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2024-04-20 19:18:14, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001184776 6348 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens seizure related 6 homolog (mouse)-like (SEZ6L),
transcript variant 5, mRNA.
ACCESSION NM_001184776
VERSION NM_001184776.1 GI:296179441
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 6348)
AUTHORS Wilk,J.B., Shrine,N.R., Loehr,L.R., Zhao,J.H., Manichaikul,A.,
Lopez,L.M., Smith,A.V., Heckbert,S.R., Smolonska,J., Tang,W.,
Loth,D.W., Curjuric,I., Hui,J., Cho,M.H., Latourelle,J.C.,
Henry,A.P., Aldrich,M., Bakke,P., Beaty,T.H., Bentley,A.R.,
Borecki,I.B., Brusselle,G.G., Burkart,K.M., Chen,T.H., Couper,D.,
Crapo,J.D., Davies,G., Dupuis,J., Franceschini,N., Gulsvik,A.,
Hancock,D.B., Harris,T.B., Hofman,A., Imboden,M., James,A.L.,
Khaw,K.T., Lahousse,L., Launer,L.J., Litonjua,A., Liu,Y.,
Lohman,K.K., Lomas,D.A., Lumley,T., Marciante,K.D., McArdle,W.L.,
Meibohm,B., Morrison,A.C., Musk,A.W., Myers,R.H., North,K.E.,
Postma,D.S., Psaty,B.M., Rich,S.S., Rivadeneira,F., Rochat,T.,
Rotter,J.I., Artigas,M.S., Starr,J.M., Uitterlinden,A.G.,
Wareham,N.J., Wijmenga,C., Zanen,P., Province,M.A., Silverman,E.K.,
Deary,I.J., Palmer,L.J., Cassano,P.A., Gudnason,V., Barr,R.G.,
Loos,R.J., Strachan,D.P., London,S.J., Boezen,H.M.,
Probst-Hensch,N., Gharib,S.A., Hall,I.P., O'Connor,G.T., Tobin,M.D.
and Stricker,B.H.
TITLE Genome-wide association studies identify CHRNA5/3 and HTR4 in the
development of airflow obstruction
JOURNAL Am. J. Respir. Crit. Care Med. 186 (7), 622-632 (2012)
PUBMED 22837378
REFERENCE 2 (bases 1 to 6348)
AUTHORS Irvin,M.R., Wineinger,N.E., Rice,T.K., Pajewski,N.M.,
Kabagambe,E.K., Gu,C.C., Pankow,J., North,K.E., Wilk,J.B.,
Freedman,B.I., Franceschini,N., Broeckel,U., Tiwari,H.K. and
Arnett,D.K.
TITLE Genome-wide detection of allele specific copy number variation
associated with insulin resistance in African Americans from the
HyperGEN study
JOURNAL PLoS ONE 6 (8), E24052 (2011)
PUBMED 21901158
REFERENCE 3 (bases 1 to 6348)
AUTHORS Bailey,S.D., Xie,C., Do,R., Montpetit,A., Diaz,R., Mohan,V.,
Keavney,B., Yusuf,S., Gerstein,H.C., Engert,J.C. and Anand,S.
CONSRTM DREAM investigators
TITLE Variation at the NFATC2 locus increases the risk of
thiazolidinedione-induced edema in the Diabetes REduction
Assessment with ramipril and rosiglitazone Medication (DREAM) study
JOURNAL Diabetes Care 33 (10), 2250-2253 (2010)
PUBMED 20628086
REMARK GeneRIF: Observational study of gene-disease association,
gene-environment interaction, and pharmacogenomic / toxicogenomic.
(HuGE Navigator)
REFERENCE 4 (bases 1 to 6348)
AUTHORS Raji,O.Y., Agbaje,O.F., Duffy,S.W., Cassidy,A. and Field,J.K.
TITLE Incorporation of a genetic factor into an epidemiologic model for
prediction of individual risk of lung cancer: the Liverpool Lung
Project
JOURNAL Cancer Prev Res (Phila) 3 (5), 664-669 (2010)
PUBMED 20424129
REMARK GeneRIF: the addition of SEZ6L improved the performance of the
Liverpool Lung Project risk model.
