Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   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

LOC101929117 (uncharacterized LOC101929117)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929117
Atlas_Id 78100
Location 10p12.1  [Link to chromosome band 10p12]
Location_base_pair Starts at 26577686 and ends at 26579307 bp from pter ( according to hg38-Dec_2013)

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)LOC101929117  101929117  uncharacterized LOC101929117
Aliases
GeneCards (Weizmann)LOC101929117
Ensembl hg19 (Hinxton)ENSG00000236894 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000236894 [Gene_View]  chr10:26577686-26579307 [Contig_View]  LOC101929117 [Vega]
ICGC DataPortalENSG00000236894
TCGA cBioPortalLOC101929117
AceView (NCBI)LOC101929117
Genatlas (Paris)LOC101929117
WikiGenes101929117
SOURCE (Princeton)LOC101929117
Genetics Home Reference (NIH)LOC101929117
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929117  -     chr10:26577686-26579307 -  10p12.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929117  -     10p12.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101929117 - 10p12.1 [CytoView hg19]  LOC101929117 - 10p12.1 [CytoView hg38]
Mapping of homologs : NCBILOC101929117 [Mapview hg19]  LOC101929117 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA935551 AI652398 AI962311
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929117
Cluster EST : UnigeneHs.734997 [ NCBI ]
CGAP (NCI)Hs.734997
Alternative Splicing GalleryENSG00000236894
Gene ExpressionLOC101929117 [ NCBI-GEO ]   LOC101929117 [ EBI - ARRAY_EXPRESS ]   LOC101929117 [ SEEK ]   LOC101929117 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929117 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929117
GTEX Portal (Tissue expression)LOC101929117
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929117
DMDM Disease mutations101929117
Blocks (Seattle)LOC101929117
Human Protein AtlasENSG00000236894
Protein Interaction databases
FunCoupENSG00000236894
BioGRIDLOC101929117
STRING (EMBL)LOC101929117
ZODIACLOC101929117
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929117
BioCentury BCIQLOC101929117
ClinGenLOC101929117
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929117
Clinical trialLOC101929117
Miscellaneous
canSAR (ICR)LOC101929117 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929117
EVEXLOC101929117
GoPubMedLOC101929117
iHOPLOC101929117
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 : Wed Jun 7 16:06:03 CEST 2017

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

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.