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  2. Clefting disorders
  3. FOXP2
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Clefting disorders

Gene: FOXP2

Red List (low evidence)
FOXP2 (forkhead box P2)
EnsemblGeneIds (GRCh38): ENSG00000128573
EnsemblGeneIds (GRCh37): ENSG00000128573
OMIM: 605317, Gene2Phenotype
FOXP2 is in 5 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Clefting disorders are not a feature of this disorder.
Created: 1 Feb 2024, 4:45 a.m. | Last Modified: 1 Feb 2024, 4:45 a.m.
Panel Version: 0.246

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Speech-language disorder-1, MIM# 602081

Publications

Created: 1 Feb 2024, 4:45 a.m.
Last Modified: 1 Feb 2024, 4:45 a.m.
Panel version: 0.246

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
  • Illumina TruGenome Clinical Sequencing Services
  • Expert list
Phenotypes
  • Speech-language disorder-1, MIM# 602081
OMIM
605317
Clinvar variants
Variants in FOXP2
Penetrance
None
Publications
Panels with this gene

History Filter Activity

1 Feb 2024, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: foxp2 has been classified as Red List (Low Evidence).

1 Feb 2024, Gel status: 1

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: FOXP2 were changed from Speech-language disorder-1, 602081 to Speech-language disorder-1, MIM# 602081

1 Feb 2024, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: foxp2 has been classified as Red List (Low Evidence).

16 Sep 2020, Gel status: 2

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: FOXP2 was added gene: FOXP2 was added to Clefting_GEL. Sources: Expert list,Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen Mode of inheritance for gene: FOXP2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: FOXP2 were set to 27734906; 15326624 Phenotypes for gene: FOXP2 were set to Speech-language disorder-1, 602081