnormal retina photoreceptor morphology
abnormal eye morphology
abnormal lens morphology
abnormal lens capsule morphology
abnormal lens development
cataract
persistent hyperplastic primary vitreous
primary vitreous hyperplasia
microphthalmia
abnormal posterior eye segment morphology
abnormal retina morphology
abnormal retina neuronal layer morphology
abnormal retina ganglion layer morphology
abnormal retina inner nuclear layer morphology
retina detachment
retina fold
blindness
binocular blindness
Availability Mouse Genotype
Cdkn2aem1Cjs/Cdkn2aem1Cjs *
Cdkn2aem2Cjs/Cdkn2aem2Cjs
Cdkn2atm1a(EUCOMM)Wtsi/Cdkn2atm1a(EUCOMM)Wtsi
Cdkn2atm1Cjs/Cdkn2atm1Cjs *
Cdkn2atm1Rdp/Cdkn2atm1Rdp
Cdkn2atm1Sxs/Cdkn2atm1Sxs
Cdkn2atm3(cre)Cjs/Cdkn2atm4Cjs  (conditional)

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
04/09/2024
MGI 6.23
The Jackson Laboratory