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2024-03-29 20:31:07, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_031895               8751 bp    mRNA    linear   PRI 07-JUL-2013
DEFINITION  Homo sapiens calcium channel, voltage-dependent, gamma subunit 8
            (CACNG8), mRNA.
ACCESSION   NM_031895
VERSION     NM_031895.5  GI:313482785
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 8751)
  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 8751)
  AUTHORS   Correia,S.S., Bassani,S., Brown,T.C., Lise,M.F., Backos,D.S.,
            El-Husseini,A., Passafaro,M. and Esteban,J.A.
  TITLE     Motor protein-dependent transport of AMPA receptors into spines
            during long-term potentiation
  JOURNAL   Nat. Neurosci. 11 (4), 457-466 (2008)
   PUBMED   18311135
REFERENCE   3  (bases 1 to 8751)
  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   4  (bases 1 to 8751)
  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 8751)
  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
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AC008440.9 and AF288388.1.
            On Dec 3, 2010 this sequence version replaced gi:24586685.
            
            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.
            The mRNA for this gene is believed to initiate translation from a
            non-AUG (CUG) start codon. [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 :: AF361354.1, AF288388.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025082, ERS025084 [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            non-AUG initiation codon :: inferred from conservation
            ##RefSeq-Attributes-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-140               AC008440.9         107400-107539
            141-1421            AF288388.1         1-1281
            1422-8751           AC008440.9         127250-134579
FEATURES             Location/Qualifiers
     source          1..8751
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="19"
                     /map="19q13.4"
     gene            1..8751
                     /gene="CACNG8"
                     /note="calcium channel, voltage-dependent, gamma subunit
                     8"
                     /db_xref="GeneID:59283"
                     /db_xref="HGNC:13628"
                     /db_xref="HPRD:06063"
                     /db_xref="MIM:606900"
     exon            1..390
                     /gene="CACNG8"
                     /inference="alignment:Splign:1.39.8"
     STS             10..1508
                     /gene="CACNG8"
                     /db_xref="UniSTS:494294"
     STS             10..1416
                     /gene="CACNG8"
                     /db_xref="UniSTS:482833"
     STS             58..1421
                     /gene="CACNG8"
                     /db_xref="UniSTS:480581"
     CDS             108..1385
                     /gene="CACNG8"
                     /note=";
                     non-AUG (CUG) translation initiation codon; neuronal
                     voltage-gated calcium channel gamma-8 subunit; TARP
                     gamma-8; transmembrane AMPAR regulatory protein gamma-8"
                     /codon_start=1
                     /product="voltage-dependent calcium channel gamma-8
                     subunit"
                     /protein_id="NP_114101.4"
                     /db_xref="GI:24586686"
                     /db_xref="CCDS:CCDS33104.1"
                     /db_xref="GeneID:59283"
                     /db_xref="HGNC:13628"
                     /db_xref="HPRD:06063"
                     /db_xref="MIM:606900"
                     /translation="
MESLKRWNEERGLWCEKGVQVLLTTVGAFAAFGLMTIAISTDYWLYTRALICNTTNLTAGGDDGTPHRGGGGASEKKDPGGLTHSGLWRICCLEGLKRGVCVKINHFPEDTDYDHDSAEYLLRVVRASSIFPILSAILLLLGGVCVAASRVYKSKRNIILGAGILFVAAGLSNIIGVIVYISANAGEPGPKRDEEKKNHYSYGWSFYFGGLSFILAEVIGVLAVNIYIERSREAHCQSRSDLLKAGGGAGGSGGSGPSAILRLPSYRFRYRRRSRSSSRSSEPSPSRDASPGGPGGPGFASTDISMYTLSRDPSKGSVAAGLAGAGGGGGGAVGAFGGAAGGAGGGGGGGGGAGAERDRGGASGFLTLHNAFPKEAGGGVTVTVTGPPAPPAPAPPAPSAPAPGTLAKEAAASNTNTLNRKTTPV
"
     misc_feature    156..776
                     /gene="CACNG8"
                     /note="PMP-22/EMP/MP20/Claudin family; Region:
                     PMP22_Claudin; cl15797"
                     /db_xref="CDD:210197"
     misc_feature    162..224
                     /gene="CACNG8"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8WXS5.3);
                     transmembrane region"
     misc_feature    492..554
                     /gene="CACNG8"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8WXS5.3);
                     transmembrane region"
     misc_feature    579..641
                     /gene="CACNG8"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8WXS5.3);
                     transmembrane region"
     misc_feature    729..791
                     /gene="CACNG8"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8WXS5.3);
                     transmembrane region"
     misc_feature    1059..1121
                     /gene="CACNG8"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8WXS5.3);
                     transmembrane region"
     variation       159
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369320889"
     variation       161
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200782558"
     variation       164
                     /gene="CACNG8"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200026820"
     variation       328
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376239386"
     exon            391..474
                     /gene="CACNG8"
                     /inference="alignment:Splign:1.39.8"
     exon            475..615
                     /gene="CACNG8"
                     /inference="alignment:Splign:1.39.8"
     variation       533
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:140141877"
     variation       544
                     /gene="CACNG8"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:202244345"
     variation       553
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370446891"
     variation       557
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145338051"
     variation       569
                     /gene="CACNG8"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:137915042"
     variation       605
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374385020"
     STS             613..800
                     /gene="CACNG8"
                     /standard_name="ECD23507"
                     /db_xref="UniSTS:304491"
     exon            616..8751
                     /gene="CACNG8"
                     /inference="alignment:Splign:1.39.8"
     variation       629
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370574892"
     variation       635
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374191792"
     variation       659
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367756450"
     variation       664
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142463241"
     variation       722
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200934814"
     variation       785
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200225520"
     variation       809
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372632681"
     variation       834
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:377228806"
     STS             1347..1859
                     /gene="CACNG8"
                     /standard_name="ECD13666"
                     /db_xref="UniSTS:294694"
     variation       1548
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:28970637"
     variation       1555
                     /gene="CACNG8"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:180860342"
     variation       1607
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186146252"
     variation       1627..1628
                     /gene="CACNG8"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:200471778"
     variation       1789
                     /gene="CACNG8"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:12973185"
     variation       1956
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189761087"
     variation       2055
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:7254456"
     variation       2093
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7257802"
     variation       2180
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115618479"
     variation       2197
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181390662"
     variation       2222
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185969955"
     variation       2234
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:73937632"
     variation       2244
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:117787324"
     variation       2287
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:117568575"
     variation       2335
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:7257865"
     variation       2491
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:73937633"
     variation       2516
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369083134"
     STS             2525..2726
                     /gene="CACNG8"
                     /standard_name="ECD23005"
                     /db_xref="UniSTS:303990"
     variation       2574
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:113686122"
     variation       2598
