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TMPPE (transmembrane protein with metallophosphoesterase domain)

Identity

Alias_symbol (synonym)FLJ45032
Other alias-
HGNC (Hugo) TMPPE
LocusID (NCBI) 643853
Atlas_Id 75006
Location 3p22.3  [Link to chromosome band 3p22]
Location_base_pair Starts at 33131908 and ends at 33138293 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)TMPPE   33865
Cards
Entrez_Gene (NCBI)TMPPE  643853  transmembrane protein with metallophosphoesterase domain
Aliases
GeneCards (Weizmann)TMPPE
Ensembl hg19 (Hinxton)ENSG00000188167 [Gene_View]  chr3:33131908-33138293 [Contig_View]  TMPPE [Vega]
Ensembl hg38 (Hinxton)ENSG00000188167 [Gene_View]  chr3:33131908-33138293 [Contig_View]  TMPPE [Vega]
ICGC DataPortalENSG00000188167
TCGA cBioPortalTMPPE
AceView (NCBI)TMPPE
Genatlas (Paris)TMPPE
WikiGenes643853
SOURCE (Princeton)TMPPE
Genetics Home Reference (NIH)TMPPE
Genomic and cartography
GoldenPath hg19 (UCSC)TMPPE  -     chr3:33131908-33138293 -  3p22.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)TMPPE  -     3p22.3   [Description]    (hg38-Dec_2013)
EnsemblTMPPE - 3p22.3 [CytoView hg19]  TMPPE - 3p22.3 [CytoView hg38]
Mapping of homologs : NCBITMPPE [Mapview hg19]  TMPPE [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK126979 AK128242 AW103036 BC136872 BC136873
RefSeq transcript (Entrez)NM_001039770 NM_001136238
RefSeq genomic (Entrez)NC_000003 NC_018914 NG_009005 NT_022517 NW_004929309
Consensus coding sequences : CCDS (NCBI)TMPPE
Cluster EST : UnigeneHs.443031 [ NCBI ]
CGAP (NCI)Hs.443031
Alternative Splicing GalleryENSG00000188167
Gene ExpressionTMPPE [ NCBI-GEO ]   TMPPE [ EBI - ARRAY_EXPRESS ]   TMPPE [ SEEK ]   TMPPE [ MEM ]
Gene Expression Viewer (FireBrowse)TMPPE [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)643853
GTEX Portal (Tissue expression)TMPPE
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6ZT21   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6ZT21  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6ZT21
Splice isoforms : SwissVarQ6ZT21
PhosPhoSitePlusQ6ZT21
Domains : Interpro (EBI)Calcineurin-like_PHP_apaH    Metallo-depent_PP-like   
Domain families : Pfam (Sanger)Metallophos (PF00149)   
Domain families : Pfam (NCBI)pfam00149   
Conserved Domain (NCBI)TMPPE
DMDM Disease mutations643853
Blocks (Seattle)TMPPE
SuperfamilyQ6ZT21
Human Protein AtlasENSG00000188167
Peptide AtlasQ6ZT21
IPIIPI00418754   IPI00885142   
Protein Interaction databases
DIP (DOE-UCLA)Q6ZT21
IntAct (EBI)Q6ZT21
FunCoupENSG00000188167
BioGRIDTMPPE
STRING (EMBL)TMPPE
ZODIACTMPPE
Ontologies - Pathways
QuickGOQ6ZT21
Ontology : AmiGOmetabolic process  integral component of membrane  hydrolase activity  metal ion binding  
Ontology : EGO-EBImetabolic process  integral component of membrane  hydrolase activity  metal ion binding  
NDEx NetworkTMPPE
Atlas of Cancer Signalling NetworkTMPPE
Wikipedia pathwaysTMPPE
Orthology - Evolution
OrthoDB643853
GeneTree (enSembl)ENSG00000188167
Phylogenetic Trees/Animal Genes : TreeFamTMPPE
HOVERGENQ6ZT21
HOGENOMQ6ZT21
Homologs : HomoloGeneTMPPE
Homology/Alignments : Family Browser (UCSC)TMPPE
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMPPE [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMPPE
dbVarTMPPE
ClinVarTMPPE
1000_GenomesTMPPE 
Exome Variant ServerTMPPE
ExAC (Exome Aggregation Consortium)TMPPE (select the gene name)
Genetic variants : HAPMAP643853
Genomic Variants (DGV)TMPPE [DGVbeta]
DECIPHER (Syndromes)3:33131908-33138293  ENSG00000188167
CONAN: Copy Number AnalysisTMPPE 
Mutations
ICGC Data PortalTMPPE 
TCGA Data PortalTMPPE 
Broad Tumor PortalTMPPE
OASIS PortalTMPPE [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMPPE  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDTMPPE
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch TMPPE
DgiDB (Drug Gene Interaction Database)TMPPE
DoCM (Curated mutations)TMPPE (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TMPPE (select a term)
intoGenTMPPE
Cancer3DTMPPE(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTMPPE
Genetic Testing Registry TMPPE
NextProtQ6ZT21 [Medical]
TSGene643853
GENETestsTMPPE
Huge Navigator TMPPE [HugePedia]
snp3D : Map Gene to Disease643853
BioCentury BCIQTMPPE
ClinGenTMPPE
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD643853
Chemical/Pharm GKB GenePA164726564
Clinical trialTMPPE
Miscellaneous
canSAR (ICR)TMPPE (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTMPPE
EVEXTMPPE
GoPubMedTMPPE
iHOPTMPPE
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:49:10 CET 2017

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