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

LOC101928775 (uncharacterized LOC101928775)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928775
Atlas_Id 67425
Location 9q33.1  [Link to chromosome band 9q33]
Location_base_pair Starts at 115739670 and ends at 115744239 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)LOC101928775  101928775  uncharacterized LOC101928775
Aliases
GeneCards (Weizmann)LOC101928775
Ensembl hg19 (Hinxton)ENSG00000228714 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000228714 [Gene_View]  chr9:115739670-115744239 [Contig_View]  LOC101928775 [Vega]
ICGC DataPortalENSG00000228714
TCGA cBioPortalLOC101928775
AceView (NCBI)LOC101928775
Genatlas (Paris)LOC101928775
WikiGenes101928775
SOURCE (Princeton)LOC101928775
Genetics Home Reference (NIH)LOC101928775
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928775  -     chr9:115739670-115744239 -  9q33.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928775  -     9q33.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101928775 - 9q33.1 [CytoView hg19]  LOC101928775 - 9q33.1 [CytoView hg38]
Mapping of homologs : NCBILOC101928775 [Mapview hg19]  LOC101928775 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BE671722
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928775
Cluster EST : UnigeneHs.522362 [ NCBI ]
CGAP (NCI)Hs.522362
Alternative Splicing GalleryENSG00000228714
Gene ExpressionLOC101928775 [ NCBI-GEO ]   LOC101928775 [ EBI - ARRAY_EXPRESS ]   LOC101928775 [ SEEK ]   LOC101928775 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928775 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928775
GTEX Portal (Tissue expression)LOC101928775
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928775
DMDM Disease mutations101928775
Blocks (Seattle)LOC101928775
Human Protein AtlasENSG00000228714
Protein Interaction databases
FunCoupENSG00000228714
BioGRIDLOC101928775
STRING (EMBL)LOC101928775
ZODIACLOC101928775
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928775
BioCentury BCIQLOC101928775
ClinGenLOC101928775
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928775
Clinical trialLOC101928775
Miscellaneous
canSAR (ICR)LOC101928775 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928775
EVEXLOC101928775
GoPubMedLOC101928775
iHOPLOC101928775
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 : Mon Sep 18 13:21:09 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.