Renal and urinary tract disorders
Gene: AMN

AMN (amnion associated transmembrane protein)
EnsemblGeneIds (GRCh38): ENSG00000166126
EnsemblGeneIds (GRCh37): ENSG00000166126
OMIM: 605799, Gene2Phenotype
AMN is in 8 panels

1 review

Sarah Leigh (Genomics England Curator)

Comment when marking as ready: Associated with phenotype in OMIM, not in G2P. At lease three variants reported
Created: 4 Aug 2016, 10:16 a.m.

Created: 4 Aug 2016, 10:16 a.m.

Panel version: Imported from End-stage renal disease - childhood onset panel version 0.161

Details

Mode of Inheritance

BIALLELIC, autosomal or pseudoautosomal

Sources

Expert Review Green

Phenotypes

Megaloblastic anemia-1, Norwegian type 261100

OMIM

605799

Clinvar variants

Variants in AMN

Penetrance

None

Publications

12590260

Panels with this gene

History Filter Activity

30 Jan 2019, Gel status: 4

Panel promoted to version 1.0

Eleanor Williams (Genomics England Curator)

Sarah Leigh: Comment when marking as ready:

30 Jan 2019, Gel status: 4

Set Phenotypes

Eleanor Williams (Genomics England Curator)

Phenotypes for gene: AMN were changed from Megaloblastic anemia-1, Norwegian type to Megaloblastic anemia-1, Norwegian type 261100

20 Dec 2018, Gel status: 4

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

Ellen McDonagh (Genomics England Curator)

gene: AMN was added gene: AMN was added to Renal and urinary tract disorders. Sources: Expert Review Green Mode of inheritance for gene: AMN was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: AMN were set to 12590260 Phenotypes for gene: AMN were set to Megaloblastic anemia-1, Norwegian type

Renal and urinary tract disorders Gene: AMN