GeneRIF: Observational study of gene-disease association and
gene-environment interaction. (HuGE Navigator)
REFERENCE 5 (bases 1 to 6348)
AUTHORS Talmud,P.J., Drenos,F., Shah,S., Shah,T., Palmen,J., Verzilli,C.,
Gaunt,T.R., Pallas,J., Lovering,R., Li,K., Casas,J.P., Sofat,R.,
Kumari,M., Rodriguez,S., Johnson,T., Newhouse,S.J., Dominiczak,A.,
Samani,N.J., Caulfield,M., Sever,P., Stanton,A., Shields,D.C.,
Padmanabhan,S., Melander,O., Hastie,C., Delles,C., Ebrahim,S.,
Marmot,M.G., Smith,G.D., Lawlor,D.A., Munroe,P.B., Day,I.N.,
Kivimaki,M., Whittaker,J., Humphries,S.E. and Hingorani,A.D.
CONSRTM ASCOT investigators; NORDIL investigators; BRIGHT Consortium
TITLE Gene-centric association signals for lipids and apolipoproteins
identified via the HumanCVD BeadChip
JOURNAL Am. J. Hum. Genet. 85 (5), 628-642 (2009)
PUBMED 19913121
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 6 (bases 1 to 6348)
AUTHORS Gorlov,I.P., Meyer,P., Liloglou,T., Myles,J., Boettger,M.B.,
Cassidy,A., Girard,L., Minna,J.D., Fischer,R., Duffy,S.,
Spitz,M.R., Haeussinger,K., Kammerer,S., Cantor,C., Dierkesmann,R.,
Field,J.K. and Amos,C.I.
TITLE Seizure 6-like (SEZ6L) gene and risk for lung cancer
JOURNAL Cancer Res. 67 (17), 8406-8411 (2007)
PUBMED 17804757
REMARK GeneRIF: A role of the SEZ6L Met430Ile polymorphic variant in
increasing lung cancer risk.
GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 7 (bases 1 to 6348)
AUTHORS Nishioka,M., Kohno,T., Takahashi,M., Niki,T., Yamada,T., Sone,S.
and Yokota,J.
TITLE Identification of a 428-kb homozygously deleted region disrupting
the SEZ6L gene at 22q12.1 in a lung cancer cell line
JOURNAL Oncogene 19 (54), 6251-6260 (2000)
PUBMED 11175339
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AY358405.1, AB023144.2, AB041736.1 and AL078460.6.
Transcript Variant: This variant (5) lacks two alternate, in-frame
segments in the coding region, compared to variant 1. The resulting
protein (isoform 5) is shorter when it is compared to isoform 1.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
##Evidence-Data-START##
Transcript exon combination :: AB023144.2 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-40 AY358405.1 1-40
41-756 AB023144.2 1-716
757-1031 AB041736.1 561-835
1032-1614 AB023144.2 992-1574
1615-1710 AB041736.1 1419-1514
1711-3016 AB023144.2 1671-2976
3017-6348 AL078460.6 524-3855
FEATURES Location/Qualifiers
source 1..6348
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="22"
/map="22q12.1"
gene 1..6348
/gene="SEZ6L"
/note="seizure related 6 homolog (mouse)-like"
/db_xref="GeneID:23544"
/db_xref="HGNC:10763"
/db_xref="MIM:607021"
exon 1..290
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
CDS 197..3046
/gene="SEZ6L"
/note="isoform 5 precursor is encoded by transcript
variant 5; seizure related gene 6-like; seizure 6-like
protein"
/codon_start=1
/product="seizure 6-like protein isoform 5 precursor"
/protein_id="NP_001171705.1"
/db_xref="GI:296179442"
/db_xref="CCDS:CCDS54511.1"
/db_xref="GeneID:23544"
/db_xref="HGNC:10763"
/db_xref="MIM:607021"
/translation="
MPAARPPAAGLRGISLFLALLLGSPAAALERDALPEGDASPLGPYLLPSGAPERGSPGKEHPEERVVTAPPSSSQSAEVLGELVLDGTAPSAHHDIPALSPLLPEEARPKHALPPKKKLPSLKQVNSARKQLRPKATSAATVQRAGSQPASQGLDLLSSSTEKPGPPGDPDPIVASEEASEVPLWLDRKESAVPTTPAPLQISPFTSQPYVAHTLPQRPEPGEPGPDMAQEAPQEDTSPMALMDKGENELTGSASEESQETTTSTIITTTVITTEQAPALCSVSFSNPEGYIDSSDYPLLPLNNFLECTYNVTVYTGYGVELQVKSVNLSDGELLSIRGVDGPTLTVLANQTLLVEGQVIRSPTNTISVYFRTFQDDGLGTFQLHYQAFMLSCNFPRRPDSGDVTVMDLHSGGVAHFHCHLGYELQGAKMLTCINASKPHWSSQEPICSAPCGGAVHNATIGRVLSPSYPENTNGSQFCIWTIEAPEGQKLHLHFERLLLHDKDRMTVHSGQTNKSALLYDSLQTESVPFEGLLSEGNTIRIEFTSDQARAASTFNIRFEAFEKGHCYEPYIQNGNFTTSDPTYNIGTIVEFTCDPGHSLEQGPAIIECINVRDPYWNDTEPLCRAMCGGELSAVAGVVLSPNWPEPYVEGEDCIWKIHVGEEKRIFLDIQFLNLSNSDILTIYDGDEVMPHILGQYLGNSGPQKLYSSTPDLTIQFHSDPAGLIFGKGQGFIMNYIEVSRNDSCSDLPEIQNGWKTTSHTELVRGARITYQCDPGYDIVGSDTLTCQWDLSWSSDPPFCEKTEESLACDNPGLPENGYQILYKRLYLPGESLTFMCYEGFELMGEVTIRCILGQPSHWNGPLPVCKVAEAAAETSLEGGNMALAIFIPVLIISLLLGGAYIYITRCRYYSNLRLPLMYSHPYSQITVETEFDNPIYETGETREYEVSI
"
sig_peptide 197..280
/gene="SEZ6L"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
misc_feature 1037..1360
/gene="SEZ6L"
/note="CUB domain; extracellular domain; present in
proteins mostly known to be involved in development; not
found in prokaryotes, plants and yeast; Region: CUB;
cd00041"
/db_xref="CDD:28922"
misc_feature order(1061..1063,1067..1069,1073..1075,1157..1159,
1172..1174,1271..1273,1343..1345,1349..1351,1355..1360)
/gene="SEZ6L"
/note="heterodimerization interface [polypeptide binding];
other site"
/db_xref="CDD:28922"
misc_feature 1373..1540
/gene="SEZ6L"
/note="Complement control protein (CCP) modules (aka short
consensus repeats SCRs or SUSHI repeats) have been
identified in several proteins of the complement system;
Region: CCP; cd00033"
/db_xref="CDD:153056"
misc_feature order(1403..1405,1454..1456)
/gene="SEZ6L"
/note="receptor-ligand interactions; other site"
/db_xref="CDD:153056"
misc_feature 1550..1879
/gene="SEZ6L"
/note="CUB domain; extracellular domain; present in
proteins mostly known to be involved in development; not
