2024-03-29 02:04:28, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_004822 5954 bp mRNA linear PRI 15-JUN-2013 DEFINITION Homo sapiens netrin 1 (NTN1), mRNA. ACCESSION NM_004822 VERSION NM_004822.2 GI:148613883 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 5954) AUTHORS Rafiq,S., Tapper,W., Collins,A., Khan,S., Politopoulos,I., Gerty,S., Blomqvist,C., Couch,F.J., Nevanlinna,H., Liu,J. and Eccles,D. TITLE Identification of inherited genetic variations influencing prognosis in early-onset breast cancer JOURNAL Cancer Res. 73 (6), 1883-1891 (2013) PUBMED 23319801 REFERENCE 2 (bases 1 to 5954) AUTHORS Shimizu,A., Nakayama,H., Wang,P., Konig,C., Akino,T., Sandlund,J., Coma,S., Italiano,J.E. Jr., Mammoto,A., Bielenberg,D.R. and Klagsbrun,M. TITLE Netrin-1 promotes glioblastoma cell invasiveness and angiogenesis by multiple pathways including activation of RhoA, cathepsin B, and cAMP-response element-binding protein JOURNAL J. Biol. Chem. 288 (4), 2210-2222 (2013) PUBMED 23195957 REMARK GeneRIF: Netrin-1 promotes glioblastoma cell invasiveness and angiogenesis by multiple pathways including activation of RhoA, cathepsin B, and cAMP-response element-binding protein REFERENCE 3 (bases 1 to 5954) AUTHORS Kefeli,U., Yildirim,M.E., Aydin,D., Madenci,O.C., Yasar,N., Sener,N., Mert,A.G., Yuksel,S., Ercelep,O.B., Korkmaz,T., Yildiz,R. and Gumus,M. TITLE Netrin-1 concentrations in patients with advanced gastric cancer and its relation with treatment JOURNAL Biomarkers 17 (7), 663-667 (2012) PUBMED 22889408 REMARK GeneRIF: There was no relationship between the basal netrin-1 and decline in netrin-1 concentrations and the progression-free survival and overall survival in gastric cancer. REFERENCE 4 (bases 1 to 5954) AUTHORS Ludwig,K.U., Mangold,E., Herms,S., Nowak,S., Reutter,H., Paul,A., Becker,J., Herberz,R., AlChawa,T., Nasser,E., Bohmer,A.C., Mattheisen,M., Alblas,M.A., Barth,S., Kluck,N., Lauster,C., Braumann,B., Reich,R.H., Hemprich,A., Potzsch,S., Blaumeiser,B., Daratsianos,N., Kreusch,T., Murray,J.C., Marazita,M.L., Ruczinski,I., Scott,A.F., Beaty,T.H., Kramer,F.J., Wienker,T.F., Steegers-Theunissen,R.P., Rubini,M., Mossey,P.A., Hoffmann,P., Lange,C., Cichon,S., Propping,P., Knapp,M. and Nothen,M.M. TITLE Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci JOURNAL Nat. Genet. 44 (9), 968-971 (2012) PUBMED 22863734 REFERENCE 5 (bases 1 to 5954) AUTHORS Delloye-Bourgeois,C., Goldschneider,D., Paradisi,A., Therizols,G., Belin,S., Hacot,S., Rosa-Calatrava,M., Scoazec,J.Y., Diaz,J.J., Bernet,A. and Mehlen,P. TITLE Nucleolar localization of a netrin-1 isoform enhances tumor cell proliferation JOURNAL Sci Signal 5 (236), RA57 (2012) PUBMED 22871610 REMARK GeneRIF: Data indicate that DeltaN-netrin-1 stimulated cell proliferation in vitro and tumor growth in vivo. Publication Status: Online-Only REFERENCE 6 (bases 1 to 5954) AUTHORS Brose,K., Bland,K.S., Wang,K.H., Arnott,D., Henzel,W., Goodman,C.S., Tessier-Lavigne,M. and Kidd,T. TITLE Slit proteins bind Robo receptors and have an evolutionarily conserved role in repulsive axon guidance JOURNAL Cell 96 (6), 795-806 (1999) PUBMED 10102268 REFERENCE 7 (bases 1 to 5954) AUTHORS Meyerhardt,J.A., Caca,K., Eckstrand,B.C., Hu,G., Lengauer,C., Banavali,S., Look,A.T. and Fearon,E.R. TITLE Netrin-1: interaction with deleted in colorectal cancer (DCC) and alterations in brain tumors and neuroblastomas JOURNAL Cell Growth Differ. 