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2024-03-29 00:27:50, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_004519              11266 bp    mRNA    linear   PRI 01-JUL-2013
DEFINITION  Homo sapiens potassium voltage-gated channel, KQT-like subfamily,
            member 3 (KCNQ3), transcript variant 1, mRNA.
ACCESSION   NM_004519
VERSION     NM_004519.3  GI:325651928
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 11266)
  AUTHORS   Zara,F., Specchio,N., Striano,P., Robbiano,A., Gennaro,E.,
            Paravidino,R., Vanni,N., Beccaria,F., Capovilla,G., Bianchi,A.,
            Caffi,L., Cardilli,V., Darra,F., Bernardina,B.D., Fusco,L.,
            Gaggero,R., Giordano,L., Guerrini,R., Incorpora,G., Mastrangelo,M.,
            Spaccini,L., Laverda,A.M., Vecchi,M., Vanadia,F., Veggiotti,P.,
            Viri,M., Occhi,G., Budetta,M., Taglialatela,M., Coviello,D.A.,
            Vigevano,F. and Minetti,C.
  TITLE     Genetic testing in benign familial epilepsies of the first year of
            life: clinical and diagnostic significance
  JOURNAL   Epilepsia 54 (3), 425-436 (2013)
   PUBMED   23360469
  REMARK    GeneRIF: KCNQ3 mutations might be involved in families with
            infantile seizures.
REFERENCE   2  (bases 1 to 11266)
  AUTHORS   Afawi,Z., Bassan,H., Heron,S., Oliver,K., Straussberg,R.,
            Scheffer,I., Leventer,R., Korczyn,A. and Berkovic,S.
  TITLE     Benign neonatal sleep myoclonus: an autosomal dominant form not
            allelic to KCNQ2 or KCNQ3
  JOURNAL   J. Child Neurol. 27 (10), 1260-1263 (2012)
   PUBMED   22447848
  REMARK    GeneRIF: This study demonistrated that benign neonatal sleep
            myoclonus can show autosomal dominant inheritance but not allelic
            to KCNQ3.
REFERENCE   3  (bases 1 to 11266)
  AUTHORS   Stewart,A.P., Gomez-Posada,J.C., McGeorge,J., Rouhani,M.J.,
            Villarroel,A., Murrell-Lagnado,R.D. and Edwardson,J.M.
  TITLE     The Kv7.2/Kv7.3 heterotetramer assembles with a random subunit
            arrangement
  JOURNAL   J. Biol. Chem. 287 (15), 11870-11877 (2012)
   PUBMED   22334706
  REMARK    GeneRIF: the Kv7.2-Kv7.3 heteromer assembles as a tetramer with a
            predominantly 2:2 subunit stoichiometry and with a random subunit
            arrangement.
REFERENCE   4  (bases 1 to 11266)
  AUTHORS   Cavaliere,S., Gillespie,J.M. and Hodge,J.J.
  TITLE     KCNQ channels show conserved ethanol block and function in ethanol
            behaviour
  JOURNAL   PLoS ONE 7 (11), E50279 (2012)
   PUBMED   23209695
  REMARK    GeneRIF: the single KCNQ channel in Drosophila (dKCNQ) has similar
            electrophysiological properties to neuronal KCNQ2/3
REFERENCE   5  (bases 1 to 11266)
  AUTHORS   Gomez-Posada,J.C., Aivar,P., Alberdi,A., Alaimo,A., Etxeberria,A.,
            Fernandez-Orth,J., Zamalloa,T., Roura-Ferrer,M., Villace,P.,
            Areso,P., Casis,O. and Villarroel,A.
  TITLE     Kv7 channels can function without constitutive calmodulin tethering
  JOURNAL   PLoS ONE 6 (9), E25508 (2011)
   PUBMED   21980481
  REMARK    GeneRIF: constitutive tethering of calmodulin is not required for
            Kv7 channel function
REFERENCE   6  (bases 1 to 11266)
  AUTHORS   Schroeder,B.C., Kubisch,C., Stein,V. and Jentsch,T.J.
  TITLE     Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+
            channels causes epilepsy
  JOURNAL   Nature 396 (6712), 687-690 (1998)
   PUBMED   9872318
REFERENCE   7  (bases 1 to 11266)
  AUTHORS   Wang,H.S., Pan,Z., Shi,W., Brown,B.S., Wymore,R.S., Cohen,I.S.,
            Dixon,J.E. and McKinnon,D.
