FAM66D
Chr 8family with sequence similarity 66 member D
Clinical Summary— FAM66D
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
0 submitted variants in ClinVar
FAM66D · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
External Resources
Links to major genomics databases and tools
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →Clinical Literature
Landmark / reviewRecent case evidence
Full-Text Mentions
NLP-detected gene mentions in article bodies · via PubTator3
LncRNA expression signature identified using genome-wide transcriptomic profiling to predict lymph node metastasis in patients with stage T1 and T2 gastric cancer
Dong ZB et al.·Gastric Cancer
2023Cohort
The potential role of long noncoding RNAs in primary open-angle glaucoma
Zhang F et al.·Graefes Arch Clin Exp Ophthalmol
2021
Blood-derived deoxyribonucleic acid methylation clusters associate with adverse social exposures and endophenotypes of stress-related psychiatric illness in a trauma-exposed cohort of women
Pfeiffer JR et al.·Front Psychiatry
2022Cohort
Identifying Critical States of Complex Diseases by Single-Sample Jensen-Shannon Divergence
Yan J et al.·Front Oncol
2021
Whole-genome sequencing revealed a novel long-range deletion mutation spanning GNAS in familial pseudohypoparathyroidism
Fei Y et al.·Mol Genet Genomic Med
2023
Top 5 full-text resultsSearch PubTator3 ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Association between Gut Microbiota Composition and Copy Number Variations in Human Genes FAM66D and TAS2R43.
Wang J et al.·J Microbiol Biotechnol
2025Open Access
Top 5 resultsSearch Europe PMC ↗
External Resources
Links to major genomics databases and tools