found in prokaryotes, plants and yeast; Region: CUB;
cd00041"
/db_xref="CDD:28922"
misc_feature order(1577..1579,1583..1585,1589..1591,1670..1672,
1685..1687,1787..1789,1862..1864,1868..1870,1874..1879)
/gene="SEZ6L"
/note="heterodimerization interface [polypeptide binding];
other site"
/db_xref="CDD:28922"
misc_feature 1895..2071
/gene="SEZ6L"
/note="Complement control protein (CCP) modules (aka short
consensus repeats SCRs or SUSHI repeats) have been
identified in several proteins of the complement system;
Region: CCP; cd00033"
/db_xref="CDD:153056"
misc_feature order(1922..1924,1979..1981)
/gene="SEZ6L"
/note="receptor-ligand interactions; other site"
/db_xref="CDD:153056"
misc_feature 2078..2404
/gene="SEZ6L"
/note="CUB domain; extracellular domain; present in
proteins mostly known to be involved in development; not
found in prokaryotes, plants and yeast; Region: CUB;
cd00041"
/db_xref="CDD:28922"
misc_feature order(2102..2104,2108..2110,2114..2116,2195..2197,
2210..2212,2309..2311,2393..2395,2399..2401)
/gene="SEZ6L"
/note="heterodimerization interface [polypeptide binding];
other site"
/db_xref="CDD:28922"
misc_feature 2429..2599
/gene="SEZ6L"
/note="Complement control protein (CCP) modules (aka short
consensus repeats SCRs or SUSHI repeats) have been
identified in several proteins of the complement system;
Region: CCP; cd00033"
/db_xref="CDD:153056"
misc_feature order(2459..2461,2516..2518)
/gene="SEZ6L"
/note="receptor-ligand interactions; other site"
/db_xref="CDD:153056"
misc_feature 2621..2797
/gene="SEZ6L"
/note="Complement control protein (CCP) modules (aka short
consensus repeats SCRs or SUSHI repeats) have been
identified in several proteins of the complement system;
Region: CCP; cd00033"
/db_xref="CDD:153056"
misc_feature order(2651..2653,2708..2710)
/gene="SEZ6L"
/note="receptor-ligand interactions; other site"
/db_xref="CDD:153056"
variation 247
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:199592259"
variation 259
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:150514257"
exon 291..1031
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 296
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:200131802"
variation 301
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:201233214"
variation 302
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:373985470"
variation 307
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:35377445"
variation 320
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:16981666"
variation 323
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:144848715"
variation 332
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:140163670"
variation 337
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:375944877"
variation 351
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:6004989"
variation 357
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:201583563"
variation 403
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:145637105"
variation 423
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:367686525"
variation 427
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:371822368"
variation 461
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:376609269"
variation 473
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:147727804"
variation 478
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:372902970"
variation 489
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:201824145"
variation 499
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:140909448"
variation 540
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:144766472"
variation 558
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:151261975"
variation 559
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:376407598"
variation 610
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:369680345"
variation 611
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:140450910"
variation 646
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:150393362"
variation 672
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:373898124"
variation 678
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:201671037"
variation 696
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:200003656"
variation 697
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:192283519"
variation 713
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:201060309"
variation 715
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:376527866"
variation 716
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:149306304"
variation 724
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:371054914"
variation 725
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:370632181"
variation 730
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:374087121"
variation 750
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:137203"
variation 753
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:111570897"
variation 757
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:17304075"
variation 759
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:146205533"
