Homo sapiens (human): 6506 Help Entry 6506              CDS       T01001                                  Symbol SLC1A2, DEE41, EAAT2, EIEE41, GLT-1, HBGT Name (RefSeq) solute carrier family 1 member 2   KO K05613   solute carrier family 1 (glial high affinity glutamate transporter), member 2 Organism hsa  Homo sapiens (human) Pathway hsa04721   Synaptic vesicle cycle hsa04724   Glutamatergic synapse hsa05014   Amyotrophic lateral sclerosis hsa05016   Huntington disease Disease H00606   Early infantile epileptic encephalopathy H01819   Early myoclonic encephalopathy Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09156 Nervous system    04724 Glutamatergic synapse     6506 (SLC1A2)    04721 Synaptic vesicle cycle     6506 (SLC1A2)  09160 Human Diseases   09164 Neurodegenerative disease    05014 Amyotrophic lateral sclerosis     6506 (SLC1A2)    05016 Huntington disease     6506 (SLC1A2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     6506 (SLC1A2) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC1: High-affinity glutamate and neutral amino acid transporter    6506 (SLC1A2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SDF BPD_transp_1_N Motif Other DBs NCBI-GeneID:  6506 NCBI-ProteinID:  NP_004162 OMIM:  600300 HGNC:  10940 Ensembl:  ENSG00000110436 Vega:  OTTHUMG00000044391 Pharos:  P43004(Tchem) UniProt:  P43004 LinkDB All DBs Position 11:complement(35251205..35420507) Genome browser AA seq 574 aa AA seqDB search MASTEGANNMPKQVEVRMHDSHLGSEEPKHRHLGLRLCDKLGKNLLLTLTVFGVILGAVC GGLLRLASPIHPDVVMLIAFPGDILMRMLKMLILPLIISSLITGLSGLDAKASGRLGTRA MVYYMSTTIIAAVLGVILVLAIHPGNPKLKKQLGPGKKNDEVSSLDAFLDLIRNLFPENL VQACFQQIQTVTKKVLVAPPPDEEANATSAVVSLLNETVTEVPEETKMVIKKGLEFKDGM NVLGLIGFFIAFGIAMGKMGDQAKLMVDFFNILNEIVMKLVIMIMWYSPLGIACLICGKI IAIKDLEVVARQLGMYMVTVIIGLIIHGGIFLPLIYFVVTRKNPFSFFAGIFQAWITALG TASSAGTLPVTFRCLEENLGIDKRVTRFVLPVGATINMDGTALYEAVAAIFIAQMNGVVL DGGQIVTVSLTATLASVGAASIPSAGLVTMLLILTAVGLPTEDISLLVAVDWLLDRMRTS VNVVGDSFGAGIVYHLSKSELDTIDSQHRVHEDIEMTKTQSIYDDMKNHRESNSNQCVYA AHNSVIVDECKVTLAANGKSADCSVEEEPWKREK NT seq 1725 nt NT seq  +upstreamnt  +downstreamnt atggcatctacggaaggtgccaacaatatgcccaagcaggtggaagtgcgaatgcacgac agtcatcttggctcagaggaacccaagcaccggcacctgggcctgcgcctgtgtgacaag ctggggaagaatctgctgctcaccctgacggtgtttggtgtcatcctgggagcagtgtgt ggagggcttcttcgcttggcatctcccatccaccctgatgtggttatgttaatagccttc ccaggggatatactcatgaggatgctaaaaatgctcattctccctctaatcatctccagc ttaatcacagggttgtcaggcctggatgctaaggctagtggccgcttgggcacgagagcc atggtgtattacatgtccacgaccatcattgctgcagtactgggggtcattctggtcttg gctatccatccaggcaatcccaagctcaagaagcagctggggcctgggaagaagaatgat gaagtgtccagcctggatgccttcctggaccttattcgaaatctcttccctgaaaacctt gtccaagcctgctttcaacagattcaaacagtgacgaagaaagtcctggttgcaccaccg ccggacgaggaggccaacgcaaccagcgctgttgtctctctgttgaacgagactgtgact gaggtgccggaggagactaagatggttatcaagaagggcctggagttcaaggatgggatg aacgtcttaggtctgatagggtttttcattgcttttggcatcgctatggggaagatggga gatcaggccaagctgatggtggatttcttcaacattttgaatgagattgtaatgaagtta gtgatcatgatcatgtggtactctcccctgggtatcgcctgcctgatctgtggaaagatc attgcaatcaaggacttagaagtggttgctaggcaactggggatgtacatggtaacagtg atcataggcctcatcatccacgggggcatctttctccccttgatttactttgtagtgacc aggaaaaaccccttctccttttttgctggcattttccaagcttggatcactgccctgggc accgcttccagtgctggaactttgcctgtcacctttcgttgcctggaagaaaatctgggg attgataagcgtgtgactagattcgtccttcctgttggagcaaccattaacatggatggt acagccctttatgaagcggtagccgccatctttatagcccaaatgaatggtgttgtcctg gatggaggacagattgtgactgtaagcctcacagccaccctggcaagcgtcggcgcggcc agtatccccagtgccgggctggtcaccatgctcctcattctgacagccgtgggcctgcca acagaggacatcagcctgctggtggctgtggactggctgctggacaggatgagaacttca gtcaatgttgtgggtgactcttttggggctgggatagtctatcacctctccaagtctgag ctggataccattgactcccagcatcgagtgcatgaagatattgaaatgaccaagactcaa tccatttatgatgacatgaagaaccacagggaaagcaactctaatcaatgtgtctatgct gcacacaactctgtcatagtagatgaatgcaaggtaactctggcagccaatggaaagtca gccgactgcagtgttgaggaagaaccttggaaacgtgagaaataa