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113059121"
     variation       2649
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367595723"
     variation       2662
                     /gene="CACNG8"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:2042177"
     STS             2667..3986
                     /gene="CACNG8"
                     /standard_name="stSG605695"
                     /db_xref="UniSTS:447854"
     variation       2955
                     /gene="CACNG8"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:190728814"
     variation       3091
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139220515"
     variation       3227
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369708843"
     STS             3231..3400
                     /gene="CACNG8"
                     /standard_name="GDB:335751"
                     /db_xref="UniSTS:156601"
     variation       3240
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2362381"
     STS             3267..3295
                     /gene="CACNG8"
                     /standard_name="D3S1674"
                     /db_xref="UniSTS:148451"
     variation       3347
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149036036"
     variation       3382
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2885498"
     variation       3418
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181778842"
     variation       3490..3491
                     /gene="CACNG8"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:144667828"
     variation       3514
                     /gene="CACNG8"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:143235938"
     variation       3527
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:187420599"
     variation       3571
                     /gene="CACNG8"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:4806678"
     variation       3575
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146702230"
     variation       3590
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:4806679"
     STS             3790..4070
                     /gene="CACNG8"
                     /standard_name="ECD20551"
                     /db_xref="UniSTS:301551"
     STS             3792..4822
                     /gene="CACNG8"
                     /standard_name="stSG605696"
                     /db_xref="UniSTS:447855"
     variation       3819
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115048955"
     variation       3850..3851
                     /gene="CACNG8"
                     /replace=""
                     /replace="gcatatggggctg"
                     /db_xref="dbSNP:150317609"
     variation       3862..3863
                     /gene="CACNG8"
                     /replace=""
                     /replace="catatggggctg"
                     /replace="gcatatggggctg"
                     /db_xref="dbSNP:56350202"
     variation       3863..3864
                     /gene="CACNG8"
                     /replace=""
                     /replace="gcatatggggctg"
                     /db_xref="dbSNP:34317654"
     variation       3863
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375126887"
     variation       3864
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368157203"
     variation       3865
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371556113"
     variation       3866
                     /gene="CACNG8"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:374888055"
     variation       3892
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:79918217"
     variation       3917
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192092466"
     variation       4014
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145832422"
     variation       4025
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151114139"
     variation       4055
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182828206"
     variation       4154
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114245623"
     variation       4252
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373498965"
     variation       4372
                     /gene="CACNG8"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:35658524"
     variation       4473..4474
                     /gene="CACNG8"
                     /replace=""
                     /replace="gaga"
                     /replace="gagaga"
                     /db_xref="dbSNP:59675502"
     variation       4474..4475
                     /gene="CACNG8"
                     /replace=""
                     /replace="ga"
                     /replace="gaga"
                     /db_xref="dbSNP:35381014"
     variation       4485..4486
                     /gene="CACNG8"
