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

LOC101929325 (uncharacterized LOC101929325)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929325
Atlas_Id 77363
Location 1q21.2  [Link to chromosome band 1q21]
Location_base_pair Starts at 147767287 and ends at 147769663 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)LOC101929325  101929325  uncharacterized LOC101929325
Aliases
GeneCards (Weizmann)LOC101929325
Ensembl hg19 (Hinxton) [Gene_View]  chr1:147767287-147769663 [Contig_View]  LOC101929325 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr1:147767287-147769663 [Contig_View]  LOC101929325 [Vega]
TCGA cBioPortalLOC101929325
AceView (NCBI)LOC101929325
Genatlas (Paris)LOC101929325
WikiGenes101929325
SOURCE (Princeton)LOC101929325
Genetics Home Reference (NIH)LOC101929325
Genomic and cartography
GoldenPath hg19 (UCSC)LOC101929325  -     chr1:147767287-147769663 +  1q21.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC101929325  -     1q21.2   [Description]    (hg38-Dec_2013)
EnsemblLOC101929325 - 1q21.2 [CytoView hg19]  LOC101929325 - 1q21.2 [CytoView hg38]
Mapping of homologs : NCBILOC101929325 [Mapview hg19]  LOC101929325 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC034299 HG492700
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000001 NC_018912 NT_004487 NW_004929293
Consensus coding sequences : CCDS (NCBI)LOC101929325
Cluster EST : UnigeneHs.568685 [ NCBI ]
CGAP (NCI)Hs.568685
Gene ExpressionLOC101929325 [ NCBI-GEO ]   LOC101929325 [ EBI - ARRAY_EXPRESS ]   LOC101929325 [ SEEK ]   LOC101929325 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929325 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929325
GTEX Portal (Tissue expression)LOC101929325
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929325
DMDM Disease mutations101929325
Blocks (Seattle)LOC101929325
Protein Interaction databases
BioGRIDLOC101929325
STRING (EMBL)LOC101929325
ZODIACLOC101929325
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929325
BioCentury BCIQLOC101929325
ClinGenLOC101929325
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929325
Clinical trialLOC101929325
Miscellaneous
canSAR (ICR)LOC101929325 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929325
EVEXLOC101929325
GoPubMedLOC101929325
iHOPLOC101929325
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 12:20:33 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.