TSC22D4-C7ORF61

Chr 7

TSC22D4-C7orf61 readthrough

NCBI Gene: 122198330

This locus represents naturally occurring readthrough transcription between the neighboring TSC22D4 (TSC22 domain family member 4) and C7orf61 (chromosome 7 open reading frame 61) genes on chromosome 7. The readthrough transcript encodes a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Aug 2021]

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Active trials
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Pathogenic / LP
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ClinVar variants
0
Pubs (1 yr)
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Missense Z
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LOEUF
Clinical Summary— TSC22D4-C7ORF61
Some data sources returned errors (2)

ensembl: Error: Ensembl fetch failed: 400 for https://rest.ensembl.org/lookup/symbol/homo_sapiens/TSC22D4-C7ORF61?content-type=application/json&expand=1

gnomad: Error: Gene not found

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

0 submitted variants in ClinVar

ClinVar

TSC22D4-C7ORF61 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

ClinicalTrials.gov

No active trials found for this gene.

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Clinical Literature
Landmark / reviewRecent case evidence
Full-Text Mentions
NLP-detected gene mentions in article bodies · via PubTator3
PubTator3
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Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found

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External Resources

Links to major genomics databases and tools

Franklin by Genoox
AI-powered variant curation and clinical analysis
DECIPHER
Genomic variants and phenotypes in rare disease patients