Genomics England
GMS Panels
Panels
Genes and Entities

INTS11

integrator complex subunit 11
OMIM: 611354
PanelMode of inheritanceDetails
4 panels
Green
in Ataxia and cerebellar anomalies - narrow panel
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 6.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities, OMIM:620428
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.15
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
INTS11-related neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities, OMIM:620428
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 7.51
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities, OMIM:620428
Green
in Severe microcephaly
R-numbers: R88
Signed-off version 6.8
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities, OMIM:620428