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2024-04-20 23:02:59, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001007098            2150 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens sterol carrier protein 2 (SCP2), transcript variant 2,
            mRNA.
ACCESSION   NM_001007098
VERSION     NM_001007098.2  GI:302318894
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 2150)
  AUTHORS   Williams,C.P., Schueller,N., Thompson,C.A., van den Berg,M., Van
            Haren,S.D., Erdmann,R., Bond,C.S., Distel,B., Schliebs,W.,
            Wilmanns,M. and Stanley,W.A.
  TITLE     The Peroxisomal Targeting Signal 1 in sterol carrier protein 2 is
            autonomous and essential for receptor recognition
  JOURNAL   BMC Biochem. 12, 12 (2011)
   PUBMED   21375735
  REMARK    GeneRIF: The Peroxisomal targeting signal 1 in Scp2 is autonomous
            and is essential for binding to pex5.
            Publication Status: Online-Only
REFERENCE   2  (bases 1 to 2150)
  AUTHORS   Shimada,M., Miyagawa,T., Kawashima,M., Tanaka,S., Honda,Y.,
            Honda,M. and Tokunaga,K.
  TITLE     An approach based on a genome-wide association study reveals
            candidate loci for narcolepsy
  JOURNAL   Hum. Genet. 128 (4), 433-441 (2010)
   PUBMED   20677014
  REMARK    GeneRIF: Statistical analysis indicated that six genes, NFATC2,
            SCP2, CACNA1C, TCRA, POLE, and FAM3D, were associated with
            narcolepsy.
            GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   3  (bases 1 to 2150)
  AUTHORS   Hendrickson,S.L., Lautenberger,J.A., Chinn,L.W., Malasky,M.,
            Sezgin,E., Kingsley,L.A., Goedert,J.J., Kirk,G.D., Gomperts,E.D.,
            Buchbinder,S.P., Troyer,J.L. and O'Brien,S.J.
  TITLE     Genetic variants in nuclear-encoded mitochondrial genes influence
            AIDS progression
  JOURNAL   PLoS ONE 5 (9), E12862 (2010)
   PUBMED   20877624
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
            Publication Status: Online-Only
REFERENCE   4  (bases 1 to 2150)
  AUTHORS   Dansen,T.B., Kops,G.J., Denis,S., Jelluma,N., Wanders,R.J.,
            Bos,J.L., Burgering,B.M. and Wirtz,K.W.
  TITLE     Regulation of sterol carrier protein gene expression by the
            forkhead transcription factor FOXO3a
  JOURNAL   J. Lipid Res. 45 (1), 81-88 (2004)
   PUBMED   14563822
  REMARK    GeneRIF: SCP2 in the cellular defense against oxidative damage and
            found that a fluorescent fatty acid analog bound to SCP2 is
            protected against H2O2/Cu2+-induced oxidative damage
REFERENCE   5  (bases 1 to 2150)
  AUTHORS   Ohba,T., Holt,J.A., Billheimer,J.T. and Strauss,J.F. III.
  TITLE     Human sterol carrier protein x/sterol carrier protein 2 gene has
            two promoters
  JOURNAL   Biochemistry 34 (33), 10660-10668 (1995)
   PUBMED   7654720
REFERENCE   6  (bases 1 to 2150)
  AUTHORS   Ohba,T., Rennert,H., Pfeifer,S.M., He,Z., Yamamoto,R., Holt,J.A.,
            Billheimer,J.T. and Strauss,J.F. III.
  TITLE     The structure of the human sterol carrier protein X/sterol carrier
            protein 2 gene (SCP2)
  JOURNAL   Genomics 24 (2), 370-374 (1994)
   PUBMED   7698762
REFERENCE   7  (bases 1 to 2150)
  AUTHORS   Seedorf,U., Brysch,P., Engel,T., Schrage,K. and Assmann,G.
  TITLE     Sterol carrier protein X is peroxisomal 3-oxoacyl coenzyme A
            thiolase with intrinsic sterol carrier and lipid transfer activity
  JOURNAL   J. Biol. Chem. 269 (33), 21277-21283 (1994)
   PUBMED   8063752
REFERENCE   8  (bases 1 to 2150)
  AUTHORS   Yamamoto,R.
  TITLE     [Localization of human sterol carrier protein 2 gene and cDNA
            expression in COS-7 cell]
  JOURNAL   Hokkaido Igaku Zasshi 67 (6), 839-848 (1992)
   PUBMED   1483685
REFERENCE   9  (bases 1 to 2150)
  AUTHORS   Heikoop,J.C., Ossendorp,B.C., Wanders,R.J., Wirtz,K.W. and
            Tager,J.M.
