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2024-03-29 14:45:54, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001001485            3712 bp    mRNA    linear   PRI 15-JUN-2013
DEFINITION  Homo sapiens ATPase, Ca++ transporting, type 2C, member 1 (ATP2C1),
            transcript variant 3, mRNA.
ACCESSION   NM_001001485
VERSION     NM_001001485.2  GI:312836760
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 3712)
  AUTHORS   Li,X., Zhang,D., Xiao,S. and Peng,Z.
  TITLE     Four novel mutations of the ATP2C1 gene in Chinese patients are
            associated with familial benign chronic pemphigus
  JOURNAL   Clin. Exp. Dermatol. 37 (7), 797-799 (2012)
   PUBMED   22607350
  REMARK    GeneRIF: we report four novel mutations of the ATP2C1 gene involved
            in HHD, expanding the repertoire of ATP2C1 mutations underlying
            HHD.
REFERENCE   2  (bases 1 to 3712)
  AUTHORS   Raiko,L., Siljamaki,E., Mahoney,M.G., Putaala,H., Suominen,E.,
            Peltonen,J. and Peltonen,S.
  TITLE     Hailey-Hailey disease and tight junctions: Claudins 1 and 4 are
            regulated by ATP2C1 gene encoding Ca(2+) /Mn(2+) ATPase SPCA1 in
            cultured keratinocytes
  JOURNAL   Exp. Dermatol. 21 (8), 586-591 (2012)
   PUBMED   22639968
  REMARK    GeneRIF: SPCA1 regulates the levels of claudins 1 and 4, but does
            not affect desmosomal protein levels in keratinocytes.
REFERENCE   3  (bases 1 to 3712)
  AUTHORS   Gu,S.Q., Bakthavachalu,B., Han,J., Patil,D.P., Otsuka,Y., Guda,C.
            and Schoenberg,D.R.
  TITLE     Identification of the human PMR1 mRNA endonuclease as an
            alternatively processed product of the gene for peroxidasin-like
            protein
  JOURNAL   RNA 18 (6), 1186-1196 (2012)
   PUBMED   22543864
  REMARK    GeneRIF: Human PMR1 bound to c-Src, was tyrosine phosphorylated,
            sedimented on polysomes, and catalyzed the selective decay of a
            PMR1 substrate mRNA. Human PMR1 expression stimulated cell
            motility.
REFERENCE   4  (bases 1 to 3712)
  AUTHORS   Zhang,D., Li,X., Xiao,S., Huo,J., Wang,S. and Zhou,P.
  TITLE     Detection and comparison of two types of ATP2C1 gene mutations in
            Chinese patients with Hailey-Hailey disease
  JOURNAL   Arch. Dermatol. Res. 304 (2), 163-170 (2012)
   PUBMED   22124882
  REMARK    GeneRIF: genetic polymorphism is associated with Hailey-Hailey
            disease in Chinese patients
REFERENCE   5  (bases 1 to 3712)
  AUTHORS   Zhang,H.Z., Tian,H.Q., Du,D.H., Wang,G.J., Yan,X.X., Liu,H.,
            Zhou,G.Z., Fu,X.A., Yu,Y.X., Yu,G.Q., Liu,H.X. and Zhang,F.R.
  TITLE     Analysis of ATP2C1 gene mutations in Chinese patients with
            Hailey-Hailey disease
  JOURNAL   Clin. Exp. Dermatol. 37 (2), 190-193 (2012)
   PUBMED   21883398
  REMARK    GeneRIF: we report five novel mutations and four recurrent
            mutations of the ATP2C1 gene in Chinese patients. This further
            expands the mutation spectrum in Hailey-Hailey Disease.
REFERENCE   6  (bases 1 to 3712)
  AUTHORS   Ton,V.K., Mandal,D., Vahadji,C. and Rao,R.
  TITLE     Functional expression in yeast of the human secretory pathway
            Ca(2+), Mn(2+)-ATPase defective in Hailey-Hailey disease
  JOURNAL   J. Biol. Chem. 277 (8), 6422-6427 (2002)
   PUBMED   11741891
REFERENCE   7  (bases 1 to 3712)
  AUTHORS   Dobson-Stone,C., Fairclough,R., Dunne,E., Brown,J., Dissanayake,M.,
            Munro,C.S., Strachan,T., Burge,S., Sudbrak,R., Monaco,A.P. and
            Hovnanian,A.
  TITLE     Hailey-Hailey disease: molecular and clinical characterization of
            novel mutations in the ATP2C1 gene
  JOURNAL   J. Invest. Dermatol. 118 (2), 338-343 (2002)
   PUBMED   11841554
  REMARK    GeneRIF: failed to yield any clear correlation between the nature
            of the mutation and clinical features of Hailey-Hailey disease.
