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economic lay-off of all the team involved in the Atlas before the begining of April 2015 (a foundation having suddenly withdrawn its commitment to support the Atlas).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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C19orf33 (chromosome 19 open reading frame 33)


Other namesH2RSP
HGNC (Hugo) C19orf33
LocusID (NCBI) 64073
Location 19q13.2
Location_base_pair Starts at 38794804 and ends at 38795646 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



External links

HGNC (Hugo)C19orf33   16668
Entrez_Gene (NCBI)C19orf33  64073  chromosome 19 open reading frame 33
GeneCards (Weizmann)C19orf33
Ensembl hg19 (Hinxton)ENSG00000167644 [Gene_View]  chr19:38794804-38795646 [Contig_View]  C19orf33 [Vega]
Ensembl hg38 (Hinxton)ENSG00000167644 [Gene_View]  chr19:38794804-38795646 [Contig_View]  C19orf33 [Vega]
ICGC DataPortalENSG00000167644
AceView (NCBI)C19orf33
Genatlas (Paris)C19orf33
SOURCE (Princeton)C19orf33
Genomic and cartography
GoldenPath hg19 (UCSC)C19orf33  -     chr19:38794804-38795646 +  19q13.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)C19orf33  -     19q13.2   [Description]    (hg38-Dec_2013)
EnsemblC19orf33 - 19q13.2 [CytoView hg19]  C19orf33 - 19q13.2 [CytoView hg38]
Mapping of homologs : NCBIC19orf33 [Mapview hg19]  C19orf33 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB038317 AB038318 AF213678 BC008888 BC014264
RefSeq transcript (Entrez)NM_022125 NM_033520
RefSeq genomic (Entrez)NC_000019 NC_018930 NT_011109 NW_004929415
Consensus coding sequences : CCDS (NCBI)C19orf33
Cluster EST : UnigeneHs.631544 [ NCBI ]
CGAP (NCI)Hs.631544
Alternative Splicing : Fast-db (Paris)GSHG0014887
Alternative Splicing GalleryENSG00000167644
Gene ExpressionC19orf33 [ NCBI-GEO ]     C19orf33 [ SEEK ]   C19orf33 [ MEM ]
SOURCE (Princeton)Expression in : [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9GZP8 (Uniprot)
NextProtQ9GZP8  [Medical]
With graphics : InterProQ9GZP8
Splice isoforms : SwissVarQ9GZP8 (Swissvar)
Domains : Interpro (EBI)IMUP   
Related proteins : CluSTrQ9GZP8
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
DMDM Disease mutations64073
Blocks (Seattle)Q9GZP8
Human Protein AtlasENSG00000167644
Peptide AtlasQ9GZP8
IPIIPI00030767   IPI00337392   
Protein Interaction databases
IntAct (EBI)Q9GZP8
Ontologies - Pathways
Ontology : AmiGOdouble-stranded DNA binding  single-stranded DNA binding  nucleus  biological_process  
Ontology : EGO-EBIdouble-stranded DNA binding  single-stranded DNA binding  nucleus  biological_process  
Protein Interaction DatabaseC19orf33
DoCM (Curated mutations)C19orf33
Wikipedia pathwaysC19orf33
Gene fusion - rearrangements
Polymorphisms : SNP, variants
NCBI Variation ViewerC19orf33 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C19orf33
Exome Variant ServerC19orf33
SNP (GeneSNP Utah)C19orf33
SNP : HGBaseC19orf33
Genetic variants : HAPMAPC19orf33
Genomic Variants (DGV)C19orf33 [DGVbeta]
ICGC Data PortalENSG00000167644 
Somatic Mutations in Cancer : COSMICC19orf33 
CONAN: Copy Number AnalysisC19orf33 
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] 
DECIPHER (Syndromes)19:38794804-38795646
Mutations and Diseases : HGMDC19orf33
NextProtQ9GZP8 [Medical]
Disease Genetic AssociationC19orf33
Huge Navigator C19orf33 [HugePedia]  C19orf33 [HugeCancerGEM]
snp3D : Map Gene to Disease64073
DGIdb (Drug Gene Interaction db)C19orf33
General knowledge
Homologs : HomoloGeneC19orf33
Homology/Alignments : Family Browser (UCSC)C19orf33
Phylogenetic Trees/Animal Genes : TreeFamC19orf33
Chemical/Protein Interactions : CTD64073
Chemical/Pharm GKB GenePA134924870
Clinical trialC19orf33
Cancer Resource (Charite)ENSG00000167644
Other databases
PubMed12 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 14:52:29 CET 2015

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