Genopathy
Gene-Disorder Association · Article
Gene
ARHGAP26
Rho GTPase Activating Protein 26
Disorder
Juvenile Myelomonocytic Leukemia
First reported 2000
Supporting publications 1
Key publication · gene–disorder The human GRAF gene is fused to MLL in a unique t(5;11)(q31;q23) and both alleles are disrupted in three cases of myelodysplastic syndrome/acute myeloid leukemia with a deletion 5q.Proceedings of the National Academy of Sciences of the United States of America · 2000
Key publication · disorder [Clinico-hematological considerations on a case of juvenile chronic myeloid leukemia].Minerva pediatrica · 1969
Manually curated
Association Review

In brief

The association between ARHGAP26 (Rho GTPase Activating Protein 26) and Juvenile Myelomonocytic Leukemia 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 3
Symptoms 4
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.

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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
ARHGAP26

The gene

1 source summary

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

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04
Juvenile Myelomonocytic Leukemia

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

1 clinical feature

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

3 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

1 publication

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

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09
Provenance

References & sources

8 references

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

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