Home > Gene Browser > GCNT7

GCNT7

Synonyms
C20orf105, dJ1153D9.2, gcnt
External resources
Summary
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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
14
Likely pathogenic
0
VUS
3,263
Likely benign
151
Benign
0

Patient phenotypes

Proportions of phenotypes among 14 patients carring pathogenic or likely pathogenic variants on GCNT7 gene are displayed below.

Phenotype class
Patients in 3billion (%)
Abnormality of the nervous system
35.7%
Abnormality of head or neck
21.4%
Abnormality of the cardiovascular system
21.4%
Abnormality of the ear
21.4%
Abnormality of blood and blood-forming tissues
14.3%
Abnormality of the eye
14.3%
Abnormality of the musculoskeletal system
14.3%
Abnormality of limbs
7.1%
Abnormality of the digestive system
7.1%
Abnormality of the endocrine system
7.1%
Abnormality of the genitourinary system
7.1%
Abnormality of the integument
7.1%
Growth abnormality
7.1%
Abnormal cellular phenotype
0%
Abnormality of metabolism homeostasis
0%
Abnormality of prenatal development or birth
0%
Abnormality of the breast
0%
Abnormality of the immune system
0%
Abnormality of the respiratory system
0%
Abnormality of the thoracic cavity
0%
Abnormality of the voice
0%
Constitutional symptom
0%
Neoplasm
0%

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