Genopathy
Gene-Disorder Association · Article
Gene
VPS35L
VPS35 Endosomal Protein Sorting Factor Like
Disorder
Ritscher-Schinzel Syndrome 3
First reported 2020
Supporting publications 2
Key publication · gene–disorder Biallelic VPS35L pathogenic variants cause 3C/Ritscher-Schinzel-like syndrome through dysfunction of retriever complex.Journal of medical genetics · 2020
Key publication · disorder Evidence for Ritscher-Schinzel syndrome in Canadian Native Indians.American journal of medical genetics · 1995
Manually curated
Association Review

In brief

The association between VPS35L (VPS35 Endosomal Protein Sorting Factor Like) and Ritscher-Schinzel Syndrome 3 is well established and manually curated, with its 3 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.

Sources 3
Clinical variants 7
Symptoms 57
Compounds 0
Trials 0
Publications 2
01
At a glance

Association overview

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

Request access
02
Provenance

Evidence and sources

3 sources

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

Request access
03
VPS35L

The gene

1 source summary

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

Request access
04
Ritscher-Schinzel Syndrome 3

The disorder

8 database identifiers

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

Request access
05
Phenotype

Clinical features

28 clinical features

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

Request access
06
ClinVar and variant evidence

Genetic basis

7 clinical variants

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

Request access
07
Mechanism overlap

Shared mechanisms

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

Request access
08
Literature

Reading

2 publications

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

Request access
09
Provenance

References & sources

7 references

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

Request access