ZC4H2 - Gene browser

ZC4H2

zinc finger C4H2-type containing

HCNC Approved Symbol: ZC4H2 (HGNC:24931)
Genomic Coordinates: 23:64,915,807 - 65,034,741 (Xq11.2)
Synonyms: HCA127, KIAA1166, WWS, MCS, MRXS4
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

8Patients

In total, 8 patients were diagnosed with a variant in the ZC4H2 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

08
Patient count

Hypotonia: 3 (37.5%)
Patient Count: 3 (37.5%)
% of total patients presenting each phenotype is shown in parentheses.
3 (37.5%)
Microcephaly: 2 (25.0%)
Patient Count: 2 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (25.0%)
Global developmental delay: 1 (12.5%)
Patient Count: 1 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
1 (12.5%)
Arthrogryposis multiplex: 1 (12.5%)
Patient Count: 1 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
1 (12.5%)
Bitemporal narrowing: 1 (12.5%)
Patient Count: 1 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
1 (12.5%)