Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10161
Gene name Gene Name - the full gene name approved by the HGNC.
Lysophosphatidic acid receptor 6
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LPAR6
Synonyms (NCBI Gene) Gene synonyms aliases
ARWH1, HYPT8, LAH3, LPA-6, P2RY5, P2Y5
Disease Acronyms (UniProt) Disease acronyms from UniProt database
ARWH1, HYPT8
Chromosome Chromosome number
13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
13q14.2
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene belongs to the family of G-protein coupled receptors, that are preferentially activated by adenosine and uridine nucleotides. This gene aligns with an internal intron of the retinoblastoma susceptibility gene in the revers
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT736565 hsa-miR-595 Western blotting, Microarray, qRT-PCR 22101077
MIRT1115496 hsa-miR-1252 CLIP-seq
MIRT1115497 hsa-miR-128 CLIP-seq
MIRT1115498 hsa-miR-27a CLIP-seq
MIRT1115499 hsa-miR-27b CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001835 Process Blastocyst hatching IEA
GO:0004930 Function G protein-coupled receptor activity IBA 21873635
GO:0005515 Function Protein binding IPI 32296183
GO:0005886 Component Plasma membrane IDA 18297070
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
609239 15520 ENSG00000139679
Protein
UniProt ID P43657
Protein name Lysophosphatidic acid receptor 6 (LPA receptor 6) (LPA-6) (Oleoyl-L-alpha-lysophosphatidic acid receptor) (P2Y purinoceptor 5) (P2Y5) (Purinergic receptor 5) (RB intron encoded G-protein coupled receptor)
Protein function Binds to oleoyl-L-alpha-lysophosphatidic acid (LPA). Intracellular cAMP is involved in the receptor activation. Important for the maintenance of hair growth and texture.
PDB 9ITB , 9ITE
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 34 291 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Expressed ubiquitously, including in skin and hair follicle cells. Detected in both Henle's and Huxley's layers of the inner root sheath of the hair follicle and in suprabasal layers of the epidermis (at protein level). Expressed at lo
Sequence
Sequence length 344
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Phospholipase D signaling pathway
Neuroactive ligand-receptor interaction
PI3K-Akt signaling pathway
Pathways in cancer
  G alpha (q) signalling events
P2Y receptors
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Cataract Cataract rs118203965, rs118203966, rs104893685, rs121908938, rs104894175, rs121909048, rs28937573, rs121909049, rs121909050, rs74315488, rs80358200, rs80358203, rs121434643, rs56141211, rs132630322
View all (150 more)
Hypotrichosis Hypotrichosis, HYPOTRICHOSIS 8 rs121434306, rs121434307, rs121434308, rs121434309, rs1325804776, rs267606775, rs786200875, rs1568062215, rs267606776, rs1462595806, rs267606777, rs267606659, rs2147483647, rs559648418, rs121917819
View all (18 more)
18461368, 18297072, 25119526, 18297070
Hypotrichosis simplex Hypotrichosis simplex rs121913026, rs201249971 18461368, 18297070
Woolly hair, with or without hypotrichosis WOOLLY HAIR, AUTOSOMAL RECESSIVE 1, WITH OR WITHOUT HYPOTRICHOSIS rs559648418, rs267607219, rs1720449752, rs201868115, rs201249971
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 34769557
Breast Neoplasms Associate 17047088, 37372960
Breast Neoplasms Inhibit 34510318
Carcinogenesis Associate 18475256
Carcinoma Hepatocellular Associate 27583415, 29211777, 31236404
Carcinoma Squamous Cell Associate 29211777
Crohn Disease Associate 19253308
Hair Diseases Associate 18803659
Hypotrichosis Associate 18803659, 19365138, 22385360, 25119526
Hypotrichosis Localized Autosomal Recessive 1 Associate 32336749