variation 771
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:138721720"
variation 772
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:368342681"
variation 783
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:141695407"
variation 816
/gene="SEZ6L"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200293457"
variation 817
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:143504590"
variation 835
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:371017350"
variation 841
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:374380587"
variation 859
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:202064668"
variation 867
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:368564640"
variation 875
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:147999138"
variation 906
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:199597034"
variation 928
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:141642477"
variation 965
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:150517564"
variation 972
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:201779919"
variation 974
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:193920876"
variation 979
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:370951707"
variation 981
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:375502842"
variation 983
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:367558456"
variation 993
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:368299217"
variation 1005
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:371478865"
variation 1013
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:372123102"
variation 1018
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:376019482"
variation 1024
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:17395296"
exon 1032..1165
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 1063
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:56042239"
variation 1082
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:200380172"
variation 1083
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:372813703"
variation 1107
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:376420402"
variation 1129
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:151335289"
variation 1130
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:375396789"
exon 1166..1358
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 1166
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:201889766"
variation 1174
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:147324317"
variation 1187
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:200655803"
variation 1225
/gene="SEZ6L"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140372463"
variation 1228
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:375660013"
variation 1234
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:112422707"
variation 1235
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:370293421"
variation 1267
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:200005508"
variation 1284
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:200639264"
variation 1301
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:144740621"
variation 1311
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:148526431"
variation 1324
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:371203903"
variation 1325
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:142863810"
variation 1338
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:146559583"
exon 1359..1544
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 1359
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:200415298"
variation 1377
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:141216329"
variation 1384
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:199849358"
variation 1411
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:143488032"
variation 1418
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:201236913"
variation 1462
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:146744873"
variation 1466
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:140350607"
variation 1481
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:150343251"
variation 1486
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:663048"
variation 1513
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:149068026"
exon 1545..1710
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 1577
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:201513330"
variation 1586
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:373919244"
variation 1588
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:200212656"
variation 1589
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:201151950"
variation 1615
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:1210894"
variation 1641
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:138692969"
variation 1642
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:142670064"
variation 1698
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:201913763"
