Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
122042
Gene name Gene Name - the full gene name approved by the HGNC.
Relaxin family peptide receptor 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RXFP2
Synonyms (NCBI Gene) Gene synonyms aliases
GPR106, GREAT, INSL3R, LGR8, LGR8.1, RXFPR2
Chromosome Chromosome number
13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
13q13.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the GPCR (G protein-coupled, 7-transmembrane receptor) family. Mutations in this gene are associated with cryptorchidism. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[pr
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1323244 hsa-miR-320a CLIP-seq
MIRT1323245 hsa-miR-320b CLIP-seq
MIRT1323246 hsa-miR-320c CLIP-seq
MIRT1323247 hsa-miR-320d CLIP-seq
MIRT1323248 hsa-miR-4429 CLIP-seq
Transcription factors
Transcription factor Regulation Reference
SOX9 Activation 19416188
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001556 Process Oocyte maturation IEA
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606655 17318 ENSG00000133105
Protein
UniProt ID Q8WXD0
Protein name Relaxin receptor 2 (G-protein coupled receptor 106) (G-protein coupled receptor affecting testicular descent) (Leucine-rich repeat-containing G-protein coupled receptor 8) (Relaxin family peptide receptor 2)
Protein function Receptor for relaxin. The activity of this receptor is mediated by G proteins leading to stimulation of adenylate cyclase and an increase of cAMP. May also be a receptor for Leydig insulin-like peptide (INSL3).
PDB 2M96
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00057 Ldl_recept_a 43 80 Low-density lipoprotein receptor domain class A Repeat
PF13855 LRR_8 137 197 Leucine rich repeat Repeat
PF13855 LRR_8 175 221 Leucine rich repeat Repeat
PF13855 LRR_8 281 341 Leucine rich repeat Repeat
PF00001 7tm_1 432 691 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Expressed mainly in the brain, kidney, muscle, testis, thyroid, uterus, peripheral blood cells and bone marrow.
Sequence
MIVFLVFKHLFSLRLITMFFLLHFIVLINVKDFALTQGSMITPSCQKGYFPCGNLTKCLP
RAFHCDGKDDCGNGADEENC
GDTSGWATIFGTVHGNANSVALTQECFLKQYPQCCDCKET
ELECVNGDLKSVPMISNNVTLLSLKKNKIHSLPDKVFIKYTKLKKIFLQHNCIRHISRKA
FFGLCNLQILYLNHNCI
TTLRPGIFKDLHQLTWLILDDNPI
TRISQRLFTGLNSLFFLSM
VNNYLEALPKQMCAQMPQLNWVDLEGNRIKYLTNSTFLSCDSLTVLFLPRNQIGFVPEKT
FSSLKNLGELDLSSNTITELSPHLFKDLKLLQKLNLSSNPL
MYLHKNQFESLKQLQSLDL
ERIEIPNINTRMFQPMKNLSHIYFKNFRYCSYAPHVRICMPLTDGISSFEDLLANNILRI
FVWVIAFITCFGNLFVIGMRSFIKAENTTHAMSIKILCCADCLMGVYLFFVGIFDIKYRG
QYQKYALLWMESVQCRLMGFLAMLSTEVSVLLLTYLTLEKFLVIVFPFSNIRPGKRQTSV
ILICIWMAGFLIAVIPFWNKDYFGNFYGKNGVCFPLYYDQTEDIGSKGYSLGIFLGVNLL
AFLIIVFSYITMFCSIQKTALQTTEVRNCFGREVAVANRFFFIVFSDAICWIPVFVVKIL
SLFRVEIPDTMTSWIVIFFLPVNSALNPILY
TLTTNFFKDKLKQLLHKHQRKSIFKIKKK
SLSTSIVWIEDSSSLKLGVLNKITLGDSIMKPVS
Sequence length 754
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Neuroactive ligand-receptor interaction
Relaxin signaling pathway
  G alpha (s) signalling events
Relaxin receptors
ADORA2B mediated anti-inflammatory cytokines production
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Breast Cancer BRCA2 mutation in breast cancer N/A N/A GWAS
Colorectal Cancer Colorectal cancer N/A N/A GWAS
Cryptorchidism cryptorchidism N/A N/A ClinVar, GenCC
Hypertension Essential hypertension (time to event), Hypertension (confirmatory factor analysis Factor 12), Hypertension (PheCode 401), Essential hypertension (PheCode 401.1), Hypertension, High blood pressure / hypertension N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Anorchia Associate 21853106
Azoospermia Associate 38430325
Coronary Artery Disease Associate 25197382
Cryptorchidism Associate 16926383, 26209787, 31167797, 38430325
Macular Degeneration Associate 32246154
Muscular Dystrophy Duchenne Associate 18433302
Obesity Associate 27421018
Osteoporosis Associate 18433302
Testicular Diseases Associate 16926383
Testicular Neoplasms Associate 16926383