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  3. RANBP17
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Autism

Gene: RANBP17

Red List (low evidence)
RANBP17 (RAN binding protein 17)
EnsemblGeneIds (GRCh38): ENSG00000204764
EnsemblGeneIds (GRCh37): ENSG00000204764
OMIM: 606141, Gene2Phenotype
RANBP17 is in 2 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Potential association with autism, but currently no firm evidence for Mendelian gene-disease association; in SFARI database.
Created: 7 Jan 2020, 10:26 p.m. | Last Modified: 7 Jan 2020, 10:26 p.m.
Panel Version: 0.30
Created: 7 Jan 2020, 10:26 p.m.
Last Modified: 7 Jan 2020, 10:26 p.m.
Panel version: 0.30

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
606141
Clinvar variants
Variants in RANBP17
Penetrance
None
Panels with this gene

History Filter Activity

7 Jan 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ranbp17 has been classified as Red List (Low Evidence).

7 Jan 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ranbp17 has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: RANBP17 was added gene: RANBP17 was added to Autism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: RANBP17 was set to Unknown