exon 1711..1877
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 1716
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:376866700"
variation 1717
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:371509981"
variation 1726
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:147328329"
variation 1741
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:367751295"
variation 1756
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:199770989"
variation 1771
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:186497116"
variation 1772
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:117917851"
variation 1776
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:200361966"
variation 1809
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:374078308"
variation 1818
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:142214073"
variation 1820
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:201153704"
variation 1822
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:144295883"
variation 1830
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:190114018"
variation 1831
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:368332411"
variation 1835
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:139354547"
variation 1845
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:150022206"
variation 1848
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:201841723"
variation 1849
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:146077946"
variation 1855
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:140029399"
exon 1878..2072
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 1878
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:143554731"
variation 1879
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:199961565"
variation 1900
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:146763740"
variation 1942
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:148910882"
variation 1953
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:201588335"
variation 1962
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:142677073"
variation 1978
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:370996675"
variation 1984
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:150994059"
variation 1985
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:375633558"
variation 2008
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:199713722"
variation 2018
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:370294088"
variation 2036
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:201869380"
exon 2073..2211
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 2109
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:201292047"
variation 2131
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:375506025"
variation 2140
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:145294635"
variation 2190
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:150114413"
variation 2209
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:586542"
exon 2212..2408
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 2245
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:200764167"
variation 2248
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:138699202"
variation 2254
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:141142000"
variation 2255
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:201856091"
variation 2257
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:371326790"
variation 2264
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:376430157"
variation 2296
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:200138174"
variation 2301
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:376290581"
exon 2409..2603
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 2413
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:149869184"
variation 2469
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:375559047"
variation 2475
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:200745477"
variation 2478
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:199970754"
variation 2493
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:137881901"
variation 2521
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:146425607"
variation 2532
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:200709491"
variation 2533
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:141377957"
variation 2534
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:375640180"
variation 2536
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:149442184"
variation 2553
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:144838560"
variation 2590
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:116806899"
variation 2597
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:367783225"
variation 2599
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:141923405"
exon 2604..2798
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 2662
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:146764929"
