Genopathy
Gene-Disorder Association · Article
Gene
SDCCAG8
SHH Signaling And Ciliogenesis Regulator SDCCAG8
Disorder
Senior-Loken Syndrome 1
First reported 1960
Supporting publications 1
Key publication · disorder Juvenile nephronophthisis. Part 1. A genetically determined nephropathy with hypotonic polyuria and azotaemia.Acta paediatrica · 1960
Manually curated
Association Review

In brief

The association between SDCCAG8 (SHH Signaling And Ciliogenesis Regulator SDCCAG8) and Senior-Loken Syndrome 1 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.

Sources 3
Clinical variants 5
Symptoms 31
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.

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
SDCCAG8

The gene

1 source summary

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

Request access
04
Senior-Loken Syndrome 1

The disorder

14 database identifiers

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

Request access
05
Phenotype

Clinical features

25 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

5 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

1 shared pathway

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

Request access
08
Literature

Reading

1 publication

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

Request access
09
Provenance

References & sources

10 references

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

Request access