Gene: PCGF2 Disease: INTELLECTUAL DISABILITY

Allelic requirement

monoallelic_autosomal

Mutation consequence summary

altered gene product structure

Mutation consequences flag

restricted repertoire of mutations

Panel Confidence category
DD strong

Gene: PCGF2

Location
Synonyms
ZNF144, RNF110
OMIM MIM
600346
Ensembl stable ID
ENSG00000277258
Variant information
ClinVar Decipher
Protein information
Decipher

Disease: INTELLECTUAL DISABILITY

Update disease information

Publications

Phenotypes

Look up phenotypes associated with PCGF2 in Decipher

Organ specificity

  • Brain/Cognition

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