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GPX7

Synonyms
CL683, GPX6, GPx-7, GSHPx-7, NPGPx
External resources

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
15
Likely pathogenic
0
VUS
352
Likely benign
3
Benign
0

Patient Phenotypes

Proportions of phenotypes among 15 patients carrying pathogenic or likely pathogenic variants on GPX7 gene are displayed below. The following symptoms were found in patients with a variant in GPX7. However, patients may have been diagnosed with a different variant.

Phenotype class
Patients in 3billion (%)
Abnormality of blood and blood forming tissues
26.7%
Abnormality of head or neck
26.7%
Abnormality of the cardiovascular system
26.7%
Abnormality of the digestive system
26.7%
Abnormality of the eye
26.7%
Abnormality of the musculoskeletal system
26.7%
Abnormality of the respiratory system
26.7%
Abnormality of the immune system
20%
Abnormality of the integument
20%
Abnormality of the nervous system
20%
Abnormality of metabolism homeostasis
13.3%
Abnormality of prenatal development or birth
13.3%
Abnormality of the endocrine system
13.3%
Growth abnormality
13.3%
Neoplasm
13.3%
Abnormal cellular phenotype
6.7%
Abnormality of the ear
6.7%
Abnormality of the genitourinary system
6.7%
Abnormality of limbs
0%
Abnormality of the breast
0%
Abnormality of the thoracic cavity
0%
Abnormality of the voice
0%
Constitutional symptom
0%

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