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2024-04-20 13:31:37, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001265590 4640 bp mRNA linear PRI 20-APR-2013
DEFINITION Homo sapiens reticulon 3 (RTN3), transcript variant 6, mRNA.
ACCESSION NM_001265590
VERSION NM_001265590.1 GI:388240769
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 4640)
AUTHORS Shi,Q., Prior,M., Zhou,X., Tang,X., He,W., Hu,X. and Yan,R.
TITLE Preventing formation of reticulon 3 immunoreactive dystrophic
neurites improves cognitive function in mice
JOURNAL J. Neurosci. 33 (7), 3059-3066 (2013)
PUBMED 23407961
REMARK GeneRIF: successful prevention of imunoreactive dystrophic neurites
formation should be initiated before RTN3 aggregation
REFERENCE 2 (bases 1 to 4640)
AUTHORS Chen,Y., Xiang,R. and Zhao,S.
TITLE The potential role of RTN3 in monocyte recruitment and
atherosclerosis
JOURNAL Mol. Cell. Biochem. 361 (1-2), 67-70 (2012)
PUBMED 21964562
REMARK GeneRIF: we hypothesis that RTN3 may participate in the continuous
process of circulating monocyte recruitment in atherosclerosis.
REFERENCE 3 (bases 1 to 4640)
AUTHORS Heath,J.E., Siedlak,S.L., Zhu,X., Lee,H.G., Thakur,A., Yan,R.,
Perry,G., Smith,M.A. and Castellani,R.J.
TITLE Widespread distribution of reticulon-3 in various neurodegenerative
diseases
JOURNAL Neuropathology 30 (6), 574-579 (2010)
PUBMED 20374499
REMARK GeneRIF: we examined reticulon-3 expression in cases of Alzheimer's
disease, Parkinson's disease, and diffuse Lewy body disease
REFERENCE 4 (bases 1 to 4640)
AUTHORS Chen,Y., Zhao,S. and Xiang,R.
TITLE RTN3 and RTN4: Candidate modulators in vascular cell apoptosis and
atherosclerosis
JOURNAL J. Cell. Biochem. 111 (4), 797-800 (2010)
PUBMED 20717916
REMARK GeneRIF: Reticulons, the only molecular so far to participate in
all three apoptosis signaling pathways, may be a novel player in
the progress of atherosclerosis.
REFERENCE 5 (bases 1 to 4640)
AUTHORS Landa,I., Ruiz-Llorente,S., Montero-Conde,C., Inglada-Perez,L.,
Schiavi,F., Leskela,S., Pita,G., Milne,R., Maravall,J., Ramos,I.,
Andia,V., Rodriguez-Poyo,P., Jara-Albarran,A., Meoro,A., del
Peso,C., Arribas,L., Iglesias,P., Caballero,J., Serrano,J.,
Pico,A., Pomares,F., Gimenez,G., Lopez-Mondejar,P., Castello,R.,
Merante-Boschin,I., Pelizzo,M.R., Mauricio,D., Opocher,G.,
Rodriguez-Antona,C., Gonzalez-Neira,A., Matias-Guiu,X.,
Santisteban,P. and Robledo,M.
TITLE The variant rs1867277 in FOXE1 gene confers thyroid cancer
susceptibility through the recruitment of USF1/USF2 transcription
factors
JOURNAL PLoS Genet. 5 (9), E1000637 (2009)
PUBMED 19730683
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 6 (bases 1 to 4640)
AUTHORS Qi,B., Qi,Y., Watari,A., Yoshioka,N., Inoue,H., Minemoto,Y.,
Yamashita,K., Sasagawa,T. and Yutsudo,M.
TITLE Pro-apoptotic ASY/Nogo-B protein associates with ASYIP
JOURNAL J. Cell. Physiol. 196 (2), 312-318 (2003)
PUBMED 12811824
REMARK GeneRIF: The ASYIP protein co-localizes with ASY in the endoplasmic
reticulum. Characterization of the ASYIP gene helps to clarify
ASY-induced apoptosis or Nogo-involved inhibition of neuronal
regeneration in the central nervous system.
