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2025-05-09 17:01:33, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_144585 3226 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens solute carrier family 22 (organic anion/urate
transporter), member 12 (SLC22A12), transcript variant 1, mRNA.
ACCESSION NM_144585
VERSION NM_144585.3 GI:444299633
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 3226)
AUTHORS Nakanishi,T., Ohya,K., Shimada,S., Anzai,N. and Tamai,I.
TITLE Functional cooperation of URAT1 (SLC22A12) and URATv1 (SLC2A9) in
renal reabsorption of urate
JOURNAL Nephrol. Dial. Transplant. 28 (3), 603-611 (2013)
PUBMED 23291366
REFERENCE 2 (bases 1 to 3226)
AUTHORS Hinohara,Y., Naito,M., Okada,R., Yin,G., Higashibata,T., Tamura,T.,
Kawai,S., Morita,E., Wakai,K., Matsuo,H., Mori,A. and Hamajima,N.
TITLE No association between MTHFR C677T and serum uric acid levels among
Japanese with ABCG2 126QQ and SLC22A12 258WW
JOURNAL Nagoya J Med Sci 75 (1-2), 93-100 (2013)
PUBMED 23544272
REMARK GeneRIF: Report no association between serum uric acid and MTHFR
C677T genotype, after the influences of ABCG2 Q126X and SLC22A12
W258X were removed.
REFERENCE 3 (bases 1 to 3226)
AUTHORS Kottgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark
C, Pistis G, Ruggiero D, O'Seaghdha CM, Haller T, Yang Q, Tanaka T,
Johnson AD, Kutalik Z, Smith AV, Shi J, Struchalin M, Middelberg
RP, Brown MJ, Gaffo AL, Pirastu N, Li G, Hayward C, Zemunik T,
Huffman J, Yengo L, Zhao JH, Demirkan A, Feitosa MF, Liu X, Malerba
G, Lopez LM, van der Harst P, Li X, Kleber ME, Hicks AA, Nolte IM,
Johansson A, Murgia F, Wild SH, Bakker SJ, Peden JF, Dehghan A,
Steri M, Tenesa A, Lagou V, Salo P, Mangino M, Rose LM, Lehtimaki
T, Woodward OM, Okada Y, Tin A, Muller C, Oldmeadow C, Putku M,
Czamara D, Kraft P, Frogheri L, Thun GA, Grotevendt A, Gislason GK,
Harris TB, Launer LJ, McArdle P, Shuldiner AR, Boerwinkle E, Coresh
J, Schmidt H, Schallert M, Martin NG, Montgomery GW, Kubo M,
Nakamura Y, Tanaka T, Munroe PB, Samani NJ, Jacobs DR Jr, Liu K,
D'Adamo P, Ulivi S, Rotter JI, Psaty BM, Vollenweider P, Waeber G,
Campbell S, Devuyst O, Navarro P, Kolcic I, Hastie N, Balkau B,
Froguel P, Esko T, Salumets A, Khaw KT, Langenberg C, Wareham NJ,
Isaacs A, Kraja A, Zhang Q, Wild PS, Scott RJ, Holliday EG, Org E,
Viigimaa M, Bandinelli S, Metter JE, Lupo A, Trabetti E, Sorice R,
Doring A, Lattka E, Strauch K, Theis F, Waldenberger M, Wichmann
HE, Davies G, Gow AJ, Bruinenberg M, Stolk RP, Kooner JS, Zhang W,
Winkelmann BR, Boehm BO, Lucae S, Penninx BW, Smit JH, Curhan G,
Mudgal P, Plenge RM, Portas L, Persico I, Kirin M, Wilson JF, Mateo
Leach I, van Gilst WH, Goel A, Ongen H, Hofman A, Rivadeneira F,
Uitterlinden AG, Imboden M, von Eckardstein A, Cucca F, Nagaraja R,
Piras MG, Nauck M, Schurmann C, Budde K, Ernst F, Farrington SM,
Theodoratou E, Prokopenko I, Stumvoll M, Jula A, Perola M, Salomaa
V, Shin SY, Spector TD, Sala C, Ridker PM, Kahonen M, Viikari J,
Hengstenberg C, Nelson CP, Meschia JF, Nalls MA, Sharma P,
Singleton AB, Kamatani N, Zeller T, Burnier M, Attia J, Laan M,
Klopp N, Hillege HL, Kloiber S, Choi H, Pirastu M, Tore S,
Probst-Hensch NM, Volzke H, Gudnason V, Parsa A, Schmidt R,
Whitfield JB, Fornage M, Gasparini P, Siscovick DS, Polasek O,
Campbell H, Rudan I, Bouatia-Naji N, Metspalu A, Loos RJ, van Duijn
CM, Borecki IB, Ferrucci L, Gambaro G, Deary IJ, Wolffenbuttel BH,
Chambers JC, Marz W, Pramstaller PP, Snieder H, Gyllensten U,
Wright AF, Navis G, Watkins H, Witteman JC, Sanna S, Schipf S,
Dunlop MG, Tonjes A, Ripatti S, Soranzo N, Toniolo D, Chasman DI,
Raitakari O, Kao WH, Ciullo M, Fox CS, Caulfield M, Bochud M and
Gieger C.
CONSRTM LifeLines Cohort Study; CARDIoGRAM Consortium; DIAGRAM Consortium;
ICBP Consortium; MAGIC Consortium
TITLE Genome-wide association analyses identify 18 new loci associated
with serum urate concentrations
JOURNAL Nat. Genet. 45 (2), 145-154 (2013)
PUBMED 23263486
REFERENCE 4 (bases 1 to 3226)
AUTHORS Takagi,S., Omae,R., Makanga,J.O., Kawahara,T. and Inazu,T.
TITLE Simple and rapid detection method for the mutations in SLC22A12
that cause hypouricemia by allele-specific real-time polymerase
chain reaction
JOURNAL Clin. Chim. Acta 415, 330-333 (2013)
PUBMED 23148994
REFERENCE 5 (bases 1 to 3226)
AUTHORS Wempe,M.F., Lightner,J.W., Miller,B., Iwen,T.J., Rice,P.J.,
Wakui,S., Anzai,N., Jutabha,P. and Endou,H.
TITLE Potent human uric acid transporter 1 inhibitors: in vitro and in
vivo metabolism and pharmacokinetic studies
JOURNAL Drug Des Devel Ther 6, 323-339 (2012)
PUBMED 23152669
REFERENCE 6 (bases 1 to 3226)
AUTHORS Anzai,N., Miyazaki,H., Noshiro,R., Khamdang,S., Chairoungdua,A.,
Shin,H.J., Enomoto,A., Sakamoto,S., Hirata,T., Tomita,K., Kanai,Y.
and Endou,H.
TITLE The multivalent PDZ domain-containing protein PDZK1 regulates
transport activity of renal urate-anion exchanger URAT1 via its C
terminus
JOURNAL J. Biol. Chem. 279 (44), 45942-45950 (2004)
PUBMED 15304510
REMARK GeneRIF: PDZK1 plays a role in regulating the functional activity
of URAT1-mediated urate transport in the apical membrane of renal
proximal tubules.
REFERENCE 7 (bases 1 to 3226)
AUTHORS Iwai,N., Mino,Y., Hosoyamada,M., Tago,N., Kokubo,Y. and Endou,H.
TITLE A high prevalence of renal hypouricemia caused by inactive SLC22A12
in Japanese
JOURNAL Kidney Int. 66 (3), 935-944 (2004)
PUBMED 15327384
REMARK GeneRIF: SLC22A12 is a major gene for hypouricemia but not
hyperuricemia in Japanese.
GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 8 (bases 1 to 3226)
AUTHORS Ichida,K., Hosoyamada,M., Hisatome,I., Enomoto,A., Hikita,M.,
Endou,H. and Hosoya,T.
TITLE Clinical and molecular analysis of patients with renal hypouricemia
in Japan-influence of URAT1 gene on urinary urate excretion
JOURNAL J. Am. Soc. Nephrol. 15 (1), 164-173 (2004)
PUBMED 14694169
REFERENCE 9 (bases 1 to 3226)
AUTHORS Gisler,S.M., Pribanic,S., Bacic,D., Forrer,P., Gantenbein,A.,
Sabourin,L.A., Tsuji,A., Zhao,Z.S., Manser,E., Biber,J. and
Murer,H.
