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LOC101060157 (uncharacterized LOC101060157)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101060157
Atlas_Id 66988
Location 13q11  [Link to chromosome band 13q11]
Location_base_pair Starts at 18236234 and ends at 18237845 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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC101060157  101060157  uncharacterized LOC101060157
Aliases
GeneCards (Weizmann)LOC101060157
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr13:18236234-18237845 [Contig_View]  LOC101060157 [Vega]
TCGA cBioPortalLOC101060157
AceView (NCBI)LOC101060157
Genatlas (Paris)LOC101060157
WikiGenes101060157
SOURCE (Princeton)LOC101060157
Genetics Home Reference (NIH)LOC101060157
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101060157  -     chr13:18236234-18237845 +  13q11   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101060157  -     13q11   [Description]    (hg19-Feb_2009)
EnsemblLOC101060157 - 13q11 [CytoView hg19]  LOC101060157 - 13q11 [CytoView hg38]
Mapping of homologs : NCBILOC101060157 [Mapview hg19]  LOC101060157 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AL117481 AL122069 AL133561
RefSeq transcript (Entrez)NM_001145711
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101060157
Cluster EST : UnigeneHs.648234 [ NCBI ]
CGAP (NCI)Hs.648234
Gene ExpressionLOC101060157 [ NCBI-GEO ]   LOC101060157 [ EBI - ARRAY_EXPRESS ]   LOC101060157 [ SEEK ]   LOC101060157 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101060157 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)101060157
GTEX Portal (Tissue expression)LOC101060157
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9UF83   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9UF83  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9UF83
Splice isoforms : SwissVarQ9UF83
PhosPhoSitePlusQ9UF83
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101060157
DMDM Disease mutations101060157
Blocks (Seattle)LOC101060157
SuperfamilyQ9UF83
Peptide AtlasQ9UF83
Protein Interaction databases
DIP (DOE-UCLA)Q9UF83
IntAct (EBI)Q9UF83
BioGRIDLOC101060157
STRING (EMBL)LOC101060157
ZODIACLOC101060157
Ontologies - Pathways
QuickGOQ9UF83
Ontology : AmiGOextracellular space  
Ontology : EGO-EBIextracellular space  
NDEx NetworkLOC101060157
Atlas of Cancer Signalling NetworkLOC101060157
Wikipedia pathwaysLOC101060157
Orthology - Evolution
OrthoDB101060157
Phylogenetic Trees/Animal Genes : TreeFam-
HOVERGENQ9UF83
HOGENOMQ9UF83
Homologs : HomoloGeneLOC101060157
Homology/Alignments : Family Browser (UCSC)LOC101060157
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerLOC101060157 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)LOC101060157
dbVarLOC101060157
ClinVarLOC101060157
1000_GenomesLOC101060157 
Exome Variant ServerLOC101060157
ExAC (Exome Aggregation Consortium)LOC101060157 (select the gene name)
Genetic variants : HAPMAP101060157
Genomic Variants (DGV)LOC101060157 [DGVbeta]
DECIPHERLOC101060157 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisLOC101060157 
Mutations
ICGC Data Portal- 
TCGA Data Portal- 
Broad Tumor Portal-
OASIS Portal- [ Somatic mutations - Copy number]
Mutations and Diseases : HGMD-
BioMutasearch LOC101060157
DgiDB (Drug Gene Interaction Database)LOC101060157
DoCM (Curated mutations)LOC101060157 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)LOC101060157 (select a term)
intoGenLOC101060157
Cancer3DLOC101060157(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenLOC101060157
Genetic Testing Registry LOC101060157
NextProtQ9UF83 [Medical]
TSGene101060157
GENETestsLOC101060157
Target ValidationLOC101060157
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101060157
BioCentury BCIQLOC101060157
ClinGenLOC101060157
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101060157
Clinical trialLOC101060157
Miscellaneous
canSAR (ICR)LOC101060157 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101060157
EVEXLOC101060157
GoPubMedLOC101060157
iHOPLOC101060157
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 : Mon Sep 18 13:19:28 CEST 2017

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