ARMC2
Chr 6ARarmadillo repeat containing 2
Also known as: SPGF38, bA787I22.1
Primary Disease Associations & Inheritance
Spermatogenic failure 38MIM #618433
AR
Clinical highlights
Gene-disease validity (ClinGen)
spermatogenic failure 38 · ARDefinitivesufficient evidence for diagnostic panels
Population Genetics & Constraint
gnomAD v4 — loss-of-function & missense intolerance
Tolerant — LoF & missense variants common in population
LoF Constraint?
0.79LOEUF
pLI 0.000
Z-score 2.56
OE 0.54 (0.38–0.79)
Typical tolerance to LoF variation
Missense Constraint?
0.74Z-score
OE missense 0.90 (0.83–0.98)
409 obs / 453.1 exp
Mild missense constraint
Observed / Expected Ratios?
LoF OE?0.54 (0.38–0.79)
0≤0.351.4
Missense OE?0.90 (0.83–0.98)
0≤0.61.4
Synonymous OE?1.09
0≤1.21.6
LoF obs/exp: 20 / 36.8Missense obs/exp: 409 / 453.1Syn Z: -0.94
ClinVar Variant Classifications
0 submitted variants in ClinVar
Protein Context — Lollipop Plot
ARMC2 · 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 →External Resources
Links to major genomics databases and tools