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TMEM133 (transmembrane protein 133)

Identity

Alias_symbol (synonym)AD031
Other alias
HGNC (Hugo) TMEM133
LocusID (NCBI) 83935
Atlas_Id 74797
Location 11q22.1  [Link to chromosome band 11q22]
Location_base_pair Starts at 100992080 and ends at 100993935 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)TMEM133   24033
Cards
Entrez_Gene (NCBI)TMEM133  83935  transmembrane protein 133
AliasesAD031
GeneCards (Weizmann)TMEM133
Ensembl hg19 (Hinxton)ENSG00000170647 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000170647 [Gene_View]  chr11:100992080-100993935 [Contig_View]  TMEM133 [Vega]
ICGC DataPortalENSG00000170647
TCGA cBioPortalTMEM133
AceView (NCBI)TMEM133
Genatlas (Paris)TMEM133
WikiGenes83935
SOURCE (Princeton)TMEM133
Genetics Home Reference (NIH)TMEM133
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM133  -     chr11:100992080-100993935 +  11q22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM133  -     11q22.1   [Description]    (hg19-Feb_2009)
EnsemblTMEM133 - 11q22.1 [CytoView hg19]  TMEM133 - 11q22.1 [CytoView hg38]
Mapping of homologs : NCBITMEM133 [Mapview hg19]  TMEM133 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF247167 AK314174 BC058024 BC093843 BC112050
RefSeq transcript (Entrez)NM_032021
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)TMEM133
Cluster EST : UnigeneHs.44004 [ NCBI ]
CGAP (NCI)Hs.44004
Alternative Splicing GalleryENSG00000170647
Gene ExpressionTMEM133 [ NCBI-GEO ]   TMEM133 [ EBI - ARRAY_EXPRESS ]   TMEM133 [ SEEK ]   TMEM133 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM133 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)83935
GTEX Portal (Tissue expression)TMEM133
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9H2Q1   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9H2Q1  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9H2Q1
Splice isoforms : SwissVarQ9H2Q1
PhosPhoSitePlusQ9H2Q1
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)TMEM133
DMDM Disease mutations83935
Blocks (Seattle)TMEM133
SuperfamilyQ9H2Q1
Human Protein AtlasENSG00000170647
Peptide AtlasQ9H2Q1
HPRD12425
IPIIPI00012458   
Protein Interaction databases
DIP (DOE-UCLA)Q9H2Q1
IntAct (EBI)Q9H2Q1
FunCoupENSG00000170647
BioGRIDTMEM133
STRING (EMBL)TMEM133
ZODIACTMEM133
Ontologies - Pathways
QuickGOQ9H2Q1
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkTMEM133
Atlas of Cancer Signalling NetworkTMEM133
Wikipedia pathwaysTMEM133
Orthology - Evolution
OrthoDB83935
GeneTree (enSembl)ENSG00000170647
Phylogenetic Trees/Animal Genes : TreeFamTMEM133
HOVERGENQ9H2Q1
HOGENOMQ9H2Q1
Homologs : HomoloGeneTMEM133
Homology/Alignments : Family Browser (UCSC)TMEM133
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM133 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM133
dbVarTMEM133
ClinVarTMEM133
1000_GenomesTMEM133 
Exome Variant ServerTMEM133
ExAC (Exome Aggregation Consortium)TMEM133 (select the gene name)
Genetic variants : HAPMAP83935
Genomic Variants (DGV)TMEM133 [DGVbeta]
DECIPHERTMEM133 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM133 
Mutations
ICGC Data PortalTMEM133 
TCGA Data PortalTMEM133 
Broad Tumor PortalTMEM133
OASIS PortalTMEM133 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM133  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDTMEM133
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch TMEM133
DgiDB (Drug Gene Interaction Database)TMEM133
DoCM (Curated mutations)TMEM133 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TMEM133 (select a term)
intoGenTMEM133
Cancer3DTMEM133(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTMEM133
Genetic Testing Registry TMEM133
NextProtQ9H2Q1 [Medical]
TSGene83935
GENETestsTMEM133
Huge Navigator TMEM133 [HugePedia]
snp3D : Map Gene to Disease83935
BioCentury BCIQTMEM133
ClinGenTMEM133
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD83935
Chemical/Pharm GKB GenePA143485656
Clinical trialTMEM133
Miscellaneous
canSAR (ICR)TMEM133 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTMEM133
EVEXTMEM133
GoPubMedTMEM133
iHOPTMEM133
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Fri May 19 11:58:22 CEST 2017

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