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TMEM155 (transmembrane protein 155)

Identity

Alias_symbol (synonym)FLJ30834
Other alias-
HGNC (Hugo) TMEM155
LocusID (NCBI) 132332
Atlas_Id 74819
Location 4q27  [Link to chromosome band 4q27]
Location_base_pair Starts at 122680085 and ends at 122686340 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)TMEM155   26418
Cards
Entrez_Gene (NCBI)TMEM155  132332  transmembrane protein 155
Aliases
GeneCards (Weizmann)TMEM155
Ensembl hg19 (Hinxton)ENSG00000164112 [Gene_View]  chr4:122680085-122686340 [Contig_View]  TMEM155 [Vega]
Ensembl hg38 (Hinxton)ENSG00000164112 [Gene_View]  chr4:122680085-122686340 [Contig_View]  TMEM155 [Vega]
ICGC DataPortalENSG00000164112
TCGA cBioPortalTMEM155
AceView (NCBI)TMEM155
Genatlas (Paris)TMEM155
WikiGenes132332
SOURCE (Princeton)TMEM155
Genetics Home Reference (NIH)TMEM155
Genomic and cartography
GoldenPath hg19 (UCSC)TMEM155  -     chr4:122680085-122686340 -  4q27   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)TMEM155  -     4q27   [Description]    (hg38-Dec_2013)
EnsemblTMEM155 - 4q27 [CytoView hg19]  TMEM155 - 4q27 [CytoView hg38]
Mapping of homologs : NCBITMEM155 [Mapview hg19]  TMEM155 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK055396 AK310583 BC047657 BC059365 BI757990
RefSeq transcript (Entrez)NM_152399
RefSeq genomic (Entrez)NC_000004 NC_018915 NT_016354 NW_004929320
Consensus coding sequences : CCDS (NCBI)TMEM155
Cluster EST : UnigeneHs.607691 [ NCBI ]
CGAP (NCI)Hs.607691
Alternative Splicing GalleryENSG00000164112
Gene ExpressionTMEM155 [ NCBI-GEO ]   TMEM155 [ EBI - ARRAY_EXPRESS ]   TMEM155 [ SEEK ]   TMEM155 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM155 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)132332
GTEX Portal (Tissue expression)TMEM155
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ4W5P6   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ4W5P6  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ4W5P6
Splice isoforms : SwissVarQ4W5P6
PhosPhoSitePlusQ4W5P6
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)TMEM155
DMDM Disease mutations132332
Blocks (Seattle)TMEM155
SuperfamilyQ4W5P6
Human Protein AtlasENSG00000164112
Peptide AtlasQ4W5P6
HPRD08089
IPIIPI00043682   IPI00966766   
Protein Interaction databases
DIP (DOE-UCLA)Q4W5P6
IntAct (EBI)Q4W5P6
FunCoupENSG00000164112
BioGRIDTMEM155
STRING (EMBL)TMEM155
ZODIACTMEM155
Ontologies - Pathways
QuickGOQ4W5P6
Ontology : AmiGOextracellular region  
Ontology : EGO-EBIextracellular region  
NDEx NetworkTMEM155
Atlas of Cancer Signalling NetworkTMEM155
Wikipedia pathwaysTMEM155
Orthology - Evolution
OrthoDB132332
GeneTree (enSembl)ENSG00000164112
Phylogenetic Trees/Animal Genes : TreeFamTMEM155
HOVERGENQ4W5P6
HOGENOMQ4W5P6
Homologs : HomoloGeneTMEM155
Homology/Alignments : Family Browser (UCSC)TMEM155
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM155 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM155
dbVarTMEM155
ClinVarTMEM155
1000_GenomesTMEM155 
Exome Variant ServerTMEM155
ExAC (Exome Aggregation Consortium)TMEM155 (select the gene name)
Genetic variants : HAPMAP132332
Genomic Variants (DGV)TMEM155 [DGVbeta]
DECIPHER (Syndromes)4:122680085-122686340  ENSG00000164112
CONAN: Copy Number AnalysisTMEM155 
Mutations
ICGC Data PortalTMEM155 
TCGA Data PortalTMEM155 
Broad Tumor PortalTMEM155
OASIS PortalTMEM155 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM155  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDTMEM155
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch TMEM155
DgiDB (Drug Gene Interaction Database)TMEM155
DoCM (Curated mutations)TMEM155 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TMEM155 (select a term)
intoGenTMEM155
Cancer3DTMEM155(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTMEM155
Genetic Testing Registry TMEM155
NextProtQ4W5P6 [Medical]
TSGene132332
GENETestsTMEM155
Huge Navigator TMEM155 [HugePedia]
snp3D : Map Gene to Disease132332
BioCentury BCIQTMEM155
ClinGenTMEM155
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD132332
Chemical/Pharm GKB GenePA145007448
Clinical trialTMEM155
Miscellaneous
canSAR (ICR)TMEM155 (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTMEM155
EVEXTMEM155
GoPubMedTMEM155
iHOPTMEM155
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 12:48:31 CET 2017

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