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TMEM262 (transmembrane protein 262)

Identity

Other alias-
HGNC (Hugo) TMEM262
LocusID (NCBI) 100130348
Atlas_Id 74927
Location 11q13.1  [Link to chromosome band 11q13]
Location_base_pair Starts at 65088372 and ends at 65089109 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)TMEM262   49389
Cards
Entrez_Gene (NCBI)TMEM262  100130348  transmembrane protein 262
Aliases
GeneCards (Weizmann)TMEM262
Ensembl hg19 (Hinxton)ENSG00000187066 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000187066 [Gene_View]  chr11:65088372-65089109 [Contig_View]  TMEM262 [Vega]
ICGC DataPortalENSG00000187066
TCGA cBioPortalTMEM262
AceView (NCBI)TMEM262
Genatlas (Paris)TMEM262
WikiGenes100130348
SOURCE (Princeton)TMEM262
Genetics Home Reference (NIH)TMEM262
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM262  -     chr11:65088372-65089109 -  11q13.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM262  -     11q13.1   [Description]    (hg19-Feb_2009)
EnsemblTMEM262 - 11q13.1 [CytoView hg19]  TMEM262 - 11q13.1 [CytoView hg38]
Mapping of homologs : NCBITMEM262 [Mapview hg19]  TMEM262 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA416856 AI015611 AK124141 BX093670 HY032040
RefSeq transcript (Entrez)NM_001242631 NM_001282448
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)TMEM262
Cluster EST : UnigeneHs.712317 [ NCBI ]
CGAP (NCI)Hs.712317
Alternative Splicing GalleryENSG00000187066
Gene ExpressionTMEM262 [ NCBI-GEO ]   TMEM262 [ EBI - ARRAY_EXPRESS ]   TMEM262 [ SEEK ]   TMEM262 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM262 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100130348
GTEX Portal (Tissue expression)TMEM262
Protein : pattern, domain, 3D structure
UniProt/SwissProtE9PQX1   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtE9PQX1  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProE9PQX1
Splice isoforms : SwissVarE9PQX1
PhosPhoSitePlusE9PQX1
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)TMEM262
DMDM Disease mutations100130348
Blocks (Seattle)TMEM262
SuperfamilyE9PQX1
Human Protein AtlasENSG00000187066
Peptide AtlasE9PQX1
Protein Interaction databases
DIP (DOE-UCLA)E9PQX1
IntAct (EBI)E9PQX1
FunCoupENSG00000187066
BioGRIDTMEM262
STRING (EMBL)TMEM262
ZODIACTMEM262
Ontologies - Pathways
QuickGOE9PQX1
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkTMEM262
Atlas of Cancer Signalling NetworkTMEM262
Wikipedia pathwaysTMEM262
Orthology - Evolution
OrthoDB100130348
GeneTree (enSembl)ENSG00000187066
Phylogenetic Trees/Animal Genes : TreeFamTMEM262
HOVERGENE9PQX1
HOGENOME9PQX1
Homologs : HomoloGeneTMEM262
Homology/Alignments : Family Browser (UCSC)TMEM262
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM262 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM262
dbVarTMEM262
ClinVarTMEM262
1000_GenomesTMEM262 
Exome Variant ServerTMEM262
ExAC (Exome Aggregation Consortium)TMEM262 (select the gene name)
Genetic variants : HAPMAP100130348
Genomic Variants (DGV)TMEM262 [DGVbeta]
DECIPHERTMEM262 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM262 
Mutations
ICGC Data PortalTMEM262 
TCGA Data PortalTMEM262 
Broad Tumor PortalTMEM262
OASIS PortalTMEM262 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDTMEM262
BioMutasearch TMEM262
DgiDB (Drug Gene Interaction Database)TMEM262
DoCM (Curated mutations)TMEM262 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TMEM262 (select a term)
intoGenTMEM262
Cancer3DTMEM262(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTMEM262
Genetic Testing Registry TMEM262
NextProtE9PQX1 [Medical]
TSGene100130348
GENETestsTMEM262
Target ValidationTMEM262
Huge Navigator TMEM262 [HugePedia]
snp3D : Map Gene to Disease100130348
BioCentury BCIQTMEM262
ClinGenTMEM262
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100130348
Chemical/Pharm GKB GenePA166123748
Clinical trialTMEM262
Miscellaneous
canSAR (ICR)TMEM262 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTMEM262
EVEXTMEM262
GoPubMedTMEM262
iHOPTMEM262
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 : Mon Sep 18 13:41:57 CEST 2017

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