TITLE PDZK1: I. a major scaffolder in brush borders of proximal tubular
cells
JOURNAL Kidney Int. 64 (5), 1733-1745 (2003)
PUBMED 14531806
REFERENCE 10 (bases 1 to 3226)
AUTHORS Enomoto,A., Kimura,H., Chairoungdua,A., Shigeta,Y., Jutabha,P.,
Cha,S.H., Hosoyamada,M., Takeda,M., Sekine,T., Igarashi,T.,
Matsuo,H., Kikuchi,Y., Oda,T., Ichida,K., Hosoya,T., Shimokata,K.,
Niwa,T., Kanai,Y. and Endou,H.
TITLE Molecular identification of a renal urate anion exchanger that
regulates blood urate levels
JOURNAL Nature 417 (6887), 447-452 (2002)
PUBMED 12024214
REMARK GeneRIF: Molecular identification of a renal urate anion exchanger
that regulates blood urate levels
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AB050269.1, AP001092.5,
DA631511.1, BC053348.1 and BX104022.1.
This sequence is a reference standard in the RefSeqGene project.
On Jan 30, 2013 this sequence version replaced gi:24497484.
Summary: The protein encoded by this gene is a member of the
organic anion transporter (OAT) family, and it acts as a urate
transporter to regulate urate levels in blood. This protein is an
integral membrane protein primarily found in epithelial cells of
the proximal tubule of the kidney. An elevated level of serum
urate, hyperuricemia, is associated with increased incidences of
gout, and mutations in this gene cause renal hypouricemia type 1.
Alternative splicing results in multiple transcript variants.
[provided by RefSeq, Jan 2013].
Transcript Variant: This variant (1) represents the longest
transcript and encodes the longest isoform (a).
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: AB050269.1, AK122599.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025088, ERS025092 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-323 AB050269.1 1-323
324-324 AP001092.5 34063-34063
325-998 AB050269.1 325-998
999-1055 DA631511.1 517-573
1056-1172 BC053348.1 599-715
1173-1173 AB050269.1 1170-1170
1174-1994 BC053348.1 717-1537
1995-1995 AP001092.5 42783-42783
1996-3202 BC053348.1 1539-2745
3203-3226 BX104022.1 228-251
FEATURES Location/Qualifiers
source 1..3226
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="11"
/map="11q13.1"
gene 1..3226
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/note="solute carrier family 22 (organic anion/urate
transporter), member 12"
/db_xref="GeneID:116085"
/db_xref="HGNC:17989"
/db_xref="MIM:607096"
exon 1..1149
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="alignment:Splign:1.39.8"
variation 30
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:9734313"
STS 94..350
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/standard_name="REN55630"
/db_xref="UniSTS:380430"
variation 202
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:191101229"
variation 279
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:71581770"
variation 282
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="g"
/db_xref="dbSNP:138511904"
variation 324
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:559946"
variation 337
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:182715759"
variation 338
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:79768170"
variation 339
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:75351039"
STS 348..588
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/standard_name="REN55631"
/db_xref="UniSTS:380431"
STS 392..575
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/standard_name="stSG635523"
/db_xref="UniSTS:460781"
variation 394
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:191077837"
variation 438
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="c"
/db_xref="dbSNP:372424252"
variation 514
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:72922827"
variation 528
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:3825018"
STS 568..819
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/standard_name="REN55632"
/db_xref="UniSTS:380432"
variation 624
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369334634"
variation 642
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:71581771"
variation 673
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369153816"
variation 703
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201365068"
misc_feature 736..738
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/note="upstream in-frame stop codon"
STS 743..972
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/standard_name="REN55633"
/db_xref="UniSTS:380433"
CDS 748..2409
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/note="isoform a is encoded by transcript variant 1;
solute carrier family 22 (organic anion/cation
transporter), member 12; urate transporter 1; urate anion
exchanger 1; renal-specific transporter; organic anion
transporter 4-like protein"
/codon_start=1
/product="solute carrier family 22 member 12 isoform a"
/protein_id="NP_653186.2"
/db_xref="GI:24497485"
/db_xref="CCDS:CCDS8075.1"
/db_xref="GeneID:116085"
/db_xref="HGNC:17989"
/db_xref="MIM:607096"
/translation="