  TITLE     Subcellular localisation and processing of non-specific lipid
            transfer protein are not aberrant in Rhizomelic Chondrodysplasia
            Punctata fibroblasts
  JOURNAL   FEBS Lett. 299 (2), 201-204 (1992)
   PUBMED   1347505
REFERENCE   10 (bases 1 to 2150)
  AUTHORS   Yamamoto,R., Kallen,C.B., Babalola,G.O., Rennert,H.,
            Billheimer,J.T. and Strauss,J.F. III.
  TITLE     Cloning and expression of a cDNA encoding human sterol carrier
            protein 2
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 88 (2), 463-467 (1991)
   PUBMED   1703300
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from AC099677.2, DC330171.1,
            BC067108.1 and AL445183.19.
            On Aug 6, 2010 this sequence version replaced gi:55956774.
            
            Summary: This gene encodes two proteins: sterol carrier protein X
            (SCPx) and sterol carrier protein 2 (SCP2), as a result of
            transcription initiation from 2 independently regulated promoters.
            The transcript initiated from the proximal promoter encodes the
            longer SCPx protein, and the transcript initiated from the distal
            promoter encodes the shorter SCP2 protein, with the 2 proteins
            sharing a common C-terminus. Evidence suggests that the SCPx
            protein is a peroxisome-associated thiolase that is involved in the
            oxidation of branched chain fatty acids, while the SCP2 protein is
            thought to be an intracellular lipid transfer protein. This gene is
            highly expressed in organs involved in lipid metabolism, and may
            play a role in Zellweger syndrome, in which cells are deficient in
            peroxisomes and have impaired bile acid synthesis. Alternative
            splicing of this gene produces multiple transcript variants, some
            encoding different isoforms.[provided by RefSeq, Aug 2010].
            
            Transcript Variant: This variant (2) has multiple differences in
            the coding region, compared to variant 1, one of which results in a
            translational frameshift. The resulting isoform (2) is shorter and
            has a distinct C-terminus, compared to isoform 1.
            
            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 :: BC067108.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025083, ERS025084 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-16                AC099677.2         88079-88094
            17-89               DC330171.1         1-73
            90-1464             BC067108.1         1-1375
            1465-1779           AL445183.19        40219-40533
            1780-2150           BC067108.1         1690-2060
FEATURES             Location/Qualifiers
     source          1..2150
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="1"
                     /map="1p32"
     gene            1..2150
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /note="sterol carrier protein 2"
                     /db_xref="GeneID:6342"
                     /db_xref="HGNC:10606"
                     /db_xref="HPRD:01700"
                     /db_xref="MIM:184755"
     exon            1..237
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /inference="alignment:Splign:1.39.8"
     variation       8
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1242331"
     variation       82
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:184943760"
     variation       89
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:115810571"
     variation       112
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140752743"
     CDS             169..1137
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /EC_number="2.3.1.176"
                     /note="isoform 2 is encoded by transcript variant 2;
                     sterol carrier protein X; non-specific lipid-transfer
                     protein; propanoyl-CoA C-acyltransferase"
                     /codon_start=1
                     /product="non-specific lipid-transfer protein isoform 2"
                     /protein_id="NP_001007099.1"
                     /db_xref="GI:55956775"
                     /db_xref="CCDS:CCDS41338.1"
                     /db_xref="GeneID:6342"
                     /db_xref="HGNC:10606"
                     /db_xref="HPRD:01700"
                     /db_xref="MIM:184755"
                     /translation="
MSSSPWEPATLRRVFVVGVGMTKFVKPGAENSRDYPDLAEEAGKKALADAQIPYSAVDQACVGYVFGVAECVLALGFEKMSKGSLGIKFSDRTIPTDKHVDLLINKYGLSAHPVAPQMFGYAGKEHMEKYGTKIEHFAKIGWKNHKHSVNNPYSQFQDEYSLDEVMASKEVFDFLTILQCCPTSDGAAAAILASEAFVQKYGLQSKAVEILAQEMMTDLPSSFEEKSIIKMVGFDMSKEAARKCYEKSGLTPNDIDVIELHDCFSTNELLTYEALGLCPEGQGATLVDRGDNTYGGKWVINPSGGLISKGHPLGATGGHSCS
"
     misc_feature    217..1134
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /note="nondecarboxylating condensing enzymes; In general,
                     thiolases catalyze the reversible thiolytic cleavage of
                     3-ketoacyl-CoA into acyl-CoA and acetyl-CoA, a 2-step
                     reaction involving a covalent intermediate formed with a
                     catalytic cysteine. There are 2...; Region:
                     nondecarbox_cond_enzymes; cd00826"
                     /db_xref="CDD:73239"
     misc_feature    625..627
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    646..648
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     variation       183
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:147697594"
     variation       185
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148709071"
     variation       202
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190197851"
     variation       223
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:140387282"
     variation       225
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:369597903"
     variation       235
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:149958725"
     exon            238..295
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /inference="alignment:Splign:1.39.8"
