Atlas of Genetics and Cytogenetics in Oncology and Haematology


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TCONS_00029157 (uncharacterized LOC101928399)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928399
Atlas_Id 76521
Location 21q22.3  [Link to chromosome band 21q22]
Location_base_pair Starts at 44777935 and ends at 44782229 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)TCONS_00029157  101928399  uncharacterized LOC101928399
Aliases
GeneCards (Weizmann)TCONS_00029157
Ensembl hg19 (Hinxton)ENSG00000237989 [Gene_View]  chr21:44777935-44782229 [Contig_View]  TCONS_00029157 [Vega]
Ensembl hg38 (Hinxton)ENSG00000237989 [Gene_View]  chr21:44777935-44782229 [Contig_View]  TCONS_00029157 [Vega]
ICGC DataPortalENSG00000237989
TCGA cBioPortalTCONS_00029157
AceView (NCBI)TCONS_00029157
Genatlas (Paris)TCONS_00029157
WikiGenes101928399
SOURCE (Princeton)TCONS_00029157
Genetics Home Reference (NIH)TCONS_00029157
Genomic and cartography
GoldenPath hg19 (UCSC)TCONS_00029157  -     chr21:44777935-44782229 -  21q22.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)TCONS_00029157  -     21q22.3   [Description]    (hg38-Dec_2013)
EnsemblTCONS_00029157 - 21q22.3 [CytoView hg19]  TCONS_00029157 - 21q22.3 [CytoView hg38]
Mapping of homologs : NCBITCONS_00029157 [Mapview hg19]  TCONS_00029157 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AL530227 BU736390 BX390224 HG511868
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000021 NC_018932 NT_011512 NW_004929427
Consensus coding sequences : CCDS (NCBI)TCONS_00029157
Cluster EST : UnigeneHs.517319 [ NCBI ]
CGAP (NCI)Hs.517319
Alternative Splicing GalleryENSG00000237989
Gene ExpressionTCONS_00029157 [ NCBI-GEO ]   TCONS_00029157 [ EBI - ARRAY_EXPRESS ]   TCONS_00029157 [ SEEK ]   TCONS_00029157 [ MEM ]
Gene Expression Viewer (FireBrowse)TCONS_00029157 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928399
GTEX Portal (Tissue expression)TCONS_00029157
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)TCONS_00029157
DMDM Disease mutations101928399
Blocks (Seattle)TCONS_00029157
Human Protein AtlasENSG00000237989
Protein Interaction databases
FunCoupENSG00000237989
BioGRIDTCONS_00029157
STRING (EMBL)TCONS_00029157
ZODIACTCONS_00029157
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928399
BioCentury BCIQTCONS_00029157
ClinGenTCONS_00029157
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928399
Clinical trialTCONS_00029157
Miscellaneous
canSAR (ICR)TCONS_00029157 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTCONS_00029157
EVEXTCONS_00029157
GoPubMedTCONS_00029157
iHOPTCONS_00029157
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Mar 14 12:47:42 CET 2017

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