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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.

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
INTS11 - Gene browser | 3billion