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2024-04-19 23:59:10, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_025139 2278 bp mRNA linear PRI 08-JUL-2013
DEFINITION Homo sapiens armadillo repeat containing 9 (ARMC9), transcript
variant 2, mRNA.
ACCESSION NM_025139 NM_024720
VERSION NM_025139.4 GI:407020536
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 2278)
AUTHORS Del-Aguila,J.L., Beitelshees,A.L., Cooper-Dehoff,R.M.,
Chapman,A.B., Gums,J.G., Bailey,K., Gong,Y., Turner,S.T.,
Johnson,J.A. and Boerwinkle,E.
TITLE Genome-wide association analyses suggest NELL1 influences adverse
metabolic response to HCTZ in African Americans
JOURNAL Pharmacogenomics J. (2013) In press
PUBMED 23400010
REMARK Publication Status: Available-Online prior to print
REFERENCE 2 (bases 1 to 2278)
AUTHORS Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B,
Yusuf S, Gerstein HC, Engert JC and Anand S.
CONSRTM DREAM investigators
TITLE Variation at the NFATC2 locus increases the risk of
thiazolidinedione-induced edema in the Diabetes REduction
Assessment with ramipril and rosiglitazone Medication (DREAM) study
JOURNAL Diabetes Care 33 (10), 2250-2253 (2010)
PUBMED 20628086
REMARK GeneRIF: Observational study of gene-disease association,
gene-environment interaction, and pharmacogenomic / toxicogenomic.
(HuGE Navigator)
REFERENCE 3 (bases 1 to 2278)
AUTHORS Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt
TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M,
Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ,
Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S,
Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD,
Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE
and Hingorani AD.
CONSRTM ASCOT investigators; NORDIL investigators; BRIGHT Consortium
TITLE Gene-centric association signals for lipids and apolipoproteins
identified via the HumanCVD BeadChip
JOURNAL Am. J. Hum. Genet. 85 (5), 628-642 (2009)
PUBMED 19913121
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 4 (bases 1 to 2278)
AUTHORS Hillier,L.W., Graves,T.A., Fulton,R.S., Fulton,L.A., Pepin,K.H.,
Minx,P., Wagner-McPherson,C., Layman,D., Wylie,K., Sekhon,M.,
Becker,M.C., Fewell,G.A., Delehaunty,K.D., Miner,T.L., Nash,W.E.,
Kremitzki,C., Oddy,L., Du,H., Sun,H., Bradshaw-Cordum,H., Ali,J.,
Carter,J., Cordes,M., Harris,A., Isak,A., van Brunt,A., Nguyen,C.,
Du,F., Courtney,L., Kalicki,J., Ozersky,P., Abbott,S.,
Armstrong,J., Belter,E.A., Caruso,L., Cedroni,M., Cotton,M.,
Davidson,T., Desai,A., Elliott,G., Erb,T., Fronick,C., Gaige,T.,
Haakenson,W., Haglund,K., Holmes,A., Harkins,R., Kim,K.,
Kruchowski,S.S., Strong,C.M., Grewal,N., Goyea,E., Hou,S., Levy,A.,
Martinka,S., Mead,K., McLellan,M.D., Meyer,R., Randall-Maher,J.,
Tomlinson,C., Dauphin-Kohlberg,S., Kozlowicz-Reilly,A., Shah,N.,
Swearengen-Shahid,S., Snider,J., Strong,J.T., Thompson,J.,
Yoakum,M., Leonard,S., Pearman,C., Trani,L., Radionenko,M.,
Waligorski,J.E., Wang,C., Rock,S.M., Tin-Wollam,A.M., Maupin,R.,
Latreille,P., Wendl,M.C., Yang,S.P., Pohl,C., Wallis,J.W.,
Spieth,J., Bieri,T.A., Berkowicz,N., Nelson,J.O., Osborne,J.,
Ding,L., Meyer,R., Sabo,A., Shotland,Y., Sinha,P., Wohldmann,P.E.,
Cook,L.L., Hickenbotham,M.T., Eldred,J., Williams,D., Jones,T.A.,
She,X., Ciccarelli,F.D., Izaurralde,E., Taylor,J., Schmutz,J.,
Myers,R.M., Cox,D.R., Huang,X., McPherson,J.D., Mardis,E.R.,
Clifton,S.W., Warren,W.C., Chinwalla,A.T., Eddy,S.R., Marra,M.A.,
Ovcharenko,I., Furey,T.S., Miller,W., Eichler,E.E., Bork,P.,
Suyama,M., Torrents,D., Waterston,R.H. and Wilson,R.K.
TITLE Generation and annotation of the DNA sequences of human chromosomes
2 and 4
JOURNAL Nature 434 (7034), 724-731 (2005)
PUBMED 15815621
REFERENCE 5 (bases 1 to 2278)
AUTHORS Kiniwa,Y., Fujita,T., Akada,M., Ito,K., Shofuda,T., Suzuki,Y.,
Yamamoto,A., Saida,T. and Kawakami,Y.
TITLE Tumor antigens isolated from a patient with vitiligo and
T-cell-infiltrated melanoma
JOURNAL Cancer Res. 61 (21), 7900-7907 (2001)
PUBMED 11691810
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
HY022484.1, BX537956.1, AC009407.8 and AC018738.4.
On Sep 26, 2012 this sequence version replaced gi:156151429.
Transcript Variant: This variant (2) represents the primary 3'UTR
extent and encodes a shorter protein isoform (2), compared to
variant 1.
##Evidence-Data-START##
Transcript exon combination :: BX537956.1, AY929062.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025085 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-51 HY022484.1 1-51
52-283 BX537956.1 2-233
284-284 AC009407.8 193826-193826
285-2239 BX537956.1 235-2189
2240-2240 AC018738.4 130234-130234
2241-2278 BX537956.1 2191-2228
FEATURES Location/Qualifiers
source 1..2278
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="2"
/map="2q37.1"
gene 1..2278
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/note="armadillo repeat containing 9"
/db_xref="GeneID:80210"
/db_xref="HGNC:20730"
exon 1..119
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 100
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="g"
/replace="t"
/db_xref="dbSNP:191013678"
exon 120..211
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 123
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371428399"
variation 130
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="g"
/replace="t"
/db_xref="dbSNP:146897446"
misc_feature 149..151
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/note="upstream in-frame stop codon"
variation 158
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373513496"
CDS 161..2158
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/note="isoform 2 is encoded by transcript variant 2; lisH
domain-containing protein ARMC9;
armadillo/beta-catenin-like repeats; melanoma/melanocyte
specific protein KU-MEL-1; NS21;
melanoma/melanocyte-specific tumor antigen KU-MEL-1"
/codon_start=1
/product="lisH domain-containing protein ARMC9 isoform 2"
/protein_id="NP_079415.3"
/db_xref="GI:156151430"
/db_xref="CCDS:CCDS2484.1"
/db_xref="GeneID:80210"
/db_xref="HGNC:20730"
/translation="
MGDILAHESELLGLVKEYLDFAEFEDTLKTFSKECKIKGKPLCKTVGGSFRDSKSLTIQKDLVAAFDNGDQKVFFDLWEEHISSSIRDGDSFAQKLEFYLHIHFAIYLLKYSVGRPDKEELDEKISYFKTYLETKGAALSQTTEFLPFYALPFVPNPMVHPSFKELFQDSWTPELKLKLEKFLALISKASNTPKLLTIYKENGQSNKEILQQLHQQLVEAERRSVTYLKRYNKIQADYHNLIGVTAELVDSLEATVