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2025-05-09 19:02:46, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001184773 6570 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens seizure related 6 homolog (mouse)-like (SEZ6L),
transcript variant 2, mRNA.
ACCESSION NM_001184773
VERSION NM_001184773.1 GI:296179435
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 6570)
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 6570)
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 6570)
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 6570)
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 6570)
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 6570)
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 6570)
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, AB041736.1 and AL078460.6.
Transcript Variant: This variant (2) uses a different splice site
in the 3' coding region, compared to variant 1. The resulting
protein (isoform 2) is shorter by 1 aa 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 :: AY358405.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025088 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-756 AY358405.1 1-756
757-1031 AB041736.1 561-835
1032-3238 AY358405.1 1032-3238
3239-6570 AL078460.6 524-3855
FEATURES Location/Qualifiers
source 1..6570
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="22"
/map="22q12.1"
gene 1..6570
/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..3268
/gene="SEZ6L"
/note="isoform 2 precursor is encoded by transcript
variant 2; seizure related gene 6-like; seizure 6-like
protein"
/codon_start=1
/product="seizure 6-like protein isoform 2 precursor"
/protein_id="NP_001171702.1"
/db_xref="GI:296179436"
/db_xref="CCDS:CCDS54508.1"
/db_xref="GeneID:23544"
/db_xref="HGNC:10763"
/db_xref="MIM:607021"
/translation="
MPAARPPAAGLRGISLFLALLLGSPAAALERDALPEGDASPLGPYLLPSGAPERGSPGKEHPEERVVTAPPSSSQSAEVLGELVLDGTAPSAHHDIPALSPLLPEEARPKHALPPKKKLPSLKQVNSARKQLRPKATSAATVQRAGSQPASQGLDLLSSSTEKPGPPGDPDPIVASEEASEVPLWLDRKESAVPTTPAPLQISPFTSQPYVAHTLPQRPEPGEPGPDMAQEAPQEDTSPMALMDKGENELTGSASEESQETTTSTIITTTVITTEQAPALCSVSFSNPEGYIDSSDYPLLPLNNFLECTYNVTVYTGYGVELQVKSVNLSDGELLSIRGVDGPTLTVLANQTLLVEGQVIRSPTNTISVYFRTFQDDGLGTFQLHYQAFMLSCNFPRRPDSGDVTVMDLHSGGVAHFHCHLGYELQGAKMLTCINASKPHWSSQEPICSAPCGGAVHNATIGRVLSPSYPENTNGSQFCIWTIEAPEGQKLHLHFERLLLHDKDRMTVHSGQTNKSALLYDSLQTESVPFEGLLSEGNTIRIEFTSDQARAASTFNIRFEAFEKGHCYEPYIQNGNFTTSDPTYNIGTIVEFTCDPGHSLEQGPAIIECINVRDPYWNDTEPLCRAMCGGELSAVAGVVLSPNWPEPYVEGEDCIWKIHVGEEKRIFLDIQFLNLSNSDILTIYDGDEVMPHILGQYLGNSGPQKLYSSTPDLTIQFHSDPAGLIFGKGQGFIMNYIEVSRNDSCSDLPEIQNGWKTTSHTELVRGARITYQCDPGYDIVGSDTLTCQWDLSWSSDPPFCEKIMYCTDPGEVDHSTRLISDPVLLVGTTIQYTCNPGFVLEGSSLLTCYSRETGTPIWTSRLPHCVSEESLACDNPGLPENGYQILYKRLYLPGESLTFMCYEGFELMGEVTIRCILGQPSHWNGPLPVCKVNQDSFEHALEAEAAAETSLEGGNMALAIFIPVLIISLLLGGAYIYITRCRYYSNLRLPLMYSHPYSQITVETEFDNPIYETGETREYEVSI
"
sig_peptide 197..280
/gene="SEZ6L"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
misc_feature 635..679
/gene="SEZ6L"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9BYH1.1);
Region: O-glycosylated at one site"
misc_feature 722..736
/gene="SEZ6L"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9BYH1.1);
Region: O-glycosylated at one site"
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 2612..2794
/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(2642..2644,2699..2701)
/gene="SEZ6L"
/note="receptor-ligand interactions; other site"
/db_xref="CDD:153056"
misc_feature 2813..2989
/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(2843..2845,2900..2902)
/gene="SEZ6L"
/note="receptor-ligand interactions; other site"
/db_xref="CDD:153056"
misc_feature 3068..3130
/gene="SEZ6L"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9BYH1.1);
transmembrane region"
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..2795
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 2614
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:371793077"
variation 2623
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:374698416"
variation 2629