MAFSELLDLVGGLGRFQVLQTMALMVSIMWLCTQSMLENFSAAVPSHRCWAPLLDNSTAQASILGSLSPEALLAISIPPGPNQRPHQCRRFRQPQWQLLDPNATATSWSEADTEPCVDGWVYDRSIFTSTIVAKWNLVCDSHALKPMAQSIYLAGILVGAAACGPASDRFGRRLVLTWSYLQMAVMGTAAAFAPAFPVYCLFRFLLAFAVAGVMMNTGTLLMEWTAARARPLVMTLNSLGFSFGHGLTAAVAYGVRDWTLLQLVVSVPFFLCFLYSWWLAESARWLLTTGRLDWGLQELWRVAAINGKGAVQDTLTPEVLLSAMREELSMGQPPASLGTLLRMPGLRFRTCISTLCWFAFGFTFFGLALDLQALGSNIFLLQMFIGVVDIPAKMGALLLLSHLGRRPTLAASLLLAGLCILANTLVPHEMGALRSALAVLGLGGVGAAFTCITIYSSELFPTVLRMTAVGLGQMAARGGAILGPLVRLLGVHGPWLPLLVYGTVPVLSGLAALLLPETQSLPLPDTIQDVQNQAVKKATHGTLGNSVLKSTQF
"
misc_feature 772..834
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96S37.1);
transmembrane region"
misc_feature 778..2325
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/note="cation transport protein; Region: 2A0119;
TIGR00898"
/db_xref="CDD:162097"
misc_feature 1111..>1584
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/note="The Major Facilitator Superfamily (MFS) is a large
and diverse group of secondary transporters that includes
uniporters, symporters, and antiporters. MFS proteins
facilitate the transport across cytoplasmic or internal
membranes of a variety of...; Region: MFS; cd06174"
/db_xref="CDD:119392"
misc_feature order(1117..1119,1126..1134,1138..1143,1192..1194,
1201..1206,1213..1215,1225..1230,1234..1239,1375..1380,
1387..1392,1399..1404,1411..1413,1447..1452,1459..1464,
1480..1482)
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/note="putative substrate translocation pore; other site"
/db_xref="CDD:119392"
misc_feature 1183..1245
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96S37.1);
transmembrane region"
misc_feature 1267..1329
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96S37.1);
transmembrane region"
misc_feature 1330..1392
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96S37.1);
transmembrane region"
misc_feature 1441..1503
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96S37.1);
transmembrane region"
misc_feature 1525..1587
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96S37.1);
transmembrane region"
misc_feature 1798..1860
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96S37.1);
transmembrane region"
misc_feature <1873..2295
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/note="The Major Facilitator Superfamily (MFS) is a large
and diverse group of secondary transporters that includes
uniporters, symporters, and antiporters. MFS proteins
facilitate the transport across cytoplasmic or internal
membranes of a variety of...; Region: MFS; cd06174"
/db_xref="CDD:119392"
misc_feature 1879..1941
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96S37.1);
transmembrane region"
misc_feature 1966..2028
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96S37.1);
transmembrane region"
misc_feature 2050..2112
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96S37.1);
transmembrane region"
misc_feature 2143..2205
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96S37.1);
transmembrane region"
misc_feature 2230..2292
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q96S37.1);
transmembrane region"
variation 759
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138704367"
variation 795
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373719760"
variation 798
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:72559738"
variation 832
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="c"
/db_xref="dbSNP:149620216"
variation 857
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369459384"
variation 870
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144313367"
variation 873
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148378818"
variation 876
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:3802948"
variation 890
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200499531"
variation 940
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="g"
/replace="t"
/db_xref="dbSNP:12800450"
variation 967
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="g"
/replace="t"
/db_xref="dbSNP:200961759"
variation 971
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141570522"
variation 981
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377022807"
variation 993
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:3825017"
variation 1005
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:3825016"
variation 1013
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201567912"
variation 1016
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:121907896"
variation 1021
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144328876"
variation 1052
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61737613"
variation 1074
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371053482"
variation 1080
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:146095398"
variation 1138
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150428327"
exon 1150..1253
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="alignment:Splign:1.39.8"
variation 1159
