Autism
Gene: RNF135EnsemblGeneIds (GRCh38): ENSG00000181481
EnsemblGeneIds (GRCh37): ENSG00000181481
OMIM: 611358, Gene2Phenotype
RNF135 is in 5 panels
2 reviews
Chirag Patel (Genetic Health Queensland)
Comment on list classification: d/w Z.Stark - see reviewCreated: 5 Dec 2019, 3:58 a.m. | Last Modified: 5 Dec 2019, 3:58 a.m.
Panel Version: 0.473
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Some early data on possible association of particular SNPs with autism/neurodevelopmental phenotypes, more recent data refuting this association.Created: 20 Nov 2019, 3:47 a.m. | Last Modified: 20 Nov 2019, 3:47 a.m.
Panel Version: 0.8
Publications
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Red
- Victorian Clinical Genetics Services
- Victorian Clinical Genetics Services
- OMIM
- 611358
- Clinvar variants
- Variants in RNF135
- Penetrance
- None
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: rnf135 has been classified as Red List (Low Evidence).
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: rnf135 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: RNF135 was added gene: RNF135 was added to Autism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: RNF135 was set to Unknown