Symbol Name ID |
Nrl
neural retina leucine zipper gene MGI:102567 |
* | 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 |
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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) |
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 |
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