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2024-04-19 21:12:02, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001265589 4976 bp mRNA linear PRI 17-JUN-2013
DEFINITION Homo sapiens reticulon 3 (RTN3), transcript variant 5, mRNA.
ACCESSION NM_001265589
VERSION NM_001265589.1 GI:388240767
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 4976)
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 4976)
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 4976)
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 4976)
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 4976)
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 4976)
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 4976)
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 4976)
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 4976)
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 4976)
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, AY750848.1 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 (5) includes two consecutive
alternate exons in the coding region, but maintains the reading
frame, compared to variant 1. The encoded isoform (e) 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 :: AY750848.1, AK304100.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025082, ERS025084 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-33 BK001681.1 6-38
34-4970 AY750848.1 1-4937
4971-4976 BC022993.1 2520-2525
FEATURES Location/Qualifiers
source 1..4976
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="11"
/map="11q13"
gene 1..4976
/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..3286
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/note="isoform e is encoded by transcript variant 5; 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 e"
/protein_id="NP_001252518.1"
/db_xref="GI:388240768"
/db_xref="CCDS:CCDS58141.1"
/db_xref="GeneID:10313"
/db_xref="HGNC:10469"
/db_xref="MIM:604249"
/translation="
MAEPSAATQSHSISSSSFGAEPSAPGGGGSPGACPALGTKSCSSSCADSFVSSSSSQPVSLFSTSQEGLSSLCSDEPSSEIMTSSFLSSSEIHNTGLTILHGEKSHVLGSQPILAKEGKDHLDLLDMKKMEKPQGTSNNVSDSSVSLAAGVHCDRPSIPASFPEHPAFLSKKIGQVEEQIDKETKNPNGVSSREAKTALDADDRFTLLTAQKPPTEYSKVEGIYTYSLSPSKVSGDDVIEKDSPESPFEVIIDKAAFDKEFKDSYKESTDDFGSWSVHTDKESSEDISETNDKLFPLRNKEAGRYPMSALLSRQFSHTNAALEEVSRCVNDMHNFTNEILTWDLVPQVKQQTDKSSDCITKTTGLDMSEYNSEIPVVNLKTSTHQKTPVCSIDGSTPITKSTGDWAEASLQQENAITGKPVPDSLNSTKEFSIKGVQGNMQKQDDTLAELPGSPPEKCDSLGSGVATVKVVLPDDHLKDEMDWQSSALGEITEADSSGESDDTVIEDITADTSFENNKIQAEKPVSIPSAVVKTGEREIKEIPSCEREEKTSKNFEELVSDSELHQDQPDILGRSPASEAACSKVPDTNVSLEDVSEVAPEKPITTENPKLPSTVSPNVFNETEFSLNVTTSAYLESLHGKNVKHIDDSSPEDLIAAFTETRDKGIVDSERNAFKAISEKMTDFKTTPPVEVLHENESGGSEIKDIGSKYSEQSKETNGSEPLGVFPTQGTPVASLDLEQEQLTIKALKELGERQVEKSTSAQRDAELPSEEVLKQTFTFAPESWPQRSYDILERNVKNGSDLGISQKPITIRETTRVDAVSSLSKTELVKKHVLARLLTDFSVHDLIFWRDVKKTGFVFGTTLIMLLSLAAFSVISVVSYLILALLSVTISFRIYKSVIQAVQKSEEGHPFKAYLDVDITLSSEAFHNYMNAAMVHINRALKLIIRLFLVEDLVDSLKLAVFMWLMTYVGAVFNGITLLILAELLIFSVPIVYEKYKTQIDHYVGIARDQTKSIVEKIQAKLPGIAKKKAE
"
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 2132..2134
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(O95197.2); phosphorylation site"
misc_feature 2135..2137
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(O95197.2); phosphorylation site"
misc_feature 2717..3229
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/note="Reticulon; Region: Reticulon; pfam02453"
/db_xref="CDD:190314"
misc_feature 3146..3283
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (O95197.2);
Region: Interaction with FADD"
misc_feature 3185..3193
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (O95197.2);
Region: Interaction with BACE1"
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..386
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 337
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368123181"
variation 364
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:75523067"
variation 376
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371340835"
variation 378
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374939027"
exon 387..2717
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 399
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:151058657"
variation 401
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:140534064"
variation 463
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201006467"
variation 465
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200571079"
variation 474
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370573807"
variation 489
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144433263"
variation 497
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143534933"
variation 545
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373926513"
variation 546
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141445845"
variation 567
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150364552"
variation 576
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375566159"
variation 605
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144921220"
variation 619
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368359917"
variation 624
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:193027719"
variation 652
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371777828"
variation 653
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:369715649"
variation 703
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149031161"
variation 728
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200098343"
variation 734
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:372752989"
variation 735
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146754567"
variation 739
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143098965"
variation 765
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140371416"
