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2024-03-28 20:05:23, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_014405               3430 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens calcium channel, voltage-dependent, gamma subunit 4
            (CACNG4), mRNA.
ACCESSION   NM_014405 NM_032659
VERSION     NM_014405.3  GI:313482782
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 3430)
  AUTHORS   Sager,C., Tapken,D., Kott,S. and Hollmann,M.
  TITLE     Functional modulation of AMPA receptors by transmembrane AMPA
            receptor regulatory proteins
  JOURNAL   Neuroscience 158 (1), 45-54 (2009)
   PUBMED   18304745
  REMARK    Review article
REFERENCE   2  (bases 1 to 3430)
  AUTHORS   Chen,R.S., Deng,T.C., Garcia,T., Sellers,Z.M. and Best,P.M.
  TITLE     Calcium channel gamma subunits: a functionally diverse protein
            family
  JOURNAL   Cell Biochem. Biophys. 47 (2), 178-186 (2007)
   PUBMED   17652770
  REMARK    Review article
REFERENCE   3  (bases 1 to 3430)
  AUTHORS   Moss,F.J., Dolphin,A.C. and Clare,J.J.
  TITLE     Human neuronal stargazin-like proteins, gamma2, gamma3 and gamma4;
            an investigation of their specific localization in human brain and
            their influence on CaV2.1 voltage-dependent calcium channels
            expressed in Xenopus oocytes
  JOURNAL   BMC Neurosci 4, 23 (2003)
   PUBMED   14505496
  REMARK    GeneRIF: examined distribution of the stargazin-like proteins
            gamma2, gamma3, and gamma4 in human CNS: gamma2 is expressed in
            cerebellum, cerebral cortex, hippocampus and thalamus, whereas
            gamma3 abounds in cerebral cortex & amygdala and gamma4 in basal
            ganglia
            Publication Status: Online-Only
REFERENCE   4  (bases 1 to 3430)
  AUTHORS   Chu,P.J., Robertson,H.M. and Best,P.M.
  TITLE     Calcium channel gamma subunits provide insights into the evolution
            of this gene family
  JOURNAL   Gene 280 (1-2), 37-48 (2001)
   PUBMED   11738816
REFERENCE   5  (bases 1 to 3430)
  AUTHORS   Burgess,D.L., Gefrides,L.A., Foreman,P.J. and Noebels,J.L.
  TITLE     A cluster of three novel Ca2+ channel gamma subunit genes on
            chromosome 19q13.4: evolution and expression profile of the gamma
            subunit gene family
  JOURNAL   Genomics 71 (3), 339-350 (2001)
   PUBMED   11170751
REFERENCE   6  (bases 1 to 3430)
  AUTHORS   Burgess,D.L., Davis,C.F., Gefrides,L.A. and Noebels,J.L.
  TITLE     Identification of three novel Ca(2+) channel gamma subunit genes
            reveals molecular diversification by tandem and chromosome
            duplication
  JOURNAL   Genome Res. 9 (12), 1204-1213 (1999)
   PUBMED   10613843
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AC005988.1, BC034532.1 and
            AC005544.1.
            On Dec 3, 2010 this sequence version replaced gi:22027547.
            
            Summary: The protein encoded by this gene is a type I transmembrane
            AMPA receptor regulatory protein (TARP). TARPs regulate both
            trafficking and channel gating of the AMPA receptors. This gene is
            part of a functionally diverse eight-member protein subfamily of
            the PMP-22/EMP/MP20 family and is located in a cluster with two
            family members, a type II TARP and a calcium channel gamma subunit.
            [provided by RefSeq, Dec 2010].
            
            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.