                     /replace=""
                     /replace="ag"
                     /replace="agagag"
                     /db_xref="dbSNP:71983854"
     variation       4511
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12983116"
     variation       4512
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12983801"
     variation       4556
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12983159"
     variation       4614
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:950799"
     variation       4631
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377472377"
     variation       4682
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370924280"
     variation       4769
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:950798"
     variation       4782
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187681590"
     variation       4785
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10412501"
     variation       4821
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141123564"
     variation       4899
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150272320"
     variation       4924
                     /gene="CACNG8"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:10412355"
     variation       4967
                     /gene="CACNG8"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:7507796"
     variation       4997
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199656921"
     STS             5014..5884
                     /gene="CACNG8"
                     /standard_name="GDB:631802"
                     /db_xref="UniSTS:158429"
     variation       5029
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10412765"
     variation       5036
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10412581"
     variation       5036
                     /gene="CACNG8"
                     /replace="a"
                     /replace="gg"
                     /db_xref="dbSNP:368649513"
     variation       5040
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147056459"
     STS             5150..5219
                     /gene="CACNG8"
                     /standard_name="D1S1423"
                     /db_xref="UniSTS:149619"
     STS             5154..5243
                     /gene="CACNG8"
                     /standard_name="PMC156606P1"
                     /db_xref="UniSTS:271408"
     variation       5186
                     /gene="CACNG8"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:367794075"
     variation       5231
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75573916"
     variation       5252
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11668271"
     variation       5253
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374742311"
     variation       5363
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138424150"
     variation       5420
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191358886"
     variation       5421
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10418582"
     variation       5450
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113862922"
     variation       5453
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142798735"
     variation       5612
                     /gene="CACNG8"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:182581826"
     STS             5707..5797
                     /gene="CACNG8"
                     /standard_name="D8S2279"
                     /db_xref="UniSTS:473907"
     variation       5743
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148455738"
     variation       5806
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187272288"
     variation       5851
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141764811"
     STS             5863..6896
                     /gene="CACNG8"
                     /standard_name="GDB:631813"
                     /db_xref="UniSTS:158430"
     variation       5981
                     /gene="CACNG8"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:199681192"
     variation       6083
                     /gene="CACNG8"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:192103883"
     variation       6116..6117
                     /gene="CACNG8"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:11405166"
     variation       6118..6119
                     /gene="CACNG8"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:199951982"
     variation       6118
                     /gene="CACNG8"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:62145090"
     variation       6136
                     /gene="CACNG8"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:189049509"
     variation       6179
