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2024-03-29 20:02:07, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_003048               5446 bp    mRNA    linear   PRI 11-MAY-2013
DEFINITION  Homo sapiens solute carrier family 9, subfamily A (NHE2, cation
            proton antiporter 2), member 2 (SLC9A2), mRNA.
ACCESSION   NM_003048
VERSION     NM_003048.3  GI:38569454
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 5446)
  AUTHORS   Muthusamy,S., Shukla,S., Amin,M.R., Cheng,M., Orenuga,T.,
            Dudeja,P.K. and Malakooti,J.
  TITLE     PKCdelta-dependent activation of ERK1/2 leads to upregulation of
            the human NHE2 transcriptional activity in intestinal epithelial
            cell line C2BBe1
  JOURNAL   Am. J. Physiol. Gastrointest. Liver Physiol. 302 (3), G317-G325
            (2012)
   PUBMED   22052014
  REMARK    GeneRIF: Phosphorylation of nPKC-delta results in activation of
            ERK1/2 kinase and subsequent induction of Egr-1. Subsequently,
            Egr-1 directly targets NHE2 promoter and promotes NHE2
            transcriptional upregulation by interaction with NHE2-PMA response
            element.
REFERENCE   2  (bases 1 to 5446)
  AUTHORS   Son,E.J., Moon,I.S., Kim,S.H., Kim,S.J. and Choi,J.Y.
  TITLE     Interferon-gamma suppresses Na+ -H+ exchanger in cultured human
            endolymphatic sac epithelial cells
  JOURNAL   J. Cell. Biochem. 107 (5), 965-972 (2009)
   PUBMED   19479940
  REMARK    GeneRIF: The functional and molecular expression of NHEs in
            cultured human endolymphatic sac (ES) epithelial cells was
            determined and the effect of IFN-gamma on NHE function, was
            examined.
REFERENCE   3  (bases 1 to 5446)
  AUTHORS   Joly,F., Mayeur,C., Messing,B., Lavergne-Slove,A., Cazals-Hatem,D.,
            Noordine,M.L., Cherbuy,C., Duee,P.H. and Thomas,M.
  TITLE     Morphological adaptation with preserved proliferation/transporter
            content in the colon of patients with short bowel syndrome
  JOURNAL   Am. J. Physiol. Gastrointest. Liver Physiol. 297 (1), G116-G123
            (2009)
   PUBMED   19389806
  REMARK    GeneRIF: Report morphological adaptation with preserved
            proliferation/NHE2 content in the colon of patients with short
            bowel syndrome.
REFERENCE   4  (bases 1 to 5446)
  AUTHORS   Musch,M.W., Arvans,D.L., Wu,G.D. and Chang,E.B.
  TITLE     Functional coupling of the downregulated in adenoma Cl-/base
            exchanger DRA and the apical Na+/H+ exchangers NHE2 and NHE3
  JOURNAL   Am. J. Physiol. Gastrointest. Liver Physiol. 296 (2), G202-G210
            (2009)
   PUBMED   19056765
  REMARK    GeneRIF: Functional coupling of the downregulated in adenoma
            Cl-/base exchanger DRA and the apical Na+/H+ exchangers NHE2 and
            NHE3 in intestinal epithelial cells.
REFERENCE   5  (bases 1 to 5446)
  AUTHORS   Beltran,A.R., Ramirez,M.A., Carraro-Lacroix,L.R., Hiraki,Y.,
            Reboucas,N.A. and Malnic,G.
  TITLE     NHE1, NHE2, and NHE4 contribute to regulation of cell pH in T84
            colon cancer cells
  JOURNAL   Pflugers Arch. 455 (5), 799-810 (2008)
   PUBMED   17943310
  REMARK    GeneRIF: T84 human colon cells contain three isoforms of the Na+/H+
            exchanger, NHE1, NHE2, and NHE4, but not the Cl-dependent NHE
REFERENCE   6  (bases 1 to 5446)
  AUTHORS   Lin,X. and Barber,D.L.
  TITLE     A calcineurin homologous protein inhibits GTPase-stimulated Na-H
            exchange
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 93 (22), 12631-12636 (1996)
   PUBMED   8901634
REFERENCE   7  (bases 1 to 5446)
  AUTHORS   Dudeja,P.K., Rao,D.D., Syed,I., Joshi,V., Dahdal,R.Y., Gardner,C.,
            Risk,M.C., Schmidt,L., Bavishi,D., Kim,K.E., Harig,J.M.,
            Goldstein,J.L., Layden,T.J. and Ramaswamy,K.