  TITLE     KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of
            the M-channel
  JOURNAL   Science 282 (5395), 1890-1893 (1998)
   PUBMED   9836639
REFERENCE   8  (bases 1 to 11266)
  AUTHORS   Yang,W.P., Levesque,P.C., Little,W.A., Conder,M.L.,
            Ramakrishnan,P., Neubauer,M.G. and Blanar,M.A.
  TITLE     Functional expression of two KvLQT1-related potassium channels
            responsible for an inherited idiopathic epilepsy
  JOURNAL   J. Biol. Chem. 273 (31), 19419-19423 (1998)
   PUBMED   9677360
REFERENCE   9  (bases 1 to 11266)
  AUTHORS   Charlier,C., Singh,N.A., Ryan,S.G., Lewis,T.B., Reus,B.E.,
            Leach,R.J. and Leppert,M.
  TITLE     A pore mutation in a novel KQT-like potassium channel gene in an
            idiopathic epilepsy family
  JOURNAL   Nat. Genet. 18 (1), 53-55 (1998)
   PUBMED   9425900
REFERENCE   10 (bases 1 to 11266)
  AUTHORS   Ryan,S.G., Wiznitzer,M., Hollman,C., Torres,M.C., Szekeresova,M.
            and Schneider,S.
  TITLE     Benign familial neonatal convulsions: evidence for clinical and
            genetic heterogeneity
  JOURNAL   Ann. Neurol. 29 (5), 469-473 (1991)
   PUBMED   1859177
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AC018540.13, AF033347.1,
            AV728013.1, AC131042.6 and BX538233.1.
            This sequence is a reference standard in the RefSeqGene project.
            On Mar 10, 2011 this sequence version replaced gi:26638651.
            
            Summary: The M channel is a slowly activating and deactivating
            potassium channel that plays a critical role in the regulation of
            neuronal excitability. The M channel is formed by the association
            of the protein encoded by this gene and one of two related proteins
            encoded by the KCNQ2 and KCNQ5 genes, both integral membrane
            proteins. M channel currents are inhibited by M1 muscarinic
            acetylcholine receptors and activated by retigabine, a novel
            anti-convulsant drug. Defects in this gene are a cause of benign
            familial neonatal convulsions type 2 (BFNC2), also known as
            epilepsy, benign neonatal type 2 (EBN2). Two variants encoding
            distinct isoforms have been found. [provided by RefSeq, Mar 2011].
            
            Transcript Variant: This variant (1) encodes the longer isoform
            (1).
            
            Sequence Note: This RefSeq record was created from transcript and
            genomic sequence data to make the sequence consistent with the
            reference genome assembly. The genomic coordinates used for the
            transcript record were based on transcript alignments.
            
            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 :: AF033347.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-366               AC018540.13        87960-88325
            367-3097            AF033347.1         1-2731
            3098-3126           AV728013.1         74-102
            3127-11068          AC131042.6         108286-116227
            11069-11266         BX538233.1         4841-5038
FEATURES             Location/Qualifiers
     source          1..11266
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="8"
                     /map="8q24"
     gene            1..11266
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /note="potassium voltage-gated channel, KQT-like
                     subfamily, member 3"
                     /db_xref="GeneID:3786"
                     /db_xref="HGNC:6297"
                     /db_xref="HPRD:09077"
