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TMEM207 (transmembrane protein 207)

Identity

Alias (NCBI)UNQ846
HGNC (Hugo) TMEM207
LocusID (NCBI) 131920
Atlas_Id 52696
Location 3q28  [Link to chromosome band 3q28]
Location_base_pair Starts at 190428656 and ends at 190449876 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)
IL1RAP (3q28) / TMEM207 (3q28)TMEM207 (3q28) / FMR1 (Xq27.3)IL1RAP 3q28 / TMEM207 3q28

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)TMEM207   33705
Cards
Entrez_Gene (NCBI)TMEM207    transmembrane protein 207
AliasesUNQ846
GeneCards (Weizmann)TMEM207
Ensembl hg19 (Hinxton)ENSG00000198398 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000198398 [Gene_View]  ENSG00000198398 [Sequence]  chr3:190428656-190449876 [Contig_View]  TMEM207 [Vega]
ICGC DataPortalENSG00000198398
TCGA cBioPortalTMEM207
AceView (NCBI)TMEM207
Genatlas (Paris)TMEM207
SOURCE (Princeton)TMEM207
Genetics Home Reference (NIH)TMEM207
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM207  -     chr3:190428656-190449876 -  3q28   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM207  -     3q28   [Description]    (hg19-Feb_2009)
GoldenPathTMEM207 - 3q28 [CytoView hg19]  TMEM207 - 3q28 [CytoView hg38]
ImmunoBaseENSG00000198398
Genome Data Viewer NCBITMEM207 [Mapview hg19]  
OMIM614786   
Gene and transcription
Genbank (Entrez)AI762254 AY358607 BC071780
RefSeq transcript (Entrez)NM_207316
Consensus coding sequences : CCDS (NCBI)TMEM207
Gene ExpressionTMEM207 [ NCBI-GEO ]   TMEM207 [ EBI - ARRAY_EXPRESS ]   TMEM207 [ SEEK ]   TMEM207 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM207 [ Firebrowse - Broad ]
GenevisibleExpression of TMEM207 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)131920
GTEX Portal (Tissue expression)TMEM207
Human Protein AtlasENSG00000198398-TMEM207 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6UWW9   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6UWW9  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6UWW9
PhosPhoSitePlusQ6UWW9
Domains : Interpro (EBI)TMEM207   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)TMEM207
SuperfamilyQ6UWW9
AlphaFold pdb e-kbQ6UWW9   
Human Protein Atlas [tissue]ENSG00000198398-TMEM207 [tissue]
HPRD15621
Protein Interaction databases
DIP (DOE-UCLA)Q6UWW9
IntAct (EBI)Q6UWW9
BioGRIDTMEM207
STRING (EMBL)TMEM207
ZODIACTMEM207
Ontologies - Pathways
QuickGOQ6UWW9
Ontology : AmiGOmolecular_function  protein binding  cellular_component  biological_process  integral component of membrane  
Ontology : EGO-EBImolecular_function  protein binding  cellular_component  biological_process  integral component of membrane  
NDEx NetworkTMEM207
Atlas of Cancer Signalling NetworkTMEM207
Wikipedia pathwaysTMEM207
Orthology - Evolution
OrthoDB131920
GeneTree (enSembl)ENSG00000198398
Phylogenetic Trees/Animal Genes : TreeFamTMEM207
Homologs : HomoloGeneTMEM207
Homology/Alignments : Family Browser (UCSC)TMEM207
Gene fusions - Rearrangements
Fusion : QuiverTMEM207
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM207 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM207
dbVarTMEM207
ClinVarTMEM207
MonarchTMEM207
1000_GenomesTMEM207 
Exome Variant ServerTMEM207
GNOMAD BrowserENSG00000198398
Varsome BrowserTMEM207
ACMGTMEM207 variants
VarityQ6UWW9
Genomic Variants (DGV)TMEM207 [DGVbeta]
DECIPHERTMEM207 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM207 
Mutations
ICGC Data PortalTMEM207 
TCGA Data PortalTMEM207 
Broad Tumor PortalTMEM207
OASIS PortalTMEM207 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM207  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTMEM207
Mutations and Diseases : HGMDTMEM207
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM207
DgiDB (Drug Gene Interaction Database)TMEM207
DoCM (Curated mutations)TMEM207
CIViC (Clinical Interpretations of Variants in Cancer)TMEM207
Cancer3DTMEM207
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM614786   
Orphanet
DisGeNETTMEM207
MedgenTMEM207
Genetic Testing Registry TMEM207
NextProtQ6UWW9 [Medical]
GENETestsTMEM207
Target ValidationTMEM207
Huge Navigator TMEM207 [HugePedia]
ClinGenTMEM207
Clinical trials, drugs, therapy
MyCancerGenomeTMEM207
Protein Interactions : CTDTMEM207
Pharm GKB GenePA162406407
PharosQ6UWW9
Clinical trialTMEM207
Miscellaneous
canSAR (ICR)TMEM207
HarmonizomeTMEM207
DataMed IndexTMEM207
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM207
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:35:29 CEST 2021

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