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TMEM212 (transmembrane protein 212)

Identity

Alias (NCBI)-
HGNC (Hugo) TMEM212
HGNC Alias symbFLJ23172
LocusID (NCBI) 389177
Atlas_Id 74877
Location 3q26.31  [Link to chromosome band 3q26]
Location_base_pair Starts at 171843349 and ends at 171859318 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)TMEM212   34295
Cards
Entrez_Gene (NCBI)TMEM212    transmembrane protein 212
Aliases
GeneCards (Weizmann)TMEM212
Ensembl hg19 (Hinxton)ENSG00000186329 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000186329 [Gene_View]  ENSG00000186329 [Sequence]  chr3:171843349-171859318 [Contig_View]  TMEM212 [Vega]
ICGC DataPortalENSG00000186329
TCGA cBioPortalTMEM212
AceView (NCBI)TMEM212
Genatlas (Paris)TMEM212
SOURCE (Princeton)TMEM212
Genetics Home Reference (NIH)TMEM212
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM212  -     chr3:171843349-171859318 +  3q26.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM212  -     3q26.31   [Description]    (hg19-Feb_2009)
GoldenPathTMEM212 - 3q26.31 [CytoView hg19]  TMEM212 - 3q26.31 [CytoView hg38]
ImmunoBaseENSG00000186329
Genome Data Viewer NCBITMEM212 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK026825 DB199311
RefSeq transcript (Entrez)NM_001164436
Consensus coding sequences : CCDS (NCBI)TMEM212
Gene ExpressionTMEM212 [ NCBI-GEO ]   TMEM212 [ EBI - ARRAY_EXPRESS ]   TMEM212 [ SEEK ]   TMEM212 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM212 [ Firebrowse - Broad ]
GenevisibleExpression of TMEM212 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)389177
GTEX Portal (Tissue expression)TMEM212
Human Protein AtlasENSG00000186329-TMEM212 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtA6NML5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA6NML5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA6NML5
PhosPhoSitePlusA6NML5
Domains : Interpro (EBI)MS4A   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)TMEM212
SuperfamilyA6NML5
AlphaFold pdb e-kbA6NML5   
Human Protein Atlas [tissue]ENSG00000186329-TMEM212 [tissue]
Protein Interaction databases
DIP (DOE-UCLA)A6NML5
IntAct (EBI)A6NML5
BioGRIDTMEM212
STRING (EMBL)TMEM212
ZODIACTMEM212
Ontologies - Pathways
QuickGOA6NML5
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkTMEM212
Atlas of Cancer Signalling NetworkTMEM212
Wikipedia pathwaysTMEM212
Orthology - Evolution
OrthoDB389177
GeneTree (enSembl)ENSG00000186329
Phylogenetic Trees/Animal Genes : TreeFamTMEM212
Homologs : HomoloGeneTMEM212
Homology/Alignments : Family Browser (UCSC)TMEM212
Gene fusions - Rearrangements
Fusion : QuiverTMEM212
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM212 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM212
dbVarTMEM212
ClinVarTMEM212
MonarchTMEM212
1000_GenomesTMEM212 
Exome Variant ServerTMEM212
GNOMAD BrowserENSG00000186329
Varsome BrowserTMEM212
ACMGTMEM212 variants
VarityA6NML5
Genomic Variants (DGV)TMEM212 [DGVbeta]
DECIPHERTMEM212 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM212 
Mutations
ICGC Data PortalTMEM212 
TCGA Data PortalTMEM212 
Broad Tumor PortalTMEM212
OASIS PortalTMEM212 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM212  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTMEM212
Mutations and Diseases : HGMDTMEM212
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM212
DgiDB (Drug Gene Interaction Database)TMEM212
DoCM (Curated mutations)TMEM212
CIViC (Clinical Interpretations of Variants in Cancer)TMEM212
Cancer3DTMEM212
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTMEM212
MedgenTMEM212
Genetic Testing Registry TMEM212
NextProtA6NML5 [Medical]
GENETestsTMEM212
Target ValidationTMEM212
Huge Navigator TMEM212 [HugePedia]
ClinGenTMEM212
Clinical trials, drugs, therapy
MyCancerGenomeTMEM212
Protein Interactions : CTDTMEM212
Pharm GKB GenePA162406475
PharosA6NML5
Clinical trialTMEM212
Miscellaneous
canSAR (ICR)TMEM212
HarmonizomeTMEM212
DataMed IndexTMEM212
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM212
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 16:26:00 CEST 2021

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