Genopathy
Gene-Disorder Association · Article
Gene
LOC126861452
CDK7 Strongly-Dependent Group 2 Enhancer GRCh37_chr12:12037195-12038394
First reported 1979
Supporting publications 11
Association Review

In brief

The association between LOC126861452 (CDK7 Strongly-Dependent Group 2 Enhancer GRCh37_chr12:12037195-12038394) and Thrombocytopenia 5 is supported by expert-curated evidence, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 9
Symptoms 13
Compounds 0
Trials 0
Publications 11
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access
02
Provenance

Evidence and sources

1 source

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

Request access
03
LOC126861452

The gene

1 source summary

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

Request access
04
Thrombocytopenia 5

The disorder

7 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access
05
Phenotype

Clinical features

8 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

Request access
06
ClinVar and variant evidence

Genetic basis

9 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

Request access
07
Literature

Reading

11 publications

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

Request access
08
Provenance

References & sources

13 references

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

Request access