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TMEM151B (transmembrane protein 151B)

Identity

Alias (NCBI)C6orf137
TMEM193
bA444E17.5
HGNC (Hugo) TMEM151B
HGNC Alias symbbA444E17.5
HGNC Previous nameC6orf137
 TMEM193
HGNC Previous namechromosome 6 open reading frame 137
 transmembrane protein 193
LocusID (NCBI) 441151
Atlas_Id 74817
Location 6p21.1  [Link to chromosome band 6p21]
Location_base_pair Starts at 44270450 and ends at 44279444 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)
MLLT4 (6q27) / TMEM151B (6p21.1)TMEM151B (6p21.1) / MT1A (16q12.2)TMEM151B (6p21.1) / RETSAT (2p11.2)
TSPAN18 (11p11.2) / TMEM151B (6p21.1)

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)TMEM151B   21315
Cards
Entrez_Gene (NCBI)TMEM151B    transmembrane protein 151B
AliasesC6orf137; TMEM193; bA444E17.5
GeneCards (Weizmann)TMEM151B
Ensembl hg19 (Hinxton)ENSG00000178233 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000178233 [Gene_View]  ENSG00000178233 [Sequence]  chr6:44270450-44279444 [Contig_View]  TMEM151B [Vega]
ICGC DataPortalENSG00000178233
TCGA cBioPortalTMEM151B
AceView (NCBI)TMEM151B
Genatlas (Paris)TMEM151B
SOURCE (Princeton)TMEM151B
Genetics Home Reference (NIH)TMEM151B
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM151B  -     chr6:44270450-44279444 +  6p21.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM151B  -     6p21.1   [Description]    (hg19-Feb_2009)
GoldenPathTMEM151B - 6p21.1 [CytoView hg19]  TMEM151B - 6p21.1 [CytoView hg38]
ImmunoBaseENSG00000178233
Genome Data Viewer NCBITMEM151B [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK094365 AK124502 AK126839 BE671218 BM664874
RefSeq transcript (Entrez)NM_001039704 NM_001137560
Consensus coding sequences : CCDS (NCBI)TMEM151B
Gene ExpressionTMEM151B [ NCBI-GEO ]   TMEM151B [ EBI - ARRAY_EXPRESS ]   TMEM151B [ SEEK ]   TMEM151B [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM151B [ Firebrowse - Broad ]
GenevisibleExpression of TMEM151B in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)441151
GTEX Portal (Tissue expression)TMEM151B
Human Protein AtlasENSG00000178233-TMEM151B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8IW70   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8IW70  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8IW70
PhosPhoSitePlusQ8IW70
Domains : Interpro (EBI)Tmem151   
Domain families : Pfam (Sanger)TMEM151 (PF14857)   
Domain families : Pfam (NCBI)pfam14857   
Conserved Domain (NCBI)TMEM151B
SuperfamilyQ8IW70
AlphaFold pdb e-kbQ8IW70   
Human Protein Atlas [tissue]ENSG00000178233-TMEM151B [tissue]
Protein Interaction databases
DIP (DOE-UCLA)Q8IW70
IntAct (EBI)Q8IW70
BioGRIDTMEM151B
STRING (EMBL)TMEM151B
ZODIACTMEM151B
Ontologies - Pathways
QuickGOQ8IW70
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkTMEM151B
Atlas of Cancer Signalling NetworkTMEM151B
Wikipedia pathwaysTMEM151B
Orthology - Evolution
OrthoDB441151
GeneTree (enSembl)ENSG00000178233
Phylogenetic Trees/Animal Genes : TreeFamTMEM151B
Homologs : HomoloGeneTMEM151B
Homology/Alignments : Family Browser (UCSC)TMEM151B
Gene fusions - Rearrangements
Fusion : QuiverTMEM151B
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM151B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM151B
dbVarTMEM151B
ClinVarTMEM151B
MonarchTMEM151B
1000_GenomesTMEM151B 
Exome Variant ServerTMEM151B
GNOMAD BrowserENSG00000178233
Varsome BrowserTMEM151B
ACMGTMEM151B variants
VarityQ8IW70
Genomic Variants (DGV)TMEM151B [DGVbeta]
DECIPHERTMEM151B [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM151B 
Mutations
ICGC Data PortalTMEM151B 
TCGA Data PortalTMEM151B 
Broad Tumor PortalTMEM151B
OASIS PortalTMEM151B [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM151B  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTMEM151B
Mutations and Diseases : HGMDTMEM151B
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM151B
DgiDB (Drug Gene Interaction Database)TMEM151B
DoCM (Curated mutations)TMEM151B
CIViC (Clinical Interpretations of Variants in Cancer)TMEM151B
Cancer3DTMEM151B
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTMEM151B
MedgenTMEM151B
Genetic Testing Registry TMEM151B
NextProtQ8IW70 [Medical]
GENETestsTMEM151B
Target ValidationTMEM151B
Huge Navigator TMEM151B [HugePedia]
ClinGenTMEM151B
Clinical trials, drugs, therapy
MyCancerGenomeTMEM151B
Protein Interactions : CTDTMEM151B
Pharm GKB GenePA162405899
PharosQ8IW70
Clinical trialTMEM151B
Miscellaneous
canSAR (ICR)TMEM151B
HarmonizomeTMEM151B
DataMed IndexTMEM151B
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM151B
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 16:25:52 CEST 2021

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