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

LOC101929350 (uncharacterized LOC101929350)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929350
Atlas_Id 76603
Location 22q11.1  [Link to chromosome band 22q11]
Location_base_pair Starts at 17227759 and ends at 17229328 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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC101929350  101929350  uncharacterized LOC101929350
Aliases
GeneCards (Weizmann)LOC101929350
Ensembl hg19 (Hinxton)ENSG00000235343 [Gene_View]  chr22:17227759-17229328 [Contig_View]  LOC101929350 [Vega]
Ensembl hg38 (Hinxton)ENSG00000235343 [Gene_View]  chr22:17227759-17229328 [Contig_View]  LOC101929350 [Vega]
ICGC DataPortalENSG00000235343
TCGA cBioPortalLOC101929350
AceView (NCBI)LOC101929350
Genatlas (Paris)LOC101929350
WikiGenes101929350
SOURCE (Princeton)LOC101929350
Genetics Home Reference (NIH)LOC101929350
Genomic and cartography
GoldenPath hg19 (UCSC)LOC101929350  -     chr22:17227759-17229328 -  22q11.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC101929350  -     22q11.1   [Description]    (hg38-Dec_2013)
EnsemblLOC101929350 - 22q11.1 [CytoView hg19]  LOC101929350 - 22q11.1 [CytoView hg38]
Mapping of homologs : NCBILOC101929350 [Mapview hg19]  LOC101929350 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC038197 HG511968
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000022 NT_187355
Consensus coding sequences : CCDS (NCBI)LOC101929350
Cluster EST : UnigeneHs.561087 [ NCBI ]
CGAP (NCI)Hs.561087
Alternative Splicing GalleryENSG00000235343
Gene ExpressionLOC101929350 [ NCBI-GEO ]   LOC101929350 [ EBI - ARRAY_EXPRESS ]   LOC101929350 [ SEEK ]   LOC101929350 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929350 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929350
GTEX Portal (Tissue expression)LOC101929350
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929350
DMDM Disease mutations101929350
Blocks (Seattle)LOC101929350
Human Protein AtlasENSG00000235343
Protein Interaction databases
FunCoupENSG00000235343
BioGRIDLOC101929350
STRING (EMBL)LOC101929350
ZODIACLOC101929350
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929350
BioCentury BCIQLOC101929350
ClinGenLOC101929350
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929350
Clinical trialLOC101929350
Miscellaneous
canSAR (ICR)LOC101929350 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929350
EVEXLOC101929350
GoPubMedLOC101929350
iHOPLOC101929350
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 12:20:35 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.