variation 2680
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:142020765"
variation 2710
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:146313552"
variation 2740
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:148908719"
variation 2775
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:139248080"
variation 2776
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:149968977"
exon 2799..2913
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 2808
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:376385912"
variation 2809
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:369690932"
variation 2821
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:146602479"
variation 2828
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:199913295"
variation 2832
/gene="SEZ6L"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200000489"
variation 2838
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:148666049"
STS 2912..3021
/gene="SEZ6L"
/standard_name="D22S988E"
/db_xref="UniSTS:90244"
exon 2914..3016
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 2934
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:201269295"
variation 2999
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:190563242"
variation 3007
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:374094771"
exon 3017..6348
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 3031
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:138281845"
variation 3057
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:375371828"
variation 3096
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:75138773"
variation 3097
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:142360994"
variation 3107
/gene="SEZ6L"
/replace=""
/replace="t"
/db_xref="dbSNP:144636647"
variation 3166
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:5997084"
variation 3247
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:184914894"
variation 3317
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:112693479"
variation 3318
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:113309050"
variation 3585..3586
/gene="SEZ6L"
/replace=""
/replace="c"
/db_xref="dbSNP:151237595"
variation 3646
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:79392905"
variation 3665
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:375923717"
variation 3716
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:60383901"
variation 3752
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:189670414"
variation 3764
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:115524791"
variation 3772
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:370558030"
variation 3806
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:183208392"
variation 3810
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:5761503"
variation 3879
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:587471"
variation 3906
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:117888300"
variation 3927
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:116578176"
variation 3979
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:138176320"
variation 4138
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:188165461"
variation 4160
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:141792319"
variation 4161
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:73879891"
variation 4225
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:5752315"
variation 4275
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:191717454"
variation 4416
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:116906183"
variation 4455
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:183544332"
STS 4462..4584
/gene="SEZ6L"
/standard_name="D22S1013E"
/db_xref="UniSTS:85568"
variation 4505
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:188874701"
variation 4514
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:192366428"
variation 4535
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:115727743"
variation 4580
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:482902"
variation 4662
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:79154331"
variation 4682
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:183837315"
variation 4736
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:601548"
variation 4780
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:377155701"
variation 4797
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:73415354"
variation 4862
/gene="SEZ6L"
/replace=""
/replace="a"
/db_xref="dbSNP:143254900"
variation 4919
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:114145797"
variation 4921..4922
/gene="SEZ6L"
/replace=""
/replace="c"
/db_xref="dbSNP:35212633"
variation 4927
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:370264622"
variation 4962
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:16981991"
variation 4977
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:372296472"
variation 4995
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:186951974"
variation 5008