            
            ##Evidence-Data-START##
            Transcript exon combination :: CD625647.1, BC034532.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025082 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-46                AC005988.1         163387-163432
            47-797              BC034532.1         1-751
            798-798             AC005544.1         110879-110879       c
            799-3426            BC034532.1         753-3380
            3427-3430           AC005544.1         108247-108250       c
FEATURES             Location/Qualifiers
     source          1..3430
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="17"
                     /map="17q24"
     gene            1..3430
                     /gene="CACNG4"
                     /note="calcium channel, voltage-dependent, gamma subunit
                     4"
                     /db_xref="GeneID:27092"
                     /db_xref="HGNC:1408"
                     /db_xref="HPRD:05911"
                     /db_xref="MIM:606404"
     exon            1..268
                     /gene="CACNG4"
                     /inference="alignment:Splign:1.39.8"
     CDS             49..1032
                     /gene="CACNG4"
                     /note="neuronal voltage-gated calcium channel gamma-4
                     subunit; TARP gamma-4; transmembrane AMPAR regulatory
                     protein gamma-4"
                     /codon_start=1
                     /product="voltage-dependent calcium channel gamma-4
                     subunit"
                     /protein_id="NP_055220.1"
                     /db_xref="GI:7656948"
                     /db_xref="CCDS:CCDS11667.1"
                     /db_xref="GeneID:27092"
                     /db_xref="HGNC:1408"
                     /db_xref="HPRD:05911"
                     /db_xref="MIM:606404"
                     /translation="
MVRCDRGLQMLLTTAGAFAAFSLMAIAIGTDYWLYSSAHICNGTNLTMDDGPPPRRARGDLTHSGLWRVCCIEGIYKGHCFRINHFPEDNDYDHDSSEYLLRIVRASSVFPILSTILLLLGGLCIGAGRIYSRKNNIVLSAGILFVAAGLSNIIGIIVYISSNTGDPSDKRDEDKKNHYNYGWSFYFGALSFIVAETVGVLAVNIYIEKNKELRFKTKREFLKASSSSPYARMPSYRYRRRRSRSSSRSTEASPSRDVSPMGLKITGAIPMGELSMYTLSREPLKVTTAASYSPDQEASFLQVHDFFQQDLKEGFHVSMLNRRTTPV
"
     misc_feature    64..654
                     /gene="CACNG4"
                     /note="PMP-22/EMP/MP20/Claudin family; Region:
                     PMP22_Claudin; cl15797"
                     /db_xref="CDD:210197"
     misc_feature    76..138
                     /gene="CACNG4"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBN1.1);
                     transmembrane region"
     misc_feature    370..432
                     /gene="CACNG4"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBN1.1);
                     transmembrane region"
     misc_feature    457..519
                     /gene="CACNG4"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBN1.1);
                     transmembrane region"
     misc_feature    607..669
                     /gene="CACNG4"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UBN1.1);
                     transmembrane region"
     variation       153
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373597428"
     variation       171
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:137917225"
     variation       246
                     /gene="CACNG4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:375744713"
     exon            269..352
                     /gene="CACNG4"
                     /inference="alignment:Splign:1.39.8"
     variation       270
                     /gene="CACNG4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372687382"
     variation       293
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201531279"
     variation       294
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112211002"
     variation       323
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200886756"
     variation       324
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:34743848"
     variation       330
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186352782"
     exon            353..493
                     /gene="CACNG4"
                     /inference="alignment:Splign:1.39.8"
     variation       357
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199620115"
     variation       358
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111539823"
     variation       361
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141844181"
     variation       372
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201073226"
     variation       373
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35104874"
     STS             379..542
                     /gene="CACNG4"
                     /standard_name="Cacng4"
                     /db_xref="UniSTS:499001"
     variation       399
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148482779"
     variation       402
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:9911891"
     variation       406
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139336374"
     variation       440
                     /gene="CACNG4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:79368381"
     variation       457
                     /gene="CACNG4"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:368186078"
     variation       459
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372072866"
     variation       471
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139952030"
     variation       483
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199794639"
     variation       489
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201426250"
     exon            494..3430
                     /gene="CACNG4"
                     /inference="alignment:Splign:1.39.8"
     variation       531
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376902766"
     variation       560
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371128228"
