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  3. INTS6
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Autism

Gene: INTS6

Red List (low evidence)
INTS6 (integrator complex subunit 6)
EnsemblGeneIds (GRCh38): ENSG00000102786
EnsemblGeneIds (GRCh37): ENSG00000102786
OMIM: 604331, Gene2Phenotype
INTS6 is in 2 panels

1 review

Elena Savva (Victorian Clinical Genetics Services)

Red List (low evidence)

No association to mendelian disease
Created: 8 Jan 2021, 2 a.m. | Last Modified: 8 Jan 2021, 2 a.m.
Panel Version: 0.128
Created: 8 Jan 2021, 2 a.m.
Last Modified: 8 Jan 2021, 2 a.m.
Panel version: 0.128

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
604331
Clinvar variants
Variants in INTS6
Penetrance
None
Panels with this gene

History Filter Activity

8 Jan 2021, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ints6 has been classified as Red List (Low Evidence).

8 Jan 2021, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ints6 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: INTS6 was added gene: INTS6 was added to Autism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: INTS6 was set to Unknown