10 (1), 35-42 (1999) PUBMED 9950216 REFERENCE 8 (bases 1 to 5954) AUTHORS Hu,G. and Fearon,E.R. TITLE Siah-1 N-terminal RING domain is required for proteolysis function, and C-terminal sequences regulate oligomerization and binding to target proteins JOURNAL Mol. Cell. Biol. 19 (1), 724-732 (1999) PUBMED 9858595 REFERENCE 9 (bases 1 to 5954) AUTHORS Serafini,T., Colamarino,S.A., Leonardo,E.D., Wang,H., Beddington,R., Skarnes,W.C. and Tessier-Lavigne,M. TITLE Netrin-1 is required for commissural axon guidance in the developing vertebrate nervous system JOURNAL Cell 87 (6), 1001-1014 (1996) PUBMED 8978605 REFERENCE 10 (bases 1 to 5954) AUTHORS Keino-Masu,K., Masu,M., Hinck,L., Leonardo,E.D., Chan,S.S., Culotti,J.G. and Tessier-Lavigne,M. TITLE Deleted in Colorectal Cancer (DCC) encodes a netrin receptor JOURNAL Cell 87 (2), 175-185 (1996) PUBMED 8861902 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from U75586.1, AC090610.6 and AC005695.1. On Jun 6, 2007 this sequence version replaced gi:4758839. Summary: Netrin is included in a family of laminin-related secreted proteins. The function of this gene has not yet been defined; however, netrin is thought to be involved in axon guidance and cell migration during development. Mutations and loss of expression of netrin suggest that variation in netrin may be involved in cancer development. [provided by RefSeq, Jul 2008]. Sequence Note: This RefSeq record was created from transcript and genomic sequence data because no single transcript was available for the full length of the gene. 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 :: U75586.1 [ECO:0000332] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-16 U75586.1 3-18 17-17 AC090610.6 63987-63987 18-1001 U75586.1 20-1003 1002-1003 AC090610.6 65697-65698 1004-1946 U75586.1 1006-1948 1947-5954 AC005695.1 103259-107266 FEATURES Location/Qualifiers source 1..5954 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="17" /map="17p13-p12" gene 1..5954 /gene="NTN1" /gene_synonym="NTN1L" /note="netrin 1" /db_xref="GeneID:9423" /db_xref="HGNC:8029" /db_xref="MIM:601614" exon 1..44 /gene="NTN1" /gene_synonym="NTN1L" /inference="alignment:Splign:1.39.8" variation 17 /gene="NTN1" /gene_synonym="NTN1L" /replace="g" /replace="t" /db_xref="dbSNP:56249806" exon 45..1125 /gene="NTN1" /gene_synonym="NTN1L" /inference="alignment:Splign:1.39.8" variation 106 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:147316711" CDS 108..1922 /gene="NTN1" /gene_synonym="NTN1L" /note="netrin 1, mouse, homolog of; Netrin-1; epididymis tissue protein Li 131P" /codon_start=1 /product="netrin-1 precursor" /protein_id="NP_004813.2" /db_xref="GI:148613884" /db_xref="CCDS:CCDS11148.1" /db_xref="GeneID:9423" /db_xref="HGNC:8029" /db_xref="MIM:601614" /translation="
MMRAVWEALAALAAVACLVGAVRGGPGLSMFAGQAAQPDPCSDENGHPRRCIPDFVNAAFGKDVRVSSTCGRPPARYCVVSERGEERLRSCHLCNASDPKKAHPPAFLTDLNNPHNLTCWQSENYLQFPHNVTLTLSLGKKFEVTYVSLQFCSPRPESMAIYKSMDYGRTWVPFQFYSTQCRKMYNRPHRAPITKQNEQEAVCTDSHTDMRPLSGGLIAFSTLDGRPSAHDFDNSPVLQDWVTATDIRVAFSRLHTFGDENEDDSELARDSYFYAVSDLQVGGRCKCNGHAARCVRDRDDSLVCDCRHNTAGPECDRCKPFHYDRPWQRATAREANECVACNCNLHARRCRFNMELYKLSGRKSGGVCLNCRHNTAGRHCHYCKEGYYRDMGKPITHRKACKACDCHPVGAAGKTCNQTTGQCPCKDGVTGITCNRCAKGYQQSRSPIAPCIKIPVAPPTTAASSVEEPEDCDSYCKASKGKLKINMKKYCKKDYAVQIHILKADKAGDWWKFTVNIISVYKQGTSRIRRGDQSLWIRSRDIACKCPKIKPLKKYLLLGNAEDSPDQSGIVADKSSLVIQWRDTWARRLRKFQQREKKGKCKKA
" sig_peptide 108..179 /gene="NTN1" /gene_synonym="NTN1L" /inference="COORDINATES: ab initio prediction:SignalP:4.0" misc_feature 243..956 /gene="NTN1" /gene_synonym="NTN1L" /note="Laminin N-terminal domain (domain VI); Region: LamNT; smart00136" /db_xref="CDD:214532" misc_feature 957..1094 /gene="NTN1" /gene_synonym="NTN1L" /note="Laminin-type epidermal growth factor-like domain; laminins are the major noncollagenous components of basement membranes that mediate cell adhesion, growth migration, and differentiation; the laminin-type epidermal growth factor-like module occurs in...; Region: EGF_Lam; cd00055" /db_xref="CDD:238012" misc_feature 960..1091 /gene="NTN1" /gene_synonym="NTN1L" /note="Laminin-type epidermal growth factor-like domai; Region: EGF_Lam; smart00180" /db_xref="CDD:214543" misc_feature order(960..962,966..968,996..998,1017..1019,1023..1025, 1050..1052) /gene="NTN1" /gene_synonym="NTN1L" /note="EGF-like motif; other site" /db_xref="CDD:238012" misc_feature 1125..1277 /gene="NTN1" /gene_synonym="NTN1L" /note="Laminin-type