variation 779
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138573713"
variation 781
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201846404"
variation 786
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141607862"
variation 799
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377110085"
variation 918
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:377437871"
variation 977
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375955099"
variation 1017
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368006117"
variation 1040
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371789344"
variation 1097
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145117207"
variation 1098
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373685794"
variation 1106
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138926393"
variation 1152
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:367597571"
variation 1182
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371391643"
variation 1189
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201167593"
variation 1193
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369922424"
variation 1199
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375692793"
variation 1243
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:75409661"
variation 1282
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:113499022"
variation 1283
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150901896"
variation 1331
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369380035"
variation 1335
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201348110"
variation 1354
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370124982"
variation 1361
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139271709"
variation 1362
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375093214"
variation 1386
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:149556717"
variation 1412
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144217345"
variation 1416
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:371257360"
variation 1460
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144097273"
variation 1489
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:375047740"
variation 1493
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373939447"
variation 1513
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112690371"
variation 1565
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201074433"
variation 1585
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144676607"
variation 1595
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202032060"
variation 1599
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:542998"
variation 1621
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139663525"
variation 1688
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:7936660"
variation 1713
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:143280633"
variation 1715
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373042364"
variation 1722
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:151006740"
variation 1765
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140739177"
variation 1802
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371240135"
variation 1862
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:150093726"
variation 1872
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:79008295"
variation 1886
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146654581"
variation 1899
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370047599"
variation 1950
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373330352"
variation 1951
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373156613"
variation 1979
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:140294717"
variation 1995
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:116807490"
variation 1999
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:375941421"
variation 2011
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140444047"
variation 2052
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:112366604"
variation 2074
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370587694"
variation 2099
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:4254075"
variation 2108
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374913700"
variation 2138
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:191736847"
variation 2178
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:202037688"
variation 2180
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201582430"
variation 2188
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149399289"
variation 2214
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200262067"
variation 2237
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:199593292"
variation 2281
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143833769"
variation 2302
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:367829558"
variation 2303
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370443746"
variation 2315
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:76989455"
variation 2316
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372725878"
variation 2372
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:148172636"
variation 2373
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377208132"
variation 2387
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141979420"
variation 2410
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147124632"
variation 2477
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147247159"
variation 2478
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138982686"
variation 2513
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:370052431"
