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Autism

Gene: MET

Red List (low evidence)
MET (MET proto-oncogene, receptor tyrosine kinase)
EnsemblGeneIds (GRCh38): ENSG00000105976
EnsemblGeneIds (GRCh37): ENSG00000105976
OMIM: 164860, Gene2Phenotype
MET is in 9 panels

1 review

Chirag Patel (Genetic Health Queensland)

Red List (low evidence)

Not ID gene.
Created: 5 Dec 2019, 12:50 a.m. | Last Modified: 5 Dec 2019, 12:50 a.m.
Panel Version: 0.416

Mode of inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal

Phenotypes
?Deafness, autosomal recessive 97, OMIM #616705; {Osteofibrous dysplasia, susceptibility to}, OMIM #607278

Created: 5 Dec 2019, 12:50 a.m.
Last Modified: 5 Dec 2019, 12:50 a.m.
Panel version: Imported from Intellectual disability, syndromic and non-syndromic_GHQ_VCGS panel version 0.416

Details

Mode of Inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Expert list
  • Victorian Clinical Genetics Services
Phenotypes
  • ?Deafness, autosomal recessive 97, OMIM #616705
  • {Osteofibrous dysplasia, susceptibility to}, OMIM #607278
OMIM
164860
Clinvar variants
Variants in MET
Penetrance
None
Panels with this gene

History Filter Activity

31 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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

31 Dec 2019, Gel status: 1

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: MET were changed from to ?Deafness, autosomal recessive 97, OMIM #616705; {Osteofibrous dysplasia, susceptibility to}, OMIM #607278

31 Dec 2019, Gel status: 1

Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Mode of inheritance for gene: MET was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal

31 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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