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TMEM267 (transmembrane protein 267)

Identity

Alias (NCBI)C5orf28
HGNC (Hugo) TMEM267
HGNC Alias symbFLJ21657
HGNC Previous nameC5orf28
HGNC Previous namechromosome 5 open reading frame 28
LocusID (NCBI) 64417
Atlas_Id 78572
Location 5p12  [Link to chromosome band 5p12]
Location_base_pair Starts at 43444252 and ends at 43483865 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)TMEM267   26139
Cards
Entrez_Gene (NCBI)TMEM267    transmembrane protein 267
AliasesC5orf28
GeneCards (Weizmann)TMEM267
Ensembl hg19 (Hinxton)ENSG00000151881 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000151881 [Gene_View]  ENSG00000151881 [Sequence]  chr5:43444252-43483865 [Contig_View]  TMEM267 [Vega]
ICGC DataPortalENSG00000151881
TCGA cBioPortalTMEM267
AceView (NCBI)TMEM267
Genatlas (Paris)TMEM267
SOURCE (Princeton)TMEM267
Genetics Home Reference (NIH)TMEM267
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM267  -     chr5:43444252-43483865 -  5p12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM267  -     5p12   [Description]    (hg19-Feb_2009)
GoldenPathTMEM267 - 5p12 [CytoView hg19]  TMEM267 - 5p12 [CytoView hg38]
ImmunoBaseENSG00000151881
Genome Data Viewer NCBITMEM267 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK025310 AK225220 AK315466 AL137306 BC013351
RefSeq transcript (Entrez)NM_001377394 NM_001377395 NM_001377396 NM_001377397 NM_001377398 NM_001377399 NM_001377400 NM_001377401 NM_001377402 NM_001377403 NM_022483
Consensus coding sequences : CCDS (NCBI)TMEM267
Gene ExpressionTMEM267 [ NCBI-GEO ]   TMEM267 [ EBI - ARRAY_EXPRESS ]   TMEM267 [ SEEK ]   TMEM267 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM267 [ Firebrowse - Broad ]
GenevisibleExpression of TMEM267 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)64417
GTEX Portal (Tissue expression)TMEM267
Human Protein AtlasENSG00000151881-TMEM267 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ0VDI3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ0VDI3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ0VDI3
PhosPhoSitePlusQ0VDI3
Domains : Interpro (EBI)TMEM267   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)TMEM267
SuperfamilyQ0VDI3
AlphaFold pdb e-kbQ0VDI3   
Human Protein Atlas [tissue]ENSG00000151881-TMEM267 [tissue]
HPRD07965
Protein Interaction databases
DIP (DOE-UCLA)Q0VDI3
IntAct (EBI)Q0VDI3
BioGRIDTMEM267
STRING (EMBL)TMEM267
ZODIACTMEM267
Ontologies - Pathways
QuickGOQ0VDI3
Ontology : AmiGOprotein binding  integral component of membrane  
Ontology : EGO-EBIprotein binding  integral component of membrane  
NDEx NetworkTMEM267
Atlas of Cancer Signalling NetworkTMEM267
Wikipedia pathwaysTMEM267
Orthology - Evolution
OrthoDB64417
GeneTree (enSembl)ENSG00000151881
Phylogenetic Trees/Animal Genes : TreeFamTMEM267
Homologs : HomoloGeneTMEM267
Homology/Alignments : Family Browser (UCSC)TMEM267
Gene fusions - Rearrangements
Fusion : QuiverTMEM267
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM267 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM267
dbVarTMEM267
ClinVarTMEM267
MonarchTMEM267
1000_GenomesTMEM267 
Exome Variant ServerTMEM267
GNOMAD BrowserENSG00000151881
Varsome BrowserTMEM267
ACMGTMEM267 variants
VarityQ0VDI3
Genomic Variants (DGV)TMEM267 [DGVbeta]
DECIPHERTMEM267 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM267 
Mutations
ICGC Data PortalTMEM267 
TCGA Data PortalTMEM267 
Broad Tumor PortalTMEM267
OASIS PortalTMEM267 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM267  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTMEM267
Mutations and Diseases : HGMDTMEM267
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM267
DgiDB (Drug Gene Interaction Database)TMEM267
DoCM (Curated mutations)TMEM267
CIViC (Clinical Interpretations of Variants in Cancer)TMEM267
Cancer3DTMEM267
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTMEM267
MedgenTMEM267
Genetic Testing Registry TMEM267
NextProtQ0VDI3 [Medical]
GENETestsTMEM267
Target ValidationTMEM267
Huge Navigator TMEM267 [HugePedia]
ClinGenTMEM267
Clinical trials, drugs, therapy
MyCancerGenomeTMEM267
Protein Interactions : CTDTMEM267
Pharm GKB GenePA162380004
PharosQ0VDI3
Clinical trialTMEM267
Miscellaneous
canSAR (ICR)TMEM267
HarmonizomeTMEM267
DataMed IndexTMEM267
Probes
Litterature
PubMed10 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM267
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 : Mon Oct 4 16:26:10 CEST 2021

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