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INTS11

integrator complex subunit 11

HCNC Approved Symbol
INTS11 (HGNC:26052)
Genomic Coordinates
1:1,311,600 - 1,324,660 (1p36.33)
Synonyms
FLJ20542, RC-68, CPSF73L, INT11, CPSF3L
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities
620428AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the INTS11 gene.

Frequently observed phenotypes

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

No Results