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ANGPTL5 (angiopoietin like 5)

Identity

Alias_namesangiopoietin-like 5
Other alias-
HGNC (Hugo) ANGPTL5
LocusID (NCBI) 253935
Atlas_Id 60295
Location 11q22.1  [Link to chromosome band 11q22]
Location_base_pair Starts at 101890674 and ends at 101916522 bp from pter ( according to hg38-Dec_2013)

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)ANGPTL5   19705
Cards
Entrez_Gene (NCBI)ANGPTL5  253935  angiopoietin like 5
Aliases
GeneCards (Weizmann)ANGPTL5
Ensembl hg19 (Hinxton)ENSG00000187151 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000187151 [Gene_View]  chr11:101890674-101916522 [Contig_View]  ANGPTL5 [Vega]
ICGC DataPortalENSG00000187151
TCGA cBioPortalANGPTL5
AceView (NCBI)ANGPTL5
Genatlas (Paris)ANGPTL5
WikiGenes253935
SOURCE (Princeton)ANGPTL5
Genetics Home Reference (NIH)ANGPTL5
Genomic and cartography
GoldenPath hg38 (UCSC)ANGPTL5  -     chr11:101890674-101916522 -  11q22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ANGPTL5  -     11q22.1   [Description]    (hg19-Feb_2009)
EnsemblANGPTL5 - 11q22.1 [CytoView hg19]  ANGPTL5 - 11q22.1 [CytoView hg38]
Mapping of homologs : NCBIANGPTL5 [Mapview hg19]  ANGPTL5 [Mapview hg38]
OMIM607666   
Gene and transcription
Genbank (Entrez)AK291523 AY169281 AY358827 BC049170 BC053957
RefSeq transcript (Entrez)NM_178127
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ANGPTL5
Cluster EST : UnigeneHs.318370 [ NCBI ]
CGAP (NCI)Hs.318370
Alternative Splicing GalleryENSG00000187151
Gene ExpressionANGPTL5 [ NCBI-GEO ]   ANGPTL5 [ EBI - ARRAY_EXPRESS ]   ANGPTL5 [ SEEK ]   ANGPTL5 [ MEM ]
Gene Expression Viewer (FireBrowse)ANGPTL5 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)253935
GTEX Portal (Tissue expression)ANGPTL5
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ86XS5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ86XS5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ86XS5
Splice isoforms : SwissVarQ86XS5
PhosPhoSitePlusQ86XS5
Domaine pattern : Prosite (Expaxy)FIBRINOGEN_C_1 (PS00514)    FIBRINOGEN_C_2 (PS51406)   
Domains : Interpro (EBI)Fibrinogen_a/b/g_C_1    Fibrinogen_a/b/g_C_2    Fibrinogen_a/b/g_C_dom    Fibrinogen_CS   
Domain families : Pfam (Sanger)Fibrinogen_C (PF00147)   
Domain families : Pfam (NCBI)pfam00147   
Domain families : Smart (EMBL)FBG (SM00186)  
Conserved Domain (NCBI)ANGPTL5
DMDM Disease mutations253935
Blocks (Seattle)ANGPTL5
SuperfamilyQ86XS5
Human Protein AtlasENSG00000187151
Peptide AtlasQ86XS5
HPRD09638
IPIIPI00328963   IPI00984776   
Protein Interaction databases
DIP (DOE-UCLA)Q86XS5
IntAct (EBI)Q86XS5
FunCoupENSG00000187151
BioGRIDANGPTL5
STRING (EMBL)ANGPTL5
ZODIACANGPTL5
Ontologies - Pathways
QuickGOQ86XS5
Ontology : AmiGOextracellular region  
Ontology : EGO-EBIextracellular region  
NDEx NetworkANGPTL5
Atlas of Cancer Signalling NetworkANGPTL5
Wikipedia pathwaysANGPTL5
Orthology - Evolution
OrthoDB253935
GeneTree (enSembl)ENSG00000187151
Phylogenetic Trees/Animal Genes : TreeFamANGPTL5
HOVERGENQ86XS5
HOGENOMQ86XS5
Homologs : HomoloGeneANGPTL5
Homology/Alignments : Family Browser (UCSC)ANGPTL5
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerANGPTL5 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ANGPTL5
dbVarANGPTL5
ClinVarANGPTL5
1000_GenomesANGPTL5 
Exome Variant ServerANGPTL5
ExAC (Exome Aggregation Consortium)ANGPTL5 (select the gene name)
Genetic variants : HAPMAP253935
Genomic Variants (DGV)ANGPTL5 [DGVbeta]
DECIPHERANGPTL5 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisANGPTL5 
Mutations
ICGC Data PortalANGPTL5 
TCGA Data PortalANGPTL5 
Broad Tumor PortalANGPTL5
OASIS PortalANGPTL5 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICANGPTL5  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDANGPTL5
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ANGPTL5
DgiDB (Drug Gene Interaction Database)ANGPTL5
DoCM (Curated mutations)ANGPTL5 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ANGPTL5 (select a term)
intoGenANGPTL5
Cancer3DANGPTL5(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM607666   
Orphanet
MedgenANGPTL5
Genetic Testing Registry ANGPTL5
NextProtQ86XS5 [Medical]
TSGene253935
GENETestsANGPTL5
Target ValidationANGPTL5
Huge Navigator ANGPTL5 [HugePedia]
snp3D : Map Gene to Disease253935
BioCentury BCIQANGPTL5
ClinGenANGPTL5
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD253935
Chemical/Pharm GKB GenePA134944139
Clinical trialANGPTL5
Miscellaneous
canSAR (ICR)ANGPTL5 (select the gene name)
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineANGPTL5
EVEXANGPTL5
GoPubMedANGPTL5
iHOPANGPTL5
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed Jun 7 15:38:04 CEST 2017
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