Neogale vison (American mink): 122909513 Help Entry 122909513         CDS       T08764                                  Symbol LPAR2 Name (RefSeq) lysophosphatidic acid receptor 2   KO K04291   lysophosphatidic acid receptor 2 Organism nvs  Neogale vison (American mink) Pathway nvs04015   Rap1 signaling pathway nvs04072   Phospholipase D signaling pathway nvs04080   Neuroactive ligand-receptor interaction nvs04151   PI3K-Akt signaling pathway nvs04810   Regulation of actin cytoskeleton nvs05200   Pathways in cancer Brite KEGG Orthology (KO) [BR:nvs00001]  09130 Environmental Information Processing   09132 Signal transduction    04015 Rap1 signaling pathway     122909513 (LPAR2)    04072 Phospholipase D signaling pathway     122909513 (LPAR2)    04151 PI3K-Akt signaling pathway     122909513 (LPAR2)   09133 Signaling molecules and interaction    04080 Neuroactive ligand-receptor interaction     122909513 (LPAR2)  09140 Cellular Processes   09142 Cell motility    04810 Regulation of actin cytoskeleton     122909513 (LPAR2)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     122909513 (LPAR2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04030 G protein-coupled receptors [BR:nvs04030]     122909513 (LPAR2) G protein-coupled receptors [BR:nvs04030]  Rhodopsin family   Lipid    Lysophosphatidic acid     122909513 (LPAR2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  7tm_1 7TM_GPCR_Srsx 7tm_4 zf-UBR 7TM_GPCR_Srt DUF2157 Motif Other DBs NCBI-GeneID:  122909513 NCBI-ProteinID:  XP_044109705 LinkDB All DBs Position 6:209474187..209478009 Genome browser AA seq 351 aa AA seqDB search MATMGRCYYNETIGFFYNNSGKELSSHWRPKDVVVVALGLTVSVLVLLTNLLVIAAIASN RRFHQPIYYLLGNLAAADLFAGVAYLFLMFHTGPRTARLSLEGWFVRQGLLDTSLTASVA TLLAIAVERHRSVMAVQLHSRLPRGRVVLLIVGVWVAALGLGLLPAHSWHCLCALDRCSR MAPLLSRSYLAVWALSSLLVFLLMVAVYTRIFFYVRRRVQRMAEHVSCHPRYRETTLSLV KTVVIILGAFVVCWTPGQVVLLLDGLGCKSCNVLAVEKYFLLLAEANSLVNAVVYSCRDA EMRRTFRRLLCCLCLRRSPHESARYAPSTRTGASTRIMLPENGHPLMDSTL NT seq 1056 nt NT seq  +upstreamnt  +downstreamnt atggccaccatgggccggtgctactacaatgagaccatcggctttttctacaacaacagt ggcaaggagctcagctcccactggcggcccaaagatgtggttgtggtggccctggggctg accgtcagcgttctggtgctcctgactaacttgctggtgatcgcagctatcgcctccaac cgccgcttccaccagcccatttactacctgctcggcaacctggccgcagccgacctcttt gcaggcgtggcctacctcttcctcatgtttcacacaggccctcgtaccgccagactctcg ctggagggctggttcgtgcggcagggcctgctggacacaagcctgaccgcctcggtggcc acactgttagccatcgccgtggagcggcaccgcagcgtgatggccgtgcagctgcacagc cgcctgccccgcggccgcgttgtcctgctcatcgtgggggtgtgggtggccgcactgggc ctggggctgctgcccgcccactcgtggcactgcctctgcgccctggaccgctgctcacgc atggcccctctgctcagccgctcctacctggctgtctgggcactgtccagcctgcttgtc ttcctgctcatggtggctgtctatacccgcattttcttctacgtgaggcggagggtgcag cgcatggcggagcacgtcagctgccacccccgctaccgagagaccacactcagcctagtc aagaccgttgtcattatcctgggagcattcgtggtctgctggacaccaggccaggtggtg ctgctcctggacggtctgggctgcaagtcctgcaacgttctggccgtggagaagtatttc ctactcttggcagaggccaactcactggtcaacgctgtggtgtactcgtgccgagacgct gagatgcgtcgcaccttccgccgcctcctctgctgtctgtgccttcgccggtcaccccac gagtctgcccgctatgctccctccacccgaacaggggccagcacgcgcatcatgcttcca gagaacggccaccccctgatggactccaccctgtag

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