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TMEM134 (transmembrane protein 134)

Identity

Alias_symbol (synonym)FLJ21749
Other alias-
HGNC (Hugo) TMEM134
LocusID (NCBI) 80194
Atlas_Id 74798
Location 11q13.2  [Link to chromosome band 11q13]
Location_base_pair Starts at 67464348 and ends at 67469277 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)TMEM134   26142
Cards
Entrez_Gene (NCBI)TMEM134  80194  transmembrane protein 134
Aliases
GeneCards (Weizmann)TMEM134
Ensembl hg19 (Hinxton)ENSG00000172663 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000172663 [Gene_View]  chr11:67464348-67469277 [Contig_View]  TMEM134 [Vega]
ICGC DataPortalENSG00000172663
TCGA cBioPortalTMEM134
AceView (NCBI)TMEM134
Genatlas (Paris)TMEM134
WikiGenes80194
SOURCE (Princeton)TMEM134
Genetics Home Reference (NIH)TMEM134
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM134  -     chr11:67464348-67469277 -  11q13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM134  -     11q13.2   [Description]    (hg19-Feb_2009)
EnsemblTMEM134 - 11q13.2 [CytoView hg19]  TMEM134 - 11q13.2 [CytoView hg38]
Mapping of homologs : NCBITMEM134 [Mapview hg19]  TMEM134 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA830850 AK025402 AK296988 AK303342 AK310743
RefSeq transcript (Entrez)NM_001078650 NM_001078651 NM_025124
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)TMEM134
Cluster EST : UnigeneHs.288761 [ NCBI ]
CGAP (NCI)Hs.288761
Alternative Splicing GalleryENSG00000172663
Gene ExpressionTMEM134 [ NCBI-GEO ]   TMEM134 [ EBI - ARRAY_EXPRESS ]   TMEM134 [ SEEK ]   TMEM134 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM134 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)80194
GTEX Portal (Tissue expression)TMEM134
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9H6X4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9H6X4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9H6X4
Splice isoforms : SwissVarQ9H6X4
PhosPhoSitePlusQ9H6X4
Domains : Interpro (EBI)DUF872_TM   
Domain families : Pfam (Sanger)DUF872 (PF05915)   
Domain families : Pfam (NCBI)pfam05915   
Conserved Domain (NCBI)TMEM134
DMDM Disease mutations80194
Blocks (Seattle)TMEM134
SuperfamilyQ9H6X4
Human Protein AtlasENSG00000172663
Peptide AtlasQ9H6X4
HPRD08642
IPIIPI00018576   IPI00815827   IPI00829874   IPI00815901   IPI00909635   IPI01010598   IPI01014921   
Protein Interaction databases
DIP (DOE-UCLA)Q9H6X4
IntAct (EBI)Q9H6X4
FunCoupENSG00000172663
BioGRIDTMEM134
STRING (EMBL)TMEM134
ZODIACTMEM134
Ontologies - Pathways
QuickGOQ9H6X4
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkTMEM134
Atlas of Cancer Signalling NetworkTMEM134
Wikipedia pathwaysTMEM134
Orthology - Evolution
OrthoDB80194
GeneTree (enSembl)ENSG00000172663
Phylogenetic Trees/Animal Genes : TreeFamTMEM134
HOVERGENQ9H6X4
HOGENOMQ9H6X4
Homologs : HomoloGeneTMEM134
Homology/Alignments : Family Browser (UCSC)TMEM134
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM134 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM134
dbVarTMEM134
ClinVarTMEM134
1000_GenomesTMEM134 
Exome Variant ServerTMEM134
ExAC (Exome Aggregation Consortium)TMEM134 (select the gene name)
Genetic variants : HAPMAP80194
Genomic Variants (DGV)TMEM134 [DGVbeta]
DECIPHERTMEM134 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM134 
Mutations
ICGC Data PortalTMEM134 
TCGA Data PortalTMEM134 
Broad Tumor PortalTMEM134
OASIS PortalTMEM134 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM134  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDTMEM134
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch TMEM134
DgiDB (Drug Gene Interaction Database)TMEM134
DoCM (Curated mutations)TMEM134 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TMEM134 (select a term)
intoGenTMEM134
Cancer3DTMEM134(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTMEM134
Genetic Testing Registry TMEM134
NextProtQ9H6X4 [Medical]
TSGene80194
GENETestsTMEM134
Target ValidationTMEM134
Huge Navigator TMEM134 [HugePedia]
snp3D : Map Gene to Disease80194
BioCentury BCIQTMEM134
ClinGenTMEM134
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD80194
Chemical/Pharm GKB GenePA143485657
Clinical trialTMEM134
Miscellaneous
canSAR (ICR)TMEM134 (select the gene name)
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTMEM134
EVEXTMEM134
GoPubMedTMEM134
iHOPTMEM134
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed May 31 15:45:51 CEST 2017

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