REFERENCE   8  (bases 1 to 3712)
  AUTHORS   Sudbrak,R., Brown,J., Dobson-Stone,C., Carter,S., Ramser,J.,
            White,J., Healy,E., Dissanayake,M., Larregue,M., Perrussel,M.,
            Lehrach,H., Munro,C.S., Strachan,T., Burge,S., Hovnanian,A. and
            Monaco,A.P.
  TITLE     Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a
            novel Ca(2+) pump
  JOURNAL   Hum. Mol. Genet. 9 (7), 1131-1140 (2000)
   PUBMED   10767338
REFERENCE   9  (bases 1 to 3712)
  AUTHORS   Hu,Z., Bonifas,J.M., Beech,J., Bench,G., Shigihara,T., Ogawa,H.,
            Ikeda,S., Mauro,T. and Epstein,E.H. Jr.
  TITLE     Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey
            disease
  JOURNAL   Nat. Genet. 24 (1), 61-65 (2000)
   PUBMED   10615129
REFERENCE   10 (bases 1 to 3712)
  AUTHORS   Ikeda,S., Welsh,E.A., Peluso,A.M., Leyden,W., Duvic,M.,
            Woodley,D.T. and Epstein,E.H. Jr.
  TITLE     Localization of the gene whose mutations underlie Hailey-Hailey
            disease to chromosome 3q
  JOURNAL   Hum. Mol. Genet. 3 (7), 1147-1150 (1994)
   PUBMED   7981684
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from DA405579.1, BC028139.1 and
            AF225981.1.
            On Nov 25, 2010 this sequence version replaced gi:48762686.
            
            Summary: The protein encoded by this gene belongs to the family of
            P-type cation transport ATPases. This magnesium-dependent enzyme
            catalyzes the hydrolysis of ATP coupled with the transport of
            calcium ions. Defects in this gene cause Hailey-Hailey disease, an
            autosomal dominant disorder. Alternatively spliced transcript
            variants encoding different isoforms have been identified.
            [provided by RefSeq, Aug 2011].
            
            Transcript Variant: This variant (3) has an alternate 5' sequence
            and lacks an internal exon in the 3' region, as compared to variant
            6. The resulting isoform (1c) has shorter and distinct N- and
            C-termini, as compared to isoform 2a. Variants 3 and 11 encode the
            same isoform 1c.
            
            Publication Note:  This RefSeq record includes a subset of the
            publications that are available for this gene. Please see the Gene
            record to access additional publications.
            
            ##Evidence-Data-START##
            Transcript exon combination :: BC028139.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025082, ERS025086 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-311               DA405579.1         1-311
            312-3665            BC028139.1         1-3354
            3666-3712           AF225981.1         3412-3458
FEATURES             Location/Qualifiers
     source          1..3712
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="3"
                     /map="3q22.1"
     gene            1..3712
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /note="ATPase, Ca++ transporting, type 2C, member 1"
                     /db_xref="GeneID:27032"
                     /db_xref="HGNC:13211"
                     /db_xref="MIM:604384"
     exon            1..323
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            324..509
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    471..473
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /note="upstream in-frame stop codon"
     CDS             504..3170
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /EC_number="3.6.3.8"
                     /note="isoform 1c is encoded by transcript variant 3;
                     secretory pathway Ca2+/Mn2+ ATPase 1; ATPase,
                     Ca(2+)-sequestering; ATPase 2C1; HUSSY-28;
                     calcium-transporting ATPase type 2C member 1;
                     ATP-dependent Ca(2+) pump PMR1"
                     /codon_start=1
                     /product="calcium-transporting ATPase type 2C member 1
                     isoform 1c"
                     /protein_id="NP_001001485.1"
                     /db_xref="GI:48762687"
                     /db_xref="CCDS:CCDS46913.1"
                     /db_xref="GeneID:27032"
                     /db_xref="HGNC:13211"
                     /db_xref="MIM:604384"
                     /translation="
