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Gene : H19 Homo sapiens

Name  ? H19 imprinted maternally expressed transcript Cytological Location  11p15.5
Brief Description  H19 imprinted maternally expressed transcript
Description  This gene is located in an imprinted region of chromosome 11 near the insulin-like growth factor 2 (IGF2) gene. This gene is only expressed from the maternally-inherited chromosome, whereas IGF2 is only expressed from the paternally-inherited chromosome. The product of this gene is a long non-coding RNA which functions as a tumor suppressor. Mutations in this gene have been associated with Beckwith-Wiedemann Syndrome and Wilms tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]
  • synonyms:
  • H19, imprinted maternally expressed transcript (non-protein coding),
  • NCRNA00008,
  • H19,
  • LINC00008,
  • H19, imprinted maternally expressed untranslated mRNA,
  • WT2,
  • ASM,
  • AF087017,
  • BWS,
  • NR_002196,
  • ASM1,
  • MIR675 host gene,
  • NCRNA00008,
  • MIR675HG,
  • OTTHUMG00000012477,
  • D11S813E,
  • LINC00008,
  • ASM1,
  • MIR675HG,
  • D11S813E,
  • uc057xvv.1,
  • adult skeletal muscle,
  • HGNC:4713,
  • non-protein coding RNA 8,
  • long intergenic non-protein coding RNA 8,
  • ASM
  • identifiers:
  • 283120,
  • ENSG00000130600,
  • H19

Genome feature

Region: gene ? Length: 6291  
Location: 11:1995176-2001466 reverse strand Cyto location: 11p15.5


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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

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Proteins

Gene --> Proteins.

SNPs

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Disease

4 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

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Expression

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Other

0 Pathways

10 SN Ps

5 Cross References

13 Data Sets

0 Homologues

0 Located Features

54 Rna Seq Results