Atlas of Genetics and Cytogenetics in Oncology and Haematology

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   
X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

C1QL3 (complement C1q like 3)

Identity

Alias (NCBI)C1QTNF13
C1ql
CTRP13
K100
HGNC (Hugo) C1QL3
HGNC Alias symbK100
C1ql
C1QTNF13
CTRP13
HGNC Previous namecomplement component 1, q subcomponent-like 3
LocusID (NCBI) 389941
Atlas_Id 61099
Location 10p13  [Link to chromosome band 10p13]
Location_base_pair Starts at 16513735 and ends at 16521879 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)C1QL3   19359
Cards
Entrez_Gene (NCBI)C1QL3    complement C1q like 3
AliasesC1QTNF13; C1ql; CTRP13; K100
GeneCards (Weizmann)C1QL3
Ensembl hg19 (Hinxton)ENSG00000165985 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000165985 [Gene_View]  ENSG00000165985 [Sequence]  chr10:16513735-16521879 [Contig_View]  C1QL3 [Vega]
ICGC DataPortalENSG00000165985
TCGA cBioPortalC1QL3
AceView (NCBI)C1QL3
Genatlas (Paris)C1QL3
SOURCE (Princeton)C1QL3
Genetics Home Reference (NIH)C1QL3
Genomic and cartography
GoldenPath hg38 (UCSC)C1QL3  -     chr10:16513735-16521879 -  10p13   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)C1QL3  -     10p13   [Description]    (hg19-Feb_2009)
GoldenPathC1QL3 - 10p13 [CytoView hg19]  C1QL3 - 10p13 [CytoView hg38]
ImmunoBaseENSG00000165985
Genome Data Viewer NCBIC1QL3 [Mapview hg19]  
OMIM615227   
Gene and transcription
Genbank (Entrez)AK094686 BC127716 BC127717
RefSeq transcript (Entrez)NM_001010908
Consensus coding sequences : CCDS (NCBI)C1QL3
Gene ExpressionC1QL3 [ NCBI-GEO ]   C1QL3 [ EBI - ARRAY_EXPRESS ]   C1QL3 [ SEEK ]   C1QL3 [ MEM ]
Gene Expression Viewer (FireBrowse)C1QL3 [ Firebrowse - Broad ]
GenevisibleExpression of C1QL3 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)389941
GTEX Portal (Tissue expression)C1QL3
Human Protein AtlasENSG00000165985-C1QL3 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5VWW1   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5VWW1  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5VWW1
PhosPhoSitePlusQ5VWW1
Domaine pattern : Prosite (Expaxy)C1Q (PS50871)   
Domains : Interpro (EBI)C1q_dom    Collagen    Tumour_necrosis_fac-like_dom   
Domain families : Pfam (Sanger)C1q (PF00386)    Collagen (PF01391)   
Domain families : Pfam (NCBI)pfam00386    pfam01391   
Domain families : Smart (EMBL)C1Q (SM00110)  
Conserved Domain (NCBI)C1QL3
SuperfamilyQ5VWW1
AlphaFold pdb e-kbQ5VWW1   
Human Protein Atlas [tissue]ENSG00000165985-C1QL3 [tissue]
HPRD16632
Protein Interaction databases
DIP (DOE-UCLA)Q5VWW1
IntAct (EBI)Q5VWW1
BioGRIDC1QL3
STRING (EMBL)C1QL3
ZODIACC1QL3
Ontologies - Pathways
QuickGOQ5VWW1
Ontology : AmiGOextracellular region  collagen trimer  identical protein binding  regulation of synapse organization  
Ontology : EGO-EBIextracellular region  collagen trimer  identical protein binding  regulation of synapse organization  
NDEx NetworkC1QL3
Atlas of Cancer Signalling NetworkC1QL3
Wikipedia pathwaysC1QL3
Orthology - Evolution
OrthoDB389941
GeneTree (enSembl)ENSG00000165985
Phylogenetic Trees/Animal Genes : TreeFamC1QL3
Homologs : HomoloGeneC1QL3
Homology/Alignments : Family Browser (UCSC)C1QL3
Gene fusions - Rearrangements
Fusion : QuiverC1QL3
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerC1QL3 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C1QL3
dbVarC1QL3
ClinVarC1QL3
MonarchC1QL3
1000_GenomesC1QL3 
Exome Variant ServerC1QL3
GNOMAD BrowserENSG00000165985
Varsome BrowserC1QL3
ACMGC1QL3 variants
VarityQ5VWW1
Genomic Variants (DGV)C1QL3 [DGVbeta]
DECIPHERC1QL3 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisC1QL3 
Mutations
ICGC Data PortalC1QL3 
TCGA Data PortalC1QL3 
Broad Tumor PortalC1QL3
OASIS PortalC1QL3 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICC1QL3  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DC1QL3
Mutations and Diseases : HGMDC1QL3
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaC1QL3
DgiDB (Drug Gene Interaction Database)C1QL3
DoCM (Curated mutations)C1QL3
CIViC (Clinical Interpretations of Variants in Cancer)C1QL3
Cancer3DC1QL3
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM615227   
Orphanet
DisGeNETC1QL3
MedgenC1QL3
Genetic Testing Registry C1QL3
NextProtQ5VWW1 [Medical]
GENETestsC1QL3
Target ValidationC1QL3
Huge Navigator C1QL3 [HugePedia]
ClinGenC1QL3
Clinical trials, drugs, therapy
MyCancerGenomeC1QL3
Protein Interactions : CTDC1QL3
Pharm GKB GenePA134891919
PharosQ5VWW1
Clinical trialC1QL3
Miscellaneous
canSAR (ICR)C1QL3
HarmonizomeC1QL3
DataMed IndexC1QL3
Probes
Litterature
PubMed12 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXC1QL3
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 15:44:07 CEST 2021
Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.