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2024-04-20 16:58:09, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_006054 2588 bp mRNA linear PRI 20-APR-2013
DEFINITION Homo sapiens reticulon 3 (RTN3), transcript variant 1, mRNA.
ACCESSION NM_006054
VERSION NM_006054.3 GI:388240761
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 2588)
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 2588)
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 2588)
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 2588)
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 2588)
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 2588)
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 2588)
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 2588)
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 2588)
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 2588)
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, BC011394.1 and
BC022993.1.
On May 22, 2012 this sequence version replaced gi:41393611.
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 (1) encodes 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 :: BK001681.1, AK075412.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025082 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-51 BK001681.1 6-56
52-2579 BC011394.1 1-2528
2580-2588 BC022993.1 2517-2525
FEATURES Location/Qualifiers
source 1..2588
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="11"
/map="11q13"
gene 1..2588
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/note="reticulon 3"
/db_xref="GeneID:10313"
/db_xref="HGNC:10469"
/db_xref="HPRD:18516"
/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..898
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/note="isoform a is encoded by transcript variant 1; 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 a"
/protein_id="NP_006045.1"
/db_xref="GI:5174655"
/db_xref="CCDS:CCDS8049.1"
/db_xref="GeneID:10313"
/db_xref="HGNC:10469"
/db_xref="HPRD:18516"
/db_xref="MIM:604249"
/translation="
MAEPSAATQSHSISSSSFGAEPSAPGGGGSPGACPALGTKSCSSSCAVHDLIFWRDVKKTGFVFGTTLIMLLSLAAFSVISVVSYLILALLSVTISFRIYKSVIQAVQKSEEGHPFKAYLDVDITLSSEAFHNYMNAAMVHINRALKLIIRLFLVEDLVDSLKLAVFMWLMTYVGAVFNGITLLILAELLIFSVPIVYEKYKTQIDHYVGIARDQTKSIVEKIQAKLPGIAKKKAE
"
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 275..277
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 329..841
/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..894
/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..676
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 540
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373638785"
variation 550
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112039472"
variation 551
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113891559"
variation 553
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201337574"
variation 639
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148694827"
variation 663
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:200363562"
exon 677..746
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 725
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="g"
/db_xref="dbSNP:35726653"
exon 747..793
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 754
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:181371695"
variation 766
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:111414035"
exon 794..852
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 820
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:146666855"
variation 821
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140229299"
variation 825
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:191695213"
variation 829
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376569243"
variation 842
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144062061"
exon 853..2588
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 878
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373844043"
variation 962
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:146447613"
variation 1003
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199515481"
variation 1010
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374545422"
STS 1186..1392
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/standard_name="D11S2301E"
/db_xref="UniSTS:58416"
variation 1222
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:11551936"
variation 1288
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:184803325"
variation 1311
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112912318"
variation 1353
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:13335"
variation 1461
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:8343"
STS 1477..1634
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/standard_name="RH91589"
