Genopathy
Gene-Disorder Association · Article
Gene
TUBB
Tubulin Beta Class I
Disorder
Cortical Dysplasia, Complex, With Other Brain Malformations 6
First reported 2021
Supporting publications 6
Key publication · gene–disorder Identification of two novel de novo TUBB variants in cases with brain malformations: case reports and literature review.Journal of human genetics · 2021
Key publication · disorder Localization of tuberous sclerosis 2 mRNA and its protein product tuberin in normal human brain and in cerebral lesions of patients with tuberous sclerosis.Brain pathology (Zurich, Switzerland) · 1996
Manually curated
Association Review

In brief

The association between TUBB (Tubulin Beta Class I) and Cortical Dysplasia, Complex, With Other Brain Malformations 6 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and causative variation.

Sources 4
Clinical variants 31
Symptoms 28
Compounds 0
Trials 0
Publications 6
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
TUBB

The gene

2 source summaries

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

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04
Cortical Dysplasia, Complex, With Other Brain Malformations 6

The disorder

8 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

15 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

31 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

6 publications

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

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09
Provenance

References & sources

13 references

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

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