1. Panels
  2. Insulin resistance (including lipodystrophy)
  3. ADRA2A
STRs in panel
Prev Next
Regions in panel
Prev Next

Insulin resistance (including lipodystrophy)

Gene: ADRA2A

Red List (low evidence)
ADRA2A (adrenoceptor alpha 2A)
EnsemblGeneIds (GRCh38): ENSG00000150594
EnsemblGeneIds (GRCh37): ENSG00000150594
OMIM: 104210, Gene2Phenotype
ADRA2A is in 2 panels

1 review

Ivone Leong (Genomics England Curator)

Red List (low evidence)

Familial partial lipodystrophy is not confirmed to be associated with ADRA2A in OMIM or Gene2Phenotype. There is only one variant reported (PMID: 27376152).
Created: 8 Jan 2019, 3:13 p.m.
Gene added as recommended by Keven Colclough (Royal Devon & Exeter Hospital).
Sources: Expert list
Created: 8 Jan 2019, 3:13 p.m.

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Phenotypes
No OMIM number; familial partial lipodystrophy

Publications

Created: 8 Jan 2019, 3:13 p.m.

Panel version: 1.7

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
Phenotypes
  • No OMIM number
  • familial partial lipodystrophy
OMIM
104210
Clinvar variants
Variants in ADRA2A
Penetrance
None
Publications
Panels with this gene

History Filter Activity

8 Jan 2019, Gel status: 1

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

Ivone Leong (Genomics England Curator)

gene: ADRA2A was added gene: ADRA2A was added to Insulin resistance (including lipodystrophy). Sources: Expert list Mode of inheritance for gene: ADRA2A was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: ADRA2A were set to 27376152 Phenotypes for gene: ADRA2A were set to No OMIM number; familial partial lipodystrophy Review for gene: ADRA2A was set to RED