epidermal growth factor-like domain; laminins are the major noncollagenous components of basement membranes that mediate cell adhesion, growth migration, and differentiation; the laminin-type epidermal growth factor-like module occurs in...; Region: EGF_Lam; cd00055" /db_xref="CDD:238012" misc_feature 1128..1310 /gene="NTN1" /gene_synonym="NTN1L" /note="Laminin EGF-like (Domains III and V); Region: Laminin_EGF; pfam00053" /db_xref="CDD:215680" misc_feature order(1128..1130,1134..1136,1155..1157,1209..1211, 1218..1220,1245..1247) /gene="NTN1" /gene_synonym="NTN1L" /note="EGF-like motif; other site" /db_xref="CDD:238012" misc_feature 1314..1460 /gene="NTN1" /gene_synonym="NTN1L" /note="Laminin-type epidermal growth factor-like domain; laminins are the major noncollagenous components of basement membranes that mediate cell adhesion, growth migration, and differentiation; the laminin-type epidermal growth factor-like module occurs in...; Region: EGF_Lam; cd00055" /db_xref="CDD:238012" misc_feature 1317..1430 /gene="NTN1" /gene_synonym="NTN1L" /note="Laminin-type epidermal growth factor-like domai; Region: EGF_Lam; smart00180" /db_xref="CDD:214543" misc_feature order(1317..1319,1323..1325,1353..1355,1374..1376, 1380..1382,1407..1409) /gene="NTN1" /gene_synonym="NTN1L" /note="EGF-like motif; other site" /db_xref="CDD:238012" misc_feature 1566..1910 /gene="NTN1" /gene_synonym="NTN1L" /note="NTR domain, Netrin-1-like subfamily; The C-terminal NTR domain of netrins is also called domain C in the context of C. elegans netrin UNC-6. Netrins are secreted proteins that function as tropic cues in the direction of axon growth and cell migration...; Region: NTR_netrin-1_like; cd03579" /db_xref="CDD:239634" misc_feature 1695..1703 /gene="NTN1" /gene_synonym="NTN1L" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O95631.2); Region: Cell attachment site (Potential)" variation 140 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:111911652" variation 227 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:376332478" variation 244 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:141044792" variation 326 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:369647326" variation 381 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="c" /db_xref="dbSNP:375380782" variation 446 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:199769574" variation 449 /gene="NTN1" /gene_synonym="NTN1L" /replace="g" /replace="t" /db_xref="dbSNP:73262152" variation 478 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="c" /db_xref="dbSNP:200187924" variation 626 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:146020999" variation 638 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:199821941" variation 704 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:138686641" variation 718 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:201736911" variation 722 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:191233754" variation 727 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:200854554" variation 735 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:199674301" variation 738 /gene="NTN1" /gene_synonym="NTN1L" /replace="g" /replace="t" /db_xref="dbSNP:34079256" variation 748 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:372642681" variation 839 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:144535726" variation 865 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:148441765" variation 901 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:142558586" variation 964 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="t" /db_xref="dbSNP:199797660" variation 992..993 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="gc" /db_xref="dbSNP:3054489" variation 1040 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:113016880" exon 1126..1314 /gene="NTN1" /gene_synonym="NTN1L" /inference="alignment:Splign:1.39.8" variation 