  TITLE     Intestinal distribution of human Na+/H+ exchanger isoforms NHE-1,
            NHE-2, and NHE-3 mRNA
  JOURNAL   Am. J. Physiol. 271 (3 PT 1), G483-G493 (1996)
   PUBMED   8843774
REFERENCE   8  (bases 1 to 5446)
  AUTHORS   Ghishan,F.K., Knobel,S.M. and Summar,M.
  TITLE     Molecular cloning, sequencing, chromosomal localization, and tissue
            distribution of the human Na+/H+ exchanger (SLC9A2)
  JOURNAL   Genomics 30 (1), 25-30 (1995)
   PUBMED   8595899
REFERENCE   9  (bases 1 to 5446)
  AUTHORS   Collins,J.F., Honda,T., Knobel,S., Bulus,N.M., Conary,J., DuBois,R.
            and Ghishan,F.K.
  TITLE     Molecular cloning, sequencing, tissue distribution, and functional
            expression of a Na+/H+ exchanger (NHE-2)
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 90 (9), 3938-3942 (1993)
   PUBMED   7683411
REFERENCE   10 (bases 1 to 5446)
  AUTHORS   Kulanthaivel,P., Furesz,T.C., Moe,A.J., Smith,C.H., Mahesh,V.B.,
            Leibach,F.H. and Ganapathy,V.
  TITLE     Human placental syncytiotrophoblast expresses two pharmacologically
            distinguishable types of Na(+)-H+ exchangers, NHE-1 in the
            maternal-facing (brush border) membrane and NHE-2 in the
            fetal-facing (basal) membrane
  JOURNAL   Biochem. J. 284 (PT 1), 33-38 (1992)
   PUBMED   1318024
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            BC035787.1, AF073299.1, AK129936.1 and AA843986.1.
            On Dec 1, 2003 this sequence version replaced gi:15529997.
            
            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 :: BC035787.1, BC136377.1 [ECO:0000332]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-199               BC035787.1         1-199
            200-2747            AF073299.1         148-2695
            2748-4767           BC035787.1         2747-4766
            4768-5257           AK129936.1         2019-2508
            5258-5387           AA843986.1         61-190              c
            5388-5446           AA843986.1         1-59                c
FEATURES             Location/Qualifiers
     source          1..5446
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="2"
                     /map="2q11.2"
     gene            1..5446
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /note="solute carrier family 9, subfamily A (NHE2, cation
                     proton antiporter 2), member 2"
                     /db_xref="GeneID:6549"
                     /db_xref="HGNC:11072"
                     /db_xref="HPRD:02756"
                     /db_xref="MIM:600530"
     exon            1..431
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="alignment:Splign:1.39.8"
     variation       23
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372115805"
     variation       64
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114579143"
     variation       96
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375752301"
     variation       103
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368856851"
     variation       135
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:190686338"
     CDS             143..2581
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /note="solute carrier family 9 (sodium/hydrogen
                     exchanger), isoform 2; sodium/hydrogen exchanger 2; NHE-2;
                     solute carrier family 9 member 2; Na(+)/H(+) exchanger 2;
                     solute carrier family 9 (sodium/hydrogen exchanger),
                     member 2"
                     /codon_start=1
                     /product="sodium/hydrogen exchanger 2 precursor"
                     /protein_id="NP_003039.2"
                     /db_xref="GI:15529998"
                     /db_xref="CCDS:CCDS2062.1"
                     /db_xref="GeneID:6549"
                     /db_xref="HGNC:11072"
                     /db_xref="HPRD:02756"
                     /db_xref="MIM:600530"
                     /translation="
MEPLGNWRSLRAPLPPMLLLLLLQVAGPVGALAETLLNAPRAMGTSSSPPSPASVVAPGTTLFEESRLPVFTLDYPHVQIPFEITLWILLASLAKIGFHLYHKLPTIVPESCLLIMVGLLLGGIIFGVDEKSPPAMKTDVFFLYLLPPIVLDAGYFMPTRPFFENIGTIFWYAVVGTLWNSIGIGVSLFGICQIEAFGLSDITLLQNLLFGSLISAVDPVAVLAVFENIHVNEQLYILVFGESLLNDAVTVVLYNLFKSFCQMKTIETIDVFAGIANFFVVGIGGVLIGIFLGFIAAFTTRFTHNIRVIEPLFVFLYSYLSYITAEMFHLSGIMAITACAMTMNKYVEENVSQKSYTTIKYFMKMLSSVSETLIFIFMGVSTVGKNHEWNWAFVCFTLAFCLMWRALGVFVLTQVINRFRTIPLTFKDQFIIAYGGLRGAICFALVFLLPAAVFPRKKLFITAAIVVIFFTVFILGITIRPLVEFLDVKRSNKKQQAVSEEIYCRLFDHVKTGIEDVCGHWGHNFWRDKFKKFDDKYLRKLLIRENQPKSSIVSLYKKLEIKHAIEMAETGMISTVPTFASLNDCREEKIRKVTSSETDEIRELLSRNLYQIRQRTLSYNRHSLTADTSERQAKEILIRRRHSLRESIRKDSSLNREHRASTSTSRYLSLPKNTKLPEKLQKRRTISIADGNSSDSDADAGTTVLNLQPRARRFLPEQFSKKSPQSYKMEWKNEVDVDSGRDMPSTPPTPHSREKGTQTSGLLQQPLLSKDQSGSEREDSLTEGIPPKPPPRLVWRASEPGSRKARFGSEKP
"
     sig_peptide     143..241
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="COORDINATES: ab initio prediction:SignalP:4.0"
     misc_feature    362..2032
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /note="sodium/hydrogen exchanger 3; Region: b_cpa1;
                     TIGR00840"
                     /db_xref="CDD:162063"
     misc_feature    461..523
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBY0.1);
                     transmembrane region"
     misc_feature    557..619
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBY0.1);