     variation       564
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145497540"
     variation       591
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374300841"
     variation       598
                     /gene="CACNG4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200930655"
     variation       638
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147716893"
     variation       645
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142496896"
     variation       675
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187099750"
     variation       682
                     /gene="CACNG4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199939691"
     variation       720
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377684890"
     variation       727
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200489504"
     variation       772
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375347933"
     variation       773
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202135500"
     variation       787
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200921531"
     variation       798
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11649752"
     variation       799
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370622371"
     variation       807
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145850219"
     variation       820
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376262241"
     variation       825
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375384748"
     variation       882
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368419631"
     variation       884
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149010646"
     variation       893
                     /gene="CACNG4"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:371870032"
     variation       913
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375114114"
     variation       927
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369344199"
     variation       931
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115238163"
     variation       941
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373248340"
     variation       960
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374952962"
     variation       983..984
                     /gene="CACNG4"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35432835"
     variation       996
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:137899115"
     variation       1016
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140902954"
     variation       1029
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372305572"
     variation       1046
                     /gene="CACNG4"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:200543453"
     variation       1052
                     /gene="CACNG4"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375156934"
     variation       1053
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368443497"
     variation       1073
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112749490"
     variation       1140
                     /gene="CACNG4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:193181650"
     variation       1184
                     /gene="CACNG4"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:144635948"
     variation       1205
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138591032"
     variation       1254
                     /gene="CACNG4"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:140217764"
     variation       1294
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112141155"
     variation       1295
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369533890"
     variation       1420
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372355692"
     variation       1452
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150301909"
     variation       1453
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:137947127"
     variation       1468
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201238001"
     variation       1516
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78430187"
     variation       1538
                     /gene="CACNG4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:58736569"
     variation       1652
                     /gene="CACNG4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:740555"
     variation       1849
                     /gene="CACNG4"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:143419199"
     variation       1854
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185149010"
     variation       1907
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143223580"
     variation       1915
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374796587"
     variation       1953
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190790284"
     variation       2101
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147471195"
     variation       2200
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77207567"
     variation       2206
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:193103950"
     variation       2253
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141909519"
     variation       2479
                     /gene="CACNG4"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:184518616"
     variation       2562
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:78886497"
     variation       2587
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:740554"
     variation       2607
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188250082"
     variation       2650
                     /gene="CACNG4"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:139718973"
     variation       2652
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:180730420"
     variation       2711
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200772549"