Homo sapiens (human): 6512 Help Entry 6512              CDS       T01001                                  Symbol SLC1A7, AAAT, EAAT5 Name (RefSeq) solute carrier family 1 member 7   KO K05618   solute carrier family 1 (glutamate transporter), member 7 Organism hsa  Homo sapiens (human) Pathway hsa04721   Synaptic vesicle cycle hsa04724   Glutamatergic synapse Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09156 Nervous system    04724 Glutamatergic synapse     6512 (SLC1A7)    04721 Synaptic vesicle cycle     6512 (SLC1A7)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     6512 (SLC1A7) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC1: High-affinity glutamate and neutral amino acid transporter    6512 (SLC1A7) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SDF DUF2417 Motif Other DBs NCBI-GeneID:  6512 NCBI-ProteinID:  NP_006662 OMIM:  604471 HGNC:  10945 Ensembl:  ENSG00000162383 Vega:  OTTHUMG00000008937 Pharos:  O00341(Tchem) UniProt:  O00341 F1T0D3 LinkDB All DBs Position 1:complement(53087183..53142638) Genome browser AA seq 560 aa AA seqDB search MVPHAILARGRDVCRRNGLLILSVLSVIVGCLLGFFLRTRRLSPQEISYFQFPGELLMRM LKMMILPLVVSSLMSGLASLDAKTSSRLGVLTVAYYLWTTFMAVIVGIFMVSIIHPGSAA QKETTEQSGKPIMSSADALLDLIRNMFPANLVEATFKQYRTKTTPVVKSPKVAPEEAPPR RILIYGVQEENGSHVQNFALDLTPPPEVVYKSEPGTSDGMNVLGIVFFSATMGIMLGRMG DSGAPLVSFCQCLNESVMKIVAVAVWYFPFGIVFLIAGKILEMDDPRAVGKKLGFYSVTV VCGLVLHGLFILPLLYFFITKKNPIVFIRGILQALLIALATSSSSATLPITFKCLLENNH IDRRIARFVLPVGATINMDGTALYEAVAAIFIAQVNNYELDFGQIITISITATAASIGAA GIPQAGLVTMVIVLTSVGLPTDDITLIIAVDWALDRFRTMINVLGDALAAGIMAHICRKD FARDTGTEKLLPCETKPVSLQEIVAAQQNGCVKSVAEASELTLGPTCPHHVPVQVEQDEE LPAASLNHCTIQISELETNV NT seq 1683 nt NT seq  +upstreamnt  +downstreamnt atggtgccgcatgccatcttggcacgggggagggacgtgtgcaggcggaatggactcctc atcctgtctgtgctgtctgtcatcgtgggctgcctcctcggcttcttcttgaggacccgg cgcctctcaccacaggaaattagttacttccagttccctggagagctcctgatgaggatg ctgaagatgatgatcctgccactggtggtctccagcttgatgtccggacttgcctccctg gatgccaagacctctagccgcctgggcgtcctcaccgtggcgtactacctgtggaccacc ttcatggctgtcatcgtgggcatcttcatggtctccatcatccacccaggcagcgcggcc cagaaggagaccacggagcagagtgggaagcccatcatgagctcagccgatgccctgttg gacctcatccggaacatgttcccagccaacctagtagaagccacattcaaacagtaccgc accaagaccaccccagttgtcaagtcccccaaggtggcaccagaggaggcccctcctcgg cggatcctcatctacggggtccaggaggagaatggctcccatgtgcagaacttcgccctg gacctgaccccgccgcccgaggtcgtttacaagtcagagccgggcaccagcgatggcatg aatgtgctgggcatcgtcttcttctctgccaccatgggcatcatgctgggccgcatgggt gacagcggggcccccctggtcagcttctgccagtgcctcaatgagtcggtcatgaagatc gtggcggtggctgtgtggtatttccccttcggcattgtgttcctcattgcgggtaagatc ctggagatggacgaccccagggccgtcggcaagaagctgggcttctactcagtcaccgtg gtgtgcgggctggtgctccacgggctctttatcctgcccctgctctacttcttcatcacc aagaagaatcccatcgtcttcatccgtggcatcctgcaggctctgctcatcgcgctggcc acctcctccagctcagccacactgcccatcaccttcaagtgcctgctggagaacaaccac atcgaccggcgcatcgctcgcttcgtgctgcccgtgggtgccaccatcaacatggacggc actgcgctctacgaggctgtggccgccatcttcatcgcccaggtcaacaactacgagctg gactttggccagatcatcaccatcagtatcacagccactgcagccagcattggggcagct ggcatcccccaggccggcctcgtcaccatggtcatcgtgctcacctccgtgggactgccc accgatgacatcaccctcatcattgccgttgactgggctctggaccgtttccgcaccatg attaacgtgctgggtgatgcgctggcagcggggatcatggcccatatatgtcggaaggat tttgcccgggacacaggcaccgagaaactgctgccctgcgagaccaagccagtgagcctc caggagatcgtggcagcccagcagaatggctgtgtgaagagtgtagccgaggcctccgag ctcaccctgggccccacctgcccccaccacgtccccgttcaagtggagcaggatgaggag ctgcccgctgcgagtctgaaccactgcaccatccagatcagtgagctggagaccaatgtc tga

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