Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

TMEM145 (transmembrane protein 145)

Identity

Alias (NCBI)-
HGNC (Hugo) TMEM145
HGNC Alias symbFLJ90805
LocusID (NCBI) 284339
Atlas_Id 74806
Location 19q13.2  [Link to chromosome band 19q13]
Location_base_pair Starts at 42313309 and ends at 42325064 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)TMEM145   26912
Cards
Entrez_Gene (NCBI)TMEM145    transmembrane protein 145
Aliases
GeneCards (Weizmann)TMEM145
Ensembl hg19 (Hinxton)ENSG00000167619 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000167619 [Gene_View]  ENSG00000167619 [Sequence]  chr19:42313309-42325064 [Contig_View]  TMEM145 [Vega]
ICGC DataPortalENSG00000167619
TCGA cBioPortalTMEM145
AceView (NCBI)TMEM145
Genatlas (Paris)TMEM145
SOURCE (Princeton)TMEM145
Genetics Home Reference (NIH)TMEM145
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM145  -     chr19:42313309-42325064 +  19q13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM145  -     19q13.2   [Description]    (hg19-Feb_2009)
GoldenPathTMEM145 - 19q13.2 [CytoView hg19]  TMEM145 - 19q13.2 [CytoView hg38]
ImmunoBaseENSG00000167619
Genome Data Viewer NCBITMEM145 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK075286 DA694683
RefSeq transcript (Entrez)NM_001366910 NM_173633
Consensus coding sequences : CCDS (NCBI)TMEM145
Gene ExpressionTMEM145 [ NCBI-GEO ]   TMEM145 [ EBI - ARRAY_EXPRESS ]   TMEM145 [ SEEK ]   TMEM145 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM145 [ Firebrowse - Broad ]
GenevisibleExpression of TMEM145 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)284339
GTEX Portal (Tissue expression)TMEM145
Human Protein AtlasENSG00000167619-TMEM145 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8NBT3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8NBT3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8NBT3
PhosPhoSitePlusQ8NBT3
Domains : Interpro (EBI)Intimal_thickness-rel_rcpt   
Domain families : Pfam (Sanger)GpcrRhopsn4 (PF10192)   
Domain families : Pfam (NCBI)pfam10192   
Conserved Domain (NCBI)TMEM145
SuperfamilyQ8NBT3
AlphaFold pdb e-kbQ8NBT3   
Human Protein Atlas [tissue]ENSG00000167619-TMEM145 [tissue]
HPRD08300
Protein Interaction databases
DIP (DOE-UCLA)Q8NBT3
IntAct (EBI)Q8NBT3
BioGRIDTMEM145
STRING (EMBL)TMEM145
ZODIACTMEM145
Ontologies - Pathways
QuickGOQ8NBT3
Ontology : AmiGOG protein-coupled receptor signaling pathway  integral component of membrane  response to pheromone  
Ontology : EGO-EBIG protein-coupled receptor signaling pathway  integral component of membrane  response to pheromone  
NDEx NetworkTMEM145
Atlas of Cancer Signalling NetworkTMEM145
Wikipedia pathwaysTMEM145
Orthology - Evolution
OrthoDB284339
GeneTree (enSembl)ENSG00000167619
Phylogenetic Trees/Animal Genes : TreeFamTMEM145
Homologs : HomoloGeneTMEM145
Homology/Alignments : Family Browser (UCSC)TMEM145
Gene fusions - Rearrangements
Fusion : QuiverTMEM145
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM145 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM145
dbVarTMEM145
ClinVarTMEM145
MonarchTMEM145
1000_GenomesTMEM145 
Exome Variant ServerTMEM145
GNOMAD BrowserENSG00000167619
Varsome BrowserTMEM145
ACMGTMEM145 variants
VarityQ8NBT3
Genomic Variants (DGV)TMEM145 [DGVbeta]
DECIPHERTMEM145 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM145 
Mutations
ICGC Data PortalTMEM145 
TCGA Data PortalTMEM145 
Broad Tumor PortalTMEM145
OASIS PortalTMEM145 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM145  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTMEM145
Mutations and Diseases : HGMDTMEM145
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM145
DgiDB (Drug Gene Interaction Database)TMEM145
DoCM (Curated mutations)TMEM145
CIViC (Clinical Interpretations of Variants in Cancer)TMEM145
Cancer3DTMEM145
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTMEM145
MedgenTMEM145
Genetic Testing Registry TMEM145
NextProtQ8NBT3 [Medical]
GENETestsTMEM145
Target ValidationTMEM145
Huge Navigator TMEM145 [HugePedia]
ClinGenTMEM145
Clinical trials, drugs, therapy
MyCancerGenomeTMEM145
Protein Interactions : CTDTMEM145
Pharm GKB GenePA144596253
PharosQ8NBT3
Clinical trialTMEM145
Miscellaneous
canSAR (ICR)TMEM145
HarmonizomeTMEM145
DataMed IndexTMEM145
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM145
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Oct 4 16:25:50 CEST 2021

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.