REFERENCE 7 (bases 1 to 4640)
AUTHORS Di Sano,F., Fazi,B., Citro,G., Lovat,P.E., Cesareni,G. and
Piacentini,M.
TITLE Glucosylceramide synthase and its functional interaction with
RTN-1C regulate chemotherapeutic-induced apoptosis in
neuroepithelioma cells
JOURNAL Cancer Res. 63 (14), 3860-3865 (2003)
PUBMED 12873973
REFERENCE 8 (bases 1 to 4640)
AUTHORS Oertle,T., Klinger,M., Stuermer,C.A. and Schwab,M.E.
TITLE A reticular rhapsody: phylogenic evolution and nomenclature of the
RTN/Nogo gene family
JOURNAL FASEB J. 17 (10), 1238-1247 (2003)
PUBMED 12832288
REFERENCE 9 (bases 1 to 4640)
AUTHORS Qu,X., Qi,Y. and Qi,B.
TITLE Generation of multiple mRNA transcripts from the novel human
apoptosis-inducing gene hap by alternative polyadenylation
utilization and the translational activation function of 3'
untranslated region
JOURNAL Arch. Biochem. Biophys. 400 (2), 233-244 (2002)
PUBMED 12054434
REFERENCE 10 (bases 1 to 4640)
AUTHORS Moreira,E.F., Jaworski,C.J. and Rodriguez,I.R.
TITLE Cloning of a novel member of the reticulon gene family (RTN3): gene
structure and chromosomal localization to 11q13
JOURNAL Genomics 58 (1), 73-81 (1999)
PUBMED 10331947
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from BK001681.1, AK309766.1,
AY427821.2 and BC022993.1.
Summary: This gene belongs to the reticulon family of highly
conserved genes that are preferentially expressed in neuroendocrine
tissues. This family of proteins interact with, and modulate the
activity of beta-amyloid converting enzyme 1 (BACE1), and the
production of amyloid-beta. An increase in the expression of any
reticulon protein substantially reduces the production of
amyloid-beta, suggesting that reticulon proteins are negative
modulators of BACE1 in cells. Alternatively spliced transcript
variants encoding different isoforms have been found for this gene,
and pseudogenes of this gene are located on chromosomes 4 and 12.
[provided by RefSeq, May 2012].
Transcript Variant: This variant (6) includes an alternate exon in
the coding region, but maintains the reading frame, compared to
variant 1. The encoded isoform (f) is longer than isoform a.
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 :: AK295758.1, AK309766.1 [ECO:0000332]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-215 BK001681.1 6-220
216-1262 AK309766.1 170-1216
1263-4634 AY427821.2 1509-4880
4635-4640 BC022993.1 2520-2525
FEATURES Location/Qualifiers
source 1..4640
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="11"
/map="11q13"
gene 1..4640
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/note="reticulon 3"
/db_xref="GeneID:10313"
/db_xref="HGNC:10469"
/db_xref="MIM:604249"
exon 1..329
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 38
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370655059"
variation 86
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:186618572"
misc_feature 95..97
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/note="upstream in-frame stop codon"
variation 145
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:11551948"
variation 162
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:11551938"
variation 179
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:11551937"
variation 180
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:372883387"
CDS 188..2950
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/note="isoform f is encoded by transcript variant 6; ASY
interacting protein; homolog of ASY protein;
neuroendocrine-specific protein-like 2; NSP-like protein
II; NSP-like protein 2; neuroendocrine-specific
protein-like II"
/codon_start=1
/product="reticulon-3 isoform f"
/protein_id="NP_001252519.1"
/db_xref="GI:388240770"
/db_xref="CCDS:CCDS58142.1"
/db_xref="GeneID:10313"
/db_xref="HGNC:10469"
/db_xref="MIM:604249"
/translation="
MAEPSAATQSHSISSSSFGAEPSAPGGGGSPGACPALGTKSCSSSCAASFPEHPAFLSKKIGQVEEQIDKETKNPNGVSSREAKTALDADDRFTLLTAQKPPTEYSKVEGIYTYSLSPSKVSGDDVIEKDSPESPFEVIIDKAAFDKEFKDSYKESTDDFGSWSVHTDKESSEDISETNDKLFPLRNKEAGRYPMSALLSRQFSHTNAALEEVSRCVNDMHNFTNEILTWDLVPQVKQQTDKSSDCITKTTGLDMSEYNSEIPVVNLKTSTHQKTPVCSIDGSTPITKSTGDWAEASLQQENAITGKPVPDSLNSTKEFSIKGVQGNMQKQDDTLAELPGSPPEKCDSLGSGVATVKVVLPDDHLKDEMDWQSSALGEITEADSSGESDDTVIEDITADTSFENNKIQAEKPVSIPSAVVKTGEREIKEIPSCEREEKTSKNFEELVSDSELHQDQPDILGRSPASEAACSKVPDTNVSLEDVSEVAPEKPITTENPKLPSTVSPNVFNETEFSLNVTTSAYLESLHGKNVKHIDDSSPEDLIAAFTETRDKGIVDSERNAFKAISEKMTDFKTTPPVEVLHENESGGSEIKDIGSKYSEQSKETNGSEPLGVFPTQGTPVASLDLEQEQLTIKALKELGERQVEKSTSAQRDAELPSEEVLKQTFTFAPESWPQRSYDILERNVKNGSDLGISQKPITIRETTRVDAVSSLSKTELVKKHVLARLLTDFSVHDLIFWRDVKKTGFVFGTTLIMLLSLAAFSVISVVSYLILALLSVTISFRIYKSVIQAVQKSEEGHPFKAYLDVDITLSSEAFHNYMNAAMVHINRALKLIIRLFLVEDLVDSLKLAVFMWLMTYVGAVFNGITLLILAELLIFSVPIVYEKYKTQIDHYVGIARDQTKSIVEKIQAKLPGIAKKKAE
"
misc_feature 191..193
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/experiment="experimental evidence, no additional details
recorded"
