FAM156B

Chr X

family with sequence similarity 156 member B

Also known as: TMEM29B

The FAM156B protein binds methylated histones and localizes to the nuclear envelope. Mutations in this gene have not been definitively associated with any recognized pediatric neurological disorders in the current literature. The clinical significance of variants in FAM156B remains uncertain.

ResearchSummary from RefSeq
Multiplemechanism
Clinical SummaryFAM156B
📋
ClinVar Variants
39 unique Pathogenic / Likely Pathogenic· 1 VUS of 40 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

DN
0.6550th %ile
GOF
0.6931th %ile
LOF
0.2777th %ile

This gene has evidence for multiple mechanisms of pathogenicity (gain-of-function and dominant-negative). Both the Badonyi & Marsh prediction and the broader genomic evidence point to gain-of-function as the predominant mechanism. Different variants in this gene may act through different mechanisms — interpret in context of the specific variant.

GOFprediction above median
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

40 submitted variants in ClinVar

Classification Summary

Pathogenic39
VUS1
39
Pathogenic
1
VUS

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
39
Likely Pathogenic
0
VUS
1
Likely Benign
0
Benign
0
Total40

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

FAM156B · 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 →
Key Publications
Landmark & review papers · by relevance
PubMed
Top 1 results · since 2015Search PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found