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PI15 (peptidase inhibitor 15)

Identity

Alias_namesprotease inhibitor 15
Alias_symbol (synonym)P25TI
Other aliasCRISP8
P24TI
HGNC (Hugo) PI15
LocusID (NCBI) 51050
Atlas_Id 71901
Location 8q21.13  [Link to chromosome band 8q21]
Location_base_pair Starts at 74824537 and ends at 74855044 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)PI15   8946
Cards
Entrez_Gene (NCBI)PI15  51050  peptidase inhibitor 15
AliasesCRISP8; P24TI; P25TI
GeneCards (Weizmann)PI15
Ensembl hg19 (Hinxton)ENSG00000137558 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000137558 [Gene_View]  chr8:74824537-74855044 [Contig_View]  PI15 [Vega]
ICGC DataPortalENSG00000137558
TCGA cBioPortalPI15
AceView (NCBI)PI15
Genatlas (Paris)PI15
WikiGenes51050
SOURCE (Princeton)PI15
Genetics Home Reference (NIH)PI15
Genomic and cartography
GoldenPath hg38 (UCSC)PI15  -     chr8:74824537-74855044 +  8q21.13   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)PI15  -     8q21.13   [Description]    (hg19-Feb_2009)
EnsemblPI15 - 8q21.13 [CytoView hg19]  PI15 - 8q21.13 [CytoView hg38]
Mapping of homologs : NCBIPI15 [Mapview hg19]  PI15 [Mapview hg38]
OMIM607076   
Gene and transcription
Genbank (Entrez)AK130318 AK130386 BC074931 BC074932 BC126290
RefSeq transcript (Entrez)NM_001324403 NM_015886
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)PI15
Cluster EST : UnigeneHs.98558 [ NCBI ]
CGAP (NCI)Hs.98558
Alternative Splicing GalleryENSG00000137558
Gene ExpressionPI15 [ NCBI-GEO ]   PI15 [ EBI - ARRAY_EXPRESS ]   PI15 [ SEEK ]   PI15 [ MEM ]
Gene Expression Viewer (FireBrowse)PI15 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)51050
GTEX Portal (Tissue expression)PI15
Protein : pattern, domain, 3D structure
UniProt/SwissProtO43692   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO43692  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO43692
Splice isoforms : SwissVarO43692
PhosPhoSitePlusO43692
Domaine pattern : Prosite (Expaxy)CRISP_2 (PS01010)   
Domains : Interpro (EBI)Allrgn_V5/Tpx1    Allrgn_V5/Tpx1_CS    CAP_domain   
Domain families : Pfam (Sanger)CAP (PF00188)   
Domain families : Pfam (NCBI)pfam00188   
Domain families : Smart (EMBL)SCP (SM00198)  
Conserved Domain (NCBI)PI15
DMDM Disease mutations51050
Blocks (Seattle)PI15
SuperfamilyO43692
Human Protein AtlasENSG00000137558
Peptide AtlasO43692
HPRD06150
IPIIPI00026303   
Protein Interaction databases
DIP (DOE-UCLA)O43692
IntAct (EBI)O43692
FunCoupENSG00000137558
BioGRIDPI15
STRING (EMBL)PI15
ZODIACPI15
Ontologies - Pathways
QuickGOO43692
Ontology : AmiGOmulticellular organism development  biological_process  negative regulation of peptidase activity  peptidase inhibitor activity  extracellular exosome  
Ontology : EGO-EBImulticellular organism development  biological_process  negative regulation of peptidase activity  peptidase inhibitor activity  extracellular exosome  
NDEx NetworkPI15
Atlas of Cancer Signalling NetworkPI15
Wikipedia pathwaysPI15
Orthology - Evolution
OrthoDB51050
GeneTree (enSembl)ENSG00000137558
Phylogenetic Trees/Animal Genes : TreeFamPI15
HOVERGENO43692
HOGENOMO43692
Homologs : HomoloGenePI15
Homology/Alignments : Family Browser (UCSC)PI15
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerPI15 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)PI15
dbVarPI15
ClinVarPI15
1000_GenomesPI15 
Exome Variant ServerPI15
ExAC (Exome Aggregation Consortium)PI15 (select the gene name)
Genetic variants : HAPMAP51050
Genomic Variants (DGV)PI15 [DGVbeta]
DECIPHERPI15 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisPI15 
Mutations
ICGC Data PortalPI15 
TCGA Data PortalPI15 
Broad Tumor PortalPI15
OASIS PortalPI15 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICPI15  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDPI15
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 PI15
DgiDB (Drug Gene Interaction Database)PI15
DoCM (Curated mutations)PI15 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)PI15 (select a term)
intoGenPI15
Cancer3DPI15(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM607076   
Orphanet
MedgenPI15
Genetic Testing Registry PI15
NextProtO43692 [Medical]
TSGene51050
GENETestsPI15
Target ValidationPI15
Huge Navigator PI15 [HugePedia]
snp3D : Map Gene to Disease51050
BioCentury BCIQPI15
ClinGenPI15
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD51050
Chemical/Pharm GKB GenePA33282
Clinical trialPI15
Miscellaneous
canSAR (ICR)PI15 (select the gene name)
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMinePI15
EVEXPI15
GoPubMedPI15
iHOPPI15
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:34:31 CEST 2017

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