RTP3

Chr 3

receptor transporter protein 3

Also known as: LTM1, TMEM7, Z3CXXC3

The protein promotes functional cell surface expression of bitter taste receptors TAS2R16 and TAS2R43. No established human disease associations have been reported for mutations in this gene. The gene shows relatively low constraint to loss-of-function variation.

OMIMResearchSummary from RefSeq, UniProt
DNmechanismLOEUF 1.53
Clinical SummaryRTP3
Population Constraint (gnomAD)
Low constraint (pLI 0.20) — loss-of-function variants are relatively tolerated in the population.
📋
ClinVar Variants
8 unique Pathogenic / Likely Pathogenic· 32 VUS of 44 total submissions

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

Tolerant — LoF & missense variants common in population
LoF Constraint
1.53LOEUF
pLI 0.201
Z-score 0.99
OE 0.36 (0.131.53)
Tolerant

Highly tolerant — LoF variants common in population

Missense Constraint
0.34Z-score
OE missense 0.91 (0.791.07)
116 obs / 126.9 exp
Tolerant

Mild missense constraint

Observed / Expected Ratios
LoF OE0.36 (0.131.53)
00.351.4
Missense OE0.91 (0.791.07)
00.61.4
Synonymous OE0.84
01.21.6
LoF obs/exp: 1 / 2.8Missense obs/exp: 116 / 126.9Syn Z: 0.87
DN
0.6452th %ile
GOF
0.6052th %ile
LOF
0.2679th %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

44 submitted variants in ClinVar

Classification Summary

Pathogenic7
Likely Pathogenic1
VUS32
Likely Benign4
7
Pathogenic
1
Likely Pathogenic
32
VUS
4
Likely Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
7
0
7
Likely Pathogenic
0
0
1
0
1
VUS
0
31
1
0
32
Likely Benign
0
4
0
0
4
Benign
0
0
0
0
0
Total0359044

LoF = frameshift, stop gained/lost, canonical splice · Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

RTP3 · 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 ↗