Genomics England
GMS Panels
Panels
Genes and Entities

VPS4A

vacuolar protein sorting 4 homolog A
OMIM: 609982
PanelMode of inheritanceDetails
6 panels
Green
in Bilateral congenital or childhood onset cataracts
R-numbers: R31
Signed-off version 8.5
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
CIMDAG syndrome
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 8.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CIMDAG Syndrome, biallelic, CIMDAG Syndrome, monoallelic
Green
in Dystonia, chorea or related movement disorder, childhood onset
R-numbers: R57
Signed-off version 8.13
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
CIMDAG syndrome
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 8.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
CIMDAG syndrome, OMIM:619273
Green
in Intellectual disability
Component of the following Super Panels:
  • - Hypotonic infant
  • - Leukodystrophy, childhood onset
  • - Paediatric disorders
Signed-off version 11.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
CIMDAG syndrome
Green
in Rare anaemia
R-numbers: R92
Signed-off version 4.7
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
CIMDAG syndrome