variation 2523
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:184286324"
variation 2545
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374498816"
variation 2564
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143160052"
variation 2570
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201862583"
variation 2593
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:375825683"
variation 2602
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371368744"
variation 2609
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375610947"
variation 2670
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:368204966"
variation 2683
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372468224"
variation 2693
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147481469"
exon 2718..2925
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 2723
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368041098"
variation 2756
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200887875"
variation 2758..2759
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="t"
/db_xref="dbSNP:34381123"
variation 2776
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199892486"
variation 2792
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139166869"
variation 2816
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371369557"
variation 2837
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149925982"
variation 2848
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:144009657"
variation 2850
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142293926"
variation 2869
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201492174"
variation 2908
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113499717"
variation 2909
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201265477"
variation 2911
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:200360547"
exon 2926..3064
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 2928
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373638785"
variation 2938
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112039472"
variation 2939
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113891559"
variation 2941
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201337574"
variation 3027
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148694827"
variation 3051
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:200363562"
exon 3065..3134
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 3113
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="g"
/db_xref="dbSNP:35726653"
exon 3135..3181
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 3142
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:181371695"
variation 3154
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:111414035"
exon 3182..3240
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 3208
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:146666855"
variation 3209
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140229299"
variation 3213
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:191695213"
variation 3217
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376569243"
variation 3230
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144062061"
exon 3241..4976
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/inference="alignment:Splign:1.39.8"
variation 3266
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373844043"
variation 3350
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="g"
/replace="t"
/db_xref="dbSNP:146447613"
variation 3391
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199515481"
variation 3398
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374545422"
STS 3574..3780
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/standard_name="D11S2301E"
/db_xref="UniSTS:58416"
variation 3610
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:11551936"
variation 3676
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="g"
/db_xref="dbSNP:184803325"
variation 3699
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112912318"
variation 3741
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:13335"
variation 3849
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:8343"
STS 3865..4022
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/standard_name="RH91589"
/db_xref="UniSTS:90037"
variation 3952
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1802332"
variation 3953
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:11954"
variation 4014
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1059619"
variation 4017
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:192934097"
variation 4030
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:377748725"
variation 4035
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1065644"
variation 4038
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1802331"
variation 4065
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375616404"
variation 4091..4092
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="a"
/db_xref="dbSNP:374981561"
variation 4136
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1059646"
variation 4239
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371205618"
variation 4314
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:11551942"
variation 4440
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:184729427"
variation 4602
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1802333"
variation 4604
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150406359"
variation 4721
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1059708"
variation 4755
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="c"
/replace="t"
/db_xref="dbSNP:189594352"
variation 4773
