Genopathy
Gene-Disorder Association · Article
Gene
TRPM1
Transient Receptor Potential Cation Channel Subfamily M Member 1
Disorder
Congenital Stationary Night Blindness
First reported 2009
Supporting publications 1
Key publication · gene–disorder Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.American journal of human genetics · 2009
Key publication · disorder Congenital stationary night blindness without ophthalmoscopic or other abnormalities.Transactions of the American Ophthalmological Society · 1952
Manually curated
Association Review

In brief

The association between TRPM1 (Transient Receptor Potential Cation Channel Subfamily M Member 1) and Congenital Stationary Night Blindness is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording likely-pathogenic variants.

Sources 2
Clinical variants 11
Symptoms 19
Compounds 0
Trials 0
Publications 1
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

2 sources

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
TRPM1

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

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04
Congenital Stationary Night Blindness

The disorder

10 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Phenotype

Clinical features

14 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
ClinVar and variant evidence

Genetic basis

11 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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07
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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08
Literature

Reading

1 publication

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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09
Provenance

References & sources

7 references

Every source and publication cited across this dossier, as one numbered reference list.

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