                     /db_xref="MIM:602232"
     exon            1..611
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    16..18
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /note="upstream in-frame stop codon"
     CDS             226..2844
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /note="isoform 1 is encoded by transcript variant 1;
                     potassium channel, voltage-gated, subfamily Q, member 3;
                     potassium channel subunit alpha KvLQT3; voltage-gated
                     potassium channel subunit Kv7.3"
                     /codon_start=1
                     /product="potassium voltage-gated channel subfamily KQT
                     member 3 isoform 1"
                     /protein_id="NP_004510.1"
                     /db_xref="GI:4758630"
                     /db_xref="CCDS:CCDS34943.1"
                     /db_xref="GeneID:3786"
                     /db_xref="HGNC:6297"
                     /db_xref="HPRD:09077"
                     /db_xref="MIM:602232"
                     /translation="
MGLKARRAAGAAGGGGDGGGGGGGAANPAGGDAAAAGDEERKVGLAPGDVEQVTLALGAGADKDGTLLLEGGGRDEGQRRTPQGIGLLAKTPLSRPVKRNNAKYRRIQTLIYDALERPRGWALLYHALVFLIVLGCLILAVLTTFKEYETVSGDWLLLLETFAIFIFGAEFALRIWAAGCCCRYKGWRGRLKFARKPLCMLDIFVLIASVPVVAVGNQGNVLATSLRSLRFLQILRMLRMDRRGGTWKLLGSAICAHSKELITAWYIGFLTLILSSFLVYLVEKDVPEVDAQGEEMKEEFETYADALWWGLITLATIGYGDKTPKTWEGRLIAATFSLIGVSFFALPAGILGSGLALKVQEQHRQKHFEKRRKPAAELIQAAWRYYATNPNRIDLVATWRFYESVVSFPFFRKEQLEAASSQKLGLLDRVRLSNPRGSNTKGKLFTPLNVDAIEESPSKEPKPVGLNNKERFRTAFRMKAYAFWQSSEDAGTGDPMAEDRGYGNDFPIEDMIPTLKAAIRAVRILQFRLYKKKFKETLRPYDVKDVIEQYSAGHLDMLSRIKYLQTRIDMIFTPGPPSTPKHKKSQKGSAFTFPSQQSPRNEPYVARPSTSEIEDQSMMGKFVKVERQVQDMGKKLDFLVDMHMQHMERLQVQVTEYYPTKGTSSPAEAEKKEDNRYSDLKTIICNYSETGPPEPPYSFHQVTIDKVSPYGFFAHDPVNLPRGGPSSGKVQATPPSSATTYVERPTVLPILTLLDSRVSCHSQADLQGPYSDRISPRQRRSITRDSDTPLSLMSVNHEELERSPSGFSISQDRDDYVFGPNGGSSWMREKRYLAEGETDTDTDPFTPSGSMPLSSTGDGISDSVWTPSNKPI
"
     misc_feature    589..651
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (O43525.2);
                     transmembrane region"
     misc_feature    682..744
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (O43525.2);
                     transmembrane region"
     misc_feature    700..1278
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /note="Ion transport protein; Region: Ion_trans;
                     pfam00520"
                     /db_xref="CDD:201279"
     misc_feature    814..876
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (O43525.2);
                     transmembrane region"
     misc_feature    901..966
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (O43525.2);
                     transmembrane region"
     misc_feature    961..963
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphothreonine; propagated from
                     UniProtKB/Swiss-Prot (O43525.2); phosphorylation site"
     misc_feature    1009..1071
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (O43525.2);
                     transmembrane region"
     misc_feature    1030..1281
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /note="Ion channel; Region: Ion_trans_2; pfam07885"
                     /db_xref="CDD:203792"
     misc_feature    1171..1188
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (O43525.2);
                     Region: Selectivity filter (By similarity)"
     misc_feature    1216..1278
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (O43525.2);
                     transmembrane region"
     misc_feature    1570..2223
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /note="KCNQ voltage-gated potassium channel; Region:
                     KCNQ_channel; pfam03520"
                     /db_xref="CDD:202676"
     misc_feature    2530..2826
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /note="Ankyrin-G binding motif of KCNQ2-3; Region:
                     KCNQC3-Ank-G_bd; pfam11956"
                     /db_xref="CDD:204795"
     exon            612..702
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     exon            703..829
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     exon            830..1002
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     exon            1003..1158
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     exon            1159..1269
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     exon            1270..1365
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     STS             1312..1550
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /standard_name="Kcnq3"
                     /db_xref="UniSTS:259499"
     exon            1366..1460
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     exon            1461..1487
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     exon            1488..1690
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     exon            1691..1793
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     exon            1794..1925
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     exon            1926..2024
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     exon            2025..2109
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     exon            2110..11248
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /inference="alignment:Splign:1.39.8"
     STS             2272..3098
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /standard_name="KCNQ3_350"
                     /db_xref="UniSTS:277435"
     variation       3879
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2957046"
     variation       4981
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2272679"
     STS             5001..5150
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /standard_name="WI-14883"
                     /db_xref="UniSTS:68066"
     variation       5876
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2469626"
     variation       5879
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2469627"
     variation       6821
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2469628"
     STS             7657..7785
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /standard_name="RH47376"
                     /db_xref="UniSTS:10355"
     variation       9184
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2469629"
     variation       9800
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2469630"
     STS             10037..10117
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
                     /standard_name="D8S1431E"
                     /db_xref="UniSTS:151220"
     polyA_signal    11225..11230
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
     polyA_site      11248
                     /gene="KCNQ3"
                     /gene_synonym="BFNC2; EBN2; KV7.3"
ORIGIN      
