LPAR1 (GeneID: 1902) | Homo sapiens
Description: lysophosphatidic acid receptor 1 [Source:HGNC Symbol;Acc:HGNC:3166]
Synonyms: Mrec1.3, Gpcr26, VZG1, ec.1.3, LPA1, EDG2, vzg-1, GPR26, edg-2
Other ID(s): HGNC:3166, ENSG00000198121
Protein Accession Numbers: NP_001374438, ENST00000441240, NP_001374446, NP_001338331, NP_001338339, NP_001338347, NP_001374404, NP_001374412, NP_001374420, NP_001374430, ENST00000358883, NP_001374443, NP_001338328, NP_001392, NP_001338336, NP_001338344, NP_001374401, NP_001374409, NP_001374417, NP_001374425, NP_001374435, NP_001374440, ENST00000541779, NP_001374448, NP_001338333, NP_001338341, NP_001338349, NP_001374406, NP_001374414, NP_001374422, NP_001374432, ENST00000374431, NP_001374445, NP_001338330, NP_001338338, NP_001338346, NP_001374403, NP_001374411, NP_001374419, NP_001374427, NP_001374437, NP_001374442, NP_001338327, NP_001374450, NP_001338335, NP_001338343, NP_001374400, NP_001374408, NP_001374416, NP_001374424, NP_001374434, NP_001374439, ENST00000538760, NP_001374447, NP_001338332, NP_001338340, NP_001338348, NP_001374405, NP_001374413, NP_001374421, NP_001374431, ENST00000374430, NP_001374444, NP_001338329, NP_476500, NP_001338337, NP_001338345, NP_001374402, NP_001374410, NP_001374418, NP_001374426, NP_001374436, NP_001374441, NP_001338326, NP_001374449, NP_001338334, NP_001338342, NP_00137439
Statistics: gnomAD(116)
gnomAD Variants By Annotation

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000358883 ENST00000374430 ENST00000374431 ENST00000441240 ENST00000538760 ENST00000541779 NP_001338326 NP_001338327 NP_001338328 NP_001338329 NP_001338330 NP_001338331 NP_001338332 NP_001338333 NP_001338334 NP_001338335 NP_001338336 NP_001338337 NP_001338338 NP_001338339 NP_001338340 NP_001338341 NP_001338342 NP_001338343 NP_001338344 NP_001338345


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
NO DOMAINS EXIST

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Anosmia Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; 0.586 0.552
Malignant neoplasm of breast Neoplasms ; Skin and Connective Tissue Diseases ; 0.586 0.552
Fetal Death Female Urogenital Diseases and Pregnancy Complications ; Pathological Conditions, Signs and Symptoms ; 0.586 0.552
Growth Disorders Pathological Conditions, Signs and Symptoms ; 0.586 0.552
Leukemia, Myelocytic, Acute Neoplasms ; 0.586 0.552
Acute Myeloid Leukemia, M1 Neoplasms ; 0.586 0.552
Prostatic Neoplasms Neoplasms ; Male Urogenital Diseases ; 0.586 0.552
Schizophrenia Mental Disorders ; 0.586 0.552
Malignant neoplasm of prostate Neoplasms ; Male Urogenital Diseases ; 0.586 0.552
Craniofacial Abnormalities Musculoskeletal Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.586 0.552
Olfaction Disorders Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; 0.586 0.552
Breast Carcinoma Neoplasms ; Skin and Connective Tissue Diseases ; 0.586 0.552
Mammary Neoplasms, Human Neoplasms ; Skin and Connective Tissue Diseases ; 0.586 0.552
Mammary Neoplasms Neoplasms ; Skin and Connective Tissue Diseases ; 0.586 0.552
Sense of smell altered Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; 0.586 0.552
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.586 0.552
Cacosmia Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; 0.586 0.552
NO RESULT FOUND
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