     variation       2854
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185613832"
     variation       2964
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1051774"
     variation       2976
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:3803816"
     variation       2996
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189491636"
     variation       3105
                     /gene="CACNG4"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:182185420"
     variation       3176
                     /gene="CACNG4"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:3803815"
     variation       3227
                     /gene="CACNG4"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372820548"
     STS             3231..3356
                     /gene="CACNG4"
                     /standard_name="RH93006"
                     /db_xref="UniSTS:85461"
     variation       3248
                     /gene="CACNG4"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:374134133"
     polyA_signal    3404..3409
                     /gene="CACNG4"
     polyA_signal    3408..3413
                     /gene="CACNG4"
     polyA_site      3426
                     /gene="CACNG4"
     polyA_site      3430
                     /gene="CACNG4"
ORIGIN      
gggcgcggcgggccgggccggcgggcggcggactatgaggcgcccaccatggtgcgatgcgaccgcgggctgcagatgctgctgaccacggccggagccttcgccgccttctcgctcatggccatcgccatcggcaccgactactggctgtactccagcgcgcacatctgcaacggcaccaacctgaccatggacgacgggcccccgccccgccgcgcccgcggcgacctcacccactctggtctgtggcgggtgtgctgcatcgaagggatctataaagggcactgcttccggatcaatcacttcccagaggacaatgactacgaccacgacagctcggagtacctcctccgcatcgtgcgagcctccagcgtcttccccatcctcagcaccatcctgctcctgctgggtggcctgtgcatcggtgctggcaggatctacagccgcaagaacaacatcgtcctcagtgccggcatcctcttcgtggctgcaggcctcagtaacatcatcggtatcatcgtctacatttccagcaacacaggtgacccgagtgacaagcgggacgaagacaaaaagaaccattacaactacggctggtctttttactttggagctctgtctttcattgtggctgagaccgtgggcgtcctggctgtaaacatttacattgagaaaaataaagagttgaggtttaagaccaaacgggaattccttaaggcgtcttcctcttctccttatgccaggatgccgagctacaggtaccggcgacggcgctcgaggtccagctcaaggtccaccgaggcctcgccctccagggacgtgtcgcccatgggcctgaagatcacaggggccatccccatgggggagctgtccatgtacacgctgtccagggagcccctcaaggtgaccaccgcagccagctacagccccgaccaggaggccagcttcctgcaggtgcatgactttttccagcaggacctgaaggaaggtttccacgtcagcatgctgaaccgacggacgacccctgtgtgagccgcctgccctttctctccgctccagcctctccccagaacggctctttttgtcacacaggatggcatgtgatcctcaagacgacgaacaatgaactaaagccaaatgcagccctccctggcctccagaggtggcgtgggctggctttgcacgaaggttgtgctgggagaccggacccggggctgcagaagaagctgaaggctgactttgtcccctccccgaaaaagggtgttttgatgcctcagggtctctgaaatctcccgggaagccccagagctttcctgaggctgcctggccttgatcaacttgggaagacaaaattgagccattatctcctcttggaaacgaatcttgccagaaaaacgggatttcagggccttccctccctgcctgggtgtcgggccaccagaaggctctgccggacgccaagaagacggtctctgggctcttgtcagctgcttttgaacctgaggttcctgcgtcgttgagccagaaatcagaccaccgaagctcactcccttcctctccatctctccctctctccaagactctggcagtggcctatgatcctgaagacagctctgcagccaactggtgctttggcctttgcgctgtcccggggccagcttccctcgacctggggaggccgtggcctgtggaggaggcccaggtaaaggctgggggctgttgctggctatcctctttgcttctggaagtttctgcctcactcagaatgggcaggacagacccactgactggacttcagagtctggagggttccatcggtcaggggaatggcggccacgtgacctcttgccgtgccccttgtcatagacccaaggagcaactctgtcccctgagcgttgggggtcccgggggagaggtggacagacacctccctccaactggcatttggcaacaggagcctggacttctgtgcaagaaagggagacctaagggtgaacagtggccaataaaaaccctagagaacaaacatccatttcctaggtggttacaaatcataacttcctgcaaatcaacgccaggagagcaacttaccttcatttctttgtcttaaaaagtagcagcaactggccccacaactcctgtcattgtaagttattctgccaccacctaacaggacggagtggagtgagtttggataaacggaccgagctgggcttctcttcctccctacagaggggagatctcagcactttgtccggagctgaggaagtggtttctgtgttttacagtttttccagccattcttttcttccccctcctgaagcaagcaaagagcgtggaggcgtgtgcaggcttggaagaagaactctccagaacatggaacttaaccctcttttgtataaaacatgtgctttctaaagaaaaattgtttcttattttttgagactccttgatccaccctggaacagtcgcctgtagtcctggtagctgttgtgcttggaaataacgagcgcatccttgcctcagctacctgctcacagcccatgggtggactcggccccctggggttcagacccaggtccgttcggcctagtgatgatgtcatcgtccatcccatcttcctttgcccccaggaaaggacgcatccaccggtagcggccccagctgactgtcgccgtgtgctggggatctgaaatgaggcctgccagggcccctgtgtgctgtgctccagagccttcgctcccatcagggttggcatcatctgatggcatgtccaagtgtgcccagcagcggatgctgaagcaccagagctcaaggccttcacctgctctaggccagccctgtcaccacctccactgccatgaccaggccgaaggcagggaacgccctccccagtcccgctgtccagcaaggccccgagacttttcttctgtgatttccaaaagcaaggcagccgtgctgttctagttcctctccatccgccacctcccctcccgctgccccagaagtttctatcattccatggagaaagctgtgttccaatgaatcctacctcttgcccagtcccaggcagagtaagcagggcccacctagggaccaagaaagagtaggaagaaggggacgagccgggagcaaaaccacctcagacacccgggccttctcagccttctccccgcggccagctgggtctccggggaccctgggccctgggccgcccattcctggccctcccgctgcatctcagacctgacacccaacggggggatgtggtggcctgtgcccaccttctctccctcctcccgacccgccccctcgcccccacccctgtgtgtttcgccagttaagcacctgtgactccagtacctactactggttttgggttggttgttctgtcttttttttaattaaataaaaacatttttaaaatgtt
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:27092 -> Molecular function: GO:0005245 [voltage-gated calcium channel activity] evidence: IEA
            GeneID:27092 -> Biological process: GO:0006810 [transport] evidence: TAS
            GeneID:27092 -> Biological process: GO:0007268 [synaptic transmission] evidence: TAS
            GeneID:27092 -> Biological process: GO:0051899 [membrane depolarization] evidence: TAS
            GeneID:27092 -> Biological process: GO:2000311 [regulation of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate selective glutamate receptor activity] evidence: IDA
            GeneID:27092 -> Cellular component: GO:0005886 [plasma membrane] evidence: TAS
            GeneID:27092 -> Cellular component: GO:0005887 [integral to plasma membrane] evidence: TAS
            GeneID:27092 -> Cellular component: GO:0005891 [voltage-gated calcium channel complex] evidence: IEA
            GeneID:27092 -> Cellular component: GO:0030666 [endocytic vesicle membrane] evidence: TAS
            GeneID:27092 -> Cellular component: GO:0032281 [alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid selective glutamate receptor complex] evidence: ISS

by @meso_cacase at DBCLS
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