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:146097392"
variation 2641
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:140063137"
variation 2671
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:111824937"
variation 2697
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:58982553"
variation 2704
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:375190155"
variation 2747
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:369993825"
variation 2791
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:200098200"
exon 2796..2990
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 2854
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:146764929"
variation 2872
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:142020765"
variation 2902
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:146313552"
variation 2932
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:148908719"
variation 2967
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:139248080"
variation 2968
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:149968977"
exon 2991..3023
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 3015
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:202010195"
exon 3024..3135
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 3030
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:376385912"
variation 3031
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:369690932"
variation 3043
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:146602479"
variation 3050
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:199913295"
variation 3054
/gene="SEZ6L"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200000489"
variation 3060
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:148666049"
STS 3134..3243
/gene="SEZ6L"
/standard_name="D22S988E"
/db_xref="UniSTS:90244"
exon 3136..3238
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 3156
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:201269295"
variation 3221
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:190563242"
variation 3229
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:374094771"
exon 3239..6570
/gene="SEZ6L"
/inference="alignment:Splign:1.39.8"
variation 3253
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:138281845"
variation 3279
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:375371828"
variation 3318
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:75138773"
variation 3319
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:142360994"
variation 3329
/gene="SEZ6L"
/replace=""
/replace="t"
/db_xref="dbSNP:144636647"
variation 3388
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:5997084"
variation 3469
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:184914894"
variation 3539
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:112693479"
variation 3540
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:113309050"
variation 3807..3808
/gene="SEZ6L"
/replace=""
/replace="c"
/db_xref="dbSNP:151237595"
variation 3868
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:79392905"
variation 3887
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:375923717"
variation 3938
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:60383901"
variation 3974
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:189670414"
variation 3986
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:115524791"
variation 3994
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:370558030"
variation 4028
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:183208392"
variation 4032
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:5761503"
variation 4101
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:587471"
variation 4128
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:117888300"
variation 4149
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:116578176"
variation 4201
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:138176320"
variation 4360
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:188165461"
