TMPRSS11A

Chr 4

transmembrane serine protease 11A

Also known as: ECRG1, HATL1, HESP

The protein is a serine protease that cleaves other proteins and may regulate cellular senescence and cell cycle progression. Mutations in this gene have not been established to cause any recognized human disease. The gene is not highly constrained against loss-of-function variants, suggesting it may be tolerant to certain types of mutations.

OMIMResearchSummary from RefSeq, UniProt
DNmechanismLOEUF 1.29
Clinical SummaryTMPRSS11A
Population Constraint (gnomAD)
Low constraint (pLI 0.00) — loss-of-function variants are relatively tolerated in the population.

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

Tolerant — LoF & missense variants common in population
LoF Constraint
1.29LOEUF
pLI 0.000
Z-score 0.41
OE 0.91 (0.661.29)
Tolerant

Highly tolerant — LoF variants common in population

Missense Constraint
0.50Z-score
OE missense 0.91 (0.811.02)
206 obs / 227.1 exp
Tolerant

Mild missense constraint

Observed / Expected Ratios
LoF OE0.91 (0.661.29)
00.351.4
Missense OE0.91 (0.811.02)
00.61.4
Synonymous OE0.99
01.21.6
LoF obs/exp: 24 / 26.2Missense obs/exp: 206 / 227.1Syn Z: 0.08
DN
0.6743th %ile
GOF
0.6053th %ile
LOF
0.3746th %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

0 submitted variants in ClinVar

Protein Context — Lollipop Plot

TMPRSS11A · 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.

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Clinical Literature
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