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TMEM37 (transmembrane protein 37)

Identity

Alias (NCBI)PR
PR1
HGNC (Hugo) TMEM37
HGNC Alias symbPR1
PR
LocusID (NCBI) 140738
Atlas_Id 74936
Location 2q14.2  [Link to chromosome band 2q14]
Location_base_pair Starts at 119431854 and ends at 119438504 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)
TMEM37 (2q14.2) / UBAP2 (9p13.3)

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)TMEM37   18216
Cards
Entrez_Gene (NCBI)TMEM37    transmembrane protein 37
AliasesPR; PR1
GeneCards (Weizmann)TMEM37
Ensembl hg19 (Hinxton)ENSG00000171227 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000171227 [Gene_View]  ENSG00000171227 [Sequence]  chr2:119431854-119438504 [Contig_View]  TMEM37 [Vega]
ICGC DataPortalENSG00000171227
TCGA cBioPortalTMEM37
AceView (NCBI)TMEM37
Genatlas (Paris)TMEM37
SOURCE (Princeton)TMEM37
Genetics Home Reference (NIH)TMEM37
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM37  -     chr2:119431854-119438504 +  2q14.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM37  -     2q14.2   [Description]    (hg19-Feb_2009)
GoldenPathTMEM37 - 2q14.2 [CytoView hg19]  TMEM37 - 2q14.2 [CytoView hg38]
ImmunoBaseENSG00000171227
Genome Data Viewer NCBITMEM37 [Mapview hg19]  
OMIM618831   
Gene and transcription
Genbank (Entrez)AF361356 AK026464 BC046362 DR003856 DR005637
RefSeq transcript (Entrez)NM_183240
Consensus coding sequences : CCDS (NCBI)TMEM37
Gene ExpressionTMEM37 [ NCBI-GEO ]   TMEM37 [ EBI - ARRAY_EXPRESS ]   TMEM37 [ SEEK ]   TMEM37 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM37 [ Firebrowse - Broad ]
GenevisibleExpression of TMEM37 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)140738
GTEX Portal (Tissue expression)TMEM37
Human Protein AtlasENSG00000171227-TMEM37 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8WXS4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8WXS4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8WXS4
PhosPhoSitePlusQ8WXS4
Domains : Interpro (EBI)Tmem37   
Domain families : Pfam (Sanger)TMEM37 (PF15108)   
Domain families : Pfam (NCBI)pfam15108   
Conserved Domain (NCBI)TMEM37
SuperfamilyQ8WXS4
AlphaFold pdb e-kbQ8WXS4   
Human Protein Atlas [tissue]ENSG00000171227-TMEM37 [tissue]
HPRD15536
Protein Interaction databases
DIP (DOE-UCLA)Q8WXS4
IntAct (EBI)Q8WXS4
BioGRIDTMEM37
STRING (EMBL)TMEM37
ZODIACTMEM37
Ontologies - Pathways
QuickGOQ8WXS4
Ontology : AmiGOvoltage-gated ion channel activity  calcium channel activity  integral component of membrane  regulation of ion transmembrane transport  calcium ion transmembrane transport  
Ontology : EGO-EBIvoltage-gated ion channel activity  calcium channel activity  integral component of membrane  regulation of ion transmembrane transport  calcium ion transmembrane transport  
NDEx NetworkTMEM37
Atlas of Cancer Signalling NetworkTMEM37
Wikipedia pathwaysTMEM37
Orthology - Evolution
OrthoDB140738
GeneTree (enSembl)ENSG00000171227
Phylogenetic Trees/Animal Genes : TreeFamTMEM37
Homologs : HomoloGeneTMEM37
Homology/Alignments : Family Browser (UCSC)TMEM37
Gene fusions - Rearrangements
Fusion : QuiverTMEM37
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM37 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM37
dbVarTMEM37
ClinVarTMEM37
MonarchTMEM37
1000_GenomesTMEM37 
Exome Variant ServerTMEM37
GNOMAD BrowserENSG00000171227
Varsome BrowserTMEM37
ACMGTMEM37 variants
VarityQ8WXS4
Genomic Variants (DGV)TMEM37 [DGVbeta]
DECIPHERTMEM37 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM37 
Mutations
ICGC Data PortalTMEM37 
TCGA Data PortalTMEM37 
Broad Tumor PortalTMEM37
OASIS PortalTMEM37 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM37  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTMEM37
Mutations and Diseases : HGMDTMEM37
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM37
DgiDB (Drug Gene Interaction Database)TMEM37
DoCM (Curated mutations)TMEM37
CIViC (Clinical Interpretations of Variants in Cancer)TMEM37
Cancer3DTMEM37
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM618831   
Orphanet
DisGeNETTMEM37
MedgenTMEM37
Genetic Testing Registry TMEM37
NextProtQ8WXS4 [Medical]
GENETestsTMEM37
Target ValidationTMEM37
Huge Navigator TMEM37 [HugePedia]
ClinGenTMEM37
Clinical trials, drugs, therapy
MyCancerGenomeTMEM37
Protein Interactions : CTDTMEM37
Pharm GKB GenePA134897608
PharosQ8WXS4
Clinical trialTMEM37
Miscellaneous
canSAR (ICR)TMEM37
HarmonizomeTMEM37
DataMed IndexTMEM37
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM37
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 16:26:14 CEST 2021

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