1139 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:377280564" variation 1148 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:370864994" variation 1149 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:375204917" variation 1150 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:368127099" variation 1153 /gene="NTN1" /gene_synonym="NTN1L" /replace="g" /replace="t" /db_xref="dbSNP:374707235" variation 1158 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:140248343" variation 1187 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:375467976" variation 1217 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:144950762" variation 1235 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:112161714" variation 1244 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:55687153" variation 1250 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:2286511" variation 1274 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:368406936" variation 1304 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:150043655" exon 1315..1464 /gene="NTN1" /gene_synonym="NTN1L" /inference="alignment:Splign:1.39.8" variation 1367 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:200644287" variation 1369..1370 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="g" /db_xref="dbSNP:34730390" variation 1391 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:140380921" variation 1396 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:199736561" variation 1402 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:367908355" variation 1418 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:145337237" exon 1465..1518 /gene="NTN1" /gene_synonym="NTN1L" /inference="alignment:Splign:1.39.8" variation 1480 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:149166851" variation 1482 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="c" /db_xref="dbSNP:376278603" variation 1483 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:370320158" variation 1484 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:368540968" variation 1486 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:201647422" exon 1519..1593 /gene="NTN1" /gene_synonym="NTN1L" /inference="alignment:Splign:1.39.8" variation 1523 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:376071535" variation 1537 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:192776775" variation 1574 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:367820405" variation 1586 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:143263899" exon 1594..5954 /gene="NTN1" /gene_synonym="NTN1L" /inference="alignment:Splign:1.39.8" variation 1605 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:146793027" variation 1628 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:140474900" variation 1649 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:145630338" variation 1656 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:372941055" variation 1665 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:201393437" variation 1697 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:377128539" variation 1724 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:138773744" variation 1727 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:112235411" variation 1754 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:372411993" variation 1778 /gene="NTN1" /gene_synonym="NTN1L" /replace="g" /replace="t" /db_xref="dbSNP:367794200" variation 1818 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:199592596" variation 1839 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:77968125" variation 1913..1914 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="t" /db_xref="dbSNP:34229722" variation 1916 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:371521051" variation 2095 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:113122856" variation 2113 