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:149722479"
variation 1173
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:11231825"
variation 1178
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148915713"
variation 1223
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374684921"
variation 1233
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376212424"
variation 1237
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201181059"
variation 1241
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370851012"
exon 1254..1408
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="alignment:Splign:1.39.8"
variation 1311
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200050310"
variation 1316
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="g"
/db_xref="dbSNP:80133078"
variation 1317
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200340948"
variation 1339
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:367825288"
variation 1351
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145285248"
variation 1354
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374743769"
variation 1355
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141975942"
variation 1362
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:71581772"
variation 1380
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61745330"
variation 1397
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:121907893"
exon 1409..1577
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="alignment:Splign:1.39.8"
variation 1424
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145738825"
variation 1426
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201136391"
variation 1430
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376338940"
variation 1431
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377128267"
variation 1479
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371087747"
variation 1500
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373029817"
variation 1507
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="g"
/replace="t"
/db_xref="dbSNP:376297536"
variation 1521
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:121907892"
variation 1525
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200690486"
variation 1560
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200680754"
variation 1576
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139316841"
exon 1578..1701
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="alignment:Splign:1.39.8"
variation 1593
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:71581775"
variation 1608
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140154051"
variation 1627
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="g"
/replace="t"
/db_xref="dbSNP:183246258"
variation 1641
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:121907894"
variation 1642
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199992707"
variation 1672
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="g"
/replace="t"
/db_xref="dbSNP:367678216"
exon 1702..1817
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="alignment:Splign:1.39.8"
variation 1720
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150255373"
variation 1721
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375040493"
variation 1750
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138889743"
variation 1772
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140376651"
variation 1779
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370083633"
variation 1786
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374858585"
variation 1808
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371005496"
exon 1818..2032
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="alignment:Splign:1.39.8"
variation 1822
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201322494"
variation 1829
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="g"
/replace="t"
/db_xref="dbSNP:121907897"
variation 1830
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368451526"
variation 1847
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="t"
/db_xref="dbSNP:372794965"
variation 1882
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372225207"
variation 1901
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149438001"
variation 1909
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146388519"
variation 1932
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138457974"
variation 1956
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142769893"
variation 1964
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372595086"
variation 1970
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:146048999"
variation 1971
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201081275"
variation 1972
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:77159242"
variation 1978
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370100606"
variation 1995
