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Gene: H19 (H19 imprinted maternally expressed transcript) Homo sapiens
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Symbol: H19
Name: H19 imprinted maternally expressed transcript
Description: Implicated in several diseases, including Beckwith-Wiedemann syndrome; Silver-Russell syndrome; ovary epithelial cancer; teratoma; and urinary system cancer (multiple). Biomarker of breast adenocarcinoma; cervix carcinoma; endometrial carcinoma; endometrial hyperplasia; and uterine cancer.
Type: ncrna
RefSeq Status: REVIEWED
Also known as: ASM; ASM1; BWS; D11S813E; H19, imprinted maternally expressed transcript; H19, imprinted maternally expressed transcript (non-protein coding); LINC00008; MGC4485; MIR675HG; NCRNA00008; PRO2605; WT2
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl111,995,176 - 2,001,470 (-)EnsemblGRCh38hg38GRCh38
GRCh38111,995,176 - 2,001,466 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37112,016,406 - 2,019,065 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36111,972,982 - 1,975,641 (-)NCBINCBI36hg18NCBI36
Celera112,055,536 - 2,058,195 (-)NCBI
Cytogenetic Map11p15.5NCBI
HuRef111,807,445 - 1,810,104 (-)NCBIHuRef
CHM1_1112,015,226 - 2,021,516 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Phenotype Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on H19
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1604187
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2020-05-19
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.