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:184106895" variation 2150 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:368067419" variation 2253 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:372235419" variation 2286 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:376515380" variation 2419 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:147972816" variation 2501 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1107361" variation 2568 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:3826394" variation 2571 /gene="NTN1" /gene_synonym="NTN1L" /replace="g" /replace="t" /db_xref="dbSNP:12453129" variation 2685..2696 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="ctgcccctgccc" /db_xref="dbSNP:6145985" variation 2685..2690 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="gggcag" /db_xref="dbSNP:3031879" variation 2694 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:372928070" variation 2726 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:374885476" variation 2771 /gene="NTN1" /gene_synonym="NTN1L" /replace="g" /replace="t" /db_xref="dbSNP:188454225" variation 2832 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="c" /db_xref="dbSNP:192604291" variation 2839 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="t" /db_xref="dbSNP:117799337" variation 2840 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:184534380" variation 2885 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:372110023" variation 3048 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:117971919" variation 3061 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:112770710" variation 3139 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:116653846" variation 3226 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:76071723" variation 3250 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:367882302" variation 3414 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="c" /db_xref="dbSNP:150517773" variation 3516 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:369025778" variation 3575 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:189010670" variation 3577 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:372758212" variation 3633..3634 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="t" /db_xref="dbSNP:34984969" variation 3728 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:372579982" variation 3760 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:374848429" variation 3823 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:57905138" variation 3844 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:142772498" variation 3859 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:116437061" variation 3860 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:77633648" variation 3981 /gene="NTN1" /gene_synonym="NTN1L" /replace="g" /replace="t" /db_xref="dbSNP:369254846" variation 3994 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="c" /db_xref="dbSNP:78537369" variation 4029 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:8074624" variation 4072 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="c" /db_xref="dbSNP:113998401" variation 4091 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:369174841" variation 4095 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:72814112" variation 4153 /gene="NTN1" /gene_synonym="NTN1L" /replace="g" /replace="t" /db_xref="dbSNP:182407078" variation 4341 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:372941392" variation 4342 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:376979448" variation 4352 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:147393486" variation 4449 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="c" /db_xref="dbSNP:113196403" variation 4473 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:7223351" variation 4481 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:186430762" variation 