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TMEM268 (transmembrane protein 268)

Identity

Other aliasC9orf91
HGNC (Hugo) TMEM268
LocusID (NCBI) 203197
Atlas_Id 78625
Location 9q32  [Link to chromosome band 9q32]
Location_base_pair Starts at 117373600 and ends at 117408704 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


External links

Nomenclature
HGNC (Hugo)TMEM268   24513
Cards
Entrez_Gene (NCBI)TMEM268  203197  transmembrane protein 268
AliasesC9orf91
GeneCards (Weizmann)TMEM268
Ensembl hg19 (Hinxton) [Gene_View]  chr9:117373600-117408704 [Contig_View]  TMEM268 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr9:117373600-117408704 [Contig_View]  TMEM268 [Vega]
TCGA cBioPortalTMEM268
AceView (NCBI)TMEM268
Genatlas (Paris)TMEM268
WikiGenes203197
SOURCE (Princeton)TMEM268
Genetics Home Reference (NIH)TMEM268
Genomic and cartography
GoldenPath hg19 (UCSC)TMEM268  -     chr9:117373600-117408704 +  9q32   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)TMEM268  -     9q32   [Description]    (hg38-Dec_2013)
EnsemblTMEM268 - 9q32 [CytoView hg19]  TMEM268 - 9q32 [CytoView hg38]
Mapping of homologs : NCBITMEM268 [Mapview hg19]  TMEM268 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF038174 AK095364 AK098022 AK289383 AL557166
RefSeq transcript (Entrez)NM_001330760 NM_153045
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)TMEM268
Cluster EST : UnigeneHs.522357 [ NCBI ]
CGAP (NCI)Hs.522357
Gene ExpressionTMEM268 [ NCBI-GEO ]   TMEM268 [ EBI - ARRAY_EXPRESS ]   TMEM268 [ SEEK ]   TMEM268 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM268 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)203197
GTEX Portal (Tissue expression)TMEM268
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5VZI3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5VZI3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5VZI3
Splice isoforms : SwissVarQ5VZI3
PhosPhoSitePlusQ5VZI3
Domains : Interpro (EBI)DUF4481   
Domain families : Pfam (Sanger)DUF4481 (PF14800)   
Domain families : Pfam (NCBI)pfam14800   
Conserved Domain (NCBI)TMEM268
DMDM Disease mutations203197
Blocks (Seattle)TMEM268
SuperfamilyQ5VZI3
Peptide AtlasQ5VZI3
HPRD12988
IPIIPI00643144   IPI00829919   IPI00337642   
Protein Interaction databases
DIP (DOE-UCLA)Q5VZI3
IntAct (EBI)Q5VZI3
BioGRIDTMEM268
STRING (EMBL)TMEM268
ZODIACTMEM268
Ontologies - Pathways
QuickGOQ5VZI3
Ontology : AmiGOmolecular_function  cellular_component  biological_process  integral component of membrane  
Ontology : EGO-EBImolecular_function  cellular_component  biological_process  integral component of membrane  
NDEx NetworkTMEM268
Atlas of Cancer Signalling NetworkTMEM268
Wikipedia pathwaysTMEM268
Orthology - Evolution
OrthoDB203197
Phylogenetic Trees/Animal Genes : TreeFamTMEM268
HOVERGENQ5VZI3
HOGENOMQ5VZI3
Homologs : HomoloGeneTMEM268
Homology/Alignments : Family Browser (UCSC)TMEM268
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM268 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM268
dbVarTMEM268
ClinVarTMEM268
1000_GenomesTMEM268 
Exome Variant ServerTMEM268
ExAC (Exome Aggregation Consortium)TMEM268 (select the gene name)
Genetic variants : HAPMAP203197
Genomic Variants (DGV)TMEM268 [DGVbeta]
DECIPHER (Syndromes)9:117373600-117408704  
CONAN: Copy Number AnalysisTMEM268 
Mutations
ICGC Data PortalTMEM268 
TCGA Data PortalTMEM268 
Broad Tumor PortalTMEM268
OASIS PortalTMEM268 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDTMEM268
BioMutasearch TMEM268
DgiDB (Drug Gene Interaction Database)TMEM268
DoCM (Curated mutations)TMEM268 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TMEM268 (select a term)
intoGenTMEM268
Cancer3DTMEM268(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTMEM268
Genetic Testing Registry TMEM268
NextProtQ5VZI3 [Medical]
TSGene203197
GENETestsTMEM268
Huge Navigator TMEM268 [HugePedia]
snp3D : Map Gene to Disease203197
BioCentury BCIQTMEM268
ClinGenTMEM268
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD203197
Chemical/Pharm GKB GenePA134931542
Clinical trialTMEM268
Miscellaneous
canSAR (ICR)TMEM268 (select the gene name)
Probes
Litterature
PubMed12 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTMEM268
EVEXTMEM268
GoPubMedTMEM268
iHOPTMEM268
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Tue Mar 14 12:48:54 CET 2017

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