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TMEM95 (transmembrane protein 95)

Identity

Alias_symbol (synonym)MGC129793
UNQ9390
Other alias
HGNC (Hugo) TMEM95
LocusID (NCBI) 339168
Atlas_Id 74995
Location 17p13.1  [Link to chromosome band 17p13]
Location_base_pair Starts at 7355136 and ends at 7357219 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)TMEM95   27898
Cards
Entrez_Gene (NCBI)TMEM95  339168  transmembrane protein 95
AliasesUNQ9390
GeneCards (Weizmann)TMEM95
Ensembl hg19 (Hinxton)ENSG00000182896 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000182896 [Gene_View]  chr17:7355136-7357219 [Contig_View]  TMEM95 [Vega]
ICGC DataPortalENSG00000182896
TCGA cBioPortalTMEM95
AceView (NCBI)TMEM95
Genatlas (Paris)TMEM95
WikiGenes339168
SOURCE (Princeton)TMEM95
Genetics Home Reference (NIH)TMEM95
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM95  -     chr17:7355136-7357219 +  17p13.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM95  -     17p13.1   [Description]    (hg19-Feb_2009)
EnsemblTMEM95 - 17p13.1 [CytoView hg19]  TMEM95 - 17p13.1 [CytoView hg38]
Mapping of homologs : NCBITMEM95 [Mapview hg19]  TMEM95 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AY358218 BC040900 BC107110
RefSeq transcript (Entrez)NM_001320435 NM_001320436 NM_198154
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)TMEM95
Cluster EST : UnigeneHs.259432 [ NCBI ]
CGAP (NCI)Hs.259432
Alternative Splicing GalleryENSG00000182896
Gene ExpressionTMEM95 [ NCBI-GEO ]   TMEM95 [ EBI - ARRAY_EXPRESS ]   TMEM95 [ SEEK ]   TMEM95 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM95 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)339168
GTEX Portal (Tissue expression)TMEM95
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ3KNT9   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ3KNT9  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ3KNT9
Splice isoforms : SwissVarQ3KNT9
PhosPhoSitePlusQ3KNT9
Domains : Interpro (EBI)TMEM95   
Domain families : Pfam (Sanger)TMEM95 (PF15203)   
Domain families : Pfam (NCBI)pfam15203   
Conserved Domain (NCBI)TMEM95
DMDM Disease mutations339168
Blocks (Seattle)TMEM95
SuperfamilyQ3KNT9
Human Protein AtlasENSG00000182896
Peptide AtlasQ3KNT9
HPRD14165
IPIIPI00845469   IPI00217162   IPI00788920   
Protein Interaction databases
DIP (DOE-UCLA)Q3KNT9
IntAct (EBI)Q3KNT9
FunCoupENSG00000182896
BioGRIDTMEM95
STRING (EMBL)TMEM95
ZODIACTMEM95
Ontologies - Pathways
QuickGOQ3KNT9
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkTMEM95
Atlas of Cancer Signalling NetworkTMEM95
Wikipedia pathwaysTMEM95
Orthology - Evolution
OrthoDB339168
GeneTree (enSembl)ENSG00000182896
Phylogenetic Trees/Animal Genes : TreeFamTMEM95
HOVERGENQ3KNT9
HOGENOMQ3KNT9
Homologs : HomoloGeneTMEM95
Homology/Alignments : Family Browser (UCSC)TMEM95
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM95 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM95
dbVarTMEM95
ClinVarTMEM95
1000_GenomesTMEM95 
Exome Variant ServerTMEM95
ExAC (Exome Aggregation Consortium)TMEM95 (select the gene name)
Genetic variants : HAPMAP339168
Genomic Variants (DGV)TMEM95 [DGVbeta]
DECIPHERTMEM95 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM95 
Mutations
ICGC Data PortalTMEM95 
TCGA Data PortalTMEM95 
Broad Tumor PortalTMEM95
OASIS PortalTMEM95 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM95  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDTMEM95
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch TMEM95
DgiDB (Drug Gene Interaction Database)TMEM95
DoCM (Curated mutations)TMEM95 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TMEM95 (select a term)
intoGenTMEM95
Cancer3DTMEM95(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTMEM95
Genetic Testing Registry TMEM95
NextProtQ3KNT9 [Medical]
TSGene339168
GENETestsTMEM95
Target ValidationTMEM95
Huge Navigator TMEM95 [HugePedia]
snp3D : Map Gene to Disease339168
BioCentury BCIQTMEM95
ClinGenTMEM95
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD339168
Chemical/Pharm GKB GenePA142670746
Clinical trialTMEM95
Miscellaneous
canSAR (ICR)TMEM95 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTMEM95
EVEXTMEM95
GoPubMedTMEM95
iHOPTMEM95
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 : Wed May 31 15:46:32 CEST 2017

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