4504 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:111931306" variation 4513 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:149949423" variation 4573 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:144160152" variation 4584 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="c" /db_xref="dbSNP:181549583" variation 4586 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:185815639" variation 4605 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:2277672" variation 4655 /gene="NTN1" /gene_synonym="NTN1L" /replace="g" /replace="t" /db_xref="dbSNP:2277673" variation 4691 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:115367030" variation 4758 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:377676392" variation 4807 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:2277674" variation 4908 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="c" /db_xref="dbSNP:191516898" variation 4919 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:374875133" variation 4983 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:367873134" variation 4994..5008 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="agttgtcctttttct" /db_xref="dbSNP:143502379" variation 5062 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:182837678" variation 5066 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:148699677" variation 5084 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:142260746" variation 5191..5192 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="ta" /db_xref="dbSNP:370234553" variation 5233..5253 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="gagggtcacagcccagggagg" /db_xref="dbSNP:373528309" variation 5292 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:78601898" variation 5296..5297 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="catgctggaga" /db_xref="dbSNP:372514933" variation 5309 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:374099708" variation 5317..5320 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="actt" /db_xref="dbSNP:147205539" variation 5329 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:186131073" variation 5378 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="g" /db_xref="dbSNP:114627346" variation 5388 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="t" /db_xref="dbSNP:200673624" variation 5389..5390 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="ggttc" /db_xref="dbSNP:61409174" variation 5390..5391 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="ggttc" /db_xref="dbSNP:375053374" variation 5395..5396 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="ggttc" /db_xref="dbSNP:72092816" variation 5395 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:149176823" variation 5396 /gene="NTN1" /gene_synonym="NTN1L" /replace="g" /replace="t" /db_xref="dbSNP:200010525" variation 5397 /gene="NTN1" /gene_synonym="NTN1L" /replace="g" /replace="t" /db_xref="dbSNP:138229637" variation 5417 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:146801050" variation 5441..5442 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="aag" /db_xref="dbSNP:371780868" variation 5459 /gene="NTN1" /gene_synonym="NTN1L" /replace="a" /replace="t" /db_xref="dbSNP:140575051" variation 5480 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:144298589" variation 5615 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:146598671" variation 5691 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:190607440" variation 5713 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="g" /db_xref="dbSNP:12450891" variation 5715 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:371248382" STS 5718..5871 /gene="NTN1" /gene_synonym="NTN1L" /standard_name="RH93073" /db_xref="UniSTS:84419" variation 5802 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:183417766" variation 5842..5843 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="gg" /db_xref="dbSNP:144530140" variation 5842 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="g" /db_xref="dbSNP:371053519" variation 5850..5851 /gene="NTN1" /gene_synonym="NTN1L" /replace="" /replace="t" /db_xref="dbSNP:373319325" variation 5896 /gene="NTN1" /gene_synonym="NTN1L" /replace="c" /replace="t" /db_xref="dbSNP:9889875" polyA_signal 5936..5941 /gene="NTN1" /gene_synonym="NTN1L" polyA_site 5954 /gene="NTN1" /gene_synonym="NTN1L" ORIGIN