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376503533"
     variation       6204
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:62145091"
     variation       6232
                     /gene="CACNG8"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:77428618"
     variation       6233
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139799177"
     variation       6240
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4806680"
     variation       6241
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79579144"
     variation       6313
                     /gene="CACNG8"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:143199187"
     variation       6371
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146690694"
     variation       6400
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116554941"
     variation       6478
                     /gene="CACNG8"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:112198010"
     variation       6495
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139243248"
     variation       6520
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144397142"
     variation       6537
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:193128086"
     variation       6557
                     /gene="CACNG8"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:374900376"
     variation       6591..6593
                     /gene="CACNG8"
                     /replace=""
                     /replace="aag"
                     /db_xref="dbSNP:58058782"
     variation       6591
                     /gene="CACNG8"
                     /replace=""
                     /replace="aag"
                     /db_xref="dbSNP:35736948"
     variation       6594
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201132784"
     variation       6808..6811
                     /gene="CACNG8"
                     /replace=""
                     /replace="gtgt"
                     /db_xref="dbSNP:148172458"
     variation       6808..6809
                     /gene="CACNG8"
                     /replace=""
                     /replace="gt"
                     /db_xref="dbSNP:371540723"
     variation       6816..6817
                     /gene="CACNG8"
                     /replace=""
                     /replace="tg"
                     /db_xref="dbSNP:5828563"
     variation       6817..6818
                     /gene="CACNG8"
                     /replace=""
                     /replace="tg"
                     /db_xref="dbSNP:34512641"
     variation       6819..6822
                     /gene="CACNG8"
                     /replace=""
                     /replace="tgtg"
                     /db_xref="dbSNP:72431906"
     STS             6820..7969
                     /gene="CACNG8"
                     /standard_name="stSG605697"
                     /db_xref="UniSTS:447856"
     variation       6832..6833
                     /gene="CACNG8"
                     /replace=""
                     /replace="gtgtgt"
                     /db_xref="dbSNP:72241376"
     variation       6838..6841
                     /gene="CACNG8"
                     /replace=""
                     /replace="gtgt"
                     /db_xref="dbSNP:57220250"
     variation       6841..6842
                     /gene="CACNG8"
                     /replace=""
                     /replace="gt"
                     /db_xref="dbSNP:60143367"
     variation       6846..6856
                     /gene="CACNG8"
                     /replace=""
                     /replace="gacacaaaggc"
                     /db_xref="dbSNP:201910959"
     variation       6889
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145298530"
     variation       6902
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373043984"
     STS             6916..7126
                     /gene="CACNG8"
                     /standard_name="RH80031"
                     /db_xref="UniSTS:91103"
     variation       6916
                     /gene="CACNG8"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:370978633"
     variation       6933
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:184409473"
     STS             6956..7591
                     /gene="CACNG8"
                     /standard_name="D8S2282"
                     /db_xref="UniSTS:473910"
     variation       6991
                     /gene="CACNG8"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:2362382"
     variation       7151..7152
                     /gene="CACNG8"
                     /replace=""
                     /replace="aa"
                     /db_xref="dbSNP:10663914"
     variation       7152..7153
                     /gene="CACNG8"
