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GEMIN4

gem nuclear organelle associated protein 4

HCNC Approved Symbol
GEMIN4 (HGNC:15717)
Genomic Coordinates
17:744,421 - 754,410 (17p13.3)
Synonyms
HHRF-1, DKFZP434B131, p97, DKFZP434D174, HC56, HCAP1
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
617913AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the GEMIN4 gene.

Frequently observed phenotypes

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

No Results