MKVARFQKIPNGENETMIPVLTSKKASELPVSEVASILQADLQNGLNKCEVSHRRAFHGWNEFDISEDEPLWKKYISQFKNPLIMLLLASAVISVLMHQFDDAVSITVAILIVVTVAFVQEYRSEKSLEELSKLVPPECHCVREGKLEHTLARDLVPGDTVCLSVGDRVPADLRLFEAVDLSIDESSLTGETTPCSKVTAPQPAATNGDLASRSNIAFMGTLVRCGKAKGVVIGTGENSEFGEVFKMMQAEEAPKTPLQKSMDLLGKQLSFYSFGIIGIIMLVGWLLGKDILEMFTISVSLAVAAIPEGLPIVVTVTLALGVMRMVKKRAIVKKLPIVETLGCCNVICSDKTGTLTKNEMTVTHIFTSDGLHAEVTGVGYNQFGEVIVDGDVVHGFYNPAVSRIVEAGCVCNDAVIRNNTLMGKPTEGALIALAMKMGLDGLQQDYIRKAEYPFSSEQKWMAVKCVHRTQQDRPEICFMKGAYEQVIKYCTTYQSKGQTLTLTQQQRDVYQQEKARMGSAGLRVLALASGPELGQLTFLGLVGIIDPPRTGVKEAVTTLIASGVSIKMITGDSQETAVAIASRLGLYSKTSQSVSGEEIDAMDVQQLSQIVPKVAVFYRASPRHKMKIIKSLQKNGSVVAMTGDGVNDAVALKAADIGVAMGQTGTDVCKEAADMILVDDDFQTIMSAIEEGKGIYNNIKNFVRFQLSTSIAALTLISLATLMNFPNPLNAMQILWINIIMDGPPAQSLGVEPVDKDVIRKPPRNWKDSILTKNLILKILVSSIIIVCGTLFVFWRELRDNVITPRDTTMTFTCFVFFDMFNALSSRSQTKSVFEIGLCSNRMFCYAVLGSIMGQLLVIYFPPLQKVFQTESLSILGLALGEEWTAAG
"
     misc_feature    570..3137
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /note="golgi membrane calcium-translocating P-type ATPase;
                     Region: ATPase-IIA2_Ca; TIGR01522"
                     /db_xref="CDD:130585"
     misc_feature    579..785
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /note="Cation transporter/ATPase, N-terminus; Region:
                     Cation_ATPase_N; pfam00690"
                     /db_xref="CDD:201397"
     misc_feature    714..776
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P98194.3);
                     transmembrane region"
     misc_feature    816..872
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P98194.3);
                     transmembrane region"
     misc_feature    861..1523
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /note="E1-E2 ATPase; Region: E1-E2_ATPase; pfam00122"
                     /db_xref="CDD:201018"
     misc_feature    1290..1349
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P98194.3);
                     transmembrane region"
     misc_feature    1386..1439
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P98194.3);
                     transmembrane region"
     misc_feature    1728..1982
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /note="Putative hydrolase of sodium-potassium ATPase alpha
                     subunit; Region: Hydrolase_like2; pfam13246"
                     /db_xref="CDD:205426"
     misc_feature    2154..2486
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /note="Haloacid dehalogenase-like hydrolases. The haloacid
                     dehalogenase-like (HAD) superfamily includes L-2-haloacid
                     dehalogenase, epoxide hydrolase, phosphoserine
                     phosphatase, phosphomannomutase, phosphoglycolate
                     phosphatase, P-type ATPase, and many others; Region:
                     HAD_like; cd01427"
                     /db_xref="CDD:119389"
     misc_feature    2211..2213
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /note="motif II; other site"
                     /db_xref="CDD:119389"
     misc_feature    2601..2660
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P98194.3);
                     transmembrane region"
     misc_feature    2679..3143
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /note="Cation transporting ATPase, C-terminus; Region:
                     Cation_ATPase_C; pfam00689"
                     /db_xref="CDD:201396"
     misc_feature    2691..2753
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P98194.3);
                     transmembrane region"
     misc_feature    2814..2882
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P98194.3);
                     transmembrane region"
     misc_feature    2928..2987
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P98194.3);
                     transmembrane region"
     misc_feature    3027..3083
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P98194.3);
                     transmembrane region"
     exon            510..620
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            621..737
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            738..827
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            828..863
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            864..925
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            926..1034
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            1035..1190
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            1191..1259
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            1260..1335
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            1336..1402
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            1403..1527
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            1528..1625
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            1626..1721
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            1722..1811
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            1812..1916
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            1917..2073
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            2074..2244
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            2245..2342
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            2343..2393
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            2394..2560
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            2561..2629
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            2630..2746
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            2747..2894
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            2895..2990
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            2991..3132
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     exon            3133..3693
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /inference="alignment:Splign:1.39.8"
     STS             3167..3316
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /standard_name="RH11935"
                     /db_xref="UniSTS:51335"
     variation       complement(3277)
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:34786162"
     polyA_signal    3655..3660
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
     polyA_site      3693
                     /gene="ATP2C1"
                     /gene_synonym="ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1"
ORIGIN      
aggagtgcggggcgcgactgggcggccggcggcggggaggggcggagcgcaggagtcggaggcgggagcagaccagcacggcctcgcggagccggcccggcggaccgtgacgggtcccctcacctcctcttctctcccctccccgcccgccctctctccctcccttcctccctcccgctcgcttcttctcacgccgggagcaggctcccgcctcgcaccgctgccccgcgagcagctcctcttctcccgaggcgcgcggggcgcccccgcgagccccgcggctgagaccccgcagcctggaggagggctgtccggggctttggatgctgctgctaggggtggtgggagcagccgtgggacgcgtggccgggagcgggggtgacagcctgggattccgggggcttctcttccttgtcctcctcctctcctctctattcccagtgtggccgtggctgacactaaagactttgtagccatcaacccgagtgcagtttcgatggaaaatgaaggttgcacgttttcaaaaaatacctaatggtgaaaatgagacaatgattcctgtattgacatcaaaaaaagcaagtgaattaccagtcagtgaagttgcaagcattctccaagctgatcttcagaatggtctaaacaaatgtgaagttagtcataggcgagcctttcatggctggaatgagtttgatattagtgaagatgagccactgtggaagaagtatatttctcagtttaaaaatccccttattatgctgcttctggcttctgcagtcatcagtgttttaatgcatcagtttgatgatgccgtcagtatcactgtggcaatacttatcgttgttacagttgcctttgttcaggaatatcgttcagaaaaatctcttgaagaattgagtaaacttgtgccaccagaatgccattgtgtgcgtgaaggaaaattggagcatacacttgcccgagacttggttccaggtgatacagtttgcctttctgttggggatagagttcctgctgacttacgcttgtttgaggctgtggatctttccattgatgagtccagcttgacaggtgagacaacgccttgttctaaggtgacagctcctcagccagctgcaactaatggagatcttgcatcgagaagtaacattgcctttatgggaacactggtcagatgtggcaaagcaaagggtgttgtcattggaacaggagaaaattctgaatttggggaggtttttaaaatgatgcaagcagaagaggcaccaaaaacccctctgcagaagagcatggacctcttaggaaaacaactttccttttactcctttggtataataggaatcatcatgttggttggctggttactgggaaaagatatcctggaaatgtttactattagtgtaagtttggctgtagcagcaattcctgaaggtctccccattgtggtcacagtgacgctagctcttggtgttatgagaatggtgaagaaaagggccattgtgaaaaagctgcctattgttgaaactctgggctgctgtaatgtgatttgttcagataaaactggaacactgacgaagaatgaaatgactgttactcacatatttacttcagatggtctgcatgctgaggttactggagttggctataatcaatttggggaagtgattgttgatggtgatgttgttcatggattctataacccagctgttagcagaattgttgaggcgggctgtgtgtgcaatgatgctgtaattagaaacaatactctaatggggaagccaacagaaggggccttaattgctcttgcaatgaagatgggtcttgatggacttcaacaagactacatcagaaaagctgaatacccttttagctctgagcaaaagtggatggctgttaagtgtgtacaccgaacacagcaggacagaccagagatttgttttatgaaaggtgcttacgaacaagtaattaagtactgtactacataccagagcaaagggcagaccttgacacttactcagcagcagagagatgtgtaccaacaagagaaggcacgcatgggctcagcgggactcagagttcttgctttggcttctggtcctgaactgggacagctgacatttcttggcttggtgggaatcattgatccacctagaactggtgtgaaagaagctgttacaacactcattgcctcaggagtatcaataaaaatgattactggagattcacaggagactgcagttgcaatcgccagtcgtctgggattgtattccaaaacttcccagtcagtctcaggagaagaaatagatgcaatggatgttcagcagctttcacaaatagtaccaaaggttgcagtattttacagagctagcccaaggcacaagatgaaaattattaagtcgctacagaagaacggttcagttgtagccatgacaggagatggagtaaatgatgcagttgctctgaaggctgcagacattggagttgcgatgggccagactggtacagatgtttgcaaagaggcagcagacatgatcctagtggatgatgattttcaaaccataatgtctgcaatcgaagagggtaaagggatttataataacattaaaaatttcgttagattccagctgagcacgagtatagcagcattaactttaatctcattggctacattaatgaactttcctaatcctctcaatgccatgcagattttgtggatcaatattattatggatggacccccagctcagagccttggagtagaaccagtggataaagatgtcattcgtaaacctcctcgcaactggaaagacagcattttgactaaaaacttgatacttaaaatacttgtttcatcaataatcattgtttgtgggactttgtttgtcttctggcgtgagctacgagacaatgtgattacacctcgagacacaacaatgaccttcacatgctttgtgttttttgacatgttcaatgcactaagttccagatcccagaccaagtctgtgtttgagattggactctgcagtaatagaatgttttgctatgcagttcttggatccatcatgggacaattactagttatttactttcctccgcttcagaaggtttttcagactgagagcctaagcatactgggtctggctctgggagaggagtggacagcagctggttgagatacatccccatctggagacaggactgccactgacagaagatgtgagctgtgtctaagtccagtcttgtgcccagccgtgtctgcgccttcactctttggaactctgcatacaacatcttagcaccatcttcctgcagctcttccttacctaaataaagaaacagcccaagggcagtatttctaaaagcactgtaacagcttttcattttctccacatatactacaaattctataaagaaagaaattaatttaaaaaaactaagatgtttttctcttctggcttcataaatgccttgctgtataaattgaaatattgatactgaactgtctttttaatgatgacctaactttattcaacccatcggaatttactttttccctgaaataagatcttttccactggtctactacctgaccataaacatgtctgcatttgaattctctaaaccctaaatctgtgtctatgaaaaatacaaatgactattaaatattattctctttactgttctctttcaccgaaaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:27032 -> Molecular function: GO:0004871 [signal transducer activity] evidence: IMP
            GeneID:27032 -> Molecular function: GO:0005388 [calcium-transporting ATPase activity] evidence: IDA
            GeneID:27032 -> Molecular function: GO:0005388 [calcium-transporting ATPase activity] evidence: IMP
            GeneID:27032 -> Molecular function: GO:0005509 [calcium ion binding] evidence: IDA
            GeneID:27032 -> Molecular function: GO:0005524 [ATP binding] evidence: IDA
            GeneID:27032 -> Molecular function: GO:0005524 [ATP binding] evidence: IEA
            GeneID:27032 -> Molecular function: GO:0015410 [manganese-transporting ATPase activity] evidence: IDA
            GeneID:27032 -> Molecular function: GO:0030145 [manganese ion binding] evidence: IDA
            GeneID:27032 -> Molecular function: GO:0046872 [metal ion binding] evidence: IEA
            GeneID:27032 -> Biological process: GO:0006816 [calcium ion transport] evidence: IDA
            GeneID:27032 -> Biological process: GO:0006816 [calcium ion transport] evidence: IMP
            GeneID:27032 -> Biological process: GO:0006828 [manganese ion transport] evidence: IDA
            GeneID:27032 -> Biological process: GO:0006874 [cellular calcium ion homeostasis] evidence: IDA
            GeneID:27032 -> Biological process: GO:0006874 [cellular calcium ion homeostasis] evidence: IMP
            GeneID:27032 -> Biological process: GO:0007165 [signal transduction] evidence: IMP
            GeneID:27032 -> Biological process: GO:0008544 [epidermis development] evidence: IMP
            GeneID:27032 -> Biological process: GO:0016339 [calcium-dependent cell-cell adhesion] evidence: IMP
            GeneID:27032 -> Biological process: GO:0030026 [cellular manganese ion homeostasis] evidence: IDA
            GeneID:27032 -> Biological process: GO:0031532 [actin cytoskeleton reorganization] evidence: IMP
            GeneID:27032 -> Biological process: GO:0032468 [Golgi calcium ion homeostasis] evidence: IMP
            GeneID:27032 -> Biological process: GO:0032472 [Golgi calcium ion transport] evidence: IMP
            GeneID:27032 -> Biological process: GO:0034220 [ion transmembrane transport] evidence: TAS
            GeneID:27032 -> Biological process: GO:0043123 [positive regulation of I-kappaB kinase/NF-kappaB cascade] evidence: IMP
            GeneID:27032 -> Biological process: GO:0055085 [transmembrane transport] evidence: TAS
            GeneID:27032 -> Cellular component: GO:0000139 [Golgi membrane] evidence: IDA
            GeneID:27032 -> Cellular component: GO:0000139 [Golgi membrane] evidence: TAS
            GeneID:27032 -> Cellular component: GO:0005794 [Golgi apparatus] evidence: IDA
            GeneID:27032 -> Cellular component: GO:0005802 [trans-Golgi network] evidence: IDA
            GeneID:27032 -> Cellular component: GO:0016021 [integral to membrane] evidence: NAS
ANNOTATIONS from NCBI Entrez Gene (20130726):
            NP_001001485 -> EC 3.6.3.8

by @meso_cacase at DBCLS
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