     exon            296..367
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /inference="alignment:Splign:1.39.8"
     variation       300
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184974273"
     variation       304
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144647557"
     variation       305
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377136053"
     variation       350
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370413647"
     exon            368..432
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /inference="alignment:Splign:1.39.8"
     variation       384
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202234745"
     variation       414
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369066062"
     exon            433..559
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /inference="alignment:Splign:1.39.8"
     variation       452
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:11552393"
     variation       455
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201992866"
     variation       468
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372729186"
     variation       490
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377683847"
     variation       517
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376277989"
     exon            560..623
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /inference="alignment:Splign:1.39.8"
     variation       567
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:143441016"
     variation       608
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372168791"
     variation       611
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200541507"
     exon            624..710
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /inference="alignment:Splign:1.39.8"
     variation       645
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:41294530"
     variation       708
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371534398"
     exon            711..861
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /inference="alignment:Splign:1.39.8"
     variation       723
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:80033039"
     variation       760
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201599199"
     variation       767
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201663646"
     variation       814
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112110457"
     variation       832
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113895458"
     variation       834
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148510961"
     exon            862..1009
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /inference="alignment:Splign:1.39.8"
     variation       891
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185811440"
     variation       920
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:370185824"
     variation       936
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148423275"
     variation       937
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374102289"
     variation       969
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368088577"
     variation       978
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:3189884"
     variation       993
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1130712"
     exon            1010..1117
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /inference="alignment:Splign:1.39.8"
     variation       1023
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:7538935"
     variation       1110
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:74638331"
     variation       1112
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201780891"
     exon            1118..2092
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /inference="alignment:Splign:1.39.8"
     variation       1121
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372915189"
     variation       1159
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201228419"
     variation       1185
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375849525"
     variation       1232
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:41294532"
     variation       1243
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182127561"
     variation       1244
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:117140349"
     variation       1321
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186801373"
     variation       1342
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:41294534"
     variation       1367
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201962271"
     variation       1369
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:115255694"
     variation       1464
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace=""
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:76633416"
     variation       1465
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:111632142"
     variation       1482
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:192166984"
     variation       1549
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:150459731"
     variation       1550
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6697076"
     variation       1618
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:75660274"
     variation       1638
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183946230"
     variation       1649
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6657017"
     variation       1705
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188594598"
     variation       1779
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116111940"
     variation       1878
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11581638"
     variation       2001
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:377498178"
     variation       2034
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:137967000"
