Genopathy
Gene-Disorder Association · Article
Gene
EPB41L1
Erythrocyte Membrane Protein Band 4.1 Like 1
Disorder
Chromosome 20q11-Q12 Deletion Syndrome
First reported 1975
Key publication · disorder Possible dominant inheritance of the idiopathic hypercalcemic syndrome.Human heredity · 1975
Manually curated
Association Review

In brief

The association between EPB41L1 (Erythrocyte Membrane Protein Band 4.1 Like 1) and Chromosome 20q11-Q12 Deletion Syndrome is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and causative variation.

Sources 3
Clinical variants 12
Symptoms 75
Compounds 0
Trials 0
Publications 0
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

3 sources

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

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03
EPB41L1

The gene

1 source summary

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

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04
Chromosome 20q11-Q12 Deletion Syndrome

The disorder

5 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

18 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

12 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
Provenance

References & sources

6 references

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

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