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LINC02912 (long intergenic non-protein coding RNA 2912)

Identity

Alias (NCBI)TMEM75
HGNC (Hugo) LINC02912
HGNC Alias symbFLJ36105
HGNC Previous nameTMEM75
HGNC Previous nametransmembrane protein 75
LocusID (NCBI) 641384
Atlas_Id 57697
Location 8q24.21  [Link to chromosome band 8q24]
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



External links

 

Nomenclature
HGNC (Hugo)LINC02912   32295
Cards
Entrez_Gene (NCBI)LINC02912    long intergenic non-protein coding RNA 2912
AliasesTMEM75
GeneCards (Weizmann)LINC02912
Ensembl hg19 (Hinxton)ENSG00000280055 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000280055 [Gene_View]  ENSG00000280055 [Sequence]  - [Contig_View]  LINC02912 [Vega]
ICGC DataPortalENSG00000280055
TCGA cBioPortalLINC02912
AceView (NCBI)LINC02912
Genatlas (Paris)LINC02912
SOURCE (Princeton)LINC02912
Genetics Home Reference (NIH)LINC02912
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02912  -  
GoldenPath hg19 (UCSC)LINC02912  -  
GoldenPathLINC02912 - [CytoView hg19]  LINC02912 - [CytoView hg38]
ImmunoBaseENSG00000280055
Genome Data Viewer NCBILINC02912 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK093424 AX748117 BC137383 BC137385
RefSeq transcript (Entrez)NM_001037234
Consensus coding sequences : CCDS (NCBI)LINC02912
Gene ExpressionLINC02912 [ NCBI-GEO ]   LINC02912 [ EBI - ARRAY_EXPRESS ]   LINC02912 [ SEEK ]   LINC02912 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02912 [ Firebrowse - Broad ]
GenevisibleExpression of LINC02912 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)641384
GTEX Portal (Tissue expression)LINC02912
Human Protein AtlasENSG00000280055-LINC02912 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N9X5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N9X5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N9X5
PhosPhoSitePlusQ8N9X5
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02912
SuperfamilyQ8N9X5
AlphaFold pdb e-kbQ8N9X5   
Human Protein Atlas [tissue]ENSG00000280055-LINC02912 [tissue]
Protein Interaction databases
DIP (DOE-UCLA)Q8N9X5
IntAct (EBI)Q8N9X5
BioGRIDLINC02912
STRING (EMBL)LINC02912
ZODIACLINC02912
Ontologies - Pathways
QuickGOQ8N9X5
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkLINC02912
Atlas of Cancer Signalling NetworkLINC02912
Wikipedia pathwaysLINC02912
Orthology - Evolution
OrthoDB641384
GeneTree (enSembl)ENSG00000280055
Phylogenetic Trees/Animal Genes : TreeFamLINC02912
Homologs : HomoloGeneLINC02912
Homology/Alignments : Family Browser (UCSC)LINC02912
Gene fusions - Rearrangements
Fusion : QuiverLINC02912
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerLINC02912 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)LINC02912
dbVarLINC02912
ClinVarLINC02912
MonarchLINC02912
1000_GenomesLINC02912 
Exome Variant ServerLINC02912
GNOMAD BrowserENSG00000280055
Varsome BrowserLINC02912
ACMGLINC02912 variants
VarityQ8N9X5
Genomic Variants (DGV)LINC02912 [DGVbeta]
DECIPHERLINC02912 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisLINC02912 
Mutations
ICGC Data PortalLINC02912 
TCGA Data PortalLINC02912 
Broad Tumor PortalLINC02912
OASIS PortalLINC02912 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDLINC02912
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaLINC02912
DgiDB (Drug Gene Interaction Database)LINC02912
DoCM (Curated mutations)LINC02912
CIViC (Clinical Interpretations of Variants in Cancer)LINC02912
Cancer3DLINC02912
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETLINC02912
MedgenLINC02912
Genetic Testing Registry LINC02912
NextProtQ8N9X5 [Medical]
GENETestsLINC02912
Target ValidationLINC02912
Huge Navigator LINC02912 [HugePedia]
ClinGenLINC02912
Clinical trials, drugs, therapy
MyCancerGenomeLINC02912
Protein Interactions : CTDLINC02912
Pharm GKB GenePA142670786
PharosQ8N9X5
Clinical trialLINC02912
Miscellaneous
canSAR (ICR)LINC02912
HarmonizomeLINC02912
DataMed IndexLINC02912
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXLINC02912
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 15:16:22 CEST 2021

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