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1630320"
variation 2000
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="g"
/replace="t"
/db_xref="dbSNP:121907895"
variation 2001
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142344676"
variation 2018
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150779326"
variation 2019
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:183551522"
variation 2032
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139140123"
exon 2033..2141
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="alignment:Splign:1.39.8"
variation 2047
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145200251"
variation 2048
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147647315"
variation 2056
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:7932775"
variation 2076
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:61743169"
variation 2085
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145454847"
variation 2096
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201423508"
exon 2142..2345
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="alignment:Splign:1.39.8"
variation 2142
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200515227"
variation 2147
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200104135"
variation 2148
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368443880"
variation 2160
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199607711"
variation 2174
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="c"
/db_xref="dbSNP:148862453"
variation 2175
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:146694365"
variation 2185
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200599563"
variation 2207
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:151308640"
variation 2223
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200072517"
variation 2238
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="c"
/db_xref="dbSNP:139224371"
variation 2256
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140671173"
variation 2295
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145764379"
variation 2319
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138485972"
variation 2320
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372091940"
variation 2322..2324
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace=""
/replace="cac"
/db_xref="dbSNP:368190173"
variation 2329
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="c"
/db_xref="dbSNP:375375872"
exon 2346..3211
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/inference="alignment:Splign:1.39.8"
variation 2353..2354
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace=""
/replace="agaaggcaacacatggca"
/replace="agaaggcacacatggta"
/db_xref="dbSNP:143874752"
variation 2359
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199535450"
variation 2363
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369797157"
variation 2373
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143053863"
variation 2434
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373528077"
variation 2439
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="c"
/db_xref="dbSNP:376221325"
STS 2442..2696
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/standard_name="REN55672"
/db_xref="UniSTS:380472"
variation 2455
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:71583717"
variation 2476
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139851336"
variation 2479
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141655625"
variation 2532
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="t"
/db_xref="dbSNP:375484950"
variation 2541
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="c"
/db_xref="dbSNP:370769782"
variation 2561
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146221674"
variation 2574..2575
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace=""
/replace="tc"
/db_xref="dbSNP:139299506"
variation 2653..2654
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace=""
/replace="ccctg"
/db_xref="dbSNP:150284736"
variation 2657..2658
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace=""
/replace="gccct"
/db_xref="dbSNP:61157735"
STS 2669..2915
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/standard_name="REN55673"
/db_xref="UniSTS:380473"
variation 2677
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148845071"
variation 2680
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="a"
/replace="g"
/db_xref="dbSNP:184983393"
variation 2696
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace=""
/replace="c"
/db_xref="dbSNP:200439262"
variation 2700
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace=""
/replace="c"
/db_xref="dbSNP:3832794"
variation 2700
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201187954"
STS 2852..3112
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/standard_name="REN55674"
/db_xref="UniSTS:380474"
variation 2859
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:146963319"
