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Symbol Name ID |
Fam151b
family with sequence similarity 151, member B MGI:1921192 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Mouse Phenotypes | vision/eye phenotype |
decreased photoreceptor outer segment number |
short photoreceptor outer segment |
photoreceptor outer segment degeneration |
retina cone cell degeneration |
retina rod cell degeneration |
abnormal retina pigmentation |
abnormal retina morphology |
decreased a-wave amplitude |
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| Availability | Mouse Genotype | |||||||||
| Fam151btm1b(EUCOMM)Hmgu/Fam151btm1b(EUCOMM)Hmgu | * | |||||||||
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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