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2024-03-29 07:39:48, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_000727               1327 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens calcium channel, voltage-dependent, gamma subunit 1
            (CACNG1), mRNA.
ACCESSION   NM_000727
VERSION     NM_000727.3  GI:313482780
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 1327)
  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   2  (bases 1 to 1327)
  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   3  (bases 1 to 1327)
  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   4  (bases 1 to 1327)
  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
REFERENCE   5  (bases 1 to 1327)
  AUTHORS   Wagner,T., Tommerup,N., Wirth,J., Leffers,H., Zimmer,J., Back,E.,
            Weissenbach,J. and Scherer,G.
  TITLE     A somatic cell hybrid panel for distal 17q: GDIA1 maps to 17q25.3
  JOURNAL   Cytogenet. Cell Genet. 76 (3-4), 172-175 (1997)
   PUBMED   9186513
REFERENCE   6  (bases 1 to 1327)
  AUTHORS   Olckers,A., Jedlicka,A.E., Powers,P.A., Hogan,K., Gregg,R.G. and
            Levitt,R.C.
  TITLE     G to A polymorphism in the CACNLG gene
  JOURNAL   Hum. Mol. Genet. 2 (12), 2198 (1993)
   PUBMED   8111396
REFERENCE   7  (bases 1 to 1327)
  AUTHORS   Powers,P.A., Liu,S., Hogan,K. and Gregg,R.G.
  TITLE     Molecular characterization of the gene encoding the gamma subunit
            of the human skeletal muscle 1,4-dihydropyridine-sensitive Ca2+
            channel (CACNLG), cDNA sequence, gene structure, and chromosomal
            location
  JOURNAL   J. Biol. Chem. 268 (13), 9275-9279 (1993)
   PUBMED   8387489
REFERENCE   8  (bases 1 to 1327)
  AUTHORS   Iles,D.E., Segers,B., Weghuis,D.O., Suikerbuijk,R. and Wieringa,B.
  TITLE     Localization of the gamma-subunit of the skeletal muscle L-type
            voltage-dependent calcium channel gene (CACNLG) to human chromosome
            band 17q24 by in situ hybridization and identification of a
            polymorphic repetitive DNA sequence at the gene locus
  JOURNAL   Cytogenet. Cell Genet. 64 (3-4), 227-230 (1993)
   PUBMED   8404045
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from DA898357.1, BC113486.1,
            AF086300.1 and AC005544.1.
            On Dec 3, 2010 this sequence version replaced gi:22027542.
            
            Summary: Voltage-dependent calcium channels are composed of five
            subunits. The protein encoded by this gene represents one of these
            subunits, gamma, and is one of two known gamma subunit proteins.
            This particular gamma subunit is part of skeletal muscle
            1,4-dihydropyridine-sensitive calcium channels and is an integral
            membrane protein that plays a role in excitation-contraction
            coupling. 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 that function as transmembrane AMPA
            receptor regulatory proteins (TARPs). [provided by RefSeq, Dec
            2010].
            
