Homo sapiens (human): 10560 Help Entry 10560             CDS       T01001                                  Symbol SLC19A2, TC1, THMD1, THT1, THTR1, TRMA Name (RefSeq) solute carrier family 19 member 2   KO K14610   solute carrier family 19 (thiamine transporter), member 2/3 Organism hsa  Homo sapiens (human) Pathway hsa04977   Vitamin digestion and absorption Disease H01183   Thiamine-responsive megaloblastic anemia H01565   Wernicke encephalopathy H02832   Thiamine metabolism dysfunction syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09154 Digestive system    04977 Vitamin digestion and absorption     10560 (SLC19A2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     10560 (SLC19A2) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC19: Folate/thiamine transporter    10560 (SLC19A2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Folate_carrier MFS_1 TMEM214 Motif Other DBs NCBI-GeneID:  10560 NCBI-ProteinID:  NP_008927 OMIM:  603941 HGNC:  10938 Ensembl:  ENSG00000117479 UniProt:  O60779 A0A024R928 Structure PDBPDBj LinkDB All DBs Position 1:complement(169463909..169485970) Genome browser AA seq 497 aa AA seqDB search MDVPGPVSRRAAAAAATVLLRTARVRRECWFLPTALLCAYGFFASLRPSEPFLTPYLLGP DKNLTEREVFNEIYPVWTYSYLVLLFPVFLATDYLRYKPVVLLQGLSLIVTWFMLLYAQG LLAIQFLEFFYGIATATEIAYYSYIYSVVDLGMYQKVTSYCRSATLVGFTVGSVLGQILV SVAGWSLFSLNVISLTCVSVAFAVAWFLPMPQKSLFFHHIPSTCQRVNGIKVQNGGIVTD TPASNHLPGWEDIESKIPLNMEEPPVEEPEPKPDRLLVLKVLWNDFLMCYSSRPLLCWSV WWALSTCGYFQVVNYTQGLWEKVMPSRYAAIYNGGVEAVSTLLGAVAVFAVGYIKISWST WGEMTLSLFSLLIAAAVYIMDTVGNIWVCYASYVVFRIIYMLLITIATFQIAANLSMERY ALVFGVNTFIALALQTLLTLIVVDASGLGLEITTQFLIYASYFALIAVVFLASGAVSVMK KCRKLEDPQSSSQVTTS NT seq 1494 nt NT seq  +upstreamnt  +downstreamnt atggatgtgcccggcccggtgtctcggcgggcggcggcggcggcggccactgtgctcctg cggaccgctcgggtccgtcgcgaatgctggttcttgccgaccgcgctgctctgcgcctac ggcttcttcgccagcctcaggccgtccgagcccttcctgaccccgtacctgctggggccg gacaagaacctgaccgagagggaggtcttcaatgaaatttatccagtatggacttactct tacctggtgctactgtttcctgtgttccttgccacagactacctccgttataaacctgtt gttctactgcaggggctcagccttattgttacatggtttatgctgctctatgcccaggga ctgctggccattcaatttctagaatttttttatggcatcgccacagccactgaaattgcc tattactcttatatctacagtgtggtggacctgggcatgtaccagaaagtcacaagttac tgtcgaagtgccactttggtgggctttacagtgggctctgtcctagggcaaatccttgtc tcagtggcaggctggtcgctgttcagcctgaatgtcatctctcttacctgtgtttcagtg gcttttgctgtggcctggtttttacctatgccacagaagagcctcttctttcaccacatt ccttctacctgccagagagtgaatggcatcaaggtacaaaatggtggcattgttactgac accccagcttctaaccaccttcctggctgggaggacattgagtcaaaaatccctctaaat atggaggagcctcccgtggaggaaccggaacccaagccagaccgtctccttgtattgaaa gtactatggaatgatttcctgatgtgctactcctctcgccctcttctctgctggtctgtg tggtgggccctctctacctgtggctattttcaagttgtgaactacacacagggcctgtgg gagaaagtgatgccttctcgctatgctgctatctataatggtggcgtggaggccgtttca accttactgggtgctgttgctgtgtttgcagttggttatataaaaatatcctggtcaact tggggagaaatgacattatctctcttttctctcctgattgctgctgcagtgtatatcatg gacactgtgggtaacatttgggtgtgctatgcatcctatgttgtcttcagaatcatctac atgttactcatcacgatagcaacttttcaaattgctgcaaacctcagcatggaacgctat gccctagtatttggtgtaaataccttcattgccctggcactgcagacgctgctcactcta attgtggtagatgccagtggccttggattagaaattaccactcagtttttgatctatgcc agttattttgcactcatcgctgtggttttcctggccagtggtgcagtcagtgttatgaag aaatgtagaaagctggaagatccacaatcaagttctcaagtaaccacttcataa

