Symbol
Name
ID

Trpm1
transient receptor potential cation channel, subfamily M, member 1
MGI:1330305

Phenotype annotations related to vision/eye

*	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

Trpm1^nob11/Trpm1^nob11

Trpm1^rd15/Trpm1^rd15

Trpm1^{tm1b(KOMP)Wtsi}/Trpm1^{tm1b(KOMP)Wtsi}

Trpm1^tm1Lex/Trpm1^tm1Lex

Trpm1^tm1Tfur/Trpm1^tm1Tfur

Trpm1^tvrm27/Trpm1^tvrm27

Trpm1^tm1Lex/Trpm1^tvrm27

Trpm1^tvrm27/Trpm1⁺

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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