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OR10H3

Synonyms
-
External resources
Summary
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. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms.

Variant Counts

Variant classification counts, according to ACMG guideline on all identified variants among our tested samples, are listed. The variants with over 5% variant frequency in population genome databases ( gnomAD, dbSNP, etc.) are excluded.

Pathogenic
1
Likely pathogenic
134
VUS
332
Likely benign
48
Benign
0

Patient Phenotypes

Proportions of phenotypes among 135 patients carrying pathogenic or likely pathogenic variants on OR10H3 gene are displayed below. The following symptoms were found in patients with a variant in OR10H3. However, patients may have been diagnosed with a different variant.

Phenotype class
Patients in 3billion (%)
Abnormality of the nervous system
38.5%
Abnormality of the musculoskeletal system
28.1%
Abnormality of the cardiovascular system
20%
Abnormality of head or neck
18.5%
Abnormality of the ear
17.8%
Abnormality of the eye
16.3%
Abnormality of the genitourinary system
14.8%
Growth abnormality
14.1%
Abnormality of metabolism homeostasis
11.9%
Abnormality of limbs
8.9%
Abnormality of blood and blood forming tissues
8.1%
Abnormality of the integument
8.1%
Abnormality of the digestive system
7.4%
Abnormality of the immune system
5.9%
Abnormality of the respiratory system
5.9%
Abnormality of prenatal development or birth
5.2%
Abnormality of the endocrine system
3%
Neoplasm
1.5%
Abnormality of the thoracic cavity
0.7%
Abnormality of the voice
0.7%
Abnormal cellular phenotype
0%
Abnormality of the breast
0%
Constitutional symptom
0%

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