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ZNF41

Synonyms
MRX89
External resources
Summary
This gene encodes a protein that contains KRAB-A and KRAB-B domains multiple zinc finger DNA binding motifs and finger linking regions characteristic of the Kruppel family. An initial study suggested that this gene may be associated with X-linked cognitive disability, but a later study has called this finding into question (PMID:23871722).

Variant counts

The variants found in rare patients tested by 3billion are classified and counted according to ACMG guidelines. The variants with over 5% variant frequency in population genome databases ( gnomAD, dbSNP, etc) are excluded.

Pathogenic
0
Likely pathogenic
0
VUS
1,859
Likely benign
457
Benign
0

Patient phenotypes

No patients carry pathogenic or likely pathogenic variants on ZNF41 gene.

Phenotype class
Patients in 3billion (%)

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