Genopathy
Gene-Disorder Association · Article
Gene
SLC51A
Solute Carrier Family 51 Member A
Disorder
Cholestasis, Progressive Familial Intrahepatic, 6
First reported 1981
Supporting publications 1
Key publication · disorder Increased cholesterol and decreased fluidity of red cell membranes (spur cell anemia) in progressive intrahepatic cholestasis.Pediatrics · 1981
Manually curated
Association Review

In brief

The association between SLC51A (Solute Carrier Family 51 Member A) and Cholestasis, Progressive Familial Intrahepatic, 6 is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.

Sources 2
Clinical variants 3
Symptoms 20
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

2 sources

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

Request access
03
SLC51A

The gene

1 source summary

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

Request access
04
Cholestasis, Progressive Familial Intrahepatic, 6

The disorder

6 database identifiers

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

Request access
05
Phenotype

Clinical features

10 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

3 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

1 publication

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

Request access
09
Provenance

References & sources

5 references

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

Request access