MYRIP

Chr 3

myosin VIIA and Rab interacting protein

Also known as: SLAC2-C, SLAC2C

MYRIP encodes a Rab effector protein that links RAB27A-containing vesicles to actin filaments and motor proteins, facilitating vesicle transport and exocytosis including insulin release. Mutations cause autosomal recessive nonsyndromic hearing loss (DFNB25), typically presenting in early childhood. The gene shows very low constraint to loss-of-function variants (pLI < 0.001, LOEUF 0.568), consistent with its recessive inheritance pattern.

OMIMResearchSummary from RefSeq, UniProt
MultiplemechanismLOEUF 0.57
Clinical SummaryMYRIP
Population Constraint (gnomAD)
Low constraint (pLI 0.00) — loss-of-function variants are relatively tolerated in the population.
📋
ClinVar Variants
9 unique Pathogenic / Likely Pathogenic· 135 VUS of 172 total submissions

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

Moderate LoF intolerance
LoF Constraint
0.57LOEUF
pLI 0.000
Z-score 3.85
OE 0.38 (0.260.57)
Moderately constrained

More LoF-intolerant than ~75% of genes

Missense Constraint
0.73Z-score
OE missense 0.91 (0.840.98)
440 obs / 485.5 exp
Tolerant

Mild missense constraint

Observed / Expected Ratios
LoF OE0.38 (0.260.57)
00.351.4
Missense OE0.91 (0.840.98)
00.61.4
Synonymous OE1.10
01.21.6
LoF obs/exp: 17 / 44.9Missense obs/exp: 440 / 485.5Syn Z: -1.07
DN
0.7034th %ile
GOF
0.6932th %ile
LOF
0.3649th %ile

This gene has evidence for multiple mechanisms of pathogenicity (dominant-negative and gain-of-function). Both the Badonyi & Marsh prediction and the broader genomic evidence point to dominant-negative as the predominant mechanism. Different variants in this gene may act through different mechanisms — interpret in context of the specific variant.

DNprediction above median
GOFprediction 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

172 submitted variants in ClinVar

Classification Summary

Pathogenic8
Likely Pathogenic1
VUS135
Likely Benign9
Benign3
8
Pathogenic
1
Likely Pathogenic
135
VUS
9
Likely Benign
3
Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
8
0
8
Likely Pathogenic
0
0
1
0
1
VUS
2
133
0
0
135
Likely Benign
0
8
0
1
9
Benign
0
1
1
1
3
Total2142102156

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

View in ClinVar →

Protein Context — Lollipop Plot

MYRIP · 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
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