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2024-04-25 20:28:50, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_002027               1710 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens farnesyltransferase, CAAX box, alpha (FNTA),
            transcript variant 1, mRNA.
ACCESSION   NM_002027
VERSION     NM_002027.2  GI:66882377
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 1710)
  AUTHORS   Ghavami,S., Mutawe,M.M., Schaafsma,D., Yeganeh,B., Unruh,H.,
            Klonisch,T. and Halayko,A.J.
  TITLE     Geranylgeranyl transferase 1 modulates autophagy and apoptosis in
            human airway smooth muscle
  JOURNAL   Am. J. Physiol. Lung Cell Mol. Physiol. 302 (4), L420-L428 (2012)
   PUBMED   22160308
  REMARK    GeneRIF: our findings identify Geranylgeranyl transferase 1 as a
            key regulator of human airway smooth muscle cell viability
REFERENCE   2  (bases 1 to 1710)
  AUTHORS   Lipkin,S.M., Chao,E.C., Moreno,V., Rozek,L.S., Rennert,H.,
            Pinchev,M., Dizon,D., Rennert,G., Kopelovich,L. and Gruber,S.B.
  TITLE     Genetic variation in 3-hydroxy-3-methylglutaryl CoA reductase
            modifies the chemopreventive activity of statins for colorectal
            cancer
  JOURNAL   Cancer Prev Res (Phila) 3 (5), 597-603 (2010)
   PUBMED   20403997
  REMARK    GeneRIF: Observational study of gene-disease association,
            gene-environment interaction, and pharmacogenomic / toxicogenomic.
            (HuGE Navigator)
REFERENCE   3  (bases 1 to 1710)
  AUTHORS   Fontaine-Bisson,B., Alessi,M.C., Saut,N., Fumeron,F., Marre,M.,
            Dutour,A., Badens,C., Levy,N., Tichet,J., Juhan-Vague,I.,
            Tregouet,D.A., Balkau,B. and Morange,P.E.
  TITLE     Polymorphisms of the lamina maturation pathway and their
            association with the metabolic syndrome: the DESIR prospective
            study
  JOURNAL   J. Mol. Med. 88 (2), 193-201 (2010)
   PUBMED   19841875
  REMARK    GeneRIF: Observational study of gene-disease association and
            gene-gene interaction. (HuGE Navigator)
REFERENCE   4  (bases 1 to 1710)
  AUTHORS   Zhou,J., Vos,C.C., Gjyrezi,A., Yoshida,M., Khuri,F.R., Tamanoi,F.
            and Giannakakou,P.
  TITLE     The protein farnesyltransferase regulates HDAC6 activity in a
            microtubule-dependent manner
  JOURNAL   J. Biol. Chem. 284 (15), 9648-9655 (2009)
   PUBMED   19228685
  REMARK    GeneRIF: FTase, via its tubulin-association, is a critical upstream
            regulator of HDAC6 activity
REFERENCE   5  (bases 1 to 1710)
  AUTHORS   Armstrong,S.A., Hannah,V.C., Goldstein,J.L. and Brown,M.S.
  TITLE     CAAX geranylgeranyl transferase transfers farnesyl as efficiently
            as geranylgeranyl to RhoB
  JOURNAL   J. Biol. Chem. 270 (14), 7864-7868 (1995)
   PUBMED   7713879
REFERENCE   6  (bases 1 to 1710)
  AUTHORS   Zhang,F.L., Diehl,R.E., Kohl,N.E., Gibbs,J.B., Giros,B., Casey,P.J.
            and Omer,C.A.
  TITLE     cDNA cloning and expression of rat and human protein
            geranylgeranyltransferase type-I
  JOURNAL   J. Biol. Chem. 269 (5), 3175-3180 (1994)
   PUBMED   8106351
REFERENCE   7  (bases 1 to 1710)
  AUTHORS   Andres,D.A., Milatovich,A., Ozcelik,T., Wenzlau,J.M., Brown,M.S.,
            Goldstein,J.L. and Francke,U.
  TITLE     cDNA cloning of the two subunits of human CAAX farnesyltransferase
            and chromosomal mapping of FNTA and FNTB loci and related sequences
  JOURNAL   Genomics 18 (1), 105-112 (1993)
   PUBMED   8276393
REFERENCE   8  (bases 1 to 1710)
  AUTHORS   Omer,C.A., Kral,A.M., Diehl,R.E., Prendergast,G.C., Powers,S.,
            Allen,C.M., Gibbs,J.B. and Kohl,N.E.