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138134656"
variation 4805
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="t"
/db_xref="dbSNP:35324379"
variation 4819
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:202157557"
variation 4892
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:545308"
variation 4898
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1059763"
variation 4953
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace="a"
/replace="t"
/db_xref="dbSNP:200644841"
variation 4954..4956
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="aaa"
/db_xref="dbSNP:201753132"
variation 4963..4964
/gene="RTN3"
/gene_synonym="ASYIP; HAP; NSPL2; NSPLII; RTN3-A1"
/replace=""
/replace="ac"
/db_xref="dbSNP:113976113"
ORIGIN
gcatgcgcgctcgcgctcccgccctctagctgcgctcggctgagtcagtcagtctgtcggagtctgtcctcggagcaggcggagtaaagggacttgagcgagccagttgccggattattctatttcccctccctctctcccgccccgtatctcttttcacccttctcccaccctcgctcgcgtagccatggcggagccgtcggcggccactcagtcccattccatctcctcgtcgtccttcggagccgagccgtccgcgcccggcggcggcgggagcccaggagcctgccccgccctggggacgaagagctgcagctcctcctgtgcggattcctttgtttcttcctcttcctctcagcctgtatctctattttcgacctcacaagagggattgagctctctttgctctgatgagccatcttcagaaattatgacttcttcctttctttcatcttctgaaatacataacactggccttacaatactacatggagaaaaaagccatgtgttagggagccagcctattttagccaaagaaggaaaagaccacttggatcttctagatatgaaaaagatggaaaagcctcaggggaccagcaacaacgtatcagactcttcagtttctcttgcagcaggagttcattgtgaccgtccttctattccagccagtttcccagagcatcctgcttttctctcaaagaaaattggtcaagtggaagagcaaatagataaagagaccaagaacccaaatggggtatcaagtagggaggctaaaactgcattggatgctgatgacagattcactttgctgacagcccagaaaccacctactgagtactctaaggtagaaggcatttatacatattctttgtctccatccaaagtttcaggagatgatgttattgaaaaggattcccctgaatcaccatttgaagtaattattgacaaagcagcatttgacaaagaatttaaagactcatataaggagagcacagatgattttggtagctggtctgtgcacactgataaagaatcatccgaagacatttcagagactaatgacaagctttttccactgagaaataaagaggcaggacgttacccaatgtctgcattgctcagtaggcagttttcacacacaaatgcagcactggaagaggtgtccagatgcgtgaatgatatgcataactttactaacgaaatactgacttgggatctggttccccaagtgaaacaacagaccgataaatcttctgactgcatcacaaaaactacaggacttgacatgagtgaatataattcagaaattccagttgtaaatcttaaaactagcactcatcagaaaactcctgtatgttctattgatgggagcactcccatcactaaatcaacaggtgattgggcagaagcatctctccagcaagaaaatgctattactggaaaacctgtacctgactctttgaattccacaaaagaattcagtatcaaaggtgtgcaaggcaatatgcagaaacaggatgacacacttgcagaattacctggatctccacctgagaaatgtgactctttgggttctggagtggccacagtgaaagtggttttacctgatgaccacctgaaagatgaaatggactggcagagctctgcattgggagaaatcacagaagctgatagttctggtgagtctgatgacacagtaatagaggacatcacagcagatacatcatttgaaaataacaaaattcaggctgaaaaacctgtttccattccaagtgctgttgtaaaaacaggtgaaagagaaatcaaagagattcccagttgtgagagagaagaaaaaacatctaaaaactttgaagaattggtcagtgactctgagctgcatcaagatcagcctgatattcttggaaggagtccagctagtgaggcagcatgttcaaaagtacccgatacgaatgtctccttagaagatgtgagtgaagttgctcctgaaaagcctattactactgagaaccccaaacttccttcaacagtgtctccaaatgtttttaatgagacagaattctcattaaatgtgacaacatctgcctatttggagtcattacatgggaaaaatgttaaacatatagatgattcctccccagaggacctgatagcagcctttacagaaaccagagataaaggaatagtagatagtgaaagaaatgcttttaaagcaatatcagagaagatgacagactttaaaacaactcctcctgtagaagtcttacatgaaaatgagtccggtggttctgaaattaaagacattggaagcaaatacagtgaacaaagcaaagaaacaaatggaagtgagcctctaggtgttttccctacccaaggtactccagtagcatctcttgacttagaacaagaacagctcacaattaaggctcttaaagaattaggtgaaagacaggttgagaagtcaacttctgcacagcgtgacgcagaattgccttctgaagaagtactgaagcaaactttcacatttgctccagaatcttggccacagagatcatatgacatcctagaacgtaatgtcaagaatggatctgatcttgggatttcccagaagcccatcactatcagagaaactactagggtagatgctgtttccagccttagcaagactgaattggtaaaaaagcatgtcctagcaagacttctgacagacttctcagtgcacgatctgattttctggagagatgtgaagaagactgggtttgtctttggcaccacgctgatcatgctgctttccctggcagctttcagtgtcatcagtgtggtttcttacctcatcctggctcttctctctgtcaccatcagcttcaggatctacaagtccgtcatccaagctgtacagaagtcagaagaaggccatccattcaaagcctacctggacgtagacattactctgtcctcagaagctttccataattacatgaatgctgccatggtgcacatcaacagggccctgaaactcattattcgtctctttctggtagaagatctggttgactccttgaagctggctgtcttcatgtggctgatgacctatgttggtgctgtttttaacggaatcacccttctaattcttgctgaactgctcattttcagtgtcccgattgtctatgagaagtacaagacccagattgatcactatgttggcatcgcccgagatcagaccaagtcaattgttgaaaagatccaagcaaaactccctggaatcgccaaaaaaaaggcagaataagtacatggaaaccagaaatgcaacagttactaaaacaccatttaatagttataacgtcgttacttgtactatgaaggaaaatactcagtgtcagcttgagcctgcattccaagctttttttttaatttggtgttttctcccatcctttccctttaaccctcagtatcaagcacaaaaattgatggactgataaaagaactatcttagaactcagaagaagaaagaatcaaattcataggataagtcaataccttaatggtggtagagcctttacctgtagcttgaaaggggaaagattggaggtaagagagaaaatgaaagaacacctctgggtccttctgtccagttttcagcactagtcttactcagctatccattatagttttgcccttaagaagtcatgattaacttatgaaaaaattatttggggacaggagtgtgataccttccttggtttttttttgcagccctcaaatcctatcttcctgccccacaatgtgagcagctacccctgatactccttttctttaatgatttaactatcaacttgataaataacttataggtgatagtgataattcctgattccaagaatgccatctgataaaaaagaatagaaatggaaagtgggactgagagggagtcagcaggcatgctgcggtggcggtcactccctctgccactatccccagggaaggaaaggctccgccatttgggaaagtggtttctacgtcactggacaccggttctgagcattagtttgagaactcgttcccgaatgtgctttcctccctctcccctgcccacctcaagtttaataaataaggttgtacttttcttactataaaataaatgtctgtaactgctgtgcactgctgtaaacttgttagagaaaaaaataacctgcatgtgggctcctcagttattgagtttttgtgatcctatctcagtctgggggggaacattctcaagaggtgaaatacagaaagcctttttttcttgatcttttcccgagattcaaatctccgattcccatttgggggcaagtttttttcttcaccttcaatatgagaattcagcgaacttgaaagaaaaatcatctgtgagttccttcaggttctcactcatagtcatgatccttcagagggaatatgcactggcgagtttaaagtaagggctatgatatttgatggtcccaaagtacggcagctgcaaaaagtagtggaaggaaattgtctacgtgtcttggaaaaattagttaggaatttggatgggtaaaaggtacccttgccttactccatcttattttcttagccccctttgagtgttttaactggtttcatgtcctagtaggaagtgcattctccatcctcatcctctgccctcccaggaagtcagtgattgtctttttgggcttcccctccaaaggaccttctgcagtggaagtgccacatccagttcttttcttttgttgctgctgtgtttagataattgaagagatctttgtgccacacaggatttttttttttttttaagaaaaacctatagatgaaaaattactaatgaaactgtgtgtacgtgtctgtgcgtgcaacataaaaatacagtagcacctaaggagcttgaatcttggttcctgtaaaatttcaaattgatgtggtattaataaaaaaaaaaaaaacacaaacaa
//
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
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