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MOSPD3

Synonyms
CDS3, NET30
External resources
Summary
This gene encodes a multi-pass membrane protein with a major sperm protein (MSP) domain. The deletion of a similar mouse gene is associated with defective cardiac development and neonatal lethality. Alternate transcriptional splice variants, encoding different isoforms, have been described.

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
0
Likely pathogenic
0
VUS
2,812
Likely benign
10
Benign
0

Patient Phenotypes

No patients carry pathogenic or likely pathogenic variants on MOSPD3 gene.

Phenotype class
Patients in 3billion (%)

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