OR10AG1

Chr 11

olfactory receptor family 10 subfamily AG member 1

Also known as: OR11-160

NCBI Gene: 282770 ENSG00000174970 UniProt: Q8NH19

Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]

Research

ResearchGenerating clinical summary…

Active trials

Pubs (1 yr)

—

P/LP submissions

—

P/LP missense

1.91

LOEUF

Multiple*

Mechanism· predicted

Some data sources returned errors (1)

omim: Error: OMIM fetch failed: 429

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

gnomAD

Tolerant — LoF & missense variants common in population

LoF Constraint?

1.91LOEUF

pLI 0.000

Z-score -0.63

OE 1.32 (0.69–1.91)

Tolerant

Highly tolerant — LoF variants common in population

Missense Constraint?

-0.29Z-score

OE missense 1.07 (0.94–1.21)

170 obs / 159.5 exp

Tolerant

Tolerant to missense variation

Observed / Expected Ratios?

LoF OE?1.32 (0.69–1.91)

0≤0.351.4

Missense OE?1.07 (0.94–1.21)

0≤0.61.4

Synonymous OE?1.14

0≤1.21.6

LoF obs/exp: 6 / 4.5Missense obs/exp: 170 / 159.5Syn Z: -0.82

Background carrier burden — how many people carry a rare variant somewhere in OR10AG1?

gnomAD v4 · ~731k individuals · PASS only

Rare means allele frequency under

Rare missense

1 in 88

462 rare PASS variants

Rare truncating (LoF)

1 in 580

78 rare PASS variants

Rare synonymous (reference)

1 in 240

156 rare PASS variants

Truncating variants are far rarer here than missense — that gap, in human units, is what constraint means for OR10AG1. A background rate for each class, not the frequency of any particular variant; thin-coverage exons undercount.

By genetic ancestry · 9 gnomAD groups · rare = under 0.1% in that group

Group	People	Missense	Truncating
European (non-Finnish)	~556k	1 in 150	1 in 1,600
South Asian	~43k	1 in 160	1 in 1,500
Remaining (unassigned)	~30k	1 in 71	1 in 320
European (Finnish)	~27k	1 in 310	≈ 1 in 10,000
Admixed American	~22k	1 in 140	1 in 260
African / African American	~21k	1 in 130	1 in 250
East Asian	~20k	1 in 120	1 in 1,100
Ashkenazi Jewish	~13k	1 in 410	≈ 1 in 13,000
Middle Eastern	~2,884	1 in 87	≈ 1 in 960

Each group is summed over the variants that are rare in that group. Grey ≈ figures rest on fewer than five expected carriers — too few to distinguish groups. Differences mostly reflect how many people were sampled and how much variation each ancestry carries, not disease risk.

Exome coverage (gnomAD): 1 of 2 coding exons well covered in gnomAD exomes; exon 1 poorly covered. Genomes: all 2.? see exons ↓