This Panel is marked as Internal
Genomic imprinting
Gene: NDN
NDN (necdin, MAGE family member)
EnsemblGeneIds (GRCh38): ENSG00000182636
EnsemblGeneIds (GRCh37): ENSG00000182636
OMIM: 602117, Gene2Phenotype
NDN is in 1 panel
EnsemblGeneIds (GRCh38): ENSG00000182636
EnsemblGeneIds (GRCh37): ENSG00000182636
OMIM: 602117, Gene2Phenotype
NDN is in 1 panel
2 reviews
Ellen McDonagh (Genomics England Curator)
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Phenotypes
From the Intellectual disability gene panel
Sarah Leigh (Genomics England Curator)
Circadian expression reported in CircaDB (http://circadb.hogeneschlab.org/human)Created: 22 Dec 2020, 6:10 p.m. | Last Modified: 22 Dec 2020, 6:10 p.m.
Panel Version: 0.26
Single variant reported in patient with Smith-Magenis-like syndrome, maternal imprinting and paternal expression were demonstratedCreated: 4 May 2017, 10:57 a.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Phenotypes
Smith-Magenis-like syndrome; Prader-Willi syndrome 176270
Publications
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
- Sources
-
- Literature
- Phenotypes
-
- Smith-Magenis-like syndrome
- Prader-Willi syndrome 176270
- OMIM
- 602117
- Clinvar variants
- Variants in NDN
- Penetrance
- Complete
- Publications
- Panels with this gene
History Filter Activity
22 Dec 2020, Gel status: 1
Set publications
Sarah Leigh (Genomics England Curator)Publications for gene NDN were updated from 28213671 to 28213671 ; 30794780; http://igc.otago.ac.nz/home.html
4 May 2017, Gel status: 0
Created
Sarah Leigh (Genomics England Curator)NDN was created by sleigh
4 May 2017, Gel status: 0
Added New Source
Sarah Leigh (Genomics England Curator)NDN was added to Imprinted Genespanel. Sources: Literature