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

LOC100507599 (uncharacterized LOC100507599)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100507599
Atlas_Id 76891
Location 22q12.1  [Link to chromosome band 22q12]
Location_base_pair Starts at 26908503 and ends at 26910531 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)LOC100507599  100507599  uncharacterized LOC100507599
Aliases
GeneCards (Weizmann)LOC100507599
Ensembl hg19 (Hinxton) [Gene_View]  chr22:26908503-26910531 [Contig_View]  LOC100507599 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr22:26908503-26910531 [Contig_View]  LOC100507599 [Vega]
TCGA cBioPortalLOC100507599
AceView (NCBI)LOC100507599
Genatlas (Paris)LOC100507599
WikiGenes100507599
SOURCE (Princeton)LOC100507599
Genetics Home Reference (NIH)LOC100507599
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100507599  -     chr22:26908503-26910531 +  22q12.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100507599  -     22q12.1   [Description]    (hg38-Dec_2013)
EnsemblLOC100507599 - 22q12.1 [CytoView hg19]  LOC100507599 - 22q12.1 [CytoView hg38]
Mapping of homologs : NCBILOC100507599 [Mapview hg19]  LOC100507599 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK057443 HG512134 HG512135
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000022 NC_018933 NT_011520 NW_004929430
Consensus coding sequences : CCDS (NCBI)LOC100507599
Cluster EST : UnigeneHs.405877 [ NCBI ]
CGAP (NCI)Hs.405877
Gene ExpressionLOC100507599 [ NCBI-GEO ]   LOC100507599 [ EBI - ARRAY_EXPRESS ]   LOC100507599 [ SEEK ]   LOC100507599 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100507599 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100507599
GTEX Portal (Tissue expression)LOC100507599
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100507599
DMDM Disease mutations100507599
Blocks (Seattle)LOC100507599
Protein Interaction databases
BioGRIDLOC100507599
STRING (EMBL)LOC100507599
ZODIACLOC100507599
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100507599
BioCentury BCIQLOC100507599
ClinGenLOC100507599
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100507599
Clinical trialLOC100507599
Miscellaneous
canSAR (ICR)LOC100507599 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100507599
EVEXLOC100507599
GoPubMedLOC100507599
iHOPLOC100507599
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 12:17:36 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.