Genes in panel
Regions in panel
Prev Next

Mendeliome

Gene: RAB23

Green List (high evidence)

RAB23 (RAB23, member RAS oncogene family)
EnsemblGeneIds (GRCh38): ENSG00000112210
EnsemblGeneIds (GRCh37): ENSG00000112210
OMIM: 606144, Gene2Phenotype
RAB23 is in 12 panels

1 review

Naomi Baker (Victorian Clinical Genetics Services)

Green List (high evidence)

Well established gene-disease association. Multiple variants reported, however there is a recurrent variant, p.L145X, that resides on a common haplotype which is indicative of a founder effect in patients of northern European descent.

PMID: 25168863 reviewed prenatal findings in patient diagnosed with Carpenter syndrome at birth, and states that Carpenter syndrome should be considered if prenatal imaging identifies bowed femora and/or cardiac defect associated with abnormal skull shape.
Created: 5 Jan 2022, 3:57 a.m. | Last Modified: 5 Jan 2022, 3:57 a.m.
Panel Version: 0.10493

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Carpenter syndrome (MIM#201000)

Publications

Details

History Filter Activity

5 Jan 2022, Gel status: 3

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: rab23 has been classified as Green List (High Evidence).

5 Jan 2022, Gel status: 3

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: RAB23 were changed from to Carpenter syndrome (MIM#201000)

5 Jan 2022, Gel status: 3

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: RAB23 were set to

5 Jan 2022, Gel status: 3

Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Mode of inheritance for gene: RAB23 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: RAB23 was added gene: RAB23 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: RAB23 was set to Unknown