variation 4382
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:141792319"
variation 4383
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:73879891"
variation 4447
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:5752315"
variation 4497
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:191717454"
variation 4638
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:116906183"
variation 4677
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:183544332"
STS 4684..4806
/gene="SEZ6L"
/standard_name="D22S1013E"
/db_xref="UniSTS:85568"
variation 4727
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:188874701"
variation 4736
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:192366428"
variation 4757
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:115727743"
variation 4802
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:482902"
variation 4884
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:79154331"
variation 4904
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:183837315"
variation 4958
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:601548"
variation 5002
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:377155701"
variation 5019
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:73415354"
variation 5084
/gene="SEZ6L"
/replace=""
/replace="a"
/db_xref="dbSNP:143254900"
variation 5141
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:114145797"
variation 5143..5144
/gene="SEZ6L"
/replace=""
/replace="c"
/db_xref="dbSNP:35212633"
variation 5149
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:370264622"
variation 5184
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:16981991"
variation 5199
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:372296472"
variation 5217
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:186951974"
variation 5230
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:77237339"
variation 5240
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:76540571"
variation 5241
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:78032966"
variation 5242
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:74382755"
variation 5254
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:149269258"
variation 5273
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:146221536"
variation 5292
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:5997085"
variation 5334
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:191420478"
variation 5337
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:75170824"
variation 5342
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:16981994"
STS 5411..5521
/gene="SEZ6L"
/standard_name="D22S1017E"
/db_xref="UniSTS:150801"
variation 5458
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:184889287"
variation 5468
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:489363"
variation 5482
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:189787384"
variation 5500
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:181806723"
variation 5516
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:7284717"
variation 5571
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:139223070"
variation 5578
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:185094410"
variation 5600
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:143967932"
variation 5627
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:145942215"
variation 5711
/gene="SEZ6L"
/replace=""
/replace="a"
/db_xref="dbSNP:71758401"
variation 5711
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:201703792"
variation 5754
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:16981995"
variation 5798
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:189355139"
variation 5839
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:375396060"
variation 5860
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:182007069"
variation 5993
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:369050660"
variation 6041..6042
/gene="SEZ6L"
/replace=""