                     /replace=""
                     /replace="aa"
                     /db_xref="dbSNP:368282772"
     variation       7155
                     /gene="CACNG8"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:5828564"
     variation       7160..7161
                     /gene="CACNG8"
                     /replace=""
                     /replace="aa"
                     /db_xref="dbSNP:374466676"
     variation       7167..7168
                     /gene="CACNG8"
                     /replace=""
                     /replace="aa"
                     /db_xref="dbSNP:367798225"
     STS             7184..7468
                     /gene="CACNG8"
                     /standard_name="ECD20439"
                     /db_xref="UniSTS:301442"
     variation       7221
                     /gene="CACNG8"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:80109311"
     variation       7285
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143378252"
     variation       7305
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189243983"
     variation       7396
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112349253"
     variation       7397
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112793050"
     variation       7407
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181172644"
     variation       7582
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151332769"
     variation       7709
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141526501"
     variation       7728
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12979217"
     variation       7812..7825
                     /gene="CACNG8"
                     /replace=""
                     /replace="aaagaaagaaagtc"
                     /db_xref="dbSNP:112369042"
     variation       7819
                     /gene="CACNG8"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:184193581"
     STS             7875..8285
                     /gene="CACNG8"
                     /standard_name="ECD17173"
                     /db_xref="UniSTS:298186"
     variation       7980
                     /gene="CACNG8"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:188919917"
     variation       8095
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147046840"
     variation       8126
                     /gene="CACNG8"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:113473219"
     variation       8161
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113434672"
     variation       8177
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114246373"
     variation       8187
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:4806479"
     variation       8202
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143888524"
     variation       8204
                     /gene="CACNG8"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:66507429"
     variation       8255
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:4806480"
     variation       8341
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150221331"
     variation       8353
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11669989"
     variation       8424
                     /gene="CACNG8"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181556677"
     variation       8448
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73937639"
     variation       8532
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138016807"
     variation       8583
                     /gene="CACNG8"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:112548616"
     STS             8590..8741
                     /gene="CACNG8"
                     /standard_name="WI-22592"
                     /db_xref="UniSTS:34463"
     variation       8650
                     /gene="CACNG8"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186959355"
     variation       8717
                     /gene="CACNG8"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:201974208"
     polyA_signal    8732..8737
                     /gene="CACNG8"
     polyA_site      8751
                     /gene="CACNG8"
ORIGIN      