                     transmembrane region"
     misc_feature    647..709
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBY0.1);
                     transmembrane region"
     misc_feature    767..829
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBY0.1);
                     transmembrane region"
     misc_feature    851..913
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBY0.1);
                     transmembrane region"
     misc_feature    974..1036
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBY0.1);
                     transmembrane region"
     misc_feature    1064..1126
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBY0.1);
                     transmembrane region"
     misc_feature    1223..1285
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBY0.1);
                     transmembrane region"
     misc_feature    1316..1378
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBY0.1);
                     transmembrane region"
     misc_feature    1517..1579
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBY0.1);
                     transmembrane region"
     variation       181
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:376555739"
     variation       189
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183972576"
     variation       195
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:373622533"
     variation       223
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199622272"
     variation       224
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376898546"
     variation       258
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201327150"
     variation       267
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:74685539"
     variation       276
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141211710"
     variation       300
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201535448"
     variation       322
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199718995"
     variation       333
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:368226194"
     variation       373
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:137906470"
     exon            432..895
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="alignment:Splign:1.39.8"
     variation       451
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199869459"
     variation       478
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61740600"
     variation       502
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368634669"
     variation       532
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147336616"
     variation       589
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143241362"
     variation       590
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372934406"
     variation       601
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200268302"
     variation       602
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201828131"
     variation       628
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201412062"
     variation       690
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140049116"
     variation       725
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61743555"
     variation       733
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139722927"
     variation       742
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199725113"
     variation       766
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147714670"
     variation       826
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369331319"
     variation       833
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373112278"
     variation       851
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376604164"
     exon            896..1146
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="alignment:Splign:1.39.8"
     variation       918
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146727651"
     variation       947
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115807121"
     variation       1003
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112646996"
     variation       1012
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373377407"
     variation       1026
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377535586"
     variation       1069
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:148004830"
     variation       1113
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370904789"
     exon            1147..1364
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="alignment:Splign:1.39.8"
     variation       1181
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368738669"
     variation       1211
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:13021567"
     variation       1222
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371266585"
     variation       1238
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:12996049"
     variation       1286
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201007398"
     variation       1292
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374484897"
     variation       1303
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373845750"
     variation       1309