/note="N-acetylalanine; propagated from
UniProtKB/Swiss-Prot (O95197.2); acetylation site"
misc_feature 2381..2893
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/note="Reticulon; Region: Reticulon; pfam02453"
/db_xref="CDD:190314"
variation 201
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:11551941"
variation 204
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:11551944"
variation 217
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:11551949"
variation 223
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:11551940"
variation 238
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142892358"
variation 247
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:199568088"
variation 253
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:11551946"
variation 259
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:11551950"
variation 276..277
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="c"
/db_xref="dbSNP:34852771"
variation 279
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:11551945"
variation 292
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371351138"
exon 330..2381
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 367
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149031161"
variation 392
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200098343"
variation 398
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:372752989"
variation 399
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146754567"
variation 403
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143098965"
variation 429
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140371416"
variation 443
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138573713"
variation 445
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201846404"
variation 450
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141607862"
variation 463
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377110085"
variation 582
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:377437871"
variation 641
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375955099"
variation 681
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368006117"
variation 704
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371789344"
variation 761
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145117207"
variation 762
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373685794"
variation 770
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138926393"
variation 816
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:367597571"
variation 846
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371391643"
variation 853
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201167593"
variation 857
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369922424"
variation 863
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375692793"
variation 907
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:75409661"
variation 946
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:113499022"
variation 947
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150901896"
variation 995
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369380035"
variation 999
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201348110"
variation 1018
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370124982"
variation 1025
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139271709"
variation 1026
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375093214"
variation 1050
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:149556717"
variation 1076
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144217345"
variation 1080
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:371257360"
variation 1124
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144097273"
variation 1153
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:375047740"
variation 1157
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373939447"
variation 1177
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112690371"
variation 1229
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201074433"
variation 1249
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144676607"
variation 1259
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202032060"
variation 1263
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:542998"
variation 1285
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139663525"
variation 1352
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:7936660"
variation 1377
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:143280633"
variation 1379
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373042364"
variation 1386
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:151006740"
variation 1429
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140739177"