Homo sapiens (human): 80704 Help Entry 80704             CDS       T01001                                  Symbol SLC19A3, BBGD, THMD2, THTR2, hTHTR2, thTr-2 Name (RefSeq) solute carrier family 19 member 3   KO K14610   solute carrier family 19 (thiamine transporter), member 2/3 Organism hsa  Homo sapiens (human) Pathway hsa04977   Vitamin digestion and absorption Disease H01231   Biotin-thiamine-responsive basal ganglia disease H02832   Thiamine metabolism dysfunction syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09154 Digestive system    04977 Vitamin digestion and absorption     80704 (SLC19A3)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     80704 (SLC19A3) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC19: Folate/thiamine transporter    80704 (SLC19A3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Folate_carrier MFS_1 Cadherin_C_2 Motif Other DBs NCBI-GeneID:  80704 NCBI-ProteinID:  NP_079519 OMIM:  606152 HGNC:  16266 Ensembl:  ENSG00000135917 UniProt:  Q9BZV2 Structure PDBPDBj LinkDB All DBs Position 2:complement(227683763..227718028) Genome browser AA seq 496 aa AA seqDB search MDCYRTSLSSSWIYPTVILCLFGFFSMMRPSEPFLIPYLSGPDKNLTSAEITNEIFPVWT YSYLVLLLPVFVLTDYVRYKPVIILQGISFIITWLLLLFGQGVKTMQVVEFFYGMVTAAE VAYYAYIYSVVSPEHYQRVSGYCRSVTLAAYTAGSVLAQLLVSLANMSYFYLNVISLASV SVAFLFSLFLPMPKKSMFFHAKPSREIKKSSSVNPVLEETHEGEAPGCEEQKPTSEILST SGKLNKGQLNSLKPSNVTVDVFVQWFQDLKECYSSKRLFYWSLWWAFATAGFNQVLNYVQ ILWDYKAPSQDSSIYNGAVEAIATFGGAVAAFAVGYVKVNWDLLGELALVVFSVVNAGSL FLMHYTANIWACYAGYLIFKSSYMLLITIAVFQIAVNLNVERYALVFGINTFIALVIQTI MTVIVVDQRGLNLPVSIQFLVYGSYFAVIAGIFLMRSMYITYSTKSQKDVQSPAPSENPD VSHPEEESNIIMSTKL NT seq 1491 nt NT seq  +upstreamnt  +downstreamnt atggattgttacagaacttcactaagcagttcctggatttaccccactgtgatcctctgc ttatttggttttttctccatgatgagaccctcagaaccattccttatcccatatttatct ggaccagataaaaacctgaccagtgcagagataacaaatgagatcttccccgtttggaca tactcctacctggtgctgctgctgcctgtgtttgtcctcaccgattatgtccgctacaag ccagtcatcatcttgcaaggtatcagtttcatcattacctggctgctgctgttgtttggc caaggagtgaagaccatgcaggttgtagagttcttctatgggatggtcaccgccgccgag gtggcctactacgcctacatatacagcgtggtcagccccgagcactaccagagagtgagc ggctactgcaggagcgtcacgctggccgcctacacagcagggtcggtgctggctcaactc ttggtatccctggcgaacatgtcgtacttttacctcaacgtcatatccttggcctctgtc tccgtggctttccttttctcacttttcctaccaatgcccaagaaaagcatgttttttcat gcaaaacccagcagagaaataaagaagtcatcaagcgtgaatccagtattagaggaaact cacgaaggtgaagcaccaggctgtgaagagcagaaacccacatcagaaatactcagcact tcagggaagctgaataagggccagctgaacagcctgaaaccaagcaatgtgactgtggac gtttttgtgcagtggttccaagatttgaaggagtgctactcctcaaaacgtcttttctac tggtctctatggtgggctttcgccacagcaggttttaaccaggttttgaactatgttcaa atcctgtgggattacaaggcgccatcccaagattcttccatctataatggggccgtagaa gctattgcaacctttggaggggctgtggctgcctttgcagtgggttatgtgaaagtcaac tgggaccttctgggagagctggctctggtggtcttctcagttgtcaatgccggttcttta tttctcatgcattacacagccaatatctgggcgtgctatgctggctatttgatattcaag tccagctatatgcttcttataaccatagcagtatttcagattgcagttaatctgaatgtg gaacgctatgccttggtatttggaatcaacacctttattgccttggtgattcagaccatc atgactgtgattgtagtagatcagagagggctcaacttgccagtcagcattcagttttta gtttatgggagctattttgcagtaattgctggaattttcctaatgagaagcatgtatatt acctactcaaccaaatcccagaaggatgtacagagccctgctccaagtgagaatccagat gtgtctcacccagaggaagagagtaatatcatcatgtcaacaaaactctaa

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