gacccgcgcgggatgtgaccccctgaccccctgcctggcctcccctgccccccagggggcccgcctttgcctgcttttgggggggggtggggaggggcgcgcggatcatggcattggagttcccgggcttgcagccgccgccgccgcctcgttcacgcaccccgagcgccccttcttcccagagcagcagcggagaaggcgaagcggccggcgggggcgaggcagatggggctcaaggcgcgcagggcggcgggggcggctggcggcggcggcgacgggggcggcggaggcggcggggcggctaacccagccggaggggacgcggcggcggccggcgacgaggagcggaaagtggggctggcgcccggcgacgtggagcaagtcaccttggcgctcggggccggagccgacaaagacgggaccctgctgctggagggcggcggccgcgacgaggggcagcggaggaccccgcagggcatcgggctcctggccaagaccccgctgagccgcccagtcaagagaaacaacgccaagtaccggcgcatccaaactttgatctacgacgccctggagagaccgcggggctgggcgctgctttaccacgcgttggtgttcctgattgtcctggggtgcttgattctggctgtcctgaccacattcaaggagtatgagactgtctcgggagactggcttctgttactggagacatttgctattttcatctttggagccgagtttgctttgaggatctgggctgctggatgttgctgccgatacaaaggctggcggggccgactgaagtttgccaggaagcccctgtgcatgttggacatctttgtgctgattgcctctgtgccagtggttgctgtgggaaaccaaggcaatgttctggccacctccctgcgaagcctgcgcttcctgcagatcctgcgcatgctgcggatggaccggagaggtggcacctggaagcttctgggctcagccatctgtgcccacagcaaagaactcatcacggcctggtacatcggtttcctgacactcatcctttcttcatttcttgtctacctggttgagaaagacgtcccagaggtggatgcacaaggagaggagatgaaagaggagtttgagacctatgcagatgccctgtggtggggcctgatcacactggccaccattggctatggagacaagacacccaaaacgtgggaaggccgtctgattgccgccaccttttccttaattggcgtctccttttttgcccttccagcgggcatcctggggtccgggctggccctcaaggtgcaggagcaacaccgtcagaagcactttgagaaaaggaggaagccagctgctgagctcattcaggctgcctggaggtattatgctaccaaccccaacaggattgacctggtggcgacatggagattttatgaatcagtcgtctcttttcctttcttcaggaaagaacagctggaggcagcatccagccaaaagctgggtctcttggatcgggttcgcctttctaatcctcgtggtagcaatactaaaggaaagctatttacccctctgaatgtagatgccatagaagaaagtccttctaaagaaccaaagcctgttggcttaaacaataaagagcgtttccgcacggccttccgcatgaaagcctacgctttctggcagagttctgaagatgccgggacaggtgaccccatggcggaagacaggggctatgggaatgacttccccatcgaagacatgatccccaccctgaaggccgccatccgagccgtcagaattctacaattccgtctctataaaaaaaaattcaaggagactttgaggccttacgatgtgaaggatgtgattgagcagtattctgccgggcatctcgacatgctttccaggataaagtaccttcagacgagaatagatatgattttcacccctggacctccctccacgccaaaacacaagaagtctcagaaagggtcagcattcaccttcccatcccagcaatctcccaggaatgaaccatatgtagccagaccatccacatcagaaatcgaagaccaaagcatgatggggaagtttgtaaaagttgaaagacaggttcaggacatggggaagaagctggacttcctcgtggatatgcacatgcaacacatggaacggttgcaggtgcaggtcacggagtattacccaaccaagggcacctcctcgccagctgaagcagagaagaaggaggacaacaggtattccgatttgaaaaccatcatctgcaactattctgagacaggccccccggaaccaccctacagcttccaccaggtgaccattgacaaagtcagcccctatgggttttttgcacatgaccctgtgaacctgccccgagggggacccagttctggaaaggttcaggcaactcctccttcctcagcaacaacgtatgtggagaggcccacggtcctgcctatcttgactcttctcgactcccgagtgagctgccactcccaggctgacctgcagggcccctactcggaccgaatctccccccggcagagacgtagcatcacgcgagacagtgacacacctctgtccctgatgtcggtcaaccacgaggagctggagaggtctccaagtggcttcagcatctcccaggacagagatgattatgtgttcggccccaatggggggtcgagctggatgagggagaagcggtacctcgccgagggtgagacggacacagacacggaccccttcacgcccagcggctccatgcctctgtcgtccacaggggatgggatttctgattcagtatggaccccttccaataagcccatttaaaagaggtcactggctgacccctccttgtaatgtagacagactttgtatagttcacttactcttacacccgacgcttaccagcggggacaccaatggctgcatcaaatgcatgcgtgtgcgtggtggccccacccaggcaggggcttcccacagcctcttcctccccatgtcaccacaacaaagtgcttccttttcagcatggtttgcatgactttacactatataaatggttccgctaatctcttctaggatacacatttatctgctgttcttacttttaatcacgattggaccagtacagggagaaattactgatgagccatgctatttgtctgtttggttggctggtttgggttttggtttggtaagcagagaaagtagtttaagttatttctaggatcactgccctcttgtgtaaaacgctccagcaattaactgtttttgaaagcaaggaaataattttctcaacaaaaccacattgtgtatcagtggggctgcctactgagctaacattaggaaaggaatgagatagtcattgtgtctctaaaacaaagaatttaaacaaatatttaaggcaaaaccttttaaaagctctccaaaagacctcacttggcctgatgttacttagtatcatgcctcagtttccttatctgtaaaaagtggtggtaatcccaagtgtagcatttctgatgagttatgaattggcagggagaaaacacacacacacacacacacacacacacacacacacacatacacaaagttaaaatagtttccaatttatgtagccaaggacaatggaatttatcagaagtgaagtgcccctctgggcaggagctgagttcagtgcctttaaaatgaatttccaactctcatttcttcccatgatactgaagtacaaaatatccatctaaaatagaaattaaagtcaagaaggcacacagaaattttctagtccaaggacttccttttataaatgaagaatcttaggctcaggtaaagtgacatacccagagtcactcagttgtcccatagagaaccaggactcaaaagtcaggtctgcccactctccctgaccttgtttcccctcaccacaccattcttccatttatataatgcatcctagagattgtgtcaagatatatgactttgtgtcgcgtggaaagcacccagtttatccagcaggagggggatttccacttttattgcaaaacatgcttgcttgatgcaatgcatttcagatctagaaaaaaataatgcaagcaagctacatttacagatgtgtaaacaggcaaaatttccagaaccgtccaattttacttttccaaatttatggaaccaacccagattttttaaatgaaaatactaaaaccatatgtaaccgtaagacaagctaaaatgtaagcagacagcctgggaagcactgccctactgtacaggtgtgatattaagcacaagccatcctctggcctcttatgagatgttgttattctctgaaaaactttgatggaaaaggtttctgttaggcttagactgaattagctaaatgaccatgccacagtattattgtatcactcttctcacacacctaggcactggttgtggatagttgccatggtgacaatcaagataatccagatgacctaaacaaatgtctgtatgcagctgacactgctattctccctcacagtcttgtcaagagccacagtagctatggcagacatttggttgatggtttcatcatttcctaatacgagagtctggcactatgttggagagaggaatcacttcctcagagataggttcctttcaactcacatgtcaacagttactgtacaaaaagctcagaatacagtaatgattagagcttgacccctgactttaggaacttagaaccaaagcccaaagtcccaggccaagggcagacattgtgagcagcagaagggtgttttttatggagagccccataaatggatgggtgtagaccttgaagtctgagatgggaaatataccagaatgctcaatgcatcagacatgaagccccacgggcttccatttgacatgctggcaatctgaaggacaaagggcatgggttatttgggccttttccccactccttcaatatggctgaaagtgccagtggggattacaacctaagaaaccctatgccccttcctgagggcttgattattgaatcctgatcttcctggaatctttcacttgagatgatcacctgcctaacatccaacatgttactatgctcttctttatgtacatgagttactggaaaccaacaataaaggagagtgagtcatactctccacatatgcgccaattaattttttaacttacttattagtattcttgaagaacttactatcttaagtattttaccaatagatgatgcattttccagcaactcaatggagttctaccttaaagtatttaccattgatccaaaattggaggaactaccttagattcttttaataacctagaaaggattggagcttgtattatttcctaaaccataggcaggcagtctagcttccctgctggatcataagaccaggacagcagagattgggtttgtattgatcagtagtagggaagtattgattgtctaacatctagtaagttgtctttatcagtatagacatagacaaaatacatgttttatgaatgaataaataataagaaccttaagagctgtttttttcccatttaagaaaacaaaaaggaaaagagaaaaatgatcttctggaataactctgctttgatattctccttttgttccccaaaaaatatattccagaaaggcaaaccaaacctgctcaagttgcctatgcacagacaatctcaacaatatggctcacagtgagcaagcagaaattcagggtctggaattgaatgtgagttatgggaagaaacagtgtgtgctttcacaaagatccttttgtcagacaagggaacagcatgataatccaatggaactggttaacatgacccaagatgacatgaccacagatatactagtcgttctgaaacttgcccaagaaattgcaatcgtttcagcagaactccatgaaatattgacaaattaattccatcatcaaactaggagtgatattatcaggtaaaactatgatctcatgtatgtatttggtctttctgggtcacaatgtgacatgaaaaattttaaaggtcatattttagcaagatcaaaatgaattagataaatcaacttcacaaatgttaagcgaaacatgatcctattgagctgagaaagaagtacttgagatcgtttgagttttgactatcaaatgtcagcacaaaagcaaatatcaaaagcttaagaaaaaaattatttcaggaaaagaaaaacacatcaaattgagaaagtgttgttgaataactttgtttttagaactggaaatttaggcttattagacatgacattgatattacaaagccctagttttcatgaaaacataactagataaccccaaggtgtataggttaaaatgaactaattaatcaacaattatgcatcctgtgtctattttgtgcaaggtacttcctagacactgtagtttgaaagaataatttcctgtagaaaaacctaatctaataggacctactcataatttggcaaaatcatcctcataattccatgctactgaaatgggggtgtaataaagaaaaaatcatttgtttattcatttaacagggtttattaagcaccaatatatgcccagaactttgcagtgcactggaagttcagagataagaaaaccacagtttctgccatcaaaatgctaggaatctagaggtctcaaacatcagaggtcccttcaaactatgtctaccaggaaaataaaatacctgatttcatccctgcaaacaactctatacagacagaaatgcttcctagcttggaaactatagaaaattgaacatgaaaatgagagcaaaggttctacatcaaaatggcaatgatccaatcagcccagtcaaggctgagtgggttgaatggggacttcgagtttggattcaatgctttgaacttcatagctccagagaagctgtgcaaaaaggggggattctagggaatctgaggaagattgttggagaaaccagctttcttcttgtctcctaatccctgctaagattgataccagtcaaggagctgagttactttcatttcattatgttgaccaagagaagcttatgatacagactatgacacagcacctatttcaagagaaagatgttactctacttatgggaacctgcagatcaaattctcctggggcaagagaagaaatttgttcagcagcctaagaagtcaactgtactttggacagtgctgccaaacacaccccaggattctcccacccctgtgctttcccagaagatgccacatagctggtatttggttttcatgaataaccaaagattcttctttgcttcctgaaccccaggcatccttaggaatttgcttcatgtcctcacttgtccttgaaggcttgtttttcaggatgaacttttaaagtctaagttgtttatattcaaatcaacccaatgctattgttgctgatattaaaccattccaaactgagccaactggcccctaaacaagccagcaggcagcccctcactaatgcccagtttagaacatgttaggaccaggctatctgcatagctttagtggttttagaagccagtaatggcagtgtaaaagaggaatcatacagagatgacctggaagaaaatttgagtttcagcacattcaaaagcatttgactcttctgccgtgttttgattttcaagtgagacaatcaatgtacacacaaagcctctagtacaatgactgatgcatactagggactgttatttatgttatttttttacagtatgcatggacttcattgtctcagtctttggtgttacttataaactctaaatttacaccaaaaaaattttttttcagaaaaagaatcgtggagaaacaatcctaattattaaatcaaatgctttcacaattgctttttaaataagtacatctctgcaaataaaaatgcttgctcttgtctaccacaataaagaacagaaggaatcttggaatgaagagaggcaggaatgttggatctcagtggctgagttgtggcaattccattggacatatagtaccagatgttgcaccatctggatgatgtgtaggagataaagccaaattgcaaaaataaaagactcatgatttcccaaggaaagtcaactgtgcatggtggctatcagacaacaccctagcaatgaatgggggaacttgcagaagaaagagttaatgcttgcttaaaccttccctggggagatttgttcccaggctttcacggctttaacctcagcaaccctgtaagaaaattgtgattcatattttgatttgttatcatagatgcaaagagacataatttcatggattctaagatacacagagcaagaagagattttgatcacccagaacaaccacctgtctttttagatcaagaagcagaagctcagagcaaagaacatcacaccacgtccctcagtgattgaagcagtgattgagtcacagaataaatctggaactcaggtcttctgatctttgctccagatgttagagacaaaactaaaagtaaaataccaagtgaaatcaaagcatcacgattgagcccagaacatgaaaaagaacttcctggcccacttgagaaactgttaaaccggacatacctttggggacttcttcccttctctggaataagattgatgtttccatgctgtgaaagacgatgatgttccttctcccagattcctgctgtcttcaaaaggcctagcaaaaaccactgctgctgggtgcagttgagaaagggaatgaagaacaatcccatggccatgcaggcactcctcccctccacctctctgccctccacccctctgccctctcctaccttgttccttcttggtcctgccatgtttggactggttcacctttttggcccatcacttgggctcattcagcaacagtcatgccttaggttgcatcctcatctataggccaattaaacagggtttcttcttgataaatccctatggttttgattttaggaagtcaggcatgatttcttttgggatctatatgacccaaagtggccagttttaccaaaggtgtccctttgcactgggatctctgggtctcatttgaacacagcttgggtcctcttgccttgtcccagagaatccccatgttgtcaggacataagcagatactctagggccttcaccaaaagctacaaagaagcagacaggactcaacttaggacatcttatggttatgtaactaagagattattttaggaagtaaacaggcctctgttggctcaaatgaacatcttcattgttagtttccacttacattgttctcgggataaatcggccagaatttggcagggctccccagcagtccttgtgaatccctgtggtaggatgtttcagttctcctgagtcaggctgaagtgaaagctcctaagagatattcagaaagaaggatggtcaagttctagaacaacaatagttggcccagtaattttaaagattgtcattctacctaagccttcatcctccagatagcactgttatgggcttaaaataagcttcaagggaaataatgaatttctttgacaccgccaaaaatcggctgtatataagaataacttgagaatggcttacaatgaggtagtcaaaagcccagctcagtgctcaggaatgtatttgtaattcctcttagacttgtcgaatggactgcaatttgatacctaagagtaataaaaaatgagaccatattttatgttaatgttcccttctcttcctctgcccacaaaagtgaggtcagggaaggggagagaaacttatcctaagcactccttatgagttgcttgtgacatgatagctctctctaaagttcatgcaatcctcatcgcaaccccatgagggagatgttattgtctccatcttatagatgaggaaactgaagacaagaccttgtcaaaggtcacacattgtaagaagtagagctgcatattcaaccaaagcccgtgtacctggaaagctcattctctct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//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:3786 -> Molecular function: GO:0005249 [voltage-gated potassium channel activity] evidence: TAS
            GeneID:3786 -> Molecular function: GO:0005251 [delayed rectifier potassium channel activity] evidence: IBA
            GeneID:3786 -> Molecular function: GO:0005267 [potassium channel activity] evidence: TAS
            GeneID:3786 -> Biological process: GO:0006813 [potassium ion transport] evidence: TAS
            GeneID:3786 -> Biological process: GO:0007268 [synaptic transmission] evidence: TAS
            GeneID:3786 -> Biological process: GO:0007411 [axon guidance] evidence: TAS
            GeneID:3786 -> Biological process: GO:0060081 [membrane hyperpolarization] evidence: IEA
            GeneID:3786 -> Cellular component: GO:0005886 [plasma membrane] evidence: ISS
            GeneID:3786 -> Cellular component: GO:0005886 [plasma membrane] evidence: TAS
            GeneID:3786 -> Cellular component: GO:0008076 [voltage-gated potassium channel complex] evidence: IEA
            GeneID:3786 -> Cellular component: GO:0033268 [node of Ranvier] evidence: ISS
            GeneID:3786 -> Cellular component: GO:0043194 [axon initial segment] evidence: ISS

by @meso_cacase at DBCLS
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