/db_xref="UniSTS:90037"
variation 1564
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1802332"
variation 1565
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:11954"
variation 1626
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1059619"
variation 1629
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:192934097"
variation 1642
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:377748725"
variation 1647
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1065644"
variation 1650
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1802331"
variation 1677
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375616404"
variation 1703..1704
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="a"
/db_xref="dbSNP:374981561"
variation 1748
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1059646"
variation 1851
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371205618"
variation 1926
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:11551942"
variation 2052
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:184729427"
variation 2214
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1802333"
variation 2216
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150406359"
variation 2333
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1059708"
variation 2367
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:189594352"
variation 2385
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138134656"
variation 2417
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="t"
/db_xref="dbSNP:35324379"
variation 2431
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:202157557"
variation 2504
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:545308"
variation 2510
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1059763"
variation 2565
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:200644841"
variation 2566..2568
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="aaa"
/db_xref="dbSNP:201753132"
variation 2575..2576
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="ac"
/db_xref="dbSNP:113976113"
ORIGIN
gcatgcgcgctcgcgctcccgccctctagctgcgctcggctgagtcagtcagtctgtcggagtctgtcctcggagcaggcggagtaaagggacttgagcgagccagttgccggattattctatttcccctccctctctcccgccccgtatctcttttcacccttctcccaccctcgctcgcgtagccatggcggagccgtcggcggccactcagtcccattccatctcctcgtcgtccttcggagccgagccgtccgcgcccggcggcggcgggagcccaggagcctgccccgccctggggacgaagagctgcagctcctcctgtgcggtgcacgatctgattttctggagagatgtgaagaagactgggtttgtctttggcaccacgctgatcatgctgctttccctggcagctttcagtgtcatcagtgtggtttcttacctcatcctggctcttctctctgtcaccatcagcttcaggatctacaagtccgtcatccaagctgtacagaagtcagaagaaggccatccattcaaagcctacctggacgtagacattactctgtcctcagaagctttccataattacatgaatgctgccatggtgcacatcaacagggccctgaaactcattattcgtctctttctggtagaagatctggttgactccttgaagctggctgtcttcatgtggctgatgacctatgttggtgctgtttttaacggaatcacccttctaattcttgctgaactgctcattttcagtgtcccgattgtctatgagaagtacaagacccagattgatcactatgttggcatcgcccgagatcagaccaagtcaattgttgaaaagatccaagcaaaactccctggaatcgccaaaaaaaaggcagaataagtacatggaaaccagaaatgcaacagttactaaaacaccatttaatagttataacgtcgttacttgtactatgaaggaaaatactcagtgtcagcttgagcctgcattccaagctttttttttaatttggtgttttctcccatcctttccctttaaccctcagtatcaagcacaaaaattgatggactgataaaagaactatcttagaactcagaagaagaaagaatcaaattcataggataagtcaataccttaatggtggtagagcctttacctgtagcttgaaaggggaaagattggaggtaagagagaaaatgaaagaacacctctgggtccttctgtccagttttcagcactagtcttactcagctatccattatagttttgcccttaagaagtcatgattaacttatgaaaaaattatttggggacaggagtgtgataccttccttggtttttttttgcagccctcaaatcctatcttcctgccccacaatgtgagcagctacccctgatactccttttctttaatgatttaactatcaacttgataaataacttataggtgatagtgataattcctgattccaagaatgccatctgataaaaaagaatagaaatggaaagtgggactgagagggagtcagcaggcatgctgcggtggcggtcactccctctgccactatccccagggaaggaaaggctccgccatttgggaaagtggtttctacgtcactggacaccggttctgagcattagtttgagaactcgttcccgaatgtgctttcctccctctcccctgcccacctcaagtttaataaataaggttgtacttttcttactataaaataaatgtctgtaactgctgtgcactgctgtaaacttgttagagaaaaaaataacctgcatgtgggctcctcagttattgagtttttgtgatcctatctcagtctgggggggaacattctcaagaggtgaaatacagaaagcctttttttcttgatcttttcccgagattcaaatctccgattcccatttgggggcaagtttttttcttcaccttcaatatgagaattcagcgaacttgaaagaaaaatcatctgtgagttccttcaggttctcactcatagtcatgatccttcagagggaatatgcactggcgagtttaaagtaagggctatgatatttgatggtcccaaagtacggcagctgcaaaaagtagtggaaggaaattgtctacgtgtcttggaaaaattagttaggaatttggatgggtaaaaggtacccttgccttactccatcttattttcttagccccctttgagtgttttaactggtttcatgtcctagtaggaagtgcattctccatcctcatcctctgccctcccaggaagtcagtgattgtctttttgggcttcccctccaaaggaccttctgcagtggaagtgccacatccagttcttttcttttgttgctgctgtgtttagataattgaagagatctttgtgccacacaggatttttttttttttttaagaaaaacctatagatgaaaaattactaatgaaactgtgtgtacgtgtctgtgcgtgcaacataaaaatacagtagcacctaaggagcttgaatcttggttcctgtaaaatttcaaattgatgtggtattaataaaaaaaaaaaaaacacaaacaa
//
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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