cttcgggggcgagcgcgcgtgtgtgtgagtgcgcgccggccagcgcgccttctgcggcaggcggacagatcctcggcgcggcagggccggggcaagctggacgcagcatgatgcgcgcagtgtgggaggcgctggcggcgctggcggcggtggcgtgcctggtgggcgcggtgcgcggcgggcccgggctcagcatgttcgcgggccaggcggcgcagcccgatccctgctcggacgagaacggccacccgcgccgctgcatcccggactttgtcaatgcggccttcggcaaggacgtgcgcgtgtccagcacctgcggccggcccccggcgcgctactgcgtggtgagcgagcgcggcgaggagcggctgcgctcgtgccacctctgcaacgcgtccgaccccaagaaggcgcacccgcccgccttcctcaccgacctcaacaacccgcacaacctgacgtgctggcagtccgagaactacctgcagttcccgcacaacgtcacgctcacactgtccctcggcaagaagttcgaagtgacctacgtgagcctgcagttctgctcgccgcggcccgagtccatggccatctacaagtccatggactacgggcgcacgtgggtgcccttccagttctactccacgcagtgccgcaagatgtacaaccggccgcaccgcgcgcccatcaccaagcagaacgagcaggaggccgtgtgcaccgactcgcacaccgacatgcgcccgctctcgggcggcctcatcgccttcagcacgctggacgggcggccctcggcgcacgacttcgacaactcgcccgtgctgcaggactgggtcacggccacagacatccgcgtggccttcagccgcctgcacacgttcggcgacgagaacgaggacgactcggagctggcgcgcgactcgtacttctacgcggtgtccgacctgcaggtgggcggccggtgcaagtgcaacggccacgcggcccgctgcgtgcgcgaccgcgacgacagcctggtgtgcgactgcaggcacaacacggccggcccggagtgcgaccgctgcaagcccttccactacgaccggccctggcagcgcgccacagcccgcgaagccaacgagtgcgtggcctgtaactgcaacctgcatgcccggcgctgccgcttcaacatggagctctacaagctttcggggcgcaagagcggaggtgtctgcctcaactgtcgccacaacaccgccggccgccactgccattactgcaaggagggctactaccgcgacatgggcaagcccatcacccaccggaaggcctgcaaagcctgtgattgccaccctgtgggtgctgctggcaaaacctgcaaccaaaccaccggccagtgtccctgcaaggacggcgtgacgggtatcacctgcaaccgctgcgccaaaggctaccagcagagccgctctcccatcgccccctgcataaagatccctgtagcgccgccgacgactgcagccagcagcgtggaggagcctgaagactgcgattcctactgcaaggcctccaaggggaagctgaagattaacatgaaaaagtactgcaagaaggactatgccgtccagatccacatcctgaaggcggacaaggcgggggactggtggaagttcacggtgaacatcatctccgtgtataagcagggcacgagccgcatccgccgcggtgaccagagcctgtggatccgctcgcgggacatcgcctgcaagtgtcccaaaatcaagcccctcaagaagtacctgctgctgggcaacgcggaggactctccggaccagagcggcatcgtggccgataaaagcagcctggtgatccagtggcgggacacgtgggcgcggcggctgcgcaagttccagcagcgtgagaagaagggcaagtgcaagaaggcctagcgccgaggcagcgggcgggcgggcgggcgggcgccagggcggggccgagcgagagcgggcgccttggcccggccgccgcggacttggcccgcgagggctttcccaggtggggggagggagggggcggggccgcacggcgcggggggcgggaccctcggcggcccctccccctacccccaccctgcgcgctctgggcgggagccgcgtgcacgcggggcggggtgcgccgccggccgggccctggagaaatgacgagacgtagctacctcacggggctccttccagagcagagacgcgcttccctgggcctgggcgcggccgccgtggaggggctgggggcagcctgccctggggcccgggggcgggcgcagaatcgcacaactggggccccaggcgcggggcgtggatggcgcggagacgtggacgggaggagaactgtgaattctcaagcccgtagtgtgggcggggcgcggagcacccaccaaaccaccacccgacacgcagccgacgggatccccccctttctccccggccccttctagcagttccccgcgggccacctggctgtcacagcctggactcctccatctgaaggggcctggcagcatttggggagtggacagctcctgtccagccagcatgccccaggcggcctctgtctccactgctacctgctgagtgggtcctactgggtgggggcttggggtcggtgagtggttcacctgtggagagaggagaggaagcccctgctgctgcctgtctctgcccctgcccctgcccctgcccagcgtggggctggcccatccggaaggcagtgggcccagggacacccctgagaagcccaagccgggtggtcaccgcctcatgctggagctgcctgttggaggaggcatcgcaaacgcaaaacctcccagagagtttccttttggaaacttggaaccagccctttttatgacgttttccagggggagggggaggggcactggctgggtttacggcagtgacactatttatgtaaatgacatcagctcccgcaaggcccctcagcaatgtcaacagctggaaagggcctgaacgggcttggagtctgcaggctgcgaaggcacttgggcctggcttggggccgggggcttgtttgagctgggatggggtttgctggctcagtgaagtaccagagtgcctgagccatgggtgggcaggggcacaggaatgaccaggttcctgggggccaaggaggccatgctggcttctccaagggaaggcacagaggctgccggcctgccccctacagctgtcttgggtctggcctgggccacaccttgaccgtgcctttccagacggtctttgtggagtctgcccgtgccctccactgtgccccagccctccttccaaaatctcctagagacacggtcctcaagcaggcagccccttttgttctgacctcctcacacagggtccattcctgtgccctggggcctcctggctccctgccttcctgggctctctgcactgcccgggcctctggcccacatcctcacacccggcgcactgaattaagaggcctggctcccctcacagtcaggaaattggtttcactttcccggccagagtttggctgctcaaaagggtcataccaagtatgaagctcggcccccggtggtctggcttccctccgccttccccacatttacccgcatcacggctgccatttattgagcacctgctgtgtgccaggcactttacccacatgctcccagtgtgtactcatgacaaccctgtgggacagggactcattatcaccagcaaggagactggagtacacgtgcccaaggtcatgctgcaaattggtggcaggactggggctcaaactccagagcccgactttctgaccaggggccacgctggccctcactgcactccagctctgcagcctacccgcccaatccctgtgcaggctgggagggtgctcttgggggagtggccaccgagcccctggccctggttactgcctcttgaggacactggcatctgggctggagaacaggagcccggggtggggtagggcatggggacaatcacatcttcagaggaggcagcaaagtggtgcgggatgcagggacggacttgccagatggcagctccaggttccaggaaggcaggccttggatgctccgaagaggtggtagaaaggtgtttttagaaaggtgttttggctgcctcagggtggttggagagactccaggagagactggcagaggtgcctcaggggcagggagcagacagacctgccctgggaaggggcatttggcttccctgaatccagcccaaggctagaagacagggcccctctccaagctgtcagcgcccctcggatgcccagtgtggtgtgctgggcgccatcagcatcacaaggcactacgctgctggggcggttgtcctatttctgtctatgccagtgtggtttcttcaccctgcccagaagggctgtggcagccccacgatatcccaccctgggtctgggtctcacgggtgtcctgtgaggggcttgcatttgtggtggtctctgaggccacctcagcaacggagctggcgacacgccaagcaacaaggcatcttgcggaaaattcagccagtgtcctgcccctcccttcggctcagcaccccgcagggcacaggctgtccgcccggtggtctggcccttggggaatgcgtcagggtgaccagatccaccatgctagcagccaggtcactgttgggattgcacggtcgtcacgagctgcctttcctatccacacacccagccaggacccagcccaccactcccgactgcagccccggcctctgcggtgagcaccatccttgggaaagcacccctcctccactccggtgccccactccaaggagcagagggaaatgggaattgaggtgtcccggtttgtacagttaggaagggatgtaaaacggaactagattttgattttgaagagtgtattaaccagaattgtgctatgtaggtgtttgtttgaagaaaaacataccagattagtctttgtttttgaaacagcttccccagttgtcctttttcttaccagctgggtggtctggtgcccctgacagctgagtgcctgctttacggacacgcagtaatgccgaagatttgcgggggaggacatagggctgtccccgggattcacctgctggctgtggtctctgcccactgcttctgtccttggaaagcagggcaggaggcagcatccccaggggcctctatgtgggagggagggacacctggggtcacaacccagggagggagggtcacagcccagggaggctgggagctgctccaaggccctggaactctgcctcagtcgcggcatgctggagaggggtacggacttactttcttggagttgtcccaggttggaatgagactgaactcaagaagagaccctaagggactggggaatggttcctgccttcaggaaagtgaaagacgcttaggctgtcaacacttaaaggaagtccccttgaagcccagagtggacagactagacccattgatggggccactggccatggtccgtggacaagacattcctgtgggccatggcacaccgggggggatcaaaatgtgtacttgtggggtctcgccccttgccaaaagccaaaccagtcccactcctgtcattggacgtttcttcccattccctcctcccaaatgcacttcccctcctccctctgccccctcctgtgttttggatttctgttcactcagaattgtaaatgtttagttgtgaccatgacgtattgtttgggtcaatgtccctttccaatgcatactaatatattatggttattatatatgaatatatttaatgacatggaaaaagttgtggattttctttctttccttttttttgggggggggtggggggttggttagagttgtaatggacccagatggaacttgtaatgtgggccccacatgatagaactaaattcagatatcattaaataaactcttgtacacta
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:9423 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:9423 -> Biological process: GO:0001764 [neuron migration] evidence: IEA GeneID:9423 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA GeneID:9423 -> Biological process: GO:0007411 [axon guidance] evidence: TAS GeneID:9423 -> Biological process: GO:0008284 [positive regulation of cell proliferation] evidence: IEA GeneID:9423 -> Biological process: GO:0016337 [cell-cell adhesion] evidence: IEA GeneID:9423 -> Biological process: GO:0030334 [regulation of cell migration] evidence: IEA GeneID:9423 -> Biological process: GO:0030517 [negative regulation of axon extension] evidence: IEA GeneID:9423 -> Biological process: GO:0033564 [anterior/posterior axon guidance] evidence: IEA GeneID:9423 -> Biological process: GO:0040023 [establishment of nucleus localization] evidence: IEA GeneID:9423 -> Biological process: GO:0042472 [inner ear morphogenesis] evidence: IEA GeneID:9423 -> Biological process: GO:0045773 [positive regulation of axon extension] evidence: IEA GeneID:9423 -> Biological process: GO:0060603 [mammary gland duct morphogenesis] evidence: IEA GeneID:9423 -> Cellular component: GO:0005576 [extracellular region] evidence: TAS GeneID:9423 -> Cellular component: GO:0005604 [basement membrane] evidence: IEA GeneID:9423 -> Cellular component: GO:0005737 [cytoplasm] evidence: IEA
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