/replace="gc"
/db_xref="dbSNP:141631869"
variation 6042
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:77779362"
variation 6043
/gene="SEZ6L"
/replace=""
/replace="t"
/db_xref="dbSNP:35749592"
variation 6044
/gene="SEZ6L"
/replace="c"
/replace="t"
/db_xref="dbSNP:78604204"
variation 6060
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:79458369"
variation 6066
/gene="SEZ6L"
/replace="a"
/replace="t"
/db_xref="dbSNP:62224568"
variation 6214
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:73158677"
variation 6236
/gene="SEZ6L"
/replace=""
/replace="t"
/db_xref="dbSNP:140605651"
variation 6259
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:2092744"
variation 6260
/gene="SEZ6L"
/replace="c"
/replace="g"
/db_xref="dbSNP:16981998"
STS 6339..6448
/gene="SEZ6L"
/standard_name="RH77725"
/db_xref="UniSTS:6770"
variation 6347
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:142481081"
variation 6379
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:73415355"
STS 6391..6550
/gene="SEZ6L"
/standard_name="A002S43"
/db_xref="UniSTS:62230"
STS 6429..6567
/gene="SEZ6L"
/standard_name="WI-18670"
/db_xref="UniSTS:83301"
variation 6438
/gene="SEZ6L"
/replace="a"
/replace="c"
/db_xref="dbSNP:8136212"
variation 6477
/gene="SEZ6L"
/replace="g"
/replace="t"
/db_xref="dbSNP:186236660"
variation 6488
/gene="SEZ6L"
/replace="a"
/replace="g"
/db_xref="dbSNP:376337208"
ORIGIN
gcgcccggcgcagctcggccagagcgaccgcggggctgagcgcgcgtccgcccagggggctccggaagctgccccggcccgcggcctcctccctcgctcccgcttcccctttctcgctcaccgccgccctccttccccagctccctcgccgtccgcccgccccacagccagcggctccgcgccccctgcagccacgatgcccgcggcccggccgcccgccgcgggactccgcgggatctcgctgttcctcgctctgctcctggggagcccggcggcagcgctggagcgagatgctcttcccgagggagatgctagccctttgggtccttacctcctgccctcaggagccccggagagaggcagtcctggcaaagagcaccctgaagagagagtggtaacagcgccccccagttcctcacagtcggcggaagtgctgggcgagctggtgctggatgggaccgcaccctctgcacatcacgacatcccagccctgtcaccgctgcttccagaggaggcccgccccaagcacgccttgccccccaagaagaaactgccttcgctcaagcaggtgaactctgccaggaagcagctgaggcccaaggccacctccgcagccactgtccaaagggcagggtcccagccagcgtcccagggcctagatctcctctcctcctccacggagaagcctggcccaccgggggacccggaccccatcgtggcctccgaggaggcatcagaagtgcccctttggctggaccgaaaggagagtgcggtccctacaacacccgcacccctgcaaatctcccccttcacttcgcagccctatgtggcccacacactcccccagaggccagaacccggggagcctgggcctgacatggcccaggaggccccccaggaggacaccagccccatggccctgatggacaaaggtgagaatgagctgactgggtcagcctcagaggagagccaggagaccactacctccaccattatcaccaccacggtcatcaccaccgagcaggcaccagctctctgcagtgtgagcttctccaatcctgaggggtacattgactccagcgactacccactgctgcccctcaacaactttctggagtgcacatacaacgtgacagtctacactggctatggggtggagctccaggtgaagagtgtgaacctgtccgatggggaactgctctccatccgcggggtggacggccctaccctgaccgtcctggccaaccagacactcctggtggaggggcaggtaatccgaagccccaccaacaccatctccgtctacttccggaccttccaggacgacggccttgggaccttccagcttcactaccaggccttcatgctgagctgcaactttccccgccggcctgactctggggatgtcacggtgatggacctgcactcaggtggggtggcccactttcactgccacctgggctatgagctccagggcgctaagatgctgacatgcatcaatgcctccaagccgcactggagcagccaggagcccatctgctcagctccttgtggaggggcagtgcacaatgccaccatcggccgcgtcctctccccaagttaccctgaaaacacaaatgggagccaattctgcatctggacgattgaagctccagagggccagaagctgcacctgcactttgagaggctgttgctgcatgacaaggacaggatgacggttcacagcgggcagaccaacaagtcagctcttctctacgactcccttcaaaccgagagtgtcccttttgagggcctgctgagcgaaggcaacaccatccgcatcgagttcacgtccgaccaggcccgggcggcctccaccttcaacatccgatttgaagcgtttgagaaaggccactgctatgagccctacatccagaatgggaacttcactacatccgacccgacctataacattgggactatagtggagttcacctgcgaccccggccactccctggagcagggcccggccatcatcgaatgcatcaatgtgcgggacccatactggaatgacacagagcccctgtgcagagccatgtgtggtggggagctctctgctgtggctggggtggtattgtccccaaactggcccgagccctacgtggaaggtgaagattgtatctggaagatccacgtgggagaagagaaacggatcttcttagatatccagttcctgaatctgagcaacagtgacatcttgaccatctacgatggcgacgaggtcatgccccacatcttggggcagtaccttgggaacagtggcccccagaaactgtactcctccacgccagacttaaccatccagttccattcggaccctgctggcctcatctttggaaagggccagggatttatcatgaactacatagaggtatcaaggaatgactcctgctcggatttacccgagatccagaatggctggaaaaccacttctcacacggagttggtgcggggagccagaatcacctaccagtgtgaccccggctatgacatcgtggggagtgacaccctcacctgccagtgggacctcagctggagcagcgaccccccattttgtgagaaaattatgtactgcaccgaccccggagaggtggatcactcgacccgcttaatttcggatcctgtgctgctggtggggaccaccatccaatacacctgcaaccccggttttgtgcttgaagggagttctcttctgacctgctacagccgtgaaacagggactcccatctggacgtctcgcctgccccactgcgtttcggaggagtccctggcatgtgacaacccagggctgcctgaaaatggataccaaatcctgtacaagcgactctacctgccaggagagtccctcaccttcatgtgctacgaaggctttgagctcatgggtgaagtgaccatccgctgcatcctgggacagccatcccactggaacgggcccctgcccgtgtgtaaagttaatcaagacagttttgaacatgctttagaagcagaagcggcagcagagacgtcgctggaaggggggaacatggccctggctatcttcatcccggtcctcatcatctccttactgctgggaggagcctacatttacatcacaagatgtcgctactattccaacctccgcctgcctctgatgtactcccacccctacagccagatcaccgtggaaaccgagtttgacaaccccatttacgagacaggggaaaccagagagtatgaggtttctatctaaagagagctacacttgagaaggggacttgtgaactcaaccacaatctcctcgagacattcatccagagaccatgtggcacttgattgaaaccccagaatgtcgactgtcttttgtttagactctttatcaaaggtttactgttttcttccctgtatttattatatttaaaagtgaaataggtgtgggtttggatgtttcgcggcctcagccaaattcatgttacagcctcaattctgaaggcaggtggaagacttgcaaaatggcaaaccgcggcagcaaaaacacaaaacagcagatggagtttctcccatcagcaatgccatgctaaggctgcattgaattgcatgcatctttgggaaccatgcccatgatgttttcagtacaaatctaagtcccaagattaggttggaaagggtatttcttgttggcttagtttgggttggaatttagcatgggtacttaaacccatttggagagctgtgctcctaaacaaattctgtgtcctctcttcccattttgccagcttctgaaaggtttttccacagcccctccctctcacggttcttctgaaggtagcaaaggtgttatataaacattgtcttttaccactctggcctcgctggacagtgacaaaacaagaaaacgttttctttctagaaaggtgataaacgaccaaaggcaatttttcagagacaaatgagagatttgagagttccaatgaagaattgggtgagggggatcattgggtaagggaattgggttaaaatgttcttttctttgacactctttcaatgatgaaagagcgtgtaatttatgctacaagtgccagaatcgatcaccatgttcagcaagccactctcaagctgtggtaataaacacacaggcttgggaggcaccagcggccccactcatacagtgacaaggatttgtgatgggaaaaaggaggtgccatgtttggaaatgcaggggtgagctctggtttctcctggggttctggaatatctcagccctcaaaatagaggagactcaagtgcactgattctctaaaaggtgtcatcttcagaatatacttgccatcaagtatttcagggggcgggagggtcccatgagaagaaactatttttctattctccaaagctgtctggatgttggagggtggtgtgaatgctgactgaggaggtgcagagaacaggggcaggggattttaaatcacagcagaccatccagtggaatcctgtatcatctgatctgaacatcaatgaagacagagagaggaatttcattcagaaaggattccatagccccacatctagtcacacgggcattcctcttattttatcagggtctgttttcccccaacccagtgaaaccggtgagtgtgtaactcttgggaagattcttttctaaatacaggtataaagagaaggtggagggtgcgggtgcatggaagaaatactatgtgtgaagcagattcaccttcctgggaccggtgacatggtggtgacagtcaatggcttggacagacagacgggcacagtggcatttggaaccctctttggtgccctcccattctctctggaattgtttcaagtctgctggttttcaaacaagaaaagacctttctggccatagggagaatagcagggagtctatgttttggtggttacattggaaacatcttaagcaagatagggaaagttgattttaggcacacatgtaccctccttgacagcaggaactcagacttcaatcttgggggtctaagaccagaatattttccttctgccagaaaagaatcttgcacatatactcctgaaggcatgagtgtgtggtccatggcaagaaatagctaaaggctgctttccaggacccaaagccccatttaatgcaagaaccagagaagtgttctaggccattagtggacaatgtcatgtttggagaaagataacaacacaaataatgtaacctttccttaaaaggcagaactcaatccattttatttgatgcttattctaaccctaaccctgggtcacctggaatgaagaactctatgaataatatttgattttacaacgtgttatggttatgtgaaaactaaacatttgccttttataaagactgacaaaatataaatctttattctaaccctatccccaaaactagccaggccacaccccagatgttcttattgactattggaaagatagaaaaggcgttgtgttttttgtttttttgttgttgttgtcattgttgtttttttcagaagaccagtgtctcagttctgtcttagtagtaccacacccgtaaccgtgttttaaaagtttgttttagcctagagacagatcatacgagttcaacaatgtacagtgtgattgaaaagacaggttggtgtctatttttctttttaaaatatctgaatgtgtatttgtaatacgtaaaggtaaaaaaaaatagtgccaaaaatgtgcaaggcatctcattacagctcatgtacgtctgtttttataagatcaatattaaaacccattgggattaaatatttttgaataggatacactcttgagaaactcgagaatggactgagccttcctacaagccactctttgtttttaaaacagtggggaaatacgtttacagagattgtgagcttcagagaatgcatgtgatggtgtgtattacatgctaattcatataagctgtatctgtcagctaccaccctgtgctttaaaaatgcacacactcaaccctctttagcttggagctcagctttttgcttttttttttttttttttgtagaattatttagctaacataagtattctgattgctacctgatggccattcttacttagtttcatagatgtgctttaactatgatcctttgaagctcaccccttggagagcctacagaacctcaggctgatagctttgaagactgccaaacagcccagaaggaagcaaagcatctgcataatcaggagggttgtataacaagtagtgatttggcaaatatgtgggtagctttaggctgaggcacgggcctcaggcaaaaatgcccttcgagtgaatccgaagggcatgatcttcctatgtccttgactaggcatgacgagtcatttgaggtcagatattatttgagttgttcagcacccccaaaggtaggcattctcctgggaaattttcatttccattttatcgccaaacaaaataaaaagcaaaacaaactttctaagctagaataatgaaattaagtcattttccactttgtatatattgatgctaataaaacagatgaaaaagac
//
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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