ggccccccgcttctgcctgcgctgtgaacccccccccagccgccggcacggccccgcccccgctgccccggtggtggcccacggccccccggctgcccgtggtcaaactggagtcgctgaagcgctggaacgaagagcggggcctctggtgcgagaagggggtgcaggtgctgctgacgacggtgggcgccttcgccgccttcggcctcatgaccatcgccatcagcactgactactggctctacacgcgcgccctcatctgcaacaccaccaacctcacggccggcggcgacgacgggaccccccaccgcgggggcggcggcgcctcggagaagaaggaccccggcggcctcacgcactcgggcctctggaggatctgctgcctggaagggttgaaaagaggcgtctgcgtgaagatcaatcatttcccggaggacacggactacgaccacgacagcgcggagtatctactccgagttgtccgggcctccagcatcttccccatccttagcgccatcctgctgctgctcgggggtgtgtgcgtggcggcctcccgcgtctacaagtccaagaggaacatcattctgggcgcagggatcctgttcgtggcagcaggcctgagcaacatcatcggcgtgatcgtgtacatctccgccaacgcgggcgagccgggcccgaagcgggacgaggagaagaaaaaccactactcgtacggctggtccttctacttcggcgggctgtcgttcatcctggccgaggtgataggcgtgctggccgtcaacatctacatcgagcgcagccgcgaggcgcactgccagtctcgctcggacctgctcaaggccggcgggggcgcgggcggcagtggcgggagcggcccctcggccatcctccgtctgcccagttaccgcttccgctaccgccgccgctcccgctctagctcccgctccagcgagccgtcgccgtcgcgggacgcgtctcccggcggccccgggggcccgggctttgcctccacggacatctccatgtacacgctcagccgcgacccctccaagggcagcgtggccgcggggctggcgggggccggcggcggcggcggcggcgccgtgggggcgttcggcggcgcggccgggggcgccgggggcggcggcggaggcggcggcggggcgggtgccgagcgggaccgcgggggggcgtccggcttcctcacgctgcacaacgccttccccaaggaggcgggcggcggcgtcacggtcacggtcaccgggccgcccgccccgcccgcgcccgcgccacccgcgccctctgcgcccgcccccgggaccctggccaaggaggccgccgcctccaacaccaacacgctcaacaggaaaaccacgcctgtgtaggggcgcggcgggggagccgaggggcgtgtccggggcgcgtgcgcgggcgcgcgtgcatcgaggctgccggggtcgggggcgcccccgctttcccccgtgagcgcgctggagactgctgggcccgccccacgcccaccctccccgcccccctccccctccgaagcagggaccccgagggagggggcaggggagggagggggccgctgtgagggagcgtcgtgttttatttttttgggggatctatggggaggggggagggccatggtgttttttgcagtttcgagatgttttctttttcatgttttgctgtgtgcatggggggcggggcggggggaggggagggagggactcccagcccagcccaactcctggagaggggcccataatacacgaatacatagttacacccacaaactatatatatgccctatataaagagacacagcgaagggatgcagaaaggcagaaagaagggttggacgcgggcattcattcatttttttcattcattattccacaagggcttattaagcacctactgtgtaccaggcactggtacataagaaggcattggagcaggggacacgaacgaggcacagaaagggccttctcattcattcattcattaccggcaatttatttgtgcgccttaaaaagctaggcattgtgctccgtgctcagcgtgcaggaggcaggaaaacagccaggggccccgacgtctcatagagtaaacatcttgtgcatgagacaggcattaatcgatcatgtacatacacaataaattacagttaggctataggagaaacgagatgctatgaaatgctccatcaggggagcctaacccagttgtgaggaagagatttcagtggacagtgaaaggatgagaagaagccagcagggcggagctggggcaggagtgtggcaggcagagcagcacgtgcaaaggccccggggcaggaaggagcttgcagcgagggctgaagggtagtgaggcaggtgagcggggatcaaggtgaggccggagacacagacagggccagattgtgcaggggctcgtaggtcaggagttcagattttattctaggagtggtgagggccgtggaacgggtttaagcaggacgctaacgtgaatggtgtacaaagggaagacaggaactcggaggcaagagtaggaggcagagatgtgctgaaatacagcatcaaacatgggcacgggcccttggagctcacactcttgtgggaggaagcacgtaattacacagatgctgaagcatagtcatggtgtctggtgtgcaggagaaagccgtggggcttagagactcatgtgtctgtcactcgttcattcagccactcacccattgccatttttggccatctgctaaggtaccaggaagtgtgttaggatccagatccccaggggtgaaacagactctagccctgctctcaagcagtttattgtcatcaaacaccgccatccaggcagggcaatcggtgctggaacccggaccaccgtgggtaccgtggcacacggtggacagagtgaccaactgccaggagtgagcagcacttggggtaggcttcctggagaatatgatgcccattctgggtcttgaagaaatgagtgggcatcttctggttgatgaaaggcatgagaaaggcttgtggggccaaagaacaacttgggtgaaaacgggaggaagtgaacgagcatgatgtattggggtcagtgctaacagttctgggatgctgatgtacaaggtggggctgggagatgaggccgggaaagtagccacaagctagagtgtaaaggtaccagggtggccgggcgcggtggctcatgcctgtaatcccagcgctttgggaggctgaggctggagtatcacttgagcccaggagtttgagaccagcctggataacatggcgaaaccctgtctctacaaaacattaaaaaaaattagccgggcgtggtggagcacacctgtggacacagctactcaggaggctgagggaggaggaccatttgactccaagagttcgaggctgcagtgagctaggatcgcggcactacactccagcctgagcaacagactgagatcctgtctcagaaaaaaagagaaaaaggtgcctgagttccaggcagagggactgaggctcttctaaggatggtgagagaggatgacagctgcgcgggggcaagggctgtgcggtgattggaggggatgggtttgaagttcactgagaaggcagaggggacagcgcccagtaggcttcccttccatatttgctcagcaagtgtttcctgaggcctcccccgaagccttgtgctgggcggtgctgggagtggagaggtgattttgatcttgccctgctctcaaggggctcccagtctggcgggaaaacaggcacagacgcagcttgaggaggacgtggcagcggtggtgccatgctgccaggggctctgcgtgcccttctcttgacggaagggtacagatcagagctgggtgttcagaatttctctccgaggcctgtgtggaaggaccaggaagagagagactgaaggtccctaggaagaattctgccaaggcggtttcaggaagagatgctgggaaatgtaggaaaaggaatacaaatcagtgagacggagaagcgctgagtgagagagacggatacgtggagagaagagggatgccggagcgggtgttaaaagagacaaatctggccgggtgctgtggctcctaatcccagcactttgggagactgaggcaggcagattgagctcaggagttccagaccagccaacatattgaaatcttgtctctaccaaaaatacaaaaattagccgggtgtggtggtgcacgcctgtagtcccggctactcaggaggctgaggtgaaaggatctcgcttgggcctgggagggtgaggctgcagtgacccgtgatggcaccactgcgctccagcctgggcgaaagagcgagactctgtctcaaaaaaaaaaaaaaaattgagagacagcaaatatttgctggaagagggagagggaactggttaggggagaatggattctagagtctgaaggccaaacagaacgagagagagagagagagagagagaaagaatgaggttgagggtaggcaggaggaagagcaagatggggagggagggggagagcaggagagaccaaactagtagagtcacagacagagaaaaagtcaaagacaggaaggtgatacagaggagagagaagaggaagaggagagactgacaggtgcacaaatcagagaagtcccagagatagcagaaacacacacagagacagagatagagagggagaggtaagccggagacagactcagagattcgcacaaaaagcaacgtggagactcagaagcaagcgcagcgtcaaggaatgctccatttctggtgtgttgttttcccagtattcaagaaatatttattgagtgccaacctgttctagacccaatctcggccaggggatgtggtggcaaatagacggacaagggcctgctctcctgaaacacactggagagataaacaataaataatatcatttcagtaaccaaaaagtgctttaaaaattaagctgaaggccgggcgcagtggctcatgcctgtaatcccagcactttgggaggccgaggctggtggatcacttgaggtcaggagttcgagaccagcctggtcaacatggtgaaacttcatctctaccaataaataaataaagtagctgggtgtgctggtgtgcctgtagtcccagctacttgggaggctgagaaagaaggatcacttgaacccaggaggcagaggttgcagtgagctgagatcgcgccactgcactccagcctgggcgacagtgagtggtaacagaatgacagagcaaggatgactttagatgaggtccttggagtagaccttgtggcagaggtcacagagatgtggattgtgagtaggaaagagaggtgagaaagtctgggggccaggcattccacccaccagaggcagccccaaagcccagaaaagtagcaggtcttcgaggaggcctgtgcggtgagcagatccaccataggacagaggcacagggtaggggctgatcagttagggccttggatccttgggaagaaatctgaattttattctagatctgatgggaagtgcttggagggttttgagcacaggcatgccatgatcatatttttattttcttatttatatttattttgaaaaagagtcttgctctgtctcaggctggagtccagtgggctgatctcggctcactgccaacctccgcctcccaagttcaagtgattctcctgcctcagcctcctgagtagctgggattacaggcatgtgccaccacgcctggctaatttttttgtatttttagtaaagacgggatttcaccgtgttggccaggccaatctgaaattcctggcttcaaatgatccacctgcctcggcctcccaaaatgctgggattacaggagtgagccactgcgcccggcctcatatttttatttaaacaagaacagcagaattacattgctgtgctgagcatacgtagacttcaggagtcaaaggggaaggaaggaggtagcgggctgttgccttcctctggttgctggaggcctggaccaaggtggagttagtgggatggaggaagtggaagaaggcatgggattttggaggctagagcctgcattggtggtgaactggatgtcatagaggagggaaggaaaaggaaccaggaagagaagaactctctgaattgggcacgcacatctctgatgggcaccgatgaggattgttaccaggaacgaggagactgggatcaggaaagtggctttgggagggaggaaccaaggcttctcttttggatgtgtcaagatagatctgccttcgagaaatccgagttgtggtatcaaatagccagttggatatgtgagactggagtttgggggaaagagaggccgtggctcaaaaacgtaagttttggaaacgtcaacataaagccacaggattgggtgacgtggcctagcaggggggtggggacagagaagcgaccctggccagagccttggggacatctacatctgggggagaaggggatgtagcaaaacgagcttaggagtgatctcgaggtaggctgaaaccaggagggttacagagggcaaatgcacctttgtgtttcaagaaggagaggagacagccagctgtgccaagggctgctgagacttggacaaggatgcagagagcagagtgaccattaggtctgatgacatggacagggttggtgatcttgataagataagatgtcagttcagtgcagtggtggggacagaagccctgctggagtggaggggagagagaatttggggggaagacagaaggaaagggaattcaggcaagtgtgtgtgtgtgtgtgtgtgtgtgtgtgtgtgtaactgacacaaaggccaggtgcgatggctcacgtgtgtaatcccagcactttgggaggccgaagtgggtggatcacttgaggtcaggagttcgagaccagcctggccaatatggtgaaaccccgtctctactaaaaatacagaaattagacaggtgcggtggtgcacacctgtaatcccagctacttgagaggctgaagcaggagaatctcttgggcccaggaggcagaggttgcagtgagccaagatcacaccactgcactctagcctgggtgacagagcaagactctgtctcaaaaaagaaaaaaggtaaaaaaaaaaaaaaatgaccctgaaaggaagtagggagacatgcagatagggagatgggaggcagaaaattgcatcctgcaattagctgtcacagcaggcaggagcaagagagatggggaagcccagggccaggaggggaagatgaattcagggggcagggaagagaggatgctgtcagctaggctctggcagatcccctagccagggatgctctgcccagctcctgtctcttgctgctgtcagcgccgggcacactctgggattccccctgtagaccctgtcaagacctattgaggtgaaggggaagaacacgttttcatcattcattttcagaaataaacattcactcagttcttggaaatactttctggccaggcttgggggctcatgcctgtaatcccagcactctgggaggccaagacaggaggattgcttgaggcttggcgtttgagaccagcctgggcaatatagtaagaccccgtctctacaaaaatgaaaaatgagctgtggcgtggtggctcacgcctgtagtcctagatactcgggaggctgaggcgggaggattgcttgagtccaggagtttaaggttgcagtgagctatgattgcaccattgcacttcaggctgggccacagagcaagaccctgtctcagaaaacagaaagaaagaaagtcaaagaaataaagtcaaagacaagaaggtgatacagagaagacagaaaaggaggaggagagagactgacaggtacacaaatcagagaagtcccagagataacaaaaacacaaccacagagatagggagacgtaagccggagaaagacccagagattcgcatagaaagcaacgtggagactcagaagcaagcacagcatcaaggaatgatcaataaaaagaaaaaaaaatatttcctgaggacttccaagtacaaggccctgcaatctcaggccacttctgtcccatctctgccttcagagggggggacaggtagtccagacaattagaatacagagggggctgtgttctgacggggccacgcgggcattgaggaaacgcagcaggcccctcccctagctggggcggggatgtctgtgtgccatcatctcactccatctggtcattcctttgcccattcatccatccattcattcaagtcaccccatgcacattttccaagactgcctgtgacctggccctgtgccgggtagagctgaggatgccaaggtgaattcctcctgtgcctggccccggccccagtctgctggaagaaccagacacagacaatcacactgcggggaaacacgtgctccatcggaaaagtccagagcagggggtgggcagagaggcccagcgtgcaccagagcctcgctcaggtcagcgccaggcctgcctggagcagccaactgtgggagaagaaggagttggtgaaaggtgggtcccacctgggccgtccacagaagggctgaggggtagggggtgaggggttgaagatcaggccctgccgccatgccacacggctgtcctctgtccctgctcctgggggagctgaaactgcatggaaggtcccccaggggtgccccgtctaataaactcgatgaagagga
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:59283 -> Molecular function: GO:0005245 [voltage-gated calcium channel activity] evidence: NAS
            GeneID:59283 -> Biological process: GO:0006816 [calcium ion transport] evidence: NAS
            GeneID:59283 -> Biological process: GO:0007268 [synaptic transmission] evidence: TAS
            GeneID:59283 -> Biological process: GO:2000311 [regulation of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate selective glutamate receptor activity] evidence: IDA
            GeneID:59283 -> Cellular component: GO:0005886 [plasma membrane] evidence: TAS
            GeneID:59283 -> Cellular component: GO:0005891 [voltage-gated calcium channel complex] evidence: NAS
            GeneID:59283 -> Cellular component: GO:0014069 [postsynaptic density] evidence: ISS
            GeneID:59283 -> Cellular component: GO:0030054 [cell junction] evidence: IEA
            GeneID:59283 -> Cellular component: GO:0030666 [endocytic vesicle membrane] evidence: TAS
            GeneID:59283 -> Cellular component: GO:0032281 [alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid selective glutamate receptor complex] evidence: ISS
            GeneID:59283 -> Cellular component: GO:0045211 [postsynaptic membrane] evidence: IEA

by @meso_cacase at DBCLS
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