Atlas of Genetics and Cytogenetics in Oncology and Haematology

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA
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economic lay-off of all the team involved in the Atlas before the begining of April 2015 (a foundation having suddenly withdrawn its commitment to support the Atlas).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)

Donate (in US Dollars)

C1orf159 (chromosome 1 open reading frame 159)


Other names-
HGNC (Hugo) C1orf159
LocusID (NCBI) 54991
Location 1p36.33
Location_base_pair Starts at 1017198 and ends at 1051736 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)C1orf159   26062
Entrez_Gene (NCBI)C1orf159  54991  chromosome 1 open reading frame 159
GeneCards (Weizmann)C1orf159
Ensembl hg19 (Hinxton)ENSG00000131591 [Gene_View]  chr1:1017198-1051736 [Contig_View]  C1orf159 [Vega]
Ensembl hg38 (Hinxton)ENSG00000131591 [Gene_View]  chr1:1017198-1051736 [Contig_View]  C1orf159 [Vega]
ICGC DataPortalENSG00000131591
AceView (NCBI)C1orf159
Genatlas (Paris)C1orf159
SOURCE (Princeton)C1orf159
Genomic and cartography
GoldenPath hg19 (UCSC)C1orf159  -     chr1:1017198-1051736 -  1p36.33   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)C1orf159  -     1p36.33   [Description]    (hg38-Dec_2013)
EnsemblC1orf159 - 1p36.33 [CytoView hg19]  C1orf159 - 1p36.33 [CytoView hg38]
Mapping of homologs : NCBIC1orf159 [Mapview hg19]  C1orf159 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI270164 AK000591 AK024796 AK054793 AK057368
RefSeq transcript (Entrez)NM_017891
RefSeq genomic (Entrez)NC_000001 NC_018912 NT_032977 NW_004929288
Consensus coding sequences : CCDS (NCBI)C1orf159
Cluster EST : UnigeneHs.235095 [ NCBI ]
CGAP (NCI)Hs.235095
Alternative Splicing : Fast-db (Paris)GSHG0001648
Alternative Splicing GalleryENSG00000131591
Gene ExpressionC1orf159 [ NCBI-GEO ]     C1orf159 [ SEEK ]   C1orf159 [ MEM ]
SOURCE (Princeton)Expression in : [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96HA4 (Uniprot)
NextProtQ96HA4  [Medical]
With graphics : InterProQ96HA4
Splice isoforms : SwissVarQ96HA4 (Swissvar)
Domains : Interpro (EBI)DUF4501   
Related proteins : CluSTrQ96HA4
Domain families : Pfam (Sanger)DUF4501 (PF14946)   
Domain families : Pfam (NCBI)pfam14946   
DMDM Disease mutations54991
Blocks (Seattle)Q96HA4
Human Protein AtlasENSG00000131591
Peptide AtlasQ96HA4
IPIIPI00515131   IPI00062955   IPI00514936   IPI00016627   IPI00909677   IPI00871670   IPI00916675   IPI00446467   IPI00883596   
Protein Interaction databases
IntAct (EBI)Q96HA4
Ontologies - Pathways
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
Protein Interaction DatabaseC1orf159
DoCM (Curated mutations)C1orf159
Wikipedia pathwaysC1orf159
Gene fusion - rearrangements
Polymorphisms : SNP, variants
NCBI Variation ViewerC1orf159 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C1orf159
Exome Variant ServerC1orf159
SNP (GeneSNP Utah)C1orf159
SNP : HGBaseC1orf159
Genetic variants : HAPMAPC1orf159
Genomic Variants (DGV)C1orf159 [DGVbeta]
ICGC Data PortalENSG00000131591 
Somatic Mutations in Cancer : COSMICC1orf159 
CONAN: Copy Number AnalysisC1orf159 
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)1:1017198-1051736
Mutations and Diseases : HGMDC1orf159
NextProtQ96HA4 [Medical]
Disease Genetic AssociationC1orf159
Huge Navigator C1orf159 [HugePedia]  C1orf159 [HugeCancerGEM]
snp3D : Map Gene to Disease54991
DGIdb (Drug Gene Interaction db)C1orf159
General knowledge
Homologs : HomoloGeneC1orf159
Homology/Alignments : Family Browser (UCSC)C1orf159
Phylogenetic Trees/Animal Genes : TreeFamC1orf159
Chemical/Protein Interactions : CTD54991
Chemical/Pharm GKB GenePA142672410
Clinical trialC1orf159
Cancer Resource (Charite)ENSG00000131591
Other databases
PubMed7 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 14:52:50 CET 2015

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us