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2024-04-24 15:36:40, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001265591 2332 bp mRNA linear PRI 20-APR-2013
DEFINITION Homo sapiens reticulon 3 (RTN3), transcript variant 7, mRNA.
ACCESSION NM_001265591
VERSION NM_001265591.1 GI:388240771
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 2332)
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 2332)
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 2332)
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 2332)
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 2332)
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 2332)
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 2332)
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 2332)
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 2332)
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 2332)
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, AK297529.1,
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 (7) lacks three consecutive exons
in the 3' coding region, which results in a frameshift, compared to
variant 1. The encoded isoform (g) is shorter and has a distinct
C-terminus, compared to 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 :: AK297529.1, BP353915.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025088 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-196 BK001681.1 6-201
197-1530 AK297529.1 74-1407
1531-2326 AY427821.2 4085-4880
2327-2332 BC022993.1 2520-2525
FEATURES Location/Qualifiers
source 1..2332
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="11"
/map="11q13"
gene 1..2332
/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..832
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/note="isoform g is encoded by transcript variant 7; 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 g"
/protein_id="NP_001252520.1"
/db_xref="GI:388240772"
/db_xref="CCDS:CCDS58143.1"
/db_xref="GeneID:10313"
/db_xref="HGNC:10469"
/db_xref="MIM:604249"
/translation="
MAEPSAATQSHSISSSSFGAEPSAPGGGGSPGACPALGTKSCSSSCAVHDLIFWRDVKKTGFVFGTTLIMLLSLAAFSVISVVSYLILALLSVTISFRIYKSVIQAVQKSEEGHPFKPRLITMLASPEIRPSQLLKRSKQNSLESPKKRQNKYMETRNATVTKTPFNSYNVVTCTMKENTQCQLEPAFQAFFLIWCFLPSFPFNPQYQAQKLMD
"
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 329..>523
/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"
STS 320..638
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/standard_name="Rtn3"
/db_xref="UniSTS:547531"
exon 330..537
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 335
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368041098"
variation 368
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200887875"
variation 370..371
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="t"
/db_xref="dbSNP:34381123"
variation 388
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199892486"
variation 404
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139166869"
variation 428
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371369557"
variation 449
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149925982"
variation 460
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:144009657"
variation 462
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142293926"
variation 481
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201492174"
variation 520
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113499717"
variation 521
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201265477"
variation 523
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:200360547"
exon 538..596
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 564
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:146666855"
variation 565
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140229299"
variation 569
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:191695213"
variation 573
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376569243"
variation 586
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144062061"
exon 597..2332
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 622
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373844043"
variation 706
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:146447613"
variation 747
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199515481"
variation 754
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374545422"
STS 930..1136
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/standard_name="D11S2301E"
/db_xref="UniSTS:58416"
variation 966
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:11551936"
variation 1032
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:184803325"
variation 1055
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112912318"
variation 1097
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:13335"
variation 1205
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:8343"
STS 1221..1378
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/standard_name="RH91589"
/db_xref="UniSTS:90037"
variation 1308
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1802332"
variation 1309
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:11954"
variation 1370
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1059619"
variation 1373
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:192934097"
variation 1386
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:377748725"
variation 1391
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1065644"
variation 1394
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1802331"
variation 1421
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375616404"
variation 1447..1448
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="a"
/db_xref="dbSNP:374981561"
variation 1492
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1059646"
variation 1595
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371205618"
variation 1670
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:11551942"
variation 1796
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:184729427"
variation 1958
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1802333"
variation 1960
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150406359"
variation 2077
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1059708"
variation 2111
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:189594352"
variation 2129
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138134656"
variation 2161
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="t"
/db_xref="dbSNP:35324379"
variation 2175
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:202157557"
variation 2248
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:545308"
variation 2254
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1059763"
variation 2309
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:200644841"
variation 2310..2312
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="aaa"
/db_xref="dbSNP:201753132"
variation 2319..2320
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="ac"
/db_xref="dbSNP:113976113"
ORIGIN
gcatgcgcgctcgcgctcccgccctctagctgcgctcggctgagtcagtcagtctgtcggagtctgtcctcggagcaggcggagtaaagggacttgagcgagccagttgccggattattctatttcccctccctctctcccgccccgtatctcttttcacccttctcccaccctcgctcgcgtagccatggcggagccgtcggcggccactcagtcccattccatctcctcgtcgtccttcggagccgagccgtccgcgcccggcggcggcgggagcccaggagcctgccccgccctggggacgaagagctgcagctcctcctgtgcggtgcacgatctgattttctggagagatgtgaagaagactgggtttgtctttggcaccacgctgatcatgctgctttccctggcagctttcagtgtcatcagtgtggtttcttacctcatcctggctcttctctctgtcaccatcagcttcaggatctacaagtccgtcatccaagctgtacagaagtcagaagaaggccatccattcaaacccagattgatcactatgttggcatcgcccgagatcagaccaagtcaattgttgaaaagatccaagcaaaactccctggaatcgccaaaaaaaaggcagaataagtacatggaaaccagaaatgcaacagttactaaaacaccatttaatagttataacgtcgttacttgtactatgaaggaaaatactcagtgtcagcttgagcctgcattccaagctttttttttaatttggtgttttctcccatcctttccctttaaccctcagtatcaagcacaaaaattgatggactgataaaagaactatcttagaactcagaagaagaaagaatcaaattcataggataagtcaataccttaatggtggtagagcctttacctgtagcttgaaaggggaaagattggaggtaagagagaaaatgaaagaacacctctgggtccttctgtccagttttcagcactagtcttactcagctatccattatagttttgcccttaagaagtcatgattaacttatgaaaaaattatttggggacaggagtgtgataccttccttggtttttttttgcagccctcaaatcctatcttcctgccccacaatgtgagcagctacccctgatactccttttctttaatgatttaactatcaacttgataaataacttataggtgatagtgataattcctgattccaagaatgccatctgataaaaaagaatagaaatggaaagtgggactgagagggagtcagcaggcatgctgcggtggcggtcactccctctgccactatccccagggaaggaaaggctccgccatttgggaaagtggtttctacgtcactggacaccggttctgagcattagtttgagaactcgttcccgaatgtgctttcctccctctcccctgcccacctcaagtttaataaataaggttgtacttttcttactataaaataaatgtctgtaactgctgtgcactgctgtaaacttgttagagaaaaaaataacctgcatgtgggctcctcagttattgagtttttgtgatcctatctcagtctgggggggaacattctcaagaggtgaaatacagaaagcctttttttcttgatcttttcccgagattcaaatctccgattcccatttgggggcaagtttttttcttcaccttcaatatgagaattcagcgaacttgaaagaaaaatcatctgtgagttccttcaggttctcactcatagtcatgatccttcagagggaatatgcactggcgagtttaaagtaagggctatgatatttgatggtcccaaagtacggcagctgcaaaaagtagtggaaggaaattgtctacgtgtcttggaaaaattagttaggaatttggatgggtaaaaggtacccttgccttactccatcttattttcttagccccctttgagtgttttaactggtttcatgtcctagtaggaagtgcattctccatcctcatcctctgccctcccaggaagtcagtgattgtctttttgggcttcccctccaaaggaccttctgcagtggaagtgccacatccagttcttttcttttgttgctgctgtgtttagataattgaagagatctttgtgccacacaggatttttttttttttttaagaaaaacctatagatgaaaaattactaatgaaactgtgtgtacgtgtctgtgcgtgcaacataaaaatacagtagcacctaaggagcttgaatcttggttcctgtaaaatttcaaattgatgtggtattaataaaaaaaaaaaaaacacaaacaa
//
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
@meso_cacase at
DBCLS
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