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138052501"
     variation       1321
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368048763"
     variation       1322
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200472482"
     variation       1326
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199631560"
     variation       1327
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148935269"
     variation       1356
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372115727"
     variation       1359
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375433711"
     exon            1365..1567
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="alignment:Splign:1.39.8"
     variation       1378
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372641100"
     variation       1411
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145744861"
     variation       1473
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377206233"
     variation       1509
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200846141"
     variation       1517
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:368185370"
     variation       1528
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201428753"
     variation       1561
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149530548"
     exon            1568..1657
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="alignment:Splign:1.39.8"
     variation       1617
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191805679"
     exon            1658..1728
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="alignment:Splign:1.39.8"
     variation       1667
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:41280603"
     variation       1714
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199687608"
     exon            1729..1890
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="alignment:Splign:1.39.8"
     variation       1747
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200485887"
     variation       1757
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371605244"
     variation       1803
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374840608"
     variation       1849
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:143332304"
     variation       1855
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374852380"
     variation       1867
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368150467"
     variation       1876
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17776702"
     variation       1883
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372340067"
     exon            1891..1987
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="alignment:Splign:1.39.8"
     variation       1899
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143663218"
     variation       1913
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372771066"
     variation       1924
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374054836"
     variation       1935
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146306086"
     variation       1969
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:146755145"
     variation       1984
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114491816"
     exon            1988..2119
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="alignment:Splign:1.39.8"
     variation       1999
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371958493"
     variation       2020
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202139053"
     variation       2061
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144961744"
     variation       2075
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201034436"
     variation       2109
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115244050"
     exon            2120..2210
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="alignment:Splign:1.39.8"
     variation       2125
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148165091"
     variation       2132
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:201372565"
     variation       2172
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376425428"
     variation       2176
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369057289"
     exon            2211..5442
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /inference="alignment:Splign:1.39.8"
     variation       2241
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199943468"
     variation       2277
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111701551"
     variation       2322
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375217344"
     variation       2385
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:150662206"
     variation       2390
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202141524"
     variation       2402
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147224345"
     variation       2453
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:56156264"
     variation       2463
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368881882"
     variation       2550
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144197023"
     variation       2557
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:112482803"
