GOLGA6L7
Chr 15golgin A6 family like 7
Also known as: GOLGA6L7P
Predicted to be located in cis-Golgi network. [provided by Alliance of Genome Resources, Jul 2025]
57
ClinVar variants
38
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— GOLGA6L7
📋
ClinVar Variants
38 Pathogenic / Likely Pathogenic· 10 VUS of 57 total submissions
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
57 submitted variants in ClinVar
Classification Summary
Pathogenic36
Likely Pathogenic2
VUS10
Likely Benign8
Conflicting1
36
Pathogenic
2
Likely Pathogenic
10
VUS
8
Likely Benign
1
Conflicting
Curated Variants Distribution
Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable
| Classification | LoF | Missense + Inframe | Non-coding | Synonymous | Total |
|---|---|---|---|---|---|
Pathogenic | — | — | — | — | 36 |
Likely Pathogenic | — | — | — | — | 2 |
VUS | — | — | — | — | 10 |
Likely Benign | — | — | — | — | 8 |
Benign | — | — | — | — | 0 |
Conflicting | — | 1 | |||
| Total | — | 57 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
GOLGA6L7 · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
OMIM — Genotype-Phenotype
No OMIM entries found.
External Resources
Links to major genomics databases and tools
Variant Interpretation
Population Databases
Gene Resources
Expert Curation
ClinGen
Expert-curated gene-disease validity
GenCC
Gene Curation Coalition — multi-curator classifications
Orphanet
Rare disease encyclopedia and gene-disease associations
PanelApp
Gene panels for rare disease diagnostics (Genomics England)
LOVD
Leiden Open Variation Database — variant listings
GeneReviews
Expert-authored summaries of heritable conditions (NCBI)
Clinical Literature
Landmark / reviewRecent case evidence
No publications found for GOLGA6L7
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →External Resources
Links to major genomics databases and tools
Variant Interpretation
Population Databases
Gene Resources
Expert Curation
ClinGen
Expert-curated gene-disease validity
GenCC
Gene Curation Coalition — multi-curator classifications
Orphanet
Rare disease encyclopedia and gene-disease associations
PanelApp
Gene panels for rare disease diagnostics (Genomics England)
LOVD
Leiden Open Variation Database — variant listings
GeneReviews
Expert-authored summaries of heritable conditions (NCBI)