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TMEM132B (transmembrane protein 132B)

Identity

Alias (NCBI)-
HGNC (Hugo) TMEM132B
HGNC Alias symbKIAA1906
KIAA1786
LocusID (NCBI) 114795
Atlas_Id 74793
Location 12q24.31  [Link to chromosome band 12q24]
Location_base_pair Starts at 125326616 and ends at 125662377 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)
C12orf66 (12q14.2) / TMEM132B (12q24.32)MON2 (12q14.1) / TMEM132B (12q24.32)

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)TMEM132B   29397
Cards
Entrez_Gene (NCBI)TMEM132B    transmembrane protein 132B
Aliases
GeneCards (Weizmann)TMEM132B
Ensembl hg19 (Hinxton)ENSG00000139364 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000139364 [Gene_View]  ENSG00000139364 [Sequence]  chr12:125326616-125662377 [Contig_View]  TMEM132B [Vega]
ICGC DataPortalENSG00000139364
TCGA cBioPortalTMEM132B
AceView (NCBI)TMEM132B
Genatlas (Paris)TMEM132B
SOURCE (Princeton)TMEM132B
Genetics Home Reference (NIH)TMEM132B
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM132B  -     chr12:125326616-125662377 +  12q24.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM132B  -     12q24.31   [Description]    (hg19-Feb_2009)
GoldenPathTMEM132B - 12q24.31 [CytoView hg19]  TMEM132B - 12q24.31 [CytoView hg38]
ImmunoBaseENSG00000139364
Genome Data Viewer NCBITMEM132B [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AB058689 AB067493 AK055283 AK090767 AK091512
RefSeq transcript (Entrez)NM_001286219 NM_001366854 NM_052907
Consensus coding sequences : CCDS (NCBI)TMEM132B
Gene ExpressionTMEM132B [ NCBI-GEO ]   TMEM132B [ EBI - ARRAY_EXPRESS ]   TMEM132B [ SEEK ]   TMEM132B [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM132B [ Firebrowse - Broad ]
GenevisibleExpression of TMEM132B in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)114795
GTEX Portal (Tissue expression)TMEM132B
Human Protein AtlasENSG00000139364-TMEM132B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ14DG7   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ14DG7  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ14DG7
PhosPhoSitePlusQ14DG7
Domains : Interpro (EBI)TMEM132    TMEM132_C    TMEM132_M    TMEM132_N   
Domain families : Pfam (Sanger)TMEM132 (PF16070)    TMEM132D_C (PF15706)    TMEM132D_N (PF15705)   
Domain families : Pfam (NCBI)pfam16070    pfam15706    pfam15705   
Conserved Domain (NCBI)TMEM132B
SuperfamilyQ14DG7
AlphaFold pdb e-kbQ14DG7   
Human Protein Atlas [tissue]ENSG00000139364-TMEM132B [tissue]
HPRD17230
Protein Interaction databases
DIP (DOE-UCLA)Q14DG7
IntAct (EBI)Q14DG7
BioGRIDTMEM132B
STRING (EMBL)TMEM132B
ZODIACTMEM132B
Ontologies - Pathways
QuickGOQ14DG7
Ontology : AmiGOmolecular_function  cellular_component  biological_process  integral component of membrane  
Ontology : EGO-EBImolecular_function  cellular_component  biological_process  integral component of membrane  
NDEx NetworkTMEM132B
Atlas of Cancer Signalling NetworkTMEM132B
Wikipedia pathwaysTMEM132B
Orthology - Evolution
OrthoDB114795
GeneTree (enSembl)ENSG00000139364
Phylogenetic Trees/Animal Genes : TreeFamTMEM132B
Homologs : HomoloGeneTMEM132B
Homology/Alignments : Family Browser (UCSC)TMEM132B
Gene fusions - Rearrangements
Fusion : QuiverTMEM132B
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM132B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM132B
dbVarTMEM132B
ClinVarTMEM132B
MonarchTMEM132B
1000_GenomesTMEM132B 
Exome Variant ServerTMEM132B
GNOMAD BrowserENSG00000139364
Varsome BrowserTMEM132B
ACMGTMEM132B variants
VarityQ14DG7
Genomic Variants (DGV)TMEM132B [DGVbeta]
DECIPHERTMEM132B [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM132B 
Mutations
ICGC Data PortalTMEM132B 
TCGA Data PortalTMEM132B 
Broad Tumor PortalTMEM132B
OASIS PortalTMEM132B [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM132B  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTMEM132B
Mutations and Diseases : HGMDTMEM132B
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM132B
DgiDB (Drug Gene Interaction Database)TMEM132B
DoCM (Curated mutations)TMEM132B
CIViC (Clinical Interpretations of Variants in Cancer)TMEM132B
Cancer3DTMEM132B
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTMEM132B
MedgenTMEM132B
Genetic Testing Registry TMEM132B
NextProtQ14DG7 [Medical]
GENETestsTMEM132B
Target ValidationTMEM132B
Huge Navigator TMEM132B [HugePedia]
ClinGenTMEM132B
Clinical trials, drugs, therapy
MyCancerGenomeTMEM132B
Protein Interactions : CTDTMEM132B
Pharm GKB GenePA143485652
PharosQ14DG7
Clinical trialTMEM132B
Miscellaneous
canSAR (ICR)TMEM132B
HarmonizomeTMEM132B
DataMed IndexTMEM132B
Probes
Litterature
PubMed10 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM132B
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 16:25:47 CEST 2021

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