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TMEM151A (transmembrane protein 151A)

Identity

Alias (NCBI)TMEM151
HGNC (Hugo) TMEM151A
HGNC Alias symbMGC33486
HGNC Previous nameTMEM151
HGNC Previous nametransmembrane protein 151
LocusID (NCBI) 256472
Atlas_Id 74816
Location 11q13.2  [Link to chromosome band 11q13]
Location_base_pair Starts at 66291894 and ends at 66296664 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)TMEM151A   28497
Cards
Entrez_Gene (NCBI)TMEM151A    transmembrane protein 151A
AliasesTMEM151
GeneCards (Weizmann)TMEM151A
Ensembl hg19 (Hinxton)ENSG00000179292 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000179292 [Gene_View]  ENSG00000179292 [Sequence]  chr11:66291894-66296664 [Contig_View]  TMEM151A [Vega]
ICGC DataPortalENSG00000179292
TCGA cBioPortalTMEM151A
AceView (NCBI)TMEM151A
Genatlas (Paris)TMEM151A
SOURCE (Princeton)TMEM151A
Genetics Home Reference (NIH)TMEM151A
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM151A  -     chr11:66291894-66296664 +  11q13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM151A  -     11q13.2   [Description]    (hg19-Feb_2009)
GoldenPathTMEM151A - 11q13.2 [CytoView hg19]  TMEM151A - 11q13.2 [CytoView hg38]
ImmunoBaseENSG00000179292
Genome Data Viewer NCBITMEM151A [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AL834459 BC033898 BC035477 BM727563 BU732410
RefSeq transcript (Entrez)NM_153266
Consensus coding sequences : CCDS (NCBI)TMEM151A
Gene ExpressionTMEM151A [ NCBI-GEO ]   TMEM151A [ EBI - ARRAY_EXPRESS ]   TMEM151A [ SEEK ]   TMEM151A [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM151A [ Firebrowse - Broad ]
GenevisibleExpression of TMEM151A in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)256472
GTEX Portal (Tissue expression)TMEM151A
Human Protein AtlasENSG00000179292-TMEM151A [pathology]   [cell]   [tissue]
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
PhosPhoSitePlusQ8N4L1
Domains : Interpro (EBI)Tmem151   
Domain families : Pfam (Sanger)TMEM151 (PF14857)   
Domain families : Pfam (NCBI)pfam14857   
Conserved Domain (NCBI)TMEM151A
SuperfamilyQ8N4L1
AlphaFold pdb e-kbQ8N4L1   
Human Protein Atlas [tissue]ENSG00000179292-TMEM151A [tissue]
HPRD14564
Protein Interaction databases
DIP (DOE-UCLA)Q8N4L1
IntAct (EBI)Q8N4L1
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
Homologs : HomoloGeneTMEM151A
Homology/Alignments : Family Browser (UCSC)TMEM151A
Gene fusions - Rearrangements
Fusion : QuiverTMEM151A
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM151A [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM151A
dbVarTMEM151A
ClinVarTMEM151A
MonarchTMEM151A
1000_GenomesTMEM151A 
Exome Variant ServerTMEM151A
GNOMAD BrowserENSG00000179292
Varsome BrowserTMEM151A
ACMGTMEM151A variants
VarityQ8N4L1
Genomic Variants (DGV)TMEM151A [DGVbeta]
DECIPHERTMEM151A [patients]   [syndromes]   [variants]   [genes]  
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]  
Somatic Mutations in Cancer : COSMIC3DTMEM151A
Mutations and Diseases : HGMDTMEM151A
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM151A
DgiDB (Drug Gene Interaction Database)TMEM151A
DoCM (Curated mutations)TMEM151A
CIViC (Clinical Interpretations of Variants in Cancer)TMEM151A
Cancer3DTMEM151A
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTMEM151A
MedgenTMEM151A
Genetic Testing Registry TMEM151A
NextProtQ8N4L1 [Medical]
GENETestsTMEM151A
Target ValidationTMEM151A
Huge Navigator TMEM151A [HugePedia]
ClinGenTMEM151A
Clinical trials, drugs, therapy
MyCancerGenomeTMEM151A
Protein Interactions : CTDTMEM151A
Pharm GKB GenePA162405898
PharosQ8N4L1
Clinical trialTMEM151A
Miscellaneous
canSAR (ICR)TMEM151A
HarmonizomeTMEM151A
DataMed IndexTMEM151A
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM151A
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 16:25:52 CEST 2021

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