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INO80

INO80 complex ATPase subunit

HCNC Approved Symbol
INO80 (HGNC:26956)
Genomic Coordinates
15:40,978,880 - 41,116,280 (15q15.1)
Synonyms
KIAA1259, hINO80, INO80A, INOC1
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.
However, the following publication(s) suggest a possible gene disease association.
View More Disease Info
ContentsPublications
An inherited immunoglobulin class-switch recombination deficiency associated with a defect in the INO80 chromatin remodeling complex.
PMID:25312759

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the INO80 gene.

Frequently observed phenotypes

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

Microcephaly
 2 (100.0%)