ZBTB6

Chr 9

zinc finger and BTB domain containing 6

Also known as: ZID, ZNF482

The protein functions as a DNA-binding transcriptional repressor that regulates RNA polymerase II transcription and is predicted to be involved in cytokine production and immune system regulation. Mutations in this gene have been associated with neurodevelopmental disorders, though the clinical phenotype and inheritance pattern are not well-established from current data. The gene shows moderate constraint against loss-of-function variants (LOEUF 0.641), suggesting some intolerance to complete protein loss.

OMIMResearchSummary from RefSeq, UniProt
DNmechanismLOEUF 0.64
Clinical SummaryZBTB6
Population Constraint (gnomAD)
Constrained for loss-of-function variants (OE-LoF 0.28) despite low pLI — interpret in context.
📋
ClinVar Variants
29 unique Pathogenic / Likely Pathogenic· 35 VUS of 68 total submissions

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

Tolerant — LoF & missense variants common in population
LoF Constraint
0.64LOEUF
pLI 0.137
Z-score 2.52
OE 0.28 (0.140.64)
Tolerant

Typical tolerance to LoF variation

Missense Constraint
1.72Z-score
OE missense 0.67 (0.580.77)
144 obs / 215.1 exp
Tolerant

Mild missense constraint

Observed / Expected Ratios
LoF OE0.28 (0.140.64)
00.351.4
Missense OE0.67 (0.580.77)
00.61.4
Synonymous OE0.96
01.21.6
LoF obs/exp: 4 / 14.3Missense obs/exp: 144 / 215.1Syn Z: 0.29
DN
0.6355th %ile
GOF
0.5170th %ile
LOF
0.4037th %ile

The highest-scoring mechanism for this gene is dominant-negative.

DNprediction above median

Note: In-silico variant effect predictors (SIFT, PolyPhen, REVEL, CADD) may underestimate pathogenicity of missense variants in genes with GOF or DN mechanisms. Consider functional evidence and clinical context.

Predictions from Badonyi M, Marsh JA. PLoS ONE. 2024;19(8):e0307312.

ClinVar Variant Classifications

68 submitted variants in ClinVar

Classification Summary

Pathogenic28
Likely Pathogenic1
VUS35
Likely Benign1
28
Pathogenic
1
Likely Pathogenic
35
VUS
1
Likely Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
28
0
28
Likely Pathogenic
0
0
1
0
1
VUS
0
32
3
0
35
Likely Benign
0
0
0
1
1
Benign
0
0
0
0
0
Total03232165

LoF = frameshift, stop gained/lost, canonical splice · Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

ZBTB6 · protein map & ClinVar variants

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

3D Protein StructureAlphaFold

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Open Research Assistant →
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC