Genopathy
Gene-Disorder Association · Article
Gene
KNSTRN
Kinetochore Localized Astrin (SPAG5) Binding Protein
Disorder
Roifman-Chitayat Syndrome
First reported 2009
Supporting publications 2
Key publication · gene–disorder Combined immunodeficiency, facial dysmorphism, optic nerve atrophy, skeletal anomalies and developmental delay: a new syndrome.Clinical genetics · 2009
Key publication · disorder Familial variable immunodeficiency: autosomal dominant pattern of inheritance with variable expression of the defect(s).The Journal of pediatrics · 1975
Manually curated
Association Review

In brief

The association between KNSTRN (Kinetochore Localized Astrin (SPAG5) Binding Protein) and Roifman-Chitayat Syndrome is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and a causative germline mutation.

Sources 4
Clinical variants 1
Symptoms 110
Compounds 0
Trials 0
Publications 2
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
KNSTRN

The gene

1 source summary

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

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04
Roifman-Chitayat Syndrome

The disorder

11 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

76 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

1 clinical variant

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

2 publications

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

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09
Provenance

References & sources

10 references

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

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