Genopathy
Gene-Disorder Association · Article
Gene
TMEM127
Transmembrane Protein 127
Disorder
Hereditary Paraganglioma-Pheochromocytoma Syndromes
First reported 2017
Supporting publications 19
Key publication · gene–disorder Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention.JAMA oncology · 2017
Key publication · disorder [Cervical paragangliomas: 4 cases].Annales d'anatomie pathologique · 1963
Manually curated
Association Review

In brief

The association between TMEM127 (Transmembrane Protein 127) and Hereditary Paraganglioma-Pheochromocytoma Syndromes is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants.

Sources 3
Clinical variants 706
Symptoms 47
Compounds 0
Trials 0
Publications 19
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
TMEM127

The gene

1 source summary

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

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04
Hereditary Paraganglioma-Pheochromocytoma Syndromes

The disorder

12 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

41 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

706 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

19 publications

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

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09
Provenance

References & sources

15 references

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

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