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  3. NTNG1
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Autism

Gene: NTNG1

Red List (low evidence)
NTNG1 (netrin G1)
EnsemblGeneIds (GRCh38): ENSG00000162631
EnsemblGeneIds (GRCh37): ENSG00000162631
OMIM: 608818, Gene2Phenotype
NTNG1 is in 3 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Cannot find evidence for Mendelian gene-disease association; association studies with schizophrenia, gene family is linked to neurodevelopmental disorders.
Created: 21 Jan 2020, 11:24 p.m. | Last Modified: 21 Jan 2020, 11:24 p.m.
Panel Version: 0.42
Created: 21 Jan 2020, 11:24 p.m.
Last Modified: 21 Jan 2020, 11:24 p.m.
Panel version: 0.42

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
608818
Clinvar variants
Variants in NTNG1
Penetrance
None
Panels with this gene

History Filter Activity

21 Jan 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ntng1 has been classified as Red List (Low Evidence).

21 Jan 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ntng1 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: NTNG1 was added gene: NTNG1 was added to Autism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: NTNG1 was set to Unknown