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:77237339"
variation 5018
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:76540571"
variation 5019
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:78032966"
variation 5020
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:74382755"
variation 5032
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:149269258"
variation 5051
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:146221536"
variation 5070
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:5997085"
variation 5112
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:191420478"
variation 5115
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:75170824"
variation 5120
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:16981994"
STS 5189..5299
/gene="SEZ6L"
/standard_name="D22S1017E"
/db_xref="UniSTS:150801"
variation 5236
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:184889287"
variation 5246
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:489363"
variation 5260
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:189787384"
variation 5278
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:181806723"
variation 5294
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:7284717"
variation 5349
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:139223070"
variation 5356
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:185094410"
variation 5378
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:143967932"
variation 5405
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:145942215"
variation 5489
/gene="SEZ6L"
/replace=""
/replace="a"
/db_xref="dbSNP:71758401"
variation 5489
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:201703792"
variation 5532
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:16981995"
variation 5576
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:189355139"
variation 5617
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:375396060"
variation 5638
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:182007069"
variation 5771
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:369050660"
variation 5819..5820
/gene="SEZ6L"
/replace=""
/replace="gc"
/db_xref="dbSNP:141631869"
variation 5820
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:77779362"
variation 5821
/gene="SEZ6L"
/replace=""
/replace="t"
/db_xref="dbSNP:35749592"
variation 5822
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:78604204"
variation 5838
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:79458369"
variation 5844
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:62224568"
variation 5992
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:73158677"
variation 6014
/gene="SEZ6L"
/replace=""
/replace="t"
/db_xref="dbSNP:140605651"
variation 6037
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:2092744"
variation 6038
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:16981998"
STS 6117..6226
/gene="SEZ6L"
/standard_name="RH77725"
/db_xref="UniSTS:6770"
variation 6125
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:142481081"
variation 6157
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:73415355"
STS 6169..6328
/gene="SEZ6L"
/standard_name="A002S43"
/db_xref="UniSTS:62230"
STS 6207..6345
/gene="SEZ6L"
/standard_name="WI-18670"
/db_xref="UniSTS:83301"
variation 6216
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:8136212"
variation 6255
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:186236660"
variation 6266
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:376337208"
ORIGIN
gcgcccggcgcagctcggccagagcgaccgcggggctgagcgcgcgtccgcccagggggctccggaagctgccccggcccgcggcctcctccctcgctcccgcttcccctttctcgctcaccgccgccctccttccccagctccctcgccgtccgcccgccccacagccagcggctccgcgccccctgcagccacgatgcccgcggcccggccgcccgccgcgggactccgcgggatctcgctgttcctcgctctgctcctggggagcccggcggcagcgctggagcgagatgctcttcccgagggagatgctagccctttgggtccttacctcctgccctcaggagccccggagagaggcagtcctggcaaagagcaccctgaagagagagtggtaacagcgccccccagttcctcacagtcggcggaagtgctgggcgagctggtgctggatgggaccgcaccctctgcacatcacgacatcccagccctgtcaccgctgcttccagaggaggcccgccccaagcacgccttgccccccaagaagaaactgccttcgctcaagcaggtgaactctgccaggaagcagctgaggcccaaggccacctccgcagccactgtccaaagggcagggtcccagccagcgtcccagggcctagatctcctctcctcctccacggagaagcctggcccaccgggggacccggaccccatcgtggcctccgaggaggcatcagaagtgcccctttggctggaccgaaaggagagtgcggtccctacaacacccgcacccctgcaaatctcccccttcacttcgcagccctatgtggcccacacactcccccagaggccagaacccggggagcctgggcctgacatggcccaggaggccccccaggaggacaccagccccatggccctgatggacaaaggtgagaatgagctgactgggtcagcctcagaggagagccaggagaccactacctccaccattatcaccaccacggtcatcaccaccgagcaggcaccagctctctgcagtgtgagcttctccaatcctgaggggtacattgactccagcgactacccactgctgcccctcaacaactttctggagtgcacatacaacgtgacagtctacactggctatggggtggagctccaggtgaagagtgtgaacctgtccgatggggaactgctctccatccgcggggtggacggccctaccctgaccgtcctggccaaccagacactcctggtggaggggcaggtaatccgaagccccaccaacaccatctccgtctacttccggaccttccaggacgacggccttgggaccttccagcttcactaccaggccttcatgctgagctgcaactttccccgccggcctgactctggggatgtcacggtgatggacctgcactcaggtggggtggcccactttcactgccacctgggctatgagctccagggcgctaagatgctgacatgcatcaatgcctccaagccgcactggagcagccaggagcccatctgctcagctccttgtggaggggcagtgcacaatgccaccatcggccgcgtcctctccccaagttaccctgaaaacacaaatgggagccaattctgcatctggacgattgaagctccagagggccagaagctgcacctgcactttgagaggctgttgctgcatgacaaggacaggatgacggttcacagcgggcagaccaacaagtcagctcttctctacgactcccttcaaaccgagagtgtcccttttgagggcctgctgagcgaaggcaacaccatccgcatcgagttcacgtccgaccaggcccgggcggcctccaccttcaacatccgatttgaagcgtttgagaaaggccactgctatgagccctacatccagaatgggaacttcactacatccgacccgacctataacattgggactatagtggagttcacctgcgaccccggccactccctggagcagggcccggccatcatcgaatgcatcaatgtgcgggacccatactggaatgacacagagcccctgtgcagagccatgtgtggtggggagctctctgctgtggctggggtggtattgtccccaaactggcccgagccctacgtggaaggtgaagattgtatctggaagatccacgtgggagaagagaaacggatcttcttagatatccagttcctgaatctgagcaacagtgacatcttgaccatctacgatggcgacgaggtcatgccccacatcttggggcagtaccttgggaacagtggcccccagaaactgtactcctccacgccagacttaaccatccagttccattcggaccctgctggcctcatctttggaaagggccagggatttatcatgaactacatagaggtatcaaggaatgactcctgctcggatttacccgagatccagaatggctggaaaaccacttctcacacggagttggtgcggggagccagaatcacctaccagtgtgaccccggctatgacatcgtggggagtgacaccctcacctgccagtgggacctcagctggagcagcgaccccccattttgtgagaaaacggaggagtccctggcatgtgacaacccagggctgcctgaaaatggataccaaatcctgtacaagcgactctacctgccaggagagtccctcaccttcatgtgctacgaaggctttgagctcatgggtgaagtgaccatccgctgcatcctgggacagccatcccactggaacgggcccctgcccgtgtgtaaagtagcagaagcggcagcagagacgtcgctggaaggggggaacatggccctggctatcttcatcccggtcctcatcatctccttactgctgggaggagcctacatttacatcacaagatgtcgctactattccaacctccgcctgcctctgatgtactcccacccctacagccagatcaccgtggaaaccgagtttgacaaccccatttacgagacaggggaaaccagagagtatgaggtttctatctaaagagagctacacttgagaaggggacttgtgaactcaaccacaatctcctcgagacattcatccagagaccatgtggcacttgattgaaaccccagaatgtcgactgtcttttgtttagactctttatcaaaggtttactgttttcttccctgtatttattatatttaaaagtgaaataggtgtgggtttggatgtttcgcggcctcagccaaattcatgttacagcctcaattctgaaggcaggtggaagacttgcaaaatggcaaaccgcggcagcaaaaacacaaaacagcagatggagtttctcccatcagcaatgccatgctaaggctgcattgaattgcatgcatctttgggaaccatgcccatgatgttttcagtacaaatctaagtcccaagattaggttggaaagggtatttcttgttggcttagtttgggttggaatttagcatgggtacttaaacccatttggagagctgtgctcctaaacaaattctgtgtcctctcttcccattttgccagcttctgaaaggtttttccacagcccctccctctcacggttcttctgaaggtagcaaaggtgttatataaacattgtcttttaccactctggcctcgctggacagtgacaaaacaagaaaacgttttctttctagaaaggtgataaacgaccaaaggcaatttttcagagacaaatgagagatttgagagttccaatgaagaattgggtgagggggatcattgggtaagggaattgggttaaaatgttcttttctttgacactctttcaatgatgaaagagcgtgtaatttatgctacaagtgccagaatcgatcaccatgttcagcaagccactctcaagctgtggtaataaacacacaggcttgggaggcaccagcggccccactcatacagtgacaaggatttgtgatgggaaaaaggaggtgccatgtttggaaatgcaggggtgagctctggtttctcctggggttctggaatatctcagccctcaaaatagaggagactcaagtgcactgattctctaaaaggtgtcatcttcagaatatacttgccatcaagtatttcagggggcgggagggtcccatgagaagaaactatttttctattctccaaagctgtctggatgttggagggtggtgtgaatgctgactgaggaggtgcagagaacaggggcaggggattttaaatcacagcagaccatccagtggaatcctgtatcatctgatctgaacatcaatgaagacagagagaggaatttcattcagaaaggattccatagccccacatctagtcacacgggcattcctcttattttatcagggtctgttttcccccaacccagtgaaaccggtgagtgtgtaactcttgggaagattcttttctaaatacaggtataaagagaaggtggagggtgcgggtgcatggaagaaatactatgtgtgaagcagattcaccttcctgggaccggtgacatggtggtgacagtcaatggcttggacagacagacgggcacagtggcatttggaaccctctttggtgccctcccattctctctggaattgtttcaagtctgctggttttcaaacaagaaaagacctttctggccatagggagaatagcagggagtctatgttttggtggttacattggaaacatcttaagcaagatagggaaagttgattttaggcacacatgtaccctccttgacagcaggaactcagacttcaatcttgggggtctaagaccagaatattttccttctgccagaaaagaatcttgcacatatactcctgaaggcatgagtgtgtggtccatggcaagaaatagctaaaggctgctttccaggacccaaagccccatttaatgcaagaaccagagaagtgttctaggccattagtggacaatgtcatgtttggagaaagataacaacacaaataatgtaacctttccttaaaaggcagaactcaatccattttatttgatgcttattctaaccctaaccctgggtcacctggaatgaagaactctatgaataatatttgattttacaacgtgttatggttatgtgaaaactaaacatttgccttttataaagactgacaaaatataaatctttattctaaccctatccccaaaactagccaggccacaccccagatgttcttattgactattggaaagatagaaaaggcgttgtgttttttgtttttttgttgttgttgtcattgttgtttttttcagaagaccagtgtctcagttctgtcttagtagtaccacacccgtaaccgtgttttaaaagtttgttttagcctagagacagatcatacgagttcaacaatgtacagtgtgattgaaaagacaggttggtgtctatttttctttttaaaatatctgaatgtgtatttgtaatacgtaaaggtaaaaaaaaatagtgccaaaaatgtgcaaggcatctcattacagctcatgtacgtctgtttttataagatcaatattaaaacccattgggattaaatatttttgaataggatacactcttgagaaactcgagaatggactgagccttcctacaagccactctttgtttttaaaacagtggggaaatacgtttacagagattgtgagcttcagagaatgcatgtgatggtgtgtattacatgctaattcatataagctgtatctgtcagctaccaccctgtgctttaaaaatgcacacactcaaccctctttagcttggagctcagctttttgcttttttttttttttttttgtagaattatttagctaacataagtattctgattgctacctgatggccattcttacttagtttcatagatgtgctttaactatgatcctttgaagctcaccccttggagagcctacagaacctcaggctgatagctttgaagactgccaaacagcccagaaggaagcaaagcatctgcataatcaggagggttgtataacaagtagtgatttggcaaatatgtgggtagctttaggctgaggcacgggcctcaggcaaaaatgcccttcgagtgaatccgaagggcatgatcttcctatgtccttgactaggcatgacgagtcatttgaggtcagatattatttgagttgttcagcacccccaaaggtaggcattctcctgggaaattttcatttccattttatcgccaaacaaaataaaaagcaaaacaaactttctaagctagaataatgaaattaagtcattttccactttgtatatattgatgctaataaaacagatgaaaaagac
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:23544 -> Cellular component: GO:0005789 [endoplasmic reticulum membrane] evidence: IEA
GeneID:23544 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
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