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INSL5 (insulin like 5)

Identity

Alias_namesinsulin-like 5
Other aliasPRO182
UNQ156
HGNC (Hugo) INSL5
LocusID (NCBI) 10022
Atlas_Id 53569
Location 1p31.3  [Link to chromosome band 1p31]
Location_base_pair Starts at 66797741 and ends at 66801259 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)INSL5   6088
Cards
Entrez_Gene (NCBI)INSL5  10022  insulin like 5
AliasesPRO182; UNQ156
GeneCards (Weizmann)INSL5
Ensembl hg19 (Hinxton)ENSG00000172410 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000172410 [Gene_View]  chr1:66797741-66801259 [Contig_View]  INSL5 [Vega]
ICGC DataPortalENSG00000172410
TCGA cBioPortalINSL5
AceView (NCBI)INSL5
Genatlas (Paris)INSL5
WikiGenes10022
SOURCE (Princeton)INSL5
Genetics Home Reference (NIH)INSL5
Genomic and cartography
GoldenPath hg38 (UCSC)INSL5  -     chr1:66797741-66801259 -  1p31.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)INSL5  -     1p31.3   [Description]    (hg19-Feb_2009)
EnsemblINSL5 - 1p31.3 [CytoView hg19]  INSL5 - 1p31.3 [CytoView hg38]
Mapping of homologs : NCBIINSL5 [Mapview hg19]  INSL5 [Mapview hg38]
OMIM606413   
Gene and transcription
Genbank (Entrez)AF133816 AY359030 BC101646 BC101648
RefSeq transcript (Entrez)NM_005478
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)INSL5
Cluster EST : UnigeneHs.251380 [ NCBI ]
CGAP (NCI)Hs.251380
Alternative Splicing GalleryENSG00000172410
Gene ExpressionINSL5 [ NCBI-GEO ]   INSL5 [ EBI - ARRAY_EXPRESS ]   INSL5 [ SEEK ]   INSL5 [ MEM ]
Gene Expression Viewer (FireBrowse)INSL5 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)10022
GTEX Portal (Tissue expression)INSL5
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9Y5Q6   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9Y5Q6  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9Y5Q6
Splice isoforms : SwissVarQ9Y5Q6
PhosPhoSitePlusQ9Y5Q6
Domaine pattern : Prosite (Expaxy)INSULIN (PS00262)   
Domains : Interpro (EBI)Insulin-like    Insulin_CS   
Domain families : Pfam (Sanger)Insulin (PF00049)   
Domain families : Pfam (NCBI)pfam00049   
Domain families : Smart (EMBL)IlGF (SM00078)  
Conserved Domain (NCBI)INSL5
DMDM Disease mutations10022
Blocks (Seattle)INSL5
PDB (SRS)2K1V    2KBC   
PDB (PDBSum)2K1V    2KBC   
PDB (IMB)2K1V    2KBC   
PDB (RSDB)2K1V    2KBC   
Structural Biology KnowledgeBase2K1V    2KBC   
SCOP (Structural Classification of Proteins)2K1V    2KBC   
CATH (Classification of proteins structures)2K1V    2KBC   
SuperfamilyQ9Y5Q6
Human Protein AtlasENSG00000172410
Peptide AtlasQ9Y5Q6
HPRD08400
IPIIPI00001717   
Protein Interaction databases
DIP (DOE-UCLA)Q9Y5Q6
IntAct (EBI)Q9Y5Q6
FunCoupENSG00000172410
BioGRIDINSL5
STRING (EMBL)INSL5
ZODIACINSL5
Ontologies - Pathways
QuickGOQ9Y5Q6
Ontology : AmiGOG-protein coupled receptor binding  hormone activity  cellular_component  extracellular region  extracellular region  biological_process  positive regulation of feeding behavior  
Ontology : EGO-EBIG-protein coupled receptor binding  hormone activity  cellular_component  extracellular region  extracellular region  biological_process  positive regulation of feeding behavior  
NDEx NetworkINSL5
Atlas of Cancer Signalling NetworkINSL5
Wikipedia pathwaysINSL5
Orthology - Evolution
OrthoDB10022
GeneTree (enSembl)ENSG00000172410
Phylogenetic Trees/Animal Genes : TreeFamINSL5
HOVERGENQ9Y5Q6
HOGENOMQ9Y5Q6
Homologs : HomoloGeneINSL5
Homology/Alignments : Family Browser (UCSC)INSL5
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerINSL5 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)INSL5
dbVarINSL5
ClinVarINSL5
1000_GenomesINSL5 
Exome Variant ServerINSL5
ExAC (Exome Aggregation Consortium)INSL5 (select the gene name)
Genetic variants : HAPMAP10022
Genomic Variants (DGV)INSL5 [DGVbeta]
DECIPHERINSL5 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisINSL5 
Mutations
ICGC Data PortalINSL5 
TCGA Data PortalINSL5 
Broad Tumor PortalINSL5
OASIS PortalINSL5 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICINSL5  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDINSL5
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 INSL5
DgiDB (Drug Gene Interaction Database)INSL5
DoCM (Curated mutations)INSL5 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)INSL5 (select a term)
intoGenINSL5
Cancer3DINSL5(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM606413   
Orphanet
MedgenINSL5
Genetic Testing Registry INSL5
NextProtQ9Y5Q6 [Medical]
TSGene10022
GENETestsINSL5
Target ValidationINSL5
Huge Navigator INSL5 [HugePedia]
snp3D : Map Gene to Disease10022
BioCentury BCIQINSL5
ClinGenINSL5
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD10022
Chemical/Pharm GKB GenePA29895
Clinical trialINSL5
Miscellaneous
canSAR (ICR)INSL5 (select the gene name)
Probes
Litterature
PubMed17 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineINSL5
EVEXINSL5
GoPubMedINSL5
iHOPINSL5
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 13:56:27 CEST 2017

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