Homo sapiens (human): 2741 Help Entry 2741              CDS       T01001                                  Symbol GLRA1, HKPX1, STHE Name (RefSeq) glycine receptor alpha 1   KO K05193   glycine receptor alpha-1 Organism hsa  Homo sapiens (human) Pathway hsa04080   Neuroactive ligand-receptor interaction hsa04082   Neuroactive ligand signaling Network nt06544  Neuroactive ligand signaling   Element N01907   Transport of chloride, GLR Disease H00769   Hyperekplexia Drug target Strychnine nitrate:  D10470 Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04080 Neuroactive ligand-receptor interaction     2741 (GLRA1)    04082 Neuroactive ligand signaling     2741 (GLRA1)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    04131 Membrane trafficking [BR:hsa04131]     2741 (GLRA1)   09183 Protein families: signaling and cellular processes    04040 Ion channels [BR:hsa04040]     2741 (GLRA1) Membrane trafficking [BR:hsa04131]  Exocytosis   Calcium ion-dependent exocytosis    Acrosomal exocytosis proteins     2741 (GLRA1) Ion channels [BR:hsa04040]  Ligand-gated channels   Glycine    2741 (GLRA1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Neur_chan_LBD Neur_chan_memb Motif Other DBs NCBI-GeneID:  2741 NCBI-ProteinID:  NP_001139512 OMIM:  138491 HGNC:  4326 Ensembl:  ENSG00000145888 UniProt:  P23415 Structure PDBPDBj LinkDB All DBs Position 5:complement(151822513..151924851) Genome browser AA seq 457 aa AA seqDB search MYSFNTLRLYLWETIVFFSLAASKEAEAARSAPKPMSPSDFLDKLMGRTSGYDARIRPNF KGPPVNVSCNIFINSFGSIAETTMDYRVNIFLRQQWNDPRLAYNEYPDDSLDLDPSMLDS IWKPDLFFANEKGAHFHEITTDNKLLRISRNGNVLYSIRITLTLACPMDLKNFPMDVQTC IMQLESFGYTMNDLIFEWQEQGAVQVADGLTLPQFILKEEKDLRYCTKHYNTGKFTCIEA RFHLERQMGYYLIQMYIPSLLIVILSWISFWINMDAAPARVGLGITTVLTMTTQSSGSRA SLPKVSYVKAIDIWMAVCLLFVFSALLEYAAVNFVSRQHKELLRFRRKRRHHKSPMLNLF QEDEAGEGRFNFSAYGMGPACLQAKDGISVKGANNSNTTNPPPAPSKSPEEMRKLFIQRA KKIDKISRIGFPMAFLIFNMFYWIIYKIVRREDVHNQ NT seq 1374 nt NT seq  +upstreamnt  +downstreamnt atgtacagcttcaatactcttcgactctacctttgggagaccattgtattcttcagcctt gctgcttctaaggaggctgaagctgctcgctccgcacccaagcctatgtcaccctcggat ttcctggataagctaatggggagaacctccggatatgatgccaggatcaggcccaatttt aaaggtcccccagtgaacgtgagctgcaacattttcatcaacagctttggttccattgct gagacaaccatggactatagggtcaacatcttcctgcggcagcaatggaacgacccccgc ctggcctataatgaataccctgacgactctctggacctggacccatccatgctggactcc atctggaaacctgacctgttctttgccaacgagaagggggcccacttccatgagatcacc acagacaacaaattgctaaggatctcccggaatgggaatgtcctctacagcatcagaatc accctgacactggcctgccccatggacttgaagaatttccccatggatgtccagacatgt atcatgcaactggaaagctttggatatacgatgaatgacctcatctttgagtggcaggaa cagggagccgtgcaggtagcagatggactaactctgccccagtttatcttgaaggaagag aaggacttgagatactgcaccaagcactacaacacaggtaaattcacctgcattgaggcc cggttccacctggagcggcagatgggttactacctgattcagatgtatattcccagcctg ctcattgtcatcctctcatggatctccttctggatcaacatggatgctgcacctgctcgt gtgggcctaggcatcaccactgtgctcaccatgaccacccagagctccggctctcgagca tctctgcccaaggtgtcctatgtgaaagccattgacatttggatggcagtttgcctgctc tttgtgttctcagccctattagaatatgctgccgttaactttgtgtctcggcaacataag gagctgctccgattcaggaggaagcggagacatcacaagagccccatgttgaatctattc caggaggatgaagctggagaaggccgctttaacttctctgcctatgggatgggcccagcc tgtctacaggccaaggatggcatctcagtcaagggcgccaacaacagtaacaccaccaac ccccctcctgcaccatctaagtccccagaggagatgcgaaaactcttcatccagagggcc aagaagatcgacaaaatatcccgcattggcttccccatggccttcctcattttcaacatg ttctactggatcatctacaagattgtccgtagagaggacgtccacaaccagtga

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