| Identity |
| Other names | ASM |
| ASM1 | |
| BWS | |
| D11S813E | |
| MGC4485 | |
| NCRNA00008 | |
| PRO2605 | |
| WT2 | |
| HGNC (Hugo) | H19 |
| Location | 11p15.5 |
| Location_base_pair | Starts at 1972983 and ends at 1975648 bp from pter ( according to hg18-March_2006) |
| Note | Non-annotated gene. Preliminary data : if you are an author |
| DNA/RNA |

| External links |
| Nomenclature | |
|---|---|
| HGNC (Hugo) | H19 4713 |
| Entrez_Gene (NCBI) | H19 283120 H19, imprinted maternally expressed transcript (non-protein coding) |
| Cards | |
| GeneCards (Weizmann) | H19 |
| Ensembl (Hinxton) | ENSG00000182053 [Gene_View] H19 [Vega] |
| AceView (NCBI) | H19 |
| Genatlas (Paris) | H19 |
| euGene (Indiana) | 283120 |
| SOURCE (Stanford) | |
| Gene Expression (Array Express) | ENSG00000182053 |
| Genomic and cartography | |
| GoldenPath (UCSC) | H19 - 11p15.5 chr11:1972983-1975648 - 11p15.5 [Description] (hg18-March_2006) |
| Ensembl | H19 - 11p15.5 [CytoView] |
| Mapping of homologs : NCBI | H19 [Mapview] |
| OMIM | 103280 130650 180860 194071 |
| Gene and transcription | |
| Gene : Genbank (Entrez) | AK056774 AK092486 AK123560 AL546946 AL548405 |
| Reference sequence (RefSeq transcript) :SRS | |
| Reference transcript : Entrez | |
| RefSeq genomic : SRS | AC_000054 AC_000143 NC_000011 NG_016165 NT_009237 NW_001838017 NW_924962 |
| RefSeq genomic : Entrez | AC_000054 AC_000143 NC_000011 NG_016165 NT_009237 NW_001838017 NW_924962 |
| Consensus coding sequences : CCDS NCBI | H19 |
| Cluster EST : Unigene | Hs.533566 [ SRS ] Hs.533566 [ NCBI ] |
| Alternative Splicing : Fast-db (Paris) | 818 |
| Protein : pattern, domain, 3D structure | |
| Domain families : Pfam SRS | |
| Domain families : Pfam Sanger | |
| Domain families : Pfam NCBI | |
| Crystal structure of protein : PDB SRS | |
| Crystal structure of protein : PDBSum | |
| Crystal structure of protein : IMB | |
| Crystal structure of protein : PDB RSDB | |
| Protein Interaction databases | |
| Polymorphism : SNP, mutations, diseases | |
| Single Nucleotide Polymorphism (SNP) : dbSNP NCBI | H19 |
| SNP : GeneSNP Utah | H19 |
| SNP : HGBase | H19 |
| Genetic variants : HAPMAP | H19 |
| Mutations and Diseases : HGMD | H19 |
| Hereditary diseases : OMIM | 103280 130650 180860 194071 |
| Hereditary diseases : GENETests | 103280 130650 180860 194071 |
| Diseases : Genetic Association | H19 |
| General knowledge | |
| Homologs : HomoloGene | H19 |
| Homology/Alignments : Family Browser UCSC | H19 |
| Phylogenetic Trees/Animal Genes : TreeFam | H19 |
| Chemical/Protein Interactions : CTD | 283120 |
| Keywords Ontology : AmiGO | |
| Keywords Ontology : EGO-EBI | |
| Pathways : BIOCARTA | |
| Pathways : KEGG | |
| Other databases | |
| Probes | |
| Probes : Imagenes | H19 Related clones (RZPD - Berlin) |
| Literature | |
| PubMed | 43 Pubmed reference(s) in Entrez |
| PubGene | H19 |
| Genes in title | automatic search in PubMed |
| REVIEW articles | automatic search in PubMed |
| Last year publications | automatic search in PubMed |
| Contributor(s) |
| Written | 09-2002 | Dessen P, Le Minor S |
| Updated | 03-2009 | Dessen P |
| © Atlas of Genetics and Cytogenetics in Oncology and Haematology | indexed on : Sat Feb 27 10:44:25 CET 2010 |
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