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TMEM151A (transmembrane protein 151A)

Identity

Alias_namesTMEM151
transmembrane protein 151
Alias_symbol (synonym)MGC33486
Other alias
HGNC (Hugo) TMEM151A
LocusID (NCBI) 256472
Atlas_Id 74816
Location 11q13.2  [Link to chromosome band 11q13]
Location_base_pair Starts at 66059373 and ends at 66064135 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)TMEM151A   28497
Cards
Entrez_Gene (NCBI)TMEM151A  256472  transmembrane protein 151A
AliasesTMEM151
GeneCards (Weizmann)TMEM151A
Ensembl hg19 (Hinxton)ENSG00000179292 [Gene_View]  chr11:66059373-66064135 [Contig_View]  TMEM151A [Vega]
Ensembl hg38 (Hinxton)ENSG00000179292 [Gene_View]  chr11:66059373-66064135 [Contig_View]  TMEM151A [Vega]
ICGC DataPortalENSG00000179292
TCGA cBioPortalTMEM151A
AceView (NCBI)TMEM151A
Genatlas (Paris)TMEM151A
WikiGenes256472
SOURCE (Princeton)TMEM151A
Genetics Home Reference (NIH)TMEM151A
Genomic and cartography
GoldenPath hg19 (UCSC)TMEM151A  -     chr11:66059373-66064135 +  11q13.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)TMEM151A  -     11q13.2   [Description]    (hg38-Dec_2013)
EnsemblTMEM151A - 11q13.2 [CytoView hg19]  TMEM151A - 11q13.2 [CytoView hg38]
Mapping of homologs : NCBITMEM151A [Mapview hg19]  TMEM151A [Mapview hg38]
Gene and transcription
Genbank (Entrez)AL834459 BC033898 BC035477 BM727563 BU732410
RefSeq transcript (Entrez)NM_153266
RefSeq genomic (Entrez)NC_000011 NC_018922 NT_167190 NW_004929380
Consensus coding sequences : CCDS (NCBI)TMEM151A
Cluster EST : UnigeneHs.399779 [ NCBI ]
CGAP (NCI)Hs.399779
Alternative Splicing GalleryENSG00000179292
Gene ExpressionTMEM151A [ NCBI-GEO ]   TMEM151A [ EBI - ARRAY_EXPRESS ]   TMEM151A [ SEEK ]   TMEM151A [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM151A [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)256472
GTEX Portal (Tissue expression)TMEM151A
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N4L1   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N4L1  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N4L1
Splice isoforms : SwissVarQ8N4L1
PhosPhoSitePlusQ8N4L1
Domains : Interpro (EBI)Tmem151   
Domain families : Pfam (Sanger)TMEM151 (PF14857)   
Domain families : Pfam (NCBI)pfam14857   
Conserved Domain (NCBI)TMEM151A
DMDM Disease mutations256472
Blocks (Seattle)TMEM151A
SuperfamilyQ8N4L1
Human Protein AtlasENSG00000179292
Peptide AtlasQ8N4L1
HPRD14564
IPIIPI00166719   
Protein Interaction databases
DIP (DOE-UCLA)Q8N4L1
IntAct (EBI)Q8N4L1
FunCoupENSG00000179292
BioGRIDTMEM151A
STRING (EMBL)TMEM151A
ZODIACTMEM151A
Ontologies - Pathways
QuickGOQ8N4L1
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkTMEM151A
Atlas of Cancer Signalling NetworkTMEM151A
Wikipedia pathwaysTMEM151A
Orthology - Evolution
OrthoDB256472
GeneTree (enSembl)ENSG00000179292
Phylogenetic Trees/Animal Genes : TreeFamTMEM151A
HOVERGENQ8N4L1
HOGENOMQ8N4L1
Homologs : HomoloGeneTMEM151A
Homology/Alignments : Family Browser (UCSC)TMEM151A
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM151A [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM151A
dbVarTMEM151A
ClinVarTMEM151A
1000_GenomesTMEM151A 
Exome Variant ServerTMEM151A
ExAC (Exome Aggregation Consortium)TMEM151A (select the gene name)
Genetic variants : HAPMAP256472
Genomic Variants (DGV)TMEM151A [DGVbeta]
DECIPHER (Syndromes)11:66059373-66064135  ENSG00000179292
CONAN: Copy Number AnalysisTMEM151A 
Mutations
ICGC Data PortalTMEM151A 
TCGA Data PortalTMEM151A 
Broad Tumor PortalTMEM151A
OASIS PortalTMEM151A [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM151A  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDTMEM151A
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch TMEM151A
DgiDB (Drug Gene Interaction Database)TMEM151A
DoCM (Curated mutations)TMEM151A (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TMEM151A (select a term)
intoGenTMEM151A
Cancer3DTMEM151A(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTMEM151A
Genetic Testing Registry TMEM151A
NextProtQ8N4L1 [Medical]
TSGene256472
GENETestsTMEM151A
Huge Navigator TMEM151A [HugePedia]
snp3D : Map Gene to Disease256472
BioCentury BCIQTMEM151A
ClinGenTMEM151A
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD256472
Chemical/Pharm GKB GenePA162405898
Clinical trialTMEM151A
Miscellaneous
canSAR (ICR)TMEM151A (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTMEM151A
EVEXTMEM151A
GoPubMedTMEM151A
iHOPTMEM151A
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:48:30 CET 2017

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