Homo sapiens (human): 2774 Help Entry 2774              CDS       T01001                                  Symbol GNAL, DYT25, HG1O Name (RefSeq) G protein subunit alpha L   KO K04633   guanine nucleotide-binding protein G(olf) subunit alpha Organism hsa  Homo sapiens (human) Pathway hsa04020   Calcium signaling pathway hsa04082   Neuroactive ligand signaling hsa04728   Dopaminergic synapse hsa04740   Olfactory transduction hsa05012   Parkinson disease hsa05142   Chagas disease hsa05146   Amoebiasis Network nt06544  Neuroactive ligand signaling   Element N01897   Dopamine-DRD-GNAQ/S signaling pathway Disease H00831   Primary dystonia Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     2774 (GNAL)   09133 Signaling molecules and interaction    04082 Neuroactive ligand signaling     2774 (GNAL)  09150 Organismal Systems   09156 Nervous system    04728 Dopaminergic synapse     2774 (GNAL)   09157 Sensory system    04740 Olfactory transduction     2774 (GNAL)  09160 Human Diseases   09174 Infectious disease: parasitic    05146 Amoebiasis     2774 (GNAL)    05142 Chagas disease     2774 (GNAL)   09164 Neurodegenerative disease    05012 Parkinson disease     2774 (GNAL)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04031 GTP-binding proteins [BR:hsa04031]     2774 (GNAL) GTP-binding proteins [BR:hsa04031]  Heterotrimeric G-proteins   Alpha Subunits    Alpha type 2 (Gs)     2774 (GNAL) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  G-alpha Arf Gtr1_RagA GTP_EFTU TniB AAA_29 AAA_14 Motif Other DBs NCBI-GeneID:  2774 NCBI-ProteinID:  NP_001135811 OMIM:  139312 HGNC:  4388 Ensembl:  ENSG00000141404 UniProt:  P38405 A8K1Y9 Structure PDBPDBj LinkDB All DBs Position 18:11689264..11885685 Genome browser AA seq 381 aa AA seqDB search MGCLGGNSKTTEDQGVDEKERREANKKIEKQLQKERLAYKATHRLLLLGAGESGKSTIVK QMRILHVNGFNPEEKKQKILDIRKNVKDAIVTIVSAMSTIIPPVPLANPENQFRSDYIKS IAPITDFEYSQEFFDHVKKLWDDEGVKACFERSNEYQLIDCAQYFLERIDSVSLVDYTPT DQDLLRCRVLTSGIFETRFQVDKVNFHMFDVGGQRDERRKWIQCFNDVTAIIYVAACSSY NMVIREDNNTNRLRESLDLFESIWNNRWLRTISIILFLNKQDMLAEKVLAGKSKIEDYFP EYANYTVPEDATPDAGEDPKVTRAKFFIRDLFLRISTATGDGKHYCYPHFTCAVDTENIR RVFNDCRDIIQRMHLKQYELL NT seq 1146 nt NT seq  +upstreamnt  +downstreamnt atggggtgtttgggcggcaacagcaagacgacggaagaccagggcgtcgatgaaaaagaa cgacgcgaggccaacaaaaagatcgagaagcagttgcagaaagagcgcctggcttacaag gctacccaccgcctgctgctcctgggggctggtgagtctgggaaaagcactatcgtcaaa cagatgaggatcctgcacgtcaatgggtttaatcccgaggaaaagaaacagaaaattctg gacatccggaaaaatgttaaagatgctatcgtgacaattgtttcagcaatgagtactata atacctccagttccgctggccaaccctgaaaaccaatttcgatcagactacatcaagagc atagcccctatcactgactttgaatattcccaggaattctttgaccatgtgaaaaaactt tgggacgatgaaggcgtgaaggcatgctttgagagatccaacgaataccagctgattgac tgtgcacaatacttcctggaaagaatcgacagcgtcagcttggttgactacacacccaca gaccaggacctcctcagatgcagagttctgacatctgggatttttgagacacgattccaa gtggacaaagtaaacttccacatgtttgatgttggtggccagagggatgagaggagaaaa tggatccagtgctttaacgatgtcacagctatcatttacgtcgcagcctgcagtagctac aacatggtgattcgagaagataacaacaccaacaggctgagagagtccctggatcttttt gaaagcatctggaacaacaggtggttacggaccatttctatcatcttgttcttgaacaaa caagatatgctggcagaaaaagtcttggcagggaaatcaaaaattgaagactatttccca gaatatgcaaattatactgttcctgaagacgcaacaccagatgcaggagaagatcccaaa gttacaagagccaagttctttatccgggacctgtttttgaggatcagcacggccaccggt gacggcaaacattactgctacccgcacttcacctgcgccgtggacacagagaacatccgc agggtgttcaacgactgccgcgacatcatccagcggatgcacctcaagcagtatgagctc ttgtga

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