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

CTC-436P18.1 (uncharacterized LOC101928630)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928630
Atlas_Id 62167
Location 5q12.1  [Link to chromosome band 5q12]
Location_base_pair Starts at 60458143 and ends at 60527907 bp from pter ( according to hg19-Feb_2009)

Note

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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)CTC-436P18.1  101928630  uncharacterized LOC101928630
Aliases
GeneCards (Weizmann)CTC-436P18.1
Ensembl hg19 (Hinxton) [Gene_View]  chr5:60458143-60527907 [Contig_View]  CTC-436P18.1 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr5:60458143-60527907 [Contig_View]  CTC-436P18.1 [Vega]
TCGA cBioPortalCTC-436P18.1
AceView (NCBI)CTC-436P18.1
Genatlas (Paris)CTC-436P18.1
WikiGenes101928630
SOURCE (Princeton)CTC-436P18.1
Genetics Home Reference (NIH)CTC-436P18.1
Genomic and cartography
GoldenPath hg19 (UCSC)CTC-436P18.1  -     chr5:60458143-60527907 +  5q12.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)CTC-436P18.1  -     5q12.1   [Description]    (hg38-Dec_2013)
EnsemblCTC-436P18.1 - 5q12.1 [CytoView hg19]  CTC-436P18.1 - 5q12.1 [CytoView hg38]
Mapping of homologs : NCBICTC-436P18.1 [Mapview hg19]  CTC-436P18.1 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX109637 HG498005
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000005 NC_018916 NT_034772 NW_004929322
Consensus coding sequences : CCDS (NCBI)CTC-436P18.1
Cluster EST : UnigeneHs.575209 [ NCBI ]
CGAP (NCI)Hs.575209
Gene ExpressionCTC-436P18.1 [ NCBI-GEO ]   CTC-436P18.1 [ EBI - ARRAY_EXPRESS ]   CTC-436P18.1 [ SEEK ]   CTC-436P18.1 [ MEM ]
Gene Expression Viewer (FireBrowse)CTC-436P18.1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928630
GTEX Portal (Tissue expression)CTC-436P18.1
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)CTC-436P18.1
DMDM Disease mutations101928630
Blocks (Seattle)CTC-436P18.1
Protein Interaction databases
BioGRIDCTC-436P18.1
STRING (EMBL)CTC-436P18.1
ZODIACCTC-436P18.1
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928630
BioCentury BCIQCTC-436P18.1
ClinGenCTC-436P18.1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928630
Clinical trialCTC-436P18.1
Miscellaneous
canSAR (ICR)CTC-436P18.1 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineCTC-436P18.1
EVEXCTC-436P18.1
GoPubMedCTC-436P18.1
iHOPCTC-436P18.1
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Mar 14 12:00:36 CET 2017

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

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.