            ##Evidence-Data-START##
            Transcript exon combination :: L07738.1, BC113486.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084, ERS025087 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-65                DA898357.1         1-65
            66-852              BC113486.1         1-787
            853-1011            AF086300.1         257-415
            1012-1012           AC005544.1         85160-85160         c
            1013-1327           AF086300.1         417-731
FEATURES             Location/Qualifiers
     source          1..1327
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="17"
                     /map="17q24"
     gene            1..1327
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /note="calcium channel, voltage-dependent, gamma subunit
                     1"
                     /db_xref="GeneID:786"
                     /db_xref="HGNC:1405"
                     /db_xref="HPRD:00249"
                     /db_xref="MIM:114209"
     exon            1..354
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /inference="alignment:Splign:1.39.8"
     STS             66..852
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /db_xref="UniSTS:484296"
     variation       69
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:35542901"
     misc_feature    72..74
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /note="upstream in-frame stop codon"
     STS             76..844
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /db_xref="UniSTS:481708"
     variation       79
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368365252"
     variation       85
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375981836"
     variation       89
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139967780"
     variation       93
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374628258"
     variation       110
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377715475"
     variation       111
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371173127"
     variation       118
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202072611"
     variation       122
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:369850574"
     CDS             126..794
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /note="neuronal dihydropyridine-sensitive calcium channel
                     gamma subunit; L-type calcium channel gamma polypeptide;
                     dihydropyridine-sensitive L-type, skeletal muscle calcium
                     channel subunit gamma"
                     /codon_start=1
                     /product="voltage-dependent calcium channel gamma-1
                     subunit"
                     /protein_id="NP_000718.1"
                     /db_xref="GI:4502539"
                     /db_xref="CCDS:CCDS11668.1"
                     /db_xref="GeneID:786"
                     /db_xref="HGNC:1405"
                     /db_xref="HPRD:00249"
                     /db_xref="MIM:114209"
                     /translation="
MSQTKMLKVRVTLFCILAGIVLAMTAVVTDHWAVLSPHMEHHNTTCEAAHFGLWRICTKRIPMDDSKTCGPITLPGEKNCSYFRHFNPGESSEIFEFTTQKEYSISAAAIAIFSLGFIILGSLCVLLSLGKKRDYLLRPASMFYAFAGLCILVSVEVMRQSVKRMIDSEDTVWIEYYYSWSFACACAAFILLFLGGLALLLFSLPRMPRNPWESCMDAEPEH
"
     misc_feature    156..212
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q06432.1);
                     transmembrane region"
     misc_feature    174..665
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /note="PMP-22/EMP/MP20/Claudin tight junction; Region:
                     Claudin_2; pfam13903"
                     /db_xref="CDD:206074"
     misc_feature    438..512
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q06432.1);
                     transmembrane region"
     misc_feature    543..590
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q06432.1);
                     transmembrane region"
     misc_feature    663..737
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q06432.1);
                     transmembrane region"
     variation       153
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144718253"
     variation       154
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200166315"
     variation       170
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138597553"
     variation       185
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200565506"
     variation       192
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370512622"
     variation       196
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374725823"
     variation       212
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141232994"
     variation       224
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150777707"
     variation       233
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138069395"
     variation       250
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200630535"
     variation       257
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367858834"
     variation       263
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140686694"
     variation       264..265
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:34848220"
     variation       269
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144676810"
     variation       280
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199612249"
     variation       286
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:202046182"
     variation       289
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200686073"
     variation       315..316
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35983508"
     variation       317
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200115411"
     variation       339
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139913144"
     exon            355..429
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /inference="alignment:Splign:1.39.8"
     variation       379
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202020889"
     variation       390
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371843031"
     variation       401
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376099391"
     exon            430..567
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /inference="alignment:Splign:1.39.8"
     variation       431
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374291670"
     variation       449
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200335785"
     variation       456
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376840748"
     variation       488
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:143842742"
     variation       498
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147258815"
     variation       506
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140836897"
     variation       513
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142384274"
     variation       545
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151308706"
     variation       563
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112631391"
     variation       564
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139399934"
     exon            568..1320
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /inference="alignment:Splign:1.39.8"
     variation       587
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114830174"
     variation       608
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201378629"
     variation       615
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:143055819"
     variation       616
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140761602"
     variation       639
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368486677"
     variation       640
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112255499"
     variation       652
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144606776"
     variation       678
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146687061"
     variation       686
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148854871"
     variation       687
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372713806"
     variation       702
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372395180"
     variation       709
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:377293425"
     variation       711
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1799938"
     variation       726
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148046092"
     variation       741
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374071089"
     variation       742
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148226819"
     variation       750
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371885900"
     variation       763
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:146071095"
     variation       786
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138929263"
     variation       803
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:9912133"
     variation       812
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115573053"
     variation       813
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201720862"
     STS             822..1148
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /standard_name="SHGC-12505"
                     /db_xref="UniSTS:50748"
     variation       827
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:141132419"
     variation       839
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202044777"
     variation       840
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:375091485"
     variation       990
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111645684"
     variation       999
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:76510674"
     variation       1011
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:833"
     variation       1012
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2684"
     variation       1078..1079
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:374936894"
     variation       1080..1085
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace=""
                     /replace="tgtccc"
                     /db_xref="dbSNP:368003478"
     variation       1087
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:374852027"
     STS             1163..1296
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /standard_name="RH17604"
                     /db_xref="UniSTS:55591"
     variation       1170
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375880771"
     variation       1256
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:369152142"
     polyA_signal    1301..1306
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
     polyA_site      1320
                     /gene="CACNG1"
                     /gene_synonym="CACNLG"
ORIGIN      
acactaaacttagtggccactcccagctcgacaaccactgccaccccccaagctcggcttgtcacctgccctaggagacgcagccgccggaccctgcccagggcacccacgcctcggcgaccaccatgtcccagaccaaaatgctgaaggtccgcgtgaccctcttctgcatcctggcaggcatcgtgctggccatgacagccgtggtaaccgaccactgggctgtgctgagcccccacatggagcaccacaacactacctgcgaggcggcccacttcggcctctggcggatttgtaccaagcgcatccccatggacgacagcaagacctgcgggcccatcaccctgcccggggagaagaactgttcctacttcaggcattttaaccccggcgagagctcggagatcttcgaattcaccactcagaaggagtacagcatctcggcagccgccatcgccatcttcagccttggcttcatcatcctgggcagcctctgtgtcctcctgtccctcgggaagaagagggactatctgctgcgacccgcgtccatgttctatgcctttgcaggtctctgcatcctcgtctcggtggaggtcatgcggcagtcggtgaagcgcatgattgacagtgaggacaccgtctggatcgagtactattactcctggtcctttgcctgcgcctgtgccgccttcatcctcctctttctcggcggtctcgccctcctgctgttctccctgcctcgaatgccccggaacccatgggagtcctgcatggatgctgagcccgagcactaaccctcctgcggccctagcgaccctcaggcttcttccccaggaagcggggtcttggcctggaaccttccagagaggaggcgggagcaattttagccccaccctgctcccatctgcccccctgcaacagtcgcaggctgcttcctctctctgagttcctctgggctgccgcaggctcccctgggaatagagcaagacgtgagtcctaacctggccacagttgggggaggcagagccagcaggtggacaggtgtttgcaggggcccaacttcccctggagctcagaggtgtccccactgtaccagcctctgataagctgcctccagttgtcctttatgaacattgcagggacaacctgtgtttgccagctgggtgttccgtgtaaatagccagcctgtctctttctcggtgataaaacacaccctctctggtgagcccagcgtcccctccttggcttccaggagccctgggaagcatttttaactgggtagaatctgactgtggcttgaaataaaaagctctcagaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:786 -> Molecular function: GO:0005245 [voltage-gated calcium channel activity] evidence: IEA
            GeneID:786 -> Biological process: GO:0006810 [transport] evidence: TAS
            GeneID:786 -> Biological process: GO:0006936 [muscle contraction] evidence: TAS
            GeneID:786 -> Biological process: GO:0070296 [sarcoplasmic reticulum calcium ion transport] evidence: IEA
            GeneID:786 -> Cellular component: GO:0005891 [voltage-gated calcium channel complex] evidence: IEA

by @meso_cacase at DBCLS
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