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C19orf70 (chromosome 19 open reading frame 70)

Identity

Alias_symbol (synonym)QIL1
P117
MIC13
Other alias
HGNC (Hugo) C19orf70
LocusID (NCBI) 125988
Atlas_Id 61037
Location 19p13.3  [Link to chromosome band 19p13]
Location_base_pair Starts at 5678414 and ends at 5680896 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
C19orf70 (19p13.3) / MLLT6 (17q12)C19orf70 (19p13.3) / TRAF3IP3 (1q32.2)TRAF3IP3 (1q32.2) / C19orf70 (19p13.3)

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)C19orf70   33702
Cards
Entrez_Gene (NCBI)C19orf70  125988  chromosome 19 open reading frame 70
AliasesMIC13; P117; QIL1
GeneCards (Weizmann)C19orf70
Ensembl hg19 (Hinxton)ENSG00000174917 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000174917 [Gene_View]  chr19:5678414-5680896 [Contig_View]  C19orf70 [Vega]
ICGC DataPortalENSG00000174917
TCGA cBioPortalC19orf70
AceView (NCBI)C19orf70
Genatlas (Paris)C19orf70
WikiGenes125988
SOURCE (Princeton)C19orf70
Genetics Home Reference (NIH)C19orf70
Genomic and cartography
GoldenPath hg38 (UCSC)C19orf70  -     chr19:5678414-5680896 -  19p13.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)C19orf70  -     19p13.3   [Description]    (hg19-Feb_2009)
EnsemblC19orf70 - 19p13.3 [CytoView hg19]  C19orf70 - 19p13.3 [CytoView hg38]
Mapping of homologs : NCBIC19orf70 [Mapview hg19]  C19orf70 [Mapview hg38]
OMIM616658   
Gene and transcription
Genbank (Entrez)AA292888 AI004554 AI300708 AJ707830 AK091768
RefSeq transcript (Entrez)NM_001308240 NM_205767
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)C19orf70
Cluster EST : UnigeneHs.356626 [ NCBI ]
CGAP (NCI)Hs.356626
Alternative Splicing GalleryENSG00000174917
Gene ExpressionC19orf70 [ NCBI-GEO ]   C19orf70 [ EBI - ARRAY_EXPRESS ]   C19orf70 [ SEEK ]   C19orf70 [ MEM ]
Gene Expression Viewer (FireBrowse)C19orf70 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)125988
GTEX Portal (Tissue expression)C19orf70
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5XKP0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5XKP0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5XKP0
Splice isoforms : SwissVarQ5XKP0
PhosPhoSitePlusQ5XKP0
Domains : Interpro (EBI)Mic13   
Domain families : Pfam (Sanger)QIL1 (PF15884)   
Domain families : Pfam (NCBI)pfam15884   
Conserved Domain (NCBI)C19orf70
DMDM Disease mutations125988
Blocks (Seattle)C19orf70
SuperfamilyQ5XKP0
Human Protein AtlasENSG00000174917
Peptide AtlasQ5XKP0
HPRD15198
IPIIPI00329373   
Protein Interaction databases
DIP (DOE-UCLA)Q5XKP0
IntAct (EBI)Q5XKP0
FunCoupENSG00000174917
BioGRIDC19orf70
STRING (EMBL)C19orf70
ZODIACC19orf70
Ontologies - Pathways
QuickGOQ5XKP0
Ontology : AmiGOnucleoplasm  mitochondrion  mitochondrial inner membrane  cristae formation  mitochondrial crista junction  MICOS complex  
Ontology : EGO-EBInucleoplasm  mitochondrion  mitochondrial inner membrane  cristae formation  mitochondrial crista junction  MICOS complex  
NDEx NetworkC19orf70
Atlas of Cancer Signalling NetworkC19orf70
Wikipedia pathwaysC19orf70
Orthology - Evolution
OrthoDB125988
GeneTree (enSembl)ENSG00000174917
Phylogenetic Trees/Animal Genes : TreeFamC19orf70
HOVERGENQ5XKP0
HOGENOMQ5XKP0
Homologs : HomoloGeneC19orf70
Homology/Alignments : Family Browser (UCSC)C19orf70
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerC19orf70 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C19orf70
dbVarC19orf70
ClinVarC19orf70
1000_GenomesC19orf70 
Exome Variant ServerC19orf70
ExAC (Exome Aggregation Consortium)C19orf70 (select the gene name)
Genetic variants : HAPMAP125988
Genomic Variants (DGV)C19orf70 [DGVbeta]
DECIPHERC19orf70 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisC19orf70 
Mutations
ICGC Data PortalC19orf70 
TCGA Data PortalC19orf70 
Broad Tumor PortalC19orf70
OASIS PortalC19orf70 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICC19orf70  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDC19orf70
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch C19orf70
DgiDB (Drug Gene Interaction Database)C19orf70
DoCM (Curated mutations)C19orf70 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)C19orf70 (select a term)
intoGenC19orf70
Cancer3DC19orf70(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM616658   
Orphanet
MedgenC19orf70
Genetic Testing Registry C19orf70
NextProtQ5XKP0 [Medical]
TSGene125988
GENETestsC19orf70
Huge Navigator C19orf70 [HugePedia]
snp3D : Map Gene to Disease125988
BioCentury BCIQC19orf70
ClinGenC19orf70
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD125988
Chemical/Pharm GKB GenePA162378863
Clinical trialC19orf70
Miscellaneous
canSAR (ICR)C19orf70 (select the gene name)
Probes
Litterature
PubMed10 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineC19orf70
EVEXC19orf70
GoPubMedC19orf70
iHOPC19orf70
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Fri May 19 11:02:56 CEST 2017

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