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Symbol
Name
ID
Nrl
neural retina leucine zipper gene
MGI:102567
Phenotype annotations related to nervous system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Photophobia
Intellectual disability
Hyperreflexia
Disease(s) Associated with NRL
retinitis pigmentosa

Mouse Phenotypes
nervous system phenotype
absent retina rod cells
increased retina cone cell number
abnormal retina photoreceptor morphology
abnormal photoreceptor outer segment morphology
short photoreceptor outer segment
abnormal retina cone cell morphology
retina cone cell degeneration
retina photoreceptor degeneration
Availability Mouse Genotype
Nrltm1.1(Thrb)Df/Nrltm1.1(Thrb)Df
Nrltm1.1Jcco/Nrltm1.1Jcco
Nrltm1Asw/Nrltm1Asw
Nrltm1Jcco/Nrltm1Jcco *
Nrltm1Jcco/Nrltm1Jcco
Tg(CAG-cre/Esr1*)5Amc/0  (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
05/14/2024
MGI 6.23
The Jackson Laboratory