Macrocephaly_Megalencephaly
Gene: RAB34EnsemblGeneIds (GRCh38): ENSG00000109113
EnsemblGeneIds (GRCh37): ENSG00000109113
OMIM: 610917, Gene2Phenotype
RAB34 is in 11 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Cannot find evidence for Mendelian gene-disease association.Created: 7 Jan 2020, 10:42 p.m. | Last Modified: 7 Jan 2020, 10:42 p.m.
Panel Version: 0.10
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Red
- Victorian Clinical Genetics Services
- OMIM
- 610917
- Clinvar variants
- Variants in RAB34
- Penetrance
- None
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: rab34 has been classified as Red List (Low Evidence).
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: rab34 has been classified as Red List (Low Evidence).
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: RAB34 was added gene: RAB34 was added to Macrocephaly/Megalencephaly_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: RAB34 was set to Unknown