     polyA_signal    2063..2068
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
     variation       2083
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376016258"
     polyA_site      2092
                     /gene="SCP2"
                     /gene_synonym="NLTP; NSL-TP; SCP-2; SCP-CHI; SCP-X; SCPX"
ORIGIN      
gcgccccaccccgccccctcctcctgcccctacgcacgcgcactctcacgcgcctgtgttgccgcccgcggccctggcttcgggcttcagggagctctggtgcagtctccgcctgtcagtgccggcagtcgtccgcggcgcccgccccggtcccgcactggtgcagccatgtcctcttccccgtgggagcctgcgaccctgcgccgggtgttcgtggtgggggttggcatgaccaagtttgtgaagcctggagctgagaattcaagagactaccctgacttggcagaagaagcaggcaagaaggctttagctgatgcacagatcccttattcagcagtggaccaggcatgtgttggctatgtttttggtgtggcagaatgtgtcttggctcttgggtttgagaagatgagtaagggaagccttggaataaaattttcagatagaaccattcccactgataagcatgttgacctcctgatcaataagtatggattgtctgctcacccagttgctcctcagatgtttgggtatgctggaaaagaacatatggaaaaatatggaacaaaaattgaacactttgcaaaaattggatggaaaaatcataaacattcagttaataacccgtattcccagttccaagatgaatacagtttagatgaagtgatggcatctaaagaagtttttgattttttgactatcttacaatgttgtcccacttcagatggtgctgcagcagcaattttggccagtgaagcatttgtacagaagtatggcctgcaatccaaagctgtggaaattttggcacaagaaatgatgactgatttgccaagctcgtttgaagaaaaaagcattattaaaatggttggctttgatatgagtaaagaagctgcaagaaaatgctatgagaaatctggcctgacaccaaatgatattgacgtaatagaacttcacgattgcttttctaccaacgaactccttacttatgaagcactgggactctgtccagaaggacaaggtgcaacgctggttgatagaggagataatacatatggaggaaagtgggtcataaatcctagtggtggactgatttcaaagggacacccactaggcgctacaggaggacattcctgctcttgaaatttcctgataacccggacaagttcatggaaagcttgatctacattcatcctaatctttgctgatgcctccatgtatgttaccttaagttgccgtgctaactgccgtccttcttcctgtgttacctgtctttgatgatccagatctgctttattaccaattaaaatcattgggaactcatcacgatcctttactctgagaatctgtctttgaaacttatagatttcttcaaaactgcctctatctgtgactgaaaagaccaacaggaagccctcgccagtcctcatatactgttctctcatggctccaagctcttcttgtcctgctgtatccaaaatatctagccgggctgctctgtcatctatcacacactgctttgtgtaagaatcttcattggttggatcataatccgttacaaaataggactcccaacttaggaaacaaaacatttgtaatatgattgaagactcctgcatgcctcctcaataatattcccctctctcctcccccagcaccaagaggtaatcaatatcctgaatttggtatctgtcattctcatgcatttatacaacattagtaatcatatgatagtattcctaagctatgttttggagaggacaccactgcaaatcttcagccctatactagcttttatcggtagccatcaattgcagttttaatagaaatacaaatacatcaagtgtctgttctttaatttgtaaagaaaatttgttttctagcgtgacaccctcaaggtaccgtatctgtatgtaaatgttgtgcccaatgctacacagacattattttaaaactattttctgcctttggtaaatagactaaactgttttctttattcctcaaaagaattagatcatacttcagtgttgattttgttgctaatgggacatggagatgtctggatgataataaatattcctgtggtatggtcactgaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:6342 -> Molecular function: GO:0000062 [fatty-acyl-CoA binding] evidence: IDA
            GeneID:6342 -> Molecular function: GO:0005102 [receptor binding] evidence: IPI
            GeneID:6342 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:6342 -> Molecular function: GO:0008526 [phosphatidylinositol transporter activity] evidence: IDA
            GeneID:6342 -> Molecular function: GO:0015485 [cholesterol binding] evidence: IDA
            GeneID:6342 -> Molecular function: GO:0033814 [propanoyl-CoA C-acyltransferase activity] evidence: IEA
            GeneID:6342 -> Molecular function: GO:0036042 [long-chain fatty acyl-CoA binding] evidence: IDA
            GeneID:6342 -> Molecular function: GO:0070538 [oleic acid binding] evidence: IDA
            GeneID:6342 -> Biological process: GO:0006694 [steroid biosynthetic process] evidence: IDA
            GeneID:6342 -> Biological process: GO:0006699 [bile acid biosynthetic process] evidence: TAS
            GeneID:6342 -> Biological process: GO:0006701 [progesterone biosynthetic process] evidence: IDA
            GeneID:6342 -> Biological process: GO:0006869 [lipid transport] evidence: IEA
            GeneID:6342 -> Biological process: GO:0007031 [peroxisome organization] evidence: IEA
            GeneID:6342 -> Biological process: GO:0008206 [bile acid metabolic process] evidence: TAS
            GeneID:6342 -> Biological process: GO:0015914 [phospholipid transport] evidence: IDA
            GeneID:6342 -> Biological process: GO:0032385 [positive regulation of intracellular cholesterol transport] evidence: IDA
            GeneID:6342 -> Biological process: GO:0032385 [positive regulation of intracellular cholesterol transport] evidence: NAS
            GeneID:6342 -> Biological process: GO:0032959 [inositol trisphosphate biosynthetic process] evidence: IDA
            GeneID:6342 -> Biological process: GO:0033540 [fatty acid beta-oxidation using acyl-CoA oxidase] evidence: TAS
            GeneID:6342 -> Biological process: GO:0033559 [unsaturated fatty acid metabolic process] evidence: TAS
            GeneID:6342 -> Biological process: GO:0036109 [alpha-linolenic acid metabolic process] evidence: TAS
            GeneID:6342 -> Biological process: GO:0044255 [cellular lipid metabolic process] evidence: TAS
            GeneID:6342 -> Biological process: GO:0044281 [small molecule metabolic process] evidence: TAS
            GeneID:6342 -> Biological process: GO:0045940 [positive regulation of steroid metabolic process] evidence: IDA
            GeneID:6342 -> Biological process: GO:0072659 [protein localization to plasma membrane] evidence: IDA
            GeneID:6342 -> Biological process: GO:1901373 [lipid hydroperoxide transport] evidence: IDA
            GeneID:6342 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
            GeneID:6342 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA
            GeneID:6342 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
            GeneID:6342 -> Cellular component: GO:0005739 [mitochondrion] evidence: IEA
            GeneID:6342 -> Cellular component: GO:0005777 [peroxisome] evidence: IDA
            GeneID:6342 -> Cellular component: GO:0005782 [peroxisomal matrix] evidence: TAS
            GeneID:6342 -> Cellular component: GO:0043231 [intracellular membrane-bounded organelle] evidence: IDA
            GeneID:6342 -> Cellular component: GO:0043234 [protein complex] evidence: IDA
ANNOTATIONS from NCBI Entrez Gene (20130726):
            NP_001007099 -> EC 2.3.1.176

by @meso_cacase at DBCLS
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