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TMEM265 (transmembrane protein 265)

Identity

Other aliasIFITMD8
HGNC (Hugo) TMEM265
LocusID (NCBI) 100862671
Atlas_Id 77539
Location 16p11.2  [Link to chromosome band 16p11]
Location_base_pair Starts at 30740191 and ends at 30745196 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)TMEM265   51241
Cards
Entrez_Gene (NCBI)TMEM265  100862671  transmembrane protein 265
AliasesIFITMD8
GeneCards (Weizmann)TMEM265
Ensembl hg19 (Hinxton)ENSG00000080603 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000080603 [Gene_View]  chr16:30740191-30745196 [Contig_View]  TMEM265 [Vega]
ICGC DataPortalENSG00000080603
TCGA cBioPortalTMEM265
AceView (NCBI)TMEM265
Genatlas (Paris)TMEM265
WikiGenes100862671
SOURCE (Princeton)TMEM265
Genetics Home Reference (NIH)TMEM265
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM265  -     chr16:30740191-30745196 +  16p11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM265  -     16p11.2   [Description]    (hg19-Feb_2009)
EnsemblTMEM265 - 16p11.2 [CytoView hg19]  TMEM265 - 16p11.2 [CytoView hg38]
Mapping of homologs : NCBITMEM265 [Mapview hg19]  TMEM265 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC073882 BC104654 CA390324 CA432634
RefSeq transcript (Entrez)NM_001256829
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)TMEM265
Cluster EST : UnigeneHs.667372 [ NCBI ]
CGAP (NCI)Hs.667372
Alternative Splicing GalleryENSG00000080603
Gene ExpressionTMEM265 [ NCBI-GEO ]   TMEM265 [ EBI - ARRAY_EXPRESS ]   TMEM265 [ SEEK ]   TMEM265 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM265 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100862671
GTEX Portal (Tissue expression)TMEM265
Protein : pattern, domain, 3D structure
UniProt/SwissProtA0A087WTH1   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA0A087WTH1  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA0A087WTH1
Splice isoforms : SwissVarA0A087WTH1
PhosPhoSitePlusA0A087WTH1
Domains : Interpro (EBI)CD225/Dispanin_fam   
Domain families : Pfam (Sanger)CD225 (PF04505)   
Domain families : Pfam (NCBI)pfam04505   
Conserved Domain (NCBI)TMEM265
DMDM Disease mutations100862671
Blocks (Seattle)TMEM265
SuperfamilyA0A087WTH1
Human Protein AtlasENSG00000080603
Peptide AtlasA0A087WTH1
Protein Interaction databases
DIP (DOE-UCLA)A0A087WTH1
IntAct (EBI)A0A087WTH1
FunCoupENSG00000080603
BioGRIDTMEM265
STRING (EMBL)TMEM265
ZODIACTMEM265
Ontologies - Pathways
QuickGOA0A087WTH1
Ontology : AmiGOresponse to biotic stimulus  integral component of membrane  
Ontology : EGO-EBIresponse to biotic stimulus  integral component of membrane  
NDEx NetworkTMEM265
Atlas of Cancer Signalling NetworkTMEM265
Wikipedia pathwaysTMEM265
Orthology - Evolution
OrthoDB100862671
GeneTree (enSembl)ENSG00000080603
Phylogenetic Trees/Animal Genes : TreeFamTMEM265
HOVERGENA0A087WTH1
HOGENOMA0A087WTH1
Homologs : HomoloGeneTMEM265
Homology/Alignments : Family Browser (UCSC)TMEM265
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM265 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM265
dbVarTMEM265
ClinVarTMEM265
1000_GenomesTMEM265 
Exome Variant ServerTMEM265
ExAC (Exome Aggregation Consortium)TMEM265 (select the gene name)
Genetic variants : HAPMAP100862671
Genomic Variants (DGV)TMEM265 [DGVbeta]
DECIPHERTMEM265 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM265 
Mutations
ICGC Data PortalTMEM265 
TCGA Data PortalTMEM265 
Broad Tumor PortalTMEM265
OASIS PortalTMEM265 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDTMEM265
BioMutasearch TMEM265
DgiDB (Drug Gene Interaction Database)TMEM265
DoCM (Curated mutations)TMEM265 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TMEM265 (select a term)
intoGenTMEM265
Cancer3DTMEM265(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTMEM265
Genetic Testing Registry TMEM265
NextProtA0A087WTH1 [Medical]
TSGene100862671
GENETestsTMEM265
Huge Navigator TMEM265 [HugePedia]
snp3D : Map Gene to Disease100862671
BioCentury BCIQTMEM265
ClinGenTMEM265
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100862671
Clinical trialTMEM265
Miscellaneous
canSAR (ICR)TMEM265 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTMEM265
EVEXTMEM265
GoPubMedTMEM265
iHOPTMEM265
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 : Fri May 19 11:58:48 CEST 2017

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