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Symbol Name ID |
Stra6
stimulated by retinoic acid gene 6 MGI:107742 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Intellectual disability |
Intellectual disability, profound |
Profound global developmental delay |
| Disease(s) Associated with STRA6 | |||
| syndromic microphthalmia 9 |
| Mouse Phenotypes | nervous system phenotype |
hydrocephaly |
dilated brain ventricle |
decreased retina cone cell number |
abnormal retina photoreceptor morphology |
short photoreceptor inner segment |
short photoreceptor outer segment |
short retina rod cell outer segment |
retina cone cell degeneration |
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| Availability | Mouse Genotype | |||||||||
| Stra6tm1.1Jvli/Stra6tm1.1Jvli | * | |||||||||
| Stra6tm1Jvli/Stra6tm1Jvli | ||||||||||
| Stra6tm1Nbg/Stra6tm1Nbg | ||||||||||
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 04/23/2024 MGI 6.23 |
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