     variation       2570
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:144642954"
     variation       2628
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145995419"
     variation       2631
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:55898548"
     variation       2775
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7585959"
     variation       2811
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17027769"
     variation       3034
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114811113"
     variation       3065
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112685831"
     variation       3067
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181320416"
     variation       3086
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115630065"
     variation       3121
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141820817"
     variation       3243
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:146277126"
     variation       3262
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:185260366"
     variation       3295
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77699823"
     variation       3378
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17027770"
     variation       3403
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:189168907"
     variation       3406
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113157216"
     variation       3420
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:139050588"
     variation       3423
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142512244"
     variation       3574
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:73944403"
     variation       3580
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181873345"
     variation       3593
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:13398092"
     variation       3860
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186316096"
     variation       3891..3892
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:201886501"
     variation       3901
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191115983"
     variation       3914
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:180676758"
     variation       4385
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185991062"
     variation       4542..4543
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace=""
                     /replace="aa"
                     /db_xref="dbSNP:143157377"
     variation       4543
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202037069"
     variation       4562
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:368630188"
     variation       4578
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191382383"
     variation       4586
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183215873"
     variation       4617
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150942924"
     variation       4704
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:72229461"
     variation       4722..4725
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace=""
                     /replace="tgac"
                     /db_xref="dbSNP:144629891"
     variation       4848
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185782261"
     variation       4874
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:17776875"
     variation       4950
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:190638642"
     variation       5027
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:77140684"
     variation       5028
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:75150031"
     variation       5029
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139508966"
     variation       5109
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11123946"
     variation       5265
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:182940775"
     variation       5275
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:7605990"
     variation       5287
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187645450"
     variation       5308
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:375310416"
     variation       5338
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149701404"
     variation       5359
                     /gene="SLC9A2"
                     /gene_synonym="NHE2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147923726"
ORIGIN      
ccggtgccgcagcagcggcgggtggctgtcgctgccctgccctgcacggggcagggcggagcgggctgagcagcccgggcgcgatgcgttgagcgctcggagggccaaccgccggtccccttggcggcaaccggcggcacccatggaaccactgggcaactggaggagcctgcgggcgccactgcctccgatgctgttgctgctgctcctgcaggtggcggggcccgtgggcgccctggcggagaccttgctgaacgcgccgagggccatgggcaccagttccagcccgcctagccctgcgagcgtggtggctcccggaacgacgctgttcgaggagagccggctgcctgtgtttacgctggattacccccacgtgcagatccccttcgagatcaccctttggatcctgctggcctccctggccaagattggcttccatctgtatcacaagttgcccacaatagtgcctgagagctgccttcttataatggttggacttctactaggtgggattatttttggtgttgatgagaagtctccccctgcaatgaagactgatgtatttttcttgtacctcctcccacccatcgtgctggatgccggctatttcatgcccactcgcccattctttgagaacattggcacgattttctggtatgctgtggtagggacactttggaattccattggcattggggtgtctttgtttggtatctgccagatcgaagcattcggcctcagcgacatcactttgctccagaacctgctctttggcagcttaatctcagctgtcgatcctgtggctgtgcttgctgtctttgagaacattcacgtcaatgagcagctctacatcctggtctttggagagtccctgctgaatgatgcagtaacagtggtcctgtacaacttgttcaagtcgttttgccagatgaaaaccattgagaccattgatgtgtttgcaggaatcgccaacttctttgttgtgggaatcggtggggtgctgattggcatcttcttgggctttatagcggcatttactactcgattcacccataatatccgagtgatcgagccactgtttgttttcctgtacagttatttgtcctacatcacagctgaaatgtttcacctctcaggcatcatggcaatcactgcttgtgcaatgactatgaataagtacgtagaagaaaatgtatctcagaaatcctacacgaccatcaagtacttcatgaagatgctgagcagtgtcagcgaaaccttgatcttcatcttcatgggtgtgtctaccgtgggcaagaaccacgagtggaactgggccttcgtctgcttcaccctggccttctgcctcatgtggcgagccctgggtgtttttgtcctgactcaggtcattaataggttccggaccattcccctgacctttaaggaccagttcatcattgcctatggaggacttcgaggtgccatctgttttgcgttagtgtttctccttcctgctgctgtgtttcctcggaaaaaattgtttattacggctgccattgttgtcatattctttactgtcttcattctgggaataactattcgaccactggtggagtttcttgatgtcaagaggtccaataagaaacaacaagctgtcagtgaagaaatctattgtcggttgtttgatcatgtgaagactggaattgaagatgtttgtggacattggggtcacaacttttggagagacaagtttaagaagtttgatgataaatatctgcggaagcttttgattcgggaaaaccaaccaaagtcaagtattgtatctttatataaaaagcttgaaataaaacatgccattgagatggcagagactgggatgataagtactgtccctacatttgcatctctaaatgattgtcgtgaagaaaaaataaggaaggtcacgtccagtgaaactgatgaaattcgagaactcttatcaagaaatctctatcaaatccgtcagcgaactttatcctacaacagacacagtctgacagccgacacaagtgagagacaagccaaggagattctgattcgccggcgacacagtttgcgagaaagcattaggaaggacagcagcttgaatcgagaacacagggcttccacttcaacctcccgatatttatccttacctaaaaatacgaagcttccagaaaagctacaaaagaggaggactatttctattgcagatggcaatagcagcgactcagacgcagatgccgggaccaccgtgctcaatttgcagcccagagccaggcgcttcttgccagaacagttctccaagaaatccccccagtcctataaaatggaatggaagaatgaggtagatgttgattctggccgagatatgcccagcacccccccaacaccccacagcagagaaaagggcacccagacgtcaggcttactacagcagccccttctctctaaagaccagtctggctcagagagggaagacagtttgactgaaggcatcccgcccaagccgccaccacggctggtctggagggcatcggaacctggaagccggaaagcccgatttgggagtgagaagccttaagagaagcagcgaaagcagatctgagtgtctgacccaggacagctgtggtttgtcactctgaaacctgatgcaacagtggaatccatgtaaaactctctgtgcatctaaatacttctggagggcgacagattcatgccacggataaatgaggcaaatccgaagaaaaggaaaatcgaataaaaaatagtcccacaaaataccttttgtgactaatgggtagcaatcgtattatttgctggcctgaagagaaaaaatggtaatgtgtgcctttattgaacttgaatgacagaacttgaaatttttaacacatccttcttggtgaagattttaatatattacttatatgcttcaaattttatttatgaaaaaatatgtatatctgtaatcagttgttaagtgaatggcactaaaagtatcgagaacagctttctttcccaggggtgaaggatggcgctcgggggtgactcctaagctcagcgtggaagcttttccctgtcctgacccgatggagcagccggtaagtgaagagcacagctggaagcagagacaccttatgactcaaactgggcaaacaatcggaacgtcatgcagaaggaatggcctgactcctgcagtgcagattggaggccccagaactcctatgaactactgagagtctactggtttttaacttgttcctctgtctactgtgtgtttgggggtgacatctaaattccatttcttcttcttgtttaaatggtgcagagagaaaggttgcccagacatccaccagcttactgtgttgacagatttgggagcagcttttgatgaagttccacccatgagggtccatgtggcaagtagggccacagggcagcacctggttacaacttgctggtgggttttatgttgtgcaatactaggaggaggaggcaggtgatctatgctgatctatgatcacctgcttcagtagaatttttctgtagagtgttgtttgaattttgagcctccaggttagaggctccaagcagacaaagaagaaagtttgtagacacaatattctaacattgcacaagttgatgagatatcaagttttgaatattattcaggaagcactttggagaatgtgggagtcctactgttttgcactagtctgtaatttgttacctctccccattcgataatatagtaactcagaattttcatataaaattgaattctactcattagagtactttttaaaagtacagcagaaagaaaagaagtggaacataagcattcaagattaatatttgattctctatctcttaactgtagattttattggcctgttttttttttctaaataattctttaaaacttgactggaacatgcctctgcatttctgagtgtagaaattaaatgaagccactcacagtcctttgatttcccactgaagataccccaaaggatgcaagtgcctacagtattatcaggaggagaacatgaaaatattaagacaaaaatcctcagcagttgttctccaccccttctccacctccaccagcaaggagaagtcaatctacacttttttctcatgttctaaagtcttagaatactgctggattgttgagcatgagacagagcaaaggttagatacacaaggtacaagttcataggagcacaattccttgattcagggaaagtagcacagaatgcaatttgaaaactacaggcttaggactctgtgccaaaaatctctattttaaatgaaaatatttatataaaaatacatttattctgcttaacacaaattaaaactgacataaaattttatgataataacatgattcaagaaatgtgatgtagatttttgagaatgccaaaaatcaggtttcagaaaagctacagtatgaaatctgaaaagcaacagaaattgaaagtgaccttaaagaataaatttcctaatttttcccagtttcctatgtttataactattataaagagtttaactttctggaactgaaggagaaaacatgaaaatgtttatattgcttcttgttaagcaggtagaccaaattccgctttcagtaattcatccatacagaatttggatgactatgtataaaggaaaacttaaatcttaattattatcagtttaaattttttttgtttgttgaatgacaaaggcaataaaaataaatttgactttagctttttttctatactttcctctttttgtaattcttaaattctagtcactagtcattatgagagtattgactaaatattttcacaatctaaatattgtcacaatctaaatttctgtagtacagagagccgtagccctttgtaaaggctttcgttcgtccaaacaacacttgatccaaccaaagttccaatgtgactgtggatctttgataggtctttggtgttggttgtaacaaaatttgatttgaactacctataaatgaaaagtcggggtttattactttatatgtaatgctgagaggagactgttgggaacagttatgtcaatgagcaaactagaaattggcttcaaagtctgatacttttaaaagcatgtgttttgtgtatatgctcacaaaatgtctgtgaagagatttctttcagcttttgctcagctttatggtggggtgtactgttttatctgggcggtgagggtattgatttacataaaaactgtagacaaacacagtacgagtctcagcacgttttgcatttattgtactgcccaaattgtttttatgttaaaagtcacgtttcataatctgcaatatttttgtcaaagtgcacactgtactttcttcttaaaaacgtgattaaagagatcactttgtccggatgaagcagctgttggcattatccgctgaggcttgaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:6549 -> Molecular function: GO:0015385 [sodium:hydrogen antiporter activity] evidence: IEA
            GeneID:6549 -> Biological process: GO:0006811 [ion transport] evidence: TAS
            GeneID:6549 -> Biological process: GO:0006885 [regulation of pH] evidence: IEA
            GeneID:6549 -> Biological process: GO:0008104 [protein localization] evidence: IEA
            GeneID:6549 -> Biological process: GO:0055085 [transmembrane transport] evidence: TAS
            GeneID:6549 -> Cellular component: GO:0005886 [plasma membrane] evidence: TAS
            GeneID:6549 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA

by @meso_cacase at DBCLS
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