  TITLE     Characterization of recombinant human farnesyl-protein transferase:
            cloning, expression, farnesyl diphosphate binding, and functional
            homology with yeast prenyl-protein transferases
  JOURNAL   Biochemistry 32 (19), 5167-5176 (1993)
   PUBMED   8494894
REFERENCE   9  (bases 1 to 1710)
  AUTHORS   Adamson,P., Marshall,C.J., Hall,A. and Tilbrook,P.A.
  TITLE     Post-translational modifications of p21rho proteins
  JOURNAL   J. Biol. Chem. 267 (28), 20033-20038 (1992)
   PUBMED   1400319
REFERENCE   10 (bases 1 to 1710)
  AUTHORS   Manne,V., Roberts,D., Tobin,A., O'Rourke,E., De Virgilio,M.,
            Meyers,C., Ahmed,N., Kurz,B., Resh,M., Kung,H.F. et al.
  TITLE     Identification and preliminary characterization of protein-cysteine
            farnesyltransferase
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 87 (19), 7541-7545 (1990)
   PUBMED   2217184
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BI913631.1 and BC084566.1.
            On Jun 2, 2005 this sequence version replaced gi:4503770.
            
            Summary: Prenyltransferases can attach either a farnesyl group or a
            geranylgeranyl group in thioether linkage to the cysteine residue
            of proteins with a C-terminal CAAX box. CAAX
            geranylgeranyltransferase and CAAX farnesyltransferase are
            heterodimers that share the same alpha subunit but have different
            beta subunits. This gene encodes the alpha subunit of these
            transferases. Alternative splicing results in multiple transcript
            variants. Related pseudogenes have been identified on chromosomes
            11 and 13. [provided by RefSeq, May 2010].
            
            Transcript Variant: This variant (1) represents the longer
            transcript and encodes the functional protein.
            
            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 :: BC084566.1, L10413.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025081, ERS025082 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-40                BI913631.1         147-186
            41-1710             BC084566.1         1-1670
FEATURES             Location/Qualifiers
     source          1..1710
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="8"
                     /map="8p11"
     gene            1..1710
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /note="farnesyltransferase, CAAX box, alpha"
                     /db_xref="GeneID:2339"
                     /db_xref="HGNC:3782"
                     /db_xref="HPRD:00607"
                     /db_xref="MIM:134635"
     exon            1..248
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /inference="alignment:Splign:1.39.8"
     variation       18
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:28384488"
     CDS             49..1188
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /EC_number="2.5.1.59"
                     /EC_number="2.5.1.58"
                     /note="protein prenyltransferase alpha subunit repeat
                     containing 2; FTase-alpha; type I protein
                     geranyl-geranyltransferase alpha subunit; GGTase-I-alpha;
                     farnesyl-protein transferase alpha-subunit; ras proteins
                     prenyltransferase subunit alpha"
                     /codon_start=1
                     /product="protein
                     farnesyltransferase/geranylgeranyltransferase type-1
                     subunit alpha"
                     /protein_id="NP_002018.1"
                     /db_xref="GI:4503771"
                     /db_xref="CCDS:CCDS6140.1"
                     /db_xref="GeneID:2339"
                     /db_xref="HGNC:3782"
                     /db_xref="HPRD:00607"
                     /db_xref="MIM:134635"
                     /translation="
MAATEGVGEAAQGGEPGQPAQPPPQPHPPPPQQQHKEEMAAEAGEAVASPMDDGFVSLDSPSYVLYRDRAEWADIDPVPQNDGPNPVVQIIYSDKFRDVYDYFRAVLQRDERSERAFKLTRDAIELNAANYTVWHFRRVLLKSLQKDLHEEMNYITAIIEEQPKNYQVWHHRRVLVEWLRDPSQELEFIADILNQDAKNYHAWQHRQWVIQEFKLWDNELQYVDQLLKEDVRNNSVWNQRYFVISNTTGYNDRAVLEREVQYTLEMIKLVPHNESAWNYLKGILQDRGLSKYPNLLNQLLDLQPSHSSPYLIAFLVDIYEDMLENQCDNKEDILNKALELCEILAKEKDTIRKEYWRYIGRSLQSKHSTENDSPTNVQQ
"
     misc_feature    238..1143
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /note="farnesyltranstransferase; Region: PLN02789"
                     /db_xref="CDD:178386"
     misc_feature    382..486
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P49354.1);
                     Region: PFTA 1"
     misc_feature    391..480
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /note="Protein prenyltransferase alpha subunit repeat;
                     Region: PPTA; pfam01239"
                     /db_xref="CDD:201678"
     misc_feature    487..588
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P49354.1);
                     Region: PFTA 2"
     misc_feature    496..585
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /note="Protein prenyltransferase alpha subunit repeat;
                     Region: PPTA; pfam01239"
                     /db_xref="CDD:201678"
     misc_feature    589..693
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P49354.1);
                     Region: PFTA 3"
     misc_feature    598..687
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /note="Protein prenyltransferase alpha subunit repeat;
                     Region: PPTA; pfam01239"
                     /db_xref="CDD:201678"
     misc_feature    694..795
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P49354.1);
                     Region: PFTA 4"
     misc_feature    700..786
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /note="Protein prenyltransferase alpha subunit repeat;
                     Region: PPTA; pfam01239"
                     /db_xref="CDD:201678"
     misc_feature    811..915
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P49354.1);
                     Region: PFTA 5"
     misc_feature    820..903
