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INSL4 (insulin like 4)

Identity

Alias (NCBI)EPIL
PLACENTIN
HGNC (Hugo) INSL4
HGNC Alias symbEPIL
HGNC Previous nameinsulin-like 4 (placenta)
LocusID (NCBI) 3641
Atlas_Id 50032
Location 9p24.1  [Link to chromosome band 9p24]
Location_base_pair Starts at 5231419 and ends at 5235304 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)INSL4   6087
Cards
Entrez_Gene (NCBI)INSL4  3641  insulin like 4
AliasesEPIL; PLACENTIN
GeneCards (Weizmann)INSL4
Ensembl hg19 (Hinxton)ENSG00000120211 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000120211 [Gene_View]  ENSG00000120211 [Sequence]  chr9:5231419-5235304 [Contig_View]  INSL4 [Vega]
ICGC DataPortalENSG00000120211
TCGA cBioPortalINSL4
AceView (NCBI)INSL4
Genatlas (Paris)INSL4
WikiGenes3641
SOURCE (Princeton)INSL4
Genetics Home Reference (NIH)INSL4
Genomic and cartography
GoldenPath hg38 (UCSC)INSL4  -     chr9:5231419-5235304 +  9p24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)INSL4  -     9p24.1   [Description]    (hg19-Feb_2009)
GoldenPathINSL4 - 9p24.1 [CytoView hg19]  INSL4 - 9p24.1 [CytoView hg38]
ImmunoBaseENSG00000120211
genome Data Viewer NCBIINSL4 [Mapview hg19]  
OMIM600910   
Gene and transcription
Genbank (Entrez)AK291543 BC026254 L34838
RefSeq transcript (Entrez)NM_002195
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)INSL4
Alternative Splicing GalleryENSG00000120211
Gene ExpressionINSL4 [ NCBI-GEO ]   INSL4 [ EBI - ARRAY_EXPRESS ]   INSL4 [ SEEK ]   INSL4 [ MEM ]
Gene Expression Viewer (FireBrowse)INSL4 [ Firebrowse - Broad ]
GenevisibleExpression of INSL4 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)3641
GTEX Portal (Tissue expression)INSL4
Human Protein AtlasENSG00000120211-INSL4 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ14641   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ14641  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ14641
Splice isoforms : SwissVarQ14641
PhosPhoSitePlusQ14641
Domaine pattern : Prosite (Expaxy)INSULIN (PS00262)   
Domains : Interpro (EBI)Placentin    Relaxin   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)INSL4
DMDM Disease mutations3641
Blocks (Seattle)INSL4
SuperfamilyQ14641
Human Protein Atlas [tissue]ENSG00000120211-INSL4 [tissue]
Peptide AtlasQ14641
HPRD02946
IPIIPI00032261   
Protein Interaction databases
DIP (DOE-UCLA)Q14641
IntAct (EBI)Q14641
FunCoupENSG00000120211
BioGRIDINSL4
STRING (EMBL)INSL4
ZODIACINSL4
Ontologies - Pathways
QuickGOQ14641
Ontology : AmiGOsignaling receptor binding  insulin-like growth factor receptor binding  hormone activity  extracellular space  signal transduction  cell-cell signaling  positive regulation of chorionic trophoblast cell proliferation  
Ontology : EGO-EBIsignaling receptor binding  insulin-like growth factor receptor binding  hormone activity  extracellular space  signal transduction  cell-cell signaling  positive regulation of chorionic trophoblast cell proliferation  
NDEx NetworkINSL4
Atlas of Cancer Signalling NetworkINSL4
Wikipedia pathwaysINSL4
Orthology - Evolution
OrthoDB3641
GeneTree (enSembl)ENSG00000120211
Phylogenetic Trees/Animal Genes : TreeFamINSL4
HOGENOMQ14641
Homologs : HomoloGeneINSL4
Homology/Alignments : Family Browser (UCSC)INSL4
Gene fusions - Rearrangements
Fusion : QuiverINSL4
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerINSL4 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)INSL4
dbVarINSL4
ClinVarINSL4
MonarchINSL4
1000_GenomesINSL4 
Exome Variant ServerINSL4
GNOMAD BrowserENSG00000120211
Varsome BrowserINSL4
Genetic variants : HAPMAP3641
Genomic Variants (DGV)INSL4 [DGVbeta]
DECIPHERINSL4 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisINSL4 
Mutations
ICGC Data PortalINSL4 
TCGA Data PortalINSL4 
Broad Tumor PortalINSL4
OASIS PortalINSL4 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICINSL4  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DINSL4
Mutations and Diseases : HGMDINSL4
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch INSL4
DgiDB (Drug Gene Interaction Database)INSL4
DoCM (Curated mutations)INSL4 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)INSL4 (select a term)
intoGenINSL4
Cancer3DINSL4(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM600910   
Orphanet
DisGeNETINSL4
MedgenINSL4
Genetic Testing Registry INSL4
NextProtQ14641 [Medical]
TSGene3641
GENETestsINSL4
Target ValidationINSL4
Huge Navigator INSL4 [HugePedia]
snp3D : Map Gene to Disease3641
BioCentury BCIQINSL4
ClinGenINSL4
Clinical trials, drugs, therapy
Protein Interactions : CTD3641
Pharm GKB GenePA29894
Clinical trialINSL4
Miscellaneous
canSAR (ICR)INSL4 (select the gene name)
HarmonizomeINSL4
DataMed IndexINSL4
Probes
Litterature
PubMed15 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineINSL4
EVEXINSL4
GoPubMedINSL4
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 14 14:15:58 CEST 2020
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