Atlas of Genetics and Cytogenetics in Oncology and Haematology

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Taking over the Atlas
Dear Colleagues,
The Atlas, once more, is in great danger, and I will have to proceed to a collective economic lay-off of all the team involved in the Atlas before the begining of April 2015 (a foundation having suddenly withdrawn its commitment to support the Atlas). I ask you herein if any Scientific Society (a Society of Cytogenetics, of Clinical Genetics, of Hematology, or a Cancer Society, or any other...), any University and/or Hospital, any Charity, or any database would be interested in taking over the Atlas, in whole or in part. If taking charge of the whole lot is too big, a consortium of various actors could be the solution (I am myself trying to find partners). Could you please spread the information, contact the relevant authorities, and find partners.
Survival of the Atlas will be critically dependant upon your ability to find solutions (and urgently!).
Kind regards.
Jean-Loup Huret
Donations are also welcome
If each casual visitor gives 3 Euros or Dollars, the Atlas is saved in a week !
If each professional gives 100 Euros or Dollars once a year (now), the Atlas is saved in 2 weeks !
Don't let the Atlas imminent demise
Note: we send fiscal receipts for donations equal or above 50 Euros or Dollars

Donate (in Euros)

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H19 (H19, imprinted maternally expressed transcript (non-protein coding))


Other namesASM
HGNC (Hugo) H19
LocusID (NCBI) 283120
Location 11p15.5
Location_base_pair Starts at 2016406 and ends at 2019065 bp from pter ( according to hg19-Feb_2009)

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute



Other Solid tumors implicated (Data extracted from papers in the Atlas)

Solid Tumors AmeloblastomID5945 MedulloblastomaID5065

External links

HGNC (Hugo)H19   4713
Entrez_Gene (NCBI)H19  283120  H19, imprinted maternally expressed transcript (non-protein coding)
GeneCards (Weizmann)H19
Ensembl hg19 (Hinxton)ENSG00000130600 [Gene_View]  chr11:2016406-2019065 [Contig_View]  H19 [Vega]
Ensembl hg38 (Hinxton)ENSG00000130600 [Gene_View]  chr11:2016406-2019065 [Contig_View]  H19 [Vega]
ICGC DataPortalENSG00000130600
AceView (NCBI)H19
Genatlas (Paris)H19
SOURCE (Princeton)H19
Genomic and cartography
GoldenPath hg19 (UCSC)H19  -     chr11:2016406-2019065 -  11p15.5   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)H19  -     11p15.5   [Description]    (hg38-Dec_2013)
EnsemblH19 - 11p15.5 [CytoView hg19]  H19 - 11p15.5 [CytoView hg38]
Mapping of homologs : NCBIH19 [Mapview hg19]  H19 [Mapview hg38]
OMIM103280   130650   180860   180860   194070   194071   
Gene and transcription
Genbank (Entrez)AK092486 AK123560 AL546946 AL548405 BC006831
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000011 NC_018922 NG_016165 NT_009237 NW_004929378
Consensus coding sequences : CCDS (NCBI)H19
Cluster EST : UnigeneHs.533566 [ NCBI ]
CGAP (NCI)Hs.533566
Alternative Splicing : Fast-db (Paris)GSHG0005466
Alternative Splicing GalleryENSG00000130600
Gene ExpressionH19 [ NCBI-GEO ]     H19 [ SEEK ]   H19 [ MEM ]
SOURCE (Princeton)Expression in : [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
DMDM Disease mutations283120
Human Protein AtlasENSG00000130600
IPIIPI00307804   IPI00001322   
Protein Interaction databases
Ontologies - Pathways
PubMed115 Pubmed reference(s) in Entrez
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI


Written09-2002Dessen P, Le Minor S
Updated02-2015Dessen P

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Sat Mar 28 15:34:01 CET 2015

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