variation 1466
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371240135"
variation 1526
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:150093726"
variation 1536
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:79008295"
variation 1550
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146654581"
variation 1563
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370047599"
variation 1614
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373330352"
variation 1615
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373156613"
variation 1643
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:140294717"
variation 1659
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:116807490"
variation 1663
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:375941421"
variation 1675
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140444047"
variation 1716
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112366604"
variation 1738
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370587694"
variation 1763
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:4254075"
variation 1772
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374913700"
variation 1802
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:191736847"
variation 1842
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:202037688"
variation 1844
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201582430"
variation 1852
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149399289"
variation 1878
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200262067"
variation 1901
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:199593292"
variation 1945
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143833769"
variation 1966
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:367829558"
variation 1967
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370443746"
variation 1979
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:76989455"
variation 1980
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372725878"
variation 2036
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:148172636"
variation 2037
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377208132"
variation 2051
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141979420"
variation 2074
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147124632"
variation 2141
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147247159"
variation 2142
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138982686"
variation 2177
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:370052431"
variation 2187
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:184286324"
variation 2209
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374498816"
variation 2228
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143160052"
variation 2234
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201862583"
variation 2257
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:375825683"
variation 2266
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371368744"
variation 2273
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375610947"
variation 2334
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:368204966"
variation 2347
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372468224"
variation 2357
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147481469"
exon 2382..2589
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 2387
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368041098"
variation 2420
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200887875"
variation 2422..2423
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="t"
/db_xref="dbSNP:34381123"
variation 2440
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199892486"
variation 2456
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139166869"
variation 2480
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371369557"
variation 2501
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149925982"
variation 2512
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:144009657"
variation 2514
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142293926"
variation 2533
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201492174"
variation 2572
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113499717"
variation 2573
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201265477"
variation 2575
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:200360547"
exon 2590..2728
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 2592
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373638785"
variation 2602
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112039472"
variation 2603
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113891559"
variation 2605
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201337574"
variation 2691
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148694827"
variation 2715
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:200363562"
exon 2729..2798
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 2777
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="g"
/db_xref="dbSNP:35726653"
exon 2799..2845
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 2806
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:181371695"
variation 2818
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:111414035"
exon 2846..2904
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 2872
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:146666855"
variation 2873
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140229299"
variation 2877
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:191695213"
variation 2881
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376569243"
variation 2894
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144062061"
exon 2905..4640
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 2930
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373844043"
variation 3014
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:146447613"
variation 3055
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199515481"
variation 3062
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374545422"
STS 3238..3444
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/standard_name="D11S2301E"
/db_xref="UniSTS:58416"
variation 3274
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:11551936"
variation 3340
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:184803325"
variation 3363
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112912318"
variation 3405
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:13335"
variation 3513
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:8343"
STS 3529..3686
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/standard_name="RH91589"
/db_xref="UniSTS:90037"
variation 3616
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1802332"
variation 3617
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:11954"
variation 3678
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1059619"
variation 3681
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:192934097"
variation 3694
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:377748725"
variation 3699
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1065644"
variation 3702
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1802331"
variation 3729
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375616404"
variation 3755..3756
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="a"
/db_xref="dbSNP:374981561"
variation 3800
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1059646"
variation 3903
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371205618"
variation 3978
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:11551942"
variation 4104
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:184729427"
variation 4266
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1802333"
variation 4268
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150406359"
variation 4385
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1059708"
variation 4419
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:189594352"
variation 4437
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138134656"
variation 4469
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="t"
/db_xref="dbSNP:35324379"
variation 4483
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:202157557"
variation 4556
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:545308"
variation 4562
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1059763"
variation 4617
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:200644841"
variation 4618..4620
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="aaa"
/db_xref="dbSNP:201753132"
variation 4627..4628
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="ac"
/db_xref="dbSNP:113976113"
ORIGIN
gcatgcgcgctcgcgctcccgccctctagctgcgctcggctgagtcagtcagtctgtcggagtctgtcctcggagcaggcggagtaaagggacttgagcgagccagttgccggattattctatttcccctccctctctcccgccccgtatctcttttcacccttctcccaccctcgctcgcgtagccatggcggagccgtcggcggccactcagtcccattccatctcctcgtcgtccttcggagccgagccgtccgcgcccggcggcggcgggagcccaggagcctgccccgccctggggacgaagagctgcagctcctcctgtgcggccagtttcccagagcatcctgcttttctctcaaagaaaattggtcaagtggaagagcaaatagataaagagaccaagaacccaaatggggtatcaagtagggaggctaaaactgcattggatgctgatgacagattcactttgctgacagcccagaaaccacctactgagtactctaaggtagaaggcatttatacatattctttgtctccatccaaagtttcaggagatgatgttattgaaaaggattcccctgaatcaccatttgaagtaattattgacaaagcagcatttgacaaagaatttaaagactcatataaggagagcacagatgattttggtagctggtctgtgcacactgataaagaatcatccgaagacatttcagagactaatgacaagctttttccactgagaaataaagaggcaggacgttacccaatgtctgcattgctcagtaggcagttttcacacacaaatgcagcactggaagaggtgtccagatgcgtgaatgatatgcataactttactaacgaaatactgacttgggatctggttccccaagtgaaacaacagaccgataaatcttctgactgcatcacaaaaactacaggacttgacatgagtgaatataattcagaaattccagttgtaaatcttaaaactagcactcatcagaaaactcctgtatgttctattgatgggagcactcccatcactaaatcaacaggtgattgggcagaagcatctctccagcaagaaaatgctattactggaaaacctgtacctgactctttgaattccacaaaagaattcagtatcaaaggtgtgcaaggcaatatgcagaaacaggatgacacacttgcagaattacctggatctccacctgagaaatgtgactctttgggttctggagtggccacagtgaaagtggttttacctgatgaccacctgaaagatgaaatggactggcagagctctgcattgggagaaatcacagaagctgatagttctggtgagtctgatgacacagtaatagaggacatcacagcagatacatcatttgaaaataacaaaattcaggctgaaaaacctgtttccattccaagtgctgttgtaaaaacaggtgaaagagaaatcaaagagattcccagttgtgagagagaagaaaaaacatctaaaaactttgaagaattggtcagtgactctgagctgcatcaagatcagcctgatattcttggaaggagtccagctagtgaggcagcatgttcaaaagtacccgatacgaatgtctccttagaagatgtgagtgaagttgctcctgaaaagcctattactactgagaaccccaaacttccttcaacagtgtctccaaatgtttttaatgagacagaattctcattaaatgtgacaacatctgcctatttggagtcattacatgggaaaaatgttaaacatatagatgattcctccccagaggacctgatagcagcctttacagaaaccagagataaaggaatagtagatagtgaaagaaatgcttttaaagcaatatcagagaagatgacagactttaaaacaactcctcctgtagaagtcttacatgaaaatgagtccggtggttctgaaattaaagacattggaagcaaatacagtgaacaaagcaaagaaacaaatggaagtgagcctctaggtgttttccctacccaaggtactccagtagcatctcttgacttagaacaagaacagctcacaattaaggctcttaaagaattaggtgaaagacaggttgagaagtcaacttctgcacagcgtgacgcagaattgccttctgaagaagtactgaagcaaactttcacatttgctccagaatcttggccacagagatcatatgacatcctagaacgtaatgtcaagaatggatctgatcttgggatttcccagaagcccatcactatcagagaaactactagggtagatgctgtttccagccttagcaagactgaattggtaaaaaagcatgtcctagcaagacttctgacagacttctcagtgcacgatctgattttctggagagatgtgaagaagactgggtttgtctttggcaccacgctgatcatgctgctttccctggcagctttcagtgtcatcagtgtggtttcttacctcatcctggctcttctctctgtcaccatcagcttcaggatctacaagtccgtcatccaagctgtacagaagtcagaagaaggccatccattcaaagcctacctggacgtagacattactctgtcctcagaagctttccataattacatgaatgctgccatggtgcacatcaacagggccctgaaactcattattcgtctctttctggtagaagatctggttgactccttgaagctggctgtcttcatgtggctgatgacctatgttggtgctgtttttaacggaatcacccttctaattcttgctgaactgctcattttcagtgtcccgattgtctatgagaagtacaagacccagattgatcactatgttggcatcgcccgagatcagaccaagtcaattgttgaaaagatccaagcaaaactccctggaatcgccaaaaaaaaggcagaataagtacatggaaaccagaaatgcaacagttactaaaacaccatttaatagttataacgtcgttacttgtactatgaaggaaaatactcagtgtcagcttgagcctgcattccaagctttttttttaatttggtgttttctcccatcctttccctttaaccctcagtatcaagcacaaaaattgatggactgataaaagaactatcttagaactcagaagaagaaagaatcaaattcataggataagtcaataccttaatggtggtagagcctttacctgtagcttgaaaggggaaagattggaggtaagagagaaaatgaaagaacacctctgggtccttctgtccagttttcagcactagtcttactcagctatccattatagttttgcccttaagaagtcatgattaacttatgaaaaaattatttggggacaggagtgtgataccttccttggtttttttttgcagccctcaaatcctatcttcctgccccacaatgtgagcagctacccctgatactccttttctttaatgatttaactatcaacttgataaataacttataggtgatagtgataattcctgattccaagaatgccatctgataaaaaagaatagaaatggaaagtgggactgagagggagtcagcaggcatgctgcggtggcggtcactccctctgccactatccccagggaaggaaaggctccgccatttgggaaagtggtttctacgtcactggacaccggttctgagcattagtttgagaactcgttcccgaatgtgctttcctccctctcccctgcccacctcaagtttaataaataaggttgtacttttcttactataaaataaatgtctgtaactgctgtgcactgctgtaaacttgttagagaaaaaaataacctgcatgtgggctcctcagttattgagtttttgtgatcctatctcagtctgggggggaacattctcaagaggtgaaatacagaaagcctttttttcttgatcttttcccgagattcaaatctccgattcccatttgggggcaagtttttttcttcaccttcaatatgagaattcagcgaacttgaaagaaaaatcatctgtgagttccttcaggttctcactcatagtcatgatccttcagagggaatatgcactggcgagtttaaagtaagggctatgatatttgatggtcccaaagtacggcagctgcaaaaagtagtggaaggaaattgtctacgtgtcttggaaaaattagttaggaatttggatgggtaaaaggtacccttgccttactccatcttattttcttagccccctttgagtgttttaactggtttcatgtcctagtaggaagtgcattctccatcctcatcctctgccctcccaggaagtcagtgattgtctttttgggcttcccctccaaaggaccttctgcagtggaagtgccacatccagttcttttcttttgttgctgctgtgtttagataattgaagagatctttgtgccacacaggatttttttttttttttaagaaaaacctatagatgaaaaattactaatgaaactgtgtgtacgtgtctgtgcgtgcaacataaaaatacagtagcacctaaggagcttgaatcttggttcctgtaaaatttcaaattgatgtggtattaataaaaaaaaaaaaaacacaaacaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:10313 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA
GeneID:10313 -> Biological process: GO:0006950 [response to stress] evidence: IEA
GeneID:10313 -> Biological process: GO:0016192 [vesicle-mediated transport] evidence: IEA
GeneID:10313 -> Biological process: GO:0019048 [modulation by virus of host morphology or physiology] evidence: IEA
GeneID:10313 -> Biological process: GO:0071786 [endoplasmic reticulum tubular network organization] evidence: IMP
GeneID:10313 -> Cellular component: GO:0000139 [Golgi membrane] evidence: IEA
GeneID:10313 -> Cellular component: GO:0005615 [extracellular space] evidence: TAS
GeneID:10313 -> Cellular component: GO:0005783 [endoplasmic reticulum] evidence: IDA
GeneID:10313 -> Cellular component: GO:0005789 [endoplasmic reticulum membrane] evidence: IEA
GeneID:10313 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
by
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