Genopathy
Gene-Disorder Association · Article
Gene
SPTA1
Spectrin Alpha, Erythrocytic 1
Disorder
Pyropoikilocytosis, Hereditary
First reported 1986
Supporting publications 25
Key publication · gene–disorder Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis.Blood · 1986
Key publication · disorder Distribution of alkaline phosphatase in the serum proteins in hypophosphatasia.Journal of clinical pathology · 1962
Manually curated
Association Review

In brief

The association between SPTA1 (Spectrin Alpha, Erythrocytic 1) and Pyropoikilocytosis, Hereditary is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.

Sources 4
Clinical variants 310
Symptoms 7
Compounds 0
Trials 0
Publications 25
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

4 sources

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

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03
SPTA1

The gene

1 source summary

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

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04
Pyropoikilocytosis, Hereditary

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

4 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

310 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

25 publications

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

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09
Provenance

References & sources

14 references

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

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