variation 2926
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="c"
/replace="t"
/db_xref="dbSNP:476037"
STS 3025..3185
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/standard_name="RH98949"
/db_xref="UniSTS:90688"
variation 3056
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
/replace="g"
/replace="t"
/db_xref="dbSNP:200126462"
polyA_signal 3185..3190
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
polyA_site 3211
/gene="SLC22A12"
/gene_synonym="OAT4L; RST; URAT1"
ORIGIN
ccacagcaggtgagtggaggcaggagccacgggtggggccaggccacacagcctgggaggcgcaggggctgggcagctgccagtgacccaagcccacacagagacttgcacagctgccccagccccaaattagggggatcccctggcccaccttctcttggctcagccactctgggaggtgggcacacaggggcaccgaagggagcaggcagccctggcatcccacagccgccaggagaaaaacttaggcctccccaagacctggcacagagcaggccggccctggcccccaagcagaggaggctgcacctccctcgcgtctgtgcctgcctcaacgcgggttaaactttgaccaaggaaatgattgctaaactcgattccataagtgtcaccggtcacactttaattccagtctaaaattaaagtcttcagtctccacattccctactttccaaattcagctttcccgggaggtctggagcagctgcctctctggggagatgctggaggtctcggaatcacctcacgcggcctcagggcccagttggagccaccccaagtgacaccagcaggcagatgaccagagagcctgagcctccggccccgagtctgtgaagcctagccgctgggctggagaagccactgtgggcaccaccgtgggggaaacaggcccgttgccctggcctctttgccctgggccagcctttgtgaagtgggcccctcttctgggccccttgagtaggttccatggcattttctgaactcctggacctcgtgggtggcctgggcaggttccaggttctccagacgatggctctgatggtctccatcatgtggctgtgtacccagagcatgctggagaacttctcggccgccgtgcccagccaccgctgctgggcacccctcctggacaacagcacggctcaggccagcatcctagggagcttgagtcctgaggccctcctggctatttccatcccgccgggccccaaccagaggccccaccagtgccgccgcttccgccagccacagtggcagctcttggaccccaatgccacggccaccagctggagcgaggccgacacggagccgtgtgtggatggctgggtctatgaccgcagcatcttcacctccacaatcgtggccaagtggaacctcgtgtgtgactctcatgctctgaagcccatggcccagtccatctacctggctgggattctggtgggagctgctgcgtgcggccctgcctcagacaggtttgggcgcaggctggtgctaacctggagctaccttcagatggctgtgatgggtacggcagctgccttcgcccctgccttccccgtgtactgcctgttccgcttcctgttggcctttgccgtggcaggcgtcatgatgaacacgggcactctcctgatggagtggacggcggcacgggcccgacccttggtgatgaccttgaactctctgggcttcagcttcggccatggcctgacagctgcagtggcctacggtgtgcgggactggacactgctgcagctggtggtctcggtccccttcttcctctgctttttgtactcctggtggctggcagagtcggcacgatggctcctcaccacaggcaggctggattggggcctgcaggagctgtggagggtggctgccatcaacggaaagggggcagtgcaggacaccctgacccctgaggtcttgctttcagccatgcgggaggagctgagcatgggccagcctcctgccagcctgggcaccctgctccgcatgcccggactgcgcttccggacctgtatctccacgttgtgctggttcgcctttggcttcaccttcttcggcctggccctggacctgcaggccctgggcagcaacatcttcctgctccaaatgttcattggtgtcgtggacatcccagccaagatgggcgccctgctgctgctgagccacctgggccgccgccccacgctggccgcatccctgttgctggcagggctctgcattctggccaacacgctggtgccccacgaaatgggggctctgcgctcagccttggccgtgctggggctgggcggggtgggggctgccttcacctgcatcaccatctacagcagcgagctcttccccactgtgctcaggatgacggcagtgggcttgggccagatggcagcccgtggaggagccatcctggggcctctggtccggctgctgggtgtccatggcccctggctgcccttgctggtgtatgggacggtgccagtgctgagtggcctggccgcactgcttctgcccgagacccagagcttgccgctgcccgacaccatccaagatgtgcagaaccaggcagtaaagaaggcaacacatggcacgctggggaactctgtcctaaaatccacacagttttagcctcctggggaacctgcgatgggacggtcagaggaagagacttcttctgttctctggagaaggcaggaggaaagcaaagacctccatttccagaggcccagaggctgccctctgaggtccccactctcccccagggctgcccctccaggtgagccctgcccctctcacagtccaaggggcccccttcaatactgaaggggaaaaggacagtttgattggcaggaggtgacccagtgcaccatcaccctgccctgccctcgtggcttcggagagcagaggggtcaggcccaggggaacgagctggccttgccaaccctctgcttgactccgcactgccacttgtccccccacacccgtccacctgcccagagctcagagctaaccaccatccatggtcaagacctctcctagctccacacaagcagtagagtctcagctccacagctttacccagaagccctgtaagcctggcccctggcccctccccatgtccctccaggcctcagccacctgcccgccacatcctctgcctgctgtccccttcccaccctcatccctgaccgactccacttaacccccaaacccagccccccttccaggggtccagggccagcctgagatgcccgtgaaactcctacccacagttacagccacaagcctgcctcctcccaccctgccagcctatgagttcccagagggttggggcagtcccatgaccccatgtcccagctccccacacagcgctgggccagagaggcattggtgcgagggattgaataaagaaacaaatgaatggctgcccaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:116085 -> Molecular function: GO:0015143 [urate transmembrane transporter activity] evidence: IDA
GeneID:116085 -> Molecular function: GO:0030165 [PDZ domain binding] evidence: IPI
GeneID:116085 -> Biological process: GO:0015747 [urate transport] evidence: IDA
GeneID:116085 -> Biological process: GO:0019725 [cellular homeostasis] evidence: NAS
GeneID:116085 -> Biological process: GO:0042493 [response to drug] evidence: IDA
GeneID:116085 -> Biological process: GO:0046415 [urate metabolic process] evidence: IMP
GeneID:116085 -> Biological process: GO:0055085 [transmembrane transport] evidence: TAS
GeneID:116085 -> Cellular component: GO:0005886 [plasma membrane] evidence: IDA
GeneID:116085 -> Cellular component: GO:0005886 [plasma membrane] evidence: TAS
GeneID:116085 -> Cellular component: GO:0016021 [integral to membrane] evidence: IDA
GeneID:116085 -> Cellular component: GO:0016324 [apical plasma membrane] evidence: IDA
GeneID:116085 -> Cellular component: GO:0031526 [brush border membrane] evidence: ISS
GeneID:116085 -> Cellular component: GO:0031526 [brush border membrane] evidence: NAS
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DBCLS
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