Polydactyly
Gene: FAM92A
FAM92A (family with sequence similarity 92 member A)
EnsemblGeneIds (GRCh38): ENSG00000188343
EnsemblGeneIds (GRCh37): ENSG00000188343
OMIM: 617273, Gene2Phenotype
FAM92A is in 3 panels
EnsemblGeneIds (GRCh38): ENSG00000188343
EnsemblGeneIds (GRCh37): ENSG00000188343
OMIM: 617273, Gene2Phenotype
FAM92A is in 3 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Single family and a mouse model reported.
Sources: Expert listCreated: 21 Jul 2020, 9:29 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Polydactyly, postaxial, type A9, MIM# 618219
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Amber
- Expert list
- Phenotypes
-
- Polydactyly, postaxial, type A9, MIM# 618219
- OMIM
- 617273
- Clinvar variants
- Variants in FAM92A
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
21 Jul 2020, Gel status: 2
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: fam92a has been classified as Amber List (Moderate Evidence).
21 Jul 2020, Gel status: 2
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: fam92a has been classified as Amber List (Moderate Evidence).
21 Jul 2020, Gel status: 1
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: FAM92A was added gene: FAM92A was added to Polydactyly. Sources: Expert list Mode of inheritance for gene: FAM92A was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: FAM92A were set to 30395363 Phenotypes for gene: FAM92A were set to Polydactyly, postaxial, type A9, MIM# 618219 Review for gene: FAM92A was set to AMBER