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /note="Protein prenyltransferase alpha subunit repeat;
                     Region: PPTA; pfam01239"
                     /db_xref="CDD:201678"
     misc_feature    1165..1167
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (P49354.1); phosphorylation site"
     variation       111..112
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:139428078"
     variation       164
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375810129"
     variation       207
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370994529"
     variation       225
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374602755"
     variation       234
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:141352327"
     variation       238
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143321089"
     exon            249..334
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /inference="alignment:Splign:1.39.8"
     variation       282
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:368366624"
     variation       302
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151278515"
     variation       319
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140513662"
     exon            335..449
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /inference="alignment:Splign:1.39.8"
     variation       350
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112910348"
     variation       366
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371752527"
     variation       374
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368301964"
     variation       380
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200186349"
     variation       381
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202069696"
     variation       390
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150424879"
     variation       399
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:138334666"
     variation       401
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201374782"
     variation       407
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200796658"
     variation       410
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375845796"
     exon            450..554
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /inference="alignment:Splign:1.39.8"
     variation       451
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143829409"
     variation       457
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200780088"
     variation       471
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:76046042"
     variation       472
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:201464015"
     variation       549
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147010452"
     exon            555..681
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /inference="alignment:Splign:1.39.8"
     variation       568
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375552449"
     variation       593
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138168688"
     variation       595
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201579996"
     variation       599
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201638101"
     variation       613
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149513620"
     variation       638
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373178685"
     variation       648
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199989190"
     variation       660
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374653329"
     variation       669
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201190121"
     exon            682..830
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /inference="alignment:Splign:1.39.8"
     variation       714
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368125629"
     variation       756
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:144005707"
     variation       796
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1803597"
     variation       805
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371393216"
     variation       813
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200228527"
     exon            831..893
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /inference="alignment:Splign:1.39.8"
     variation       863
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148659497"
     variation       873
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375620813"
     variation       874
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375711846"
     exon            894..1065
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /inference="alignment:Splign:1.39.8"
     variation       895
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370193930"
     variation       907
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369359760"
     variation       917
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:141224054"
     variation       938
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202246754"
     variation       942
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373852144"
     variation       975
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:2230266"
     variation       1027
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377755753"
     variation       1030
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139144868"
     exon            1066..1694
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /inference="alignment:Splign:1.39.8"
     STS             1114..1308
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /standard_name="RH68982"
                     /db_xref="UniSTS:91779"
     variation       1155
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374000931"
     variation       1171
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191418964"
     variation       1189
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:371907116"
