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INTS1

integrator complex subunit 1

HCNC Approved Symbol
INTS1 (HGNC:24555)
Genomic Coordinates
7:1,470,277 - 1,504,389 (7p22.3)
Synonyms
DKFZp586J0619, KIAA1440, INT1, NET28
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies
618571AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the INTS1 gene.

Frequently observed phenotypes

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

No Results