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TMEM132E (transmembrane protein 132E)

Identity

Alias (NCBI)DFNB99
HGNC (Hugo) TMEM132E
HGNC Alias symbDFNB99
LocusID (NCBI) 124842
Atlas_Id 74796
Location 17q12  [Link to chromosome band 17q12]
Location_base_pair Starts at 34579582 and ends at 34639318 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)
PIP4K2B (17q12) / TMEM132E (17q12)TMEM132E (17q12) / GPATCH8 (17q21.31)

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)TMEM132E   26991
Cards
Entrez_Gene (NCBI)TMEM132E    transmembrane protein 132E
AliasesDFNB99
GeneCards (Weizmann)TMEM132E
Ensembl hg19 (Hinxton)ENSG00000181291 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000181291 [Gene_View]  ENSG00000181291 [Sequence]  chr17:34579582-34639318 [Contig_View]  TMEM132E [Vega]
ICGC DataPortalENSG00000181291
TCGA cBioPortalTMEM132E
AceView (NCBI)TMEM132E
Genatlas (Paris)TMEM132E
SOURCE (Princeton)TMEM132E
Genetics Home Reference (NIH)TMEM132E
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM132E  -     chr17:34579582-34639318 +  17q12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM132E  -     17q12   [Description]    (hg19-Feb_2009)
GoldenPathTMEM132E - 17q12 [CytoView hg19]  TMEM132E - 17q12 [CytoView hg38]
ImmunoBaseENSG00000181291
Genome Data Viewer NCBITMEM132E [Mapview hg19]  
OMIM616178   618481   
Gene and transcription
Genbank (Entrez)BC018318 BC020591 BN000149 N34927
RefSeq transcript (Entrez)NM_001304438 NM_207313
Consensus coding sequences : CCDS (NCBI)TMEM132E
Gene ExpressionTMEM132E [ NCBI-GEO ]   TMEM132E [ EBI - ARRAY_EXPRESS ]   TMEM132E [ SEEK ]   TMEM132E [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM132E [ Firebrowse - Broad ]
GenevisibleExpression of TMEM132E in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)124842
GTEX Portal (Tissue expression)TMEM132E
Human Protein AtlasENSG00000181291-TMEM132E [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6IEE7   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6IEE7  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6IEE7
PhosPhoSitePlusQ6IEE7
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)TMEM132E
SuperfamilyQ6IEE7
AlphaFold pdb e-kbQ6IEE7   
Human Protein Atlas [tissue]ENSG00000181291-TMEM132E [tissue]
HPRD14030
Protein Interaction databases
DIP (DOE-UCLA)Q6IEE7
IntAct (EBI)Q6IEE7
BioGRIDTMEM132E
STRING (EMBL)TMEM132E
ZODIACTMEM132E
Ontologies - Pathways
QuickGOQ6IEE7
Ontology : AmiGOmolecular_function  integral component of membrane  posterior lateral line neuromast hair cell development  cell body  
Ontology : EGO-EBImolecular_function  integral component of membrane  posterior lateral line neuromast hair cell development  cell body  
NDEx NetworkTMEM132E
Atlas of Cancer Signalling NetworkTMEM132E
Wikipedia pathwaysTMEM132E
Orthology - Evolution
OrthoDB124842
GeneTree (enSembl)ENSG00000181291
Phylogenetic Trees/Animal Genes : TreeFamTMEM132E
Homologs : HomoloGeneTMEM132E
Homology/Alignments : Family Browser (UCSC)TMEM132E
Gene fusions - Rearrangements
Fusion : QuiverTMEM132E
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM132E [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM132E
dbVarTMEM132E
ClinVarTMEM132E
MonarchTMEM132E
1000_GenomesTMEM132E 
Exome Variant ServerTMEM132E
GNOMAD BrowserENSG00000181291
Varsome BrowserTMEM132E
ACMGTMEM132E variants
VarityQ6IEE7
Genomic Variants (DGV)TMEM132E [DGVbeta]
DECIPHERTMEM132E [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM132E 
Mutations
ICGC Data PortalTMEM132E 
TCGA Data PortalTMEM132E 
Broad Tumor PortalTMEM132E
OASIS PortalTMEM132E [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM132E  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTMEM132E
Mutations and Diseases : HGMDTMEM132E
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM132E
DgiDB (Drug Gene Interaction Database)TMEM132E
DoCM (Curated mutations)TMEM132E
CIViC (Clinical Interpretations of Variants in Cancer)TMEM132E
Cancer3DTMEM132E
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM616178    618481   
Orphanet
DisGeNETTMEM132E
MedgenTMEM132E
Genetic Testing Registry TMEM132E
NextProtQ6IEE7 [Medical]
GENETestsTMEM132E
Target ValidationTMEM132E
Huge Navigator TMEM132E [HugePedia]
ClinGenTMEM132E
Clinical trials, drugs, therapy
MyCancerGenomeTMEM132E
Protein Interactions : CTDTMEM132E
Pharm GKB GenePA143485655
PharosQ6IEE7
Clinical trialTMEM132E
Miscellaneous
canSAR (ICR)TMEM132E
HarmonizomeTMEM132E
DataMed IndexTMEM132E
Probes
Litterature
PubMed11 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM132E
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 16:25:48 CEST 2021

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