     STS             1195..1652
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /standard_name="RH27289"
                     /db_xref="UniSTS:87023"
     variation       1237
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:374884999"
     variation       1238
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145361728"
     STS             1254..1599
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /standard_name="D8S1675"
                     /db_xref="UniSTS:9626"
     STS             1254..1428
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /standard_name="D8S1675"
                     /db_xref="UniSTS:9627"
     variation       1255
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182388872"
     variation       1271
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111906132"
     variation       1303
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142364879"
     variation       1412
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146781943"
     variation       1513
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377746719"
     variation       1576
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:11554712"
     variation       1610
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187422693"
     variation       1631
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:3196850"
     polyA_signal    1666..1671
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
     variation       1666
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190378282"
     polyA_site      1694
                     /gene="FNTA"
                     /gene_synonym="FPTA; PGGT1A; PTAR2"
ORIGIN      
gggaggggcggggcctccgccaccacctcagctgcggaccgaggcgagatggcggccaccgagggggtcggggaggctgcgcaagggggcgagcccgggcagccggcgcaacccccgccccagccgcacccaccgccgccccagcagcagcacaaggaagagatggcggccgaggctggggaagccgtggcgtcccccatggacgacgggtttgtgagcctggactcgccctcctatgtcctgtacagggacagagcagaatgggctgatatagatccggtgccgcagaatgatggccccaatcccgtggtccagatcatttatagtgacaaatttagagatgtttatgattacttccgagctgtcctgcagcgtgatgaaagaagtgaacgagcttttaagctaacccgggatgctattgagttaaatgcagccaattatacagtgtggcatttccggagagttcttttgaagtcacttcagaaggatctacatgaggaaatgaactacatcactgcaataattgaggagcagcccaaaaactatcaagtttggcatcataggcgagtattagtggaatggctaagagatccatctcaggagcttgaatttattgctgatattcttaatcaggatgcaaagaattatcatgcctggcagcatcgacaatgggttattcaggaatttaaactttgggataatgagctgcagtatgtggaccaacttctgaaagaggatgtgagaaataactctgtctggaaccaaagatacttcgttatttctaacaccactggctacaatgatcgtgctgtattggagagagaagtccaatacactctggaaatgattaaactagtaccacataatgaaagtgcatggaactatttgaaagggattttgcaggatcgtggtctttccaaatatcctaatctgttaaatcaattacttgatttacaaccaagtcatagttccccctacctaattgcctttcttgtggatatctatgaagacatgctagaaaatcagtgtgacaataaggaagacattcttaataaagcattagagttatgtgaaatcctagctaaagaaaaggacactataagaaaggaatattggagatacattggaagatcccttcaaagcaaacacagcacagaaaatgactcaccaacaaatgtacagcaataacaccatccagaagaacttgatggaatgcttttattttttattaagggaccctgcaggagtttcacacgagagtggtccttccctttgcctgtggtgtaaaagtgcatcacacaggtattgctttttaacaagaactgatgctccttgggtgctgctgctactcagactagctctaagtaatgtgattcttctaaagcaaagtcattggatgggaggaggaagaaaaagtcccataaaggaacttttgtagtcttatcaacatataatctaatcccttagcatcagctcctccctcagtggtacatgcgtcaagatttgtagcagtaataactgcaggtcacttgtatgtaatggatgtgaggtagccgaagtttggttcagtaagcagggaatacagtcgttccatcagagctggtctgcacactcacattatcttgctatcactgtaaccaactaatgccaaaagaacggttttgtaataaaattatagctgtatctaaaaacaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:2339 -> Molecular function: GO:0004660 [protein farnesyltransferase activity] evidence: IDA
            GeneID:2339 -> Molecular function: GO:0004661 [protein geranylgeranyltransferase activity] evidence: TAS
            GeneID:2339 -> Molecular function: GO:0004662 [CAAX-protein geranylgeranyltransferase activity] evidence: IEA
            GeneID:2339 -> Molecular function: GO:0004663 [Rab geranylgeranyltransferase activity] evidence: IEA
            GeneID:2339 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:2339 -> Molecular function: GO:0008017 [microtubule binding] evidence: IDA
            GeneID:2339 -> Molecular function: GO:0030548 [acetylcholine receptor regulator activity] evidence: IEA
            GeneID:2339 -> Molecular function: GO:0030971 [receptor tyrosine kinase binding] evidence: IEA
            GeneID:2339 -> Molecular function: GO:0043014 [alpha-tubulin binding] evidence: IDA
            GeneID:2339 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
            GeneID:2339 -> Biological process: GO:0006921 [cellular component disassembly involved in execution phase of apoptosis] evidence: TAS
            GeneID:2339 -> Biological process: GO:0007179 [transforming growth factor beta receptor signaling pathway] evidence: TAS
            GeneID:2339 -> Biological process: GO:0007603 [phototransduction, visible light] evidence: TAS
            GeneID:2339 -> Biological process: GO:0016056 [rhodopsin mediated signaling pathway] evidence: TAS
            GeneID:2339 -> Biological process: GO:0018343 [protein farnesylation] evidence: IDA
            GeneID:2339 -> Biological process: GO:0018344 [protein geranylgeranylation] evidence: TAS
            GeneID:2339 -> Biological process: GO:0022400 [regulation of rhodopsin mediated signaling pathway] evidence: TAS
            GeneID:2339 -> Biological process: GO:0045213 [neurotransmitter receptor metabolic process] evidence: IEA
            GeneID:2339 -> Biological process: GO:0090044 [positive regulation of tubulin deacetylation] evidence: IDA
            GeneID:2339 -> Biological process: GO:0090045 [positive regulation of deacetylase activity] evidence: IDA
            GeneID:2339 -> Cellular component: GO:0005737 [cytoplasm] evidence: TAS
            GeneID:2339 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
            GeneID:2339 -> Cellular component: GO:0005875 [microtubule associated complex] evidence: IDA
ANNOTATIONS from NCBI Entrez Gene (20130726):
            NP_002018 -> EC 2.5.1.58
            NP_002018 -> EC 2.5.1.59

by @meso_cacase at DBCLS
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