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RLN1 (relaxin 1)

Identity

Alias_namesrelaxin 1 (H1)
Alias_symbol (synonym)H1
Other aliasH1RLX
RLXH1
bA12D24.3.1
bA12D24.3.2
HGNC (Hugo) RLN1
LocusID (NCBI) 6013
Atlas_Id 43920
Location 9p24.1  [Link to chromosome band 9p24]
Location_base_pair Starts at 5334932 and ends at 5339873 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)RLN1   10026
Cards
Entrez_Gene (NCBI)RLN1  6013  relaxin 1
AliasesH1; H1RLX; RLXH1; bA12D24.3.1; 
bA12D24.3.2
GeneCards (Weizmann)RLN1
Ensembl hg19 (Hinxton)ENSG00000107018 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000107018 [Gene_View]  chr9:5334932-5339873 [Contig_View]  RLN1 [Vega]
ICGC DataPortalENSG00000107018
TCGA cBioPortalRLN1
AceView (NCBI)RLN1
Genatlas (Paris)RLN1
WikiGenes6013
SOURCE (Princeton)RLN1
Genetics Home Reference (NIH)RLN1
Genomic and cartography
GoldenPath hg38 (UCSC)RLN1  -     chr9:5334932-5339873 -  9p24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)RLN1  -     9p24.1   [Description]    (hg19-Feb_2009)
EnsemblRLN1 - 9p24.1 [CytoView hg19]  RLN1 - 9p24.1 [CytoView hg38]
Mapping of homologs : NCBIRLN1 [Mapview hg19]  RLN1 [Mapview hg38]
OMIM179730   
Gene and transcription
Genbank (Entrez)A06846 A06926 A17329 AF057705 AI363233
RefSeq transcript (Entrez)NM_006911
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)RLN1
Cluster EST : UnigeneHs.368996 [ NCBI ]
CGAP (NCI)Hs.368996
Alternative Splicing GalleryENSG00000107018
Gene ExpressionRLN1 [ NCBI-GEO ]   RLN1 [ EBI - ARRAY_EXPRESS ]   RLN1 [ SEEK ]   RLN1 [ MEM ]
Gene Expression Viewer (FireBrowse)RLN1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)6013
GTEX Portal (Tissue expression)RLN1
Protein : pattern, domain, 3D structure
UniProt/SwissProtP04808   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP04808  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP04808
Splice isoforms : SwissVarP04808
PhosPhoSitePlusP04808
Domaine pattern : Prosite (Expaxy)INSULIN (PS00262)   
Domains : Interpro (EBI)Insulin-like    Insulin_CS    Insulin_family    Relaxin   
Domain families : Pfam (Sanger)Insulin (PF00049)   
Domain families : Pfam (NCBI)pfam00049   
Domain families : Smart (EMBL)IlGF (SM00078)  
Conserved Domain (NCBI)RLN1
DMDM Disease mutations6013
Blocks (Seattle)RLN1
SuperfamilyP04808
Human Protein AtlasENSG00000107018
Peptide AtlasP04808
HPRD01560
IPIIPI00025853   IPI00219641   
Protein Interaction databases
DIP (DOE-UCLA)P04808
IntAct (EBI)P04808
FunCoupENSG00000107018
BioGRIDRLN1
STRING (EMBL)RLN1
ZODIACRLN1
Ontologies - Pathways
QuickGOP04808
Ontology : AmiGOhormone activity  extracellular region  signal transduction  female pregnancy  
Ontology : EGO-EBIhormone activity  extracellular region  signal transduction  female pregnancy  
NDEx NetworkRLN1
Atlas of Cancer Signalling NetworkRLN1
Wikipedia pathwaysRLN1
Orthology - Evolution
OrthoDB6013
GeneTree (enSembl)ENSG00000107018
Phylogenetic Trees/Animal Genes : TreeFamRLN1
HOVERGENP04808
HOGENOMP04808
Homologs : HomoloGeneRLN1
Homology/Alignments : Family Browser (UCSC)RLN1
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerRLN1 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)RLN1
dbVarRLN1
ClinVarRLN1
1000_GenomesRLN1 
Exome Variant ServerRLN1
ExAC (Exome Aggregation Consortium)RLN1 (select the gene name)
Genetic variants : HAPMAP6013
Genomic Variants (DGV)RLN1 [DGVbeta]
DECIPHERRLN1 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisRLN1 
Mutations
ICGC Data PortalRLN1 
TCGA Data PortalRLN1 
Broad Tumor PortalRLN1
OASIS PortalRLN1 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICRLN1  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDRLN1
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch RLN1
DgiDB (Drug Gene Interaction Database)RLN1
DoCM (Curated mutations)RLN1 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)RLN1 (select a term)
intoGenRLN1
Cancer3DRLN1(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM179730   
Orphanet
MedgenRLN1
Genetic Testing Registry RLN1
NextProtP04808 [Medical]
TSGene6013
GENETestsRLN1
Target ValidationRLN1
Huge Navigator RLN1 [HugePedia]
snp3D : Map Gene to Disease6013
BioCentury BCIQRLN1
ClinGenRLN1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD6013
Chemical/Pharm GKB GenePA34399
Clinical trialRLN1
Miscellaneous
canSAR (ICR)RLN1 (select the gene name)
Probes
Litterature
PubMed62 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineRLN1
EVEXRLN1
GoPubMedRLN1
iHOPRLN1
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Aug 1 17:13:06 CEST 2017

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