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TRIM49C (tripartite motif containing 49C)

Identity

Alias (NCBI)TRIM49L2
HGNC (Hugo) TRIM49C
HGNC Previous nameTRIM49L2
HGNC Previous nametripartite motif containing 49-like 2
LocusID (NCBI) 642612
Atlas_Id 75163
Location 11q14.3  [Link to chromosome band 11q14]
Location_base_pair Starts at 90031106 and ends at 90042025 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)
DPF2 (11q13.1) / TRIM49C (11q14.3)

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)TRIM49C   38877
Cards
Entrez_Gene (NCBI)TRIM49C    tripartite motif containing 49C
AliasesTRIM49L2
GeneCards (Weizmann)TRIM49C
Ensembl hg19 (Hinxton)ENSG00000204449 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000204449 [Gene_View]  ENSG00000204449 [Sequence]  chr11:90031106-90042025 [Contig_View]  TRIM49C [Vega]
ICGC DataPortalENSG00000204449
TCGA cBioPortalTRIM49C
AceView (NCBI)TRIM49C
Genatlas (Paris)TRIM49C
SOURCE (Princeton)TRIM49C
Genetics Home Reference (NIH)TRIM49C
Genomic and cartography
GoldenPath hg38 (UCSC)TRIM49C  -     chr11:90031106-90042025 +  11q14.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TRIM49C  -     11q14.3   [Description]    (hg19-Feb_2009)
GoldenPathTRIM49C - 11q14.3 [CytoView hg19]  TRIM49C - 11q14.3 [CytoView hg38]
ImmunoBaseENSG00000204449
Genome Data Viewer NCBITRIM49C [Mapview hg19]  
Gene and transcription
Genbank (Entrez)BC126470 JF968462
RefSeq transcript (Entrez)NM_001195234
Consensus coding sequences : CCDS (NCBI)TRIM49C
Gene ExpressionTRIM49C [ NCBI-GEO ]   TRIM49C [ EBI - ARRAY_EXPRESS ]   TRIM49C [ SEEK ]   TRIM49C [ MEM ]
Gene Expression Viewer (FireBrowse)TRIM49C [ Firebrowse - Broad ]
GenevisibleExpression of TRIM49C in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)642612
GTEX Portal (Tissue expression)TRIM49C
Human Protein AtlasENSG00000204449-TRIM49C [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtP0CI26   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP0CI26  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP0CI26
PhosPhoSitePlusP0CI26
Domaine pattern : Prosite (Expaxy)B302_SPRY (PS50188)    ZF_BBOX (PS50119)    ZF_RING_2 (PS50089)   
Domains : Interpro (EBI)B30.2/SPRY    B30.2/SPRY_sf    Butyrophylin_SPRY    ConA-like_dom_sf    SPRY_dom    Znf_B-box    Znf_RING    Znf_RING/FYVE/PHD   
Domain families : Pfam (Sanger)SPRY (PF00622)    zf-B_box (PF00643)   
Domain families : Pfam (NCBI)pfam00622    pfam00643   
Domain families : Smart (EMBL)BBOX (SM00336)  RING (SM00184)  SPRY (SM00449)  
Conserved Domain (NCBI)TRIM49C
SuperfamilyP0CI26
AlphaFold pdb e-kbP0CI26   
Human Protein Atlas [tissue]ENSG00000204449-TRIM49C [tissue]
Protein Interaction databases
DIP (DOE-UCLA)P0CI26
IntAct (EBI)P0CI26
BioGRIDTRIM49C
STRING (EMBL)TRIM49C
ZODIACTRIM49C
Ontologies - Pathways
QuickGOP0CI26
Ontology : AmiGOprotein binding  cytoplasm  zinc ion binding  regulation of gene expression  protein ubiquitination  innate immune response  ubiquitin protein ligase activity  
Ontology : EGO-EBIprotein binding  cytoplasm  zinc ion binding  regulation of gene expression  protein ubiquitination  innate immune response  ubiquitin protein ligase activity  
NDEx NetworkTRIM49C
Atlas of Cancer Signalling NetworkTRIM49C
Wikipedia pathwaysTRIM49C
Orthology - Evolution
OrthoDB642612
GeneTree (enSembl)ENSG00000204449
Phylogenetic Trees/Animal Genes : TreeFamTRIM49C
Homologs : HomoloGeneTRIM49C
Homology/Alignments : Family Browser (UCSC)TRIM49C
Gene fusions - Rearrangements
Fusion : QuiverTRIM49C
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTRIM49C [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TRIM49C
dbVarTRIM49C
ClinVarTRIM49C
MonarchTRIM49C
1000_GenomesTRIM49C 
Exome Variant ServerTRIM49C
GNOMAD BrowserENSG00000204449
Varsome BrowserTRIM49C
ACMGTRIM49C variants
VarityP0CI26
Genomic Variants (DGV)TRIM49C [DGVbeta]
DECIPHERTRIM49C [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTRIM49C 
Mutations
ICGC Data PortalTRIM49C 
TCGA Data PortalTRIM49C 
Broad Tumor PortalTRIM49C
OASIS PortalTRIM49C [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTRIM49C  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTRIM49C
Mutations and Diseases : HGMDTRIM49C
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTRIM49C
DgiDB (Drug Gene Interaction Database)TRIM49C
DoCM (Curated mutations)TRIM49C
CIViC (Clinical Interpretations of Variants in Cancer)TRIM49C
Cancer3DTRIM49C
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTRIM49C
MedgenTRIM49C
Genetic Testing Registry TRIM49C
NextProtP0CI26 [Medical]
GENETestsTRIM49C
Target ValidationTRIM49C
Huge Navigator TRIM49C [HugePedia]
ClinGenTRIM49C
Clinical trials, drugs, therapy
MyCancerGenomeTRIM49C
Protein Interactions : CTDTRIM49C
Pharm GKB GenePA166049036
PharosP0CI26
Clinical trialTRIM49C
Miscellaneous
canSAR (ICR)TRIM49C
HarmonizomeTRIM49C
DataMed IndexTRIM49C
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTRIM49C
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 16:26:55 CEST 2021
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