Symbol Name ID |
Trpm1
transient receptor potential cation channel, subfamily M, member 1 MGI:1330305 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of retinal pigmentation |
Congenital stationary night blindness |
Congenital stationary night blindness with abnormal fundus |
Congenital stationary night blindness with normal fundus |
Retinal thinning |
Abnormal electroretinogram |
Abnormal dark-adapted electroretinogram |
Electronegative electroretinogram |
Reduced amplitude of dark-adapted bright flash electroretinogram a-wave |
Strabismus |
Nystagmus |
Compensatory head posture |
Hypermetropia |
Myopia |
Color vision defect |
Nyctalopia |
Reduced visual acuity |
Disease(s) Associated with TRPM1 | |||||||||||||||||
congenital stationary night blindness | |||||||||||||||||
congenital stationary night blindness 1C |
Mouse Phenotypes | vision/eye phenotype |
impaired pupillary reflex |
mydriasis |
abnormal retina outer plexiform layer morphology |
thin retina outer plexiform layer |
retina degeneration |
retina spots |
abnormal eye physiology |
abnormal electroretinogram waveform feature |
absent b-wave |
abnormal eye electrophysiology |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
abnormal vision |
|
Availability | Mouse Genotype | ||||||||||||||
Trpm1nob11/Trpm1nob11 | |||||||||||||||
Trpm1rd15/Trpm1rd15 | |||||||||||||||
Trpm1tm1b(KOMP)Wtsi/Trpm1tm1b(KOMP)Wtsi | |||||||||||||||
Trpm1tm1Lex/Trpm1tm1Lex | |||||||||||||||
Trpm1tm1Tfur/Trpm1tm1Tfur | |||||||||||||||
Trpm1tvrm27/Trpm1tvrm27 | * | ||||||||||||||
Trpm1tm1Lex/Trpm1tvrm27 | |||||||||||||||
Trpm1tvrm27/Trpm1+ |
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 08/02/2024 MGI 6.24 |
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