Gene: CNOT3 Disease: CNOT3 syndrome

Allelic requirement

monoallelic_autosomal

Mutation consequence summary

absent gene product

Panel Confidence category
DD definitive

Gene: CNOT3

Location
Synonyms
NOT3
OMIM MIM
604910
Ensembl stable ID
ENSG00000088038
Variant information
ClinVar Decipher
Protein information
Decipher

Disease: CNOT3 syndrome

Update disease information

Publications

Phenotypes

Look up phenotypes associated with CNOT3 in Decipher

Organ specificity

Edit organ specificity list:


Bone Marrow/Immune
Brain/Cognition
Cancer predisposition
Ear
Endocrine
Endocrine/Metabolic
Eye
Eye: Connective tissue
Eye: Cornea
Eye: Lens
Eye: Optic nerve
Eye: Physiology
Eye: Retina
Eye: Structure
Eye: Vasculature
Eye: Vitreous
Face
GI tract
Genitalia
Hair/Nails
Heart/Cardiovasculature/Lymphatic
Kidney Renal Tract
Liver
Lungs
Multisystem
Musculature
Peripheral nerves
Respiratory tract
Skeleton
Skin
Spinal cord/Peripheral nerves
Teeth and Dentition
breast
growth