IUGR and IGF abnormalities

Gene: H19

Red List (low evidence)

H19 (H19, imprinted maternally expressed transcript (non-protein coding))
EnsemblGeneIds (GRCh38): ENSG00000130600
EnsemblGeneIds (GRCh37): ENSG00000130600
OMIM: 103280, Gene2Phenotype
H19 is in 6 panels

2 reviews

Ellen McDonagh (Genomics England Curator)

Added tag to explain why there is no Ensembl gene ID for this entity.
Created: 6 Jan 2017, 3:28 p.m.

emma baple (Genomics England Curator)

H19 hypomethylation causes Russell Silver syndrome
Created: 10 May 2016, 10:03 a.m.

Details

Mode of Inheritance
Other - please specifiy in evaluation comments
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Russell-Silver syndrome
Tags
locus-type-rna-long-non-coding
OMIM
103280
Clinvar variants
Variants in H19
Penetrance
Complete
Panels with this gene

History Filter Activity

10 May 2016, Gel status: 1

Gene classified by Genomics England curator

emma baple (Genomics England Curator)

This gene has been classified as Red List (Low Evidence).

10 May 2016, Gel status: 0

Added New Source

emma baple (Genomics England Curator)

H19 was added to IUGR and IGF abnormalitiespanel. Sources: Literature

10 May 2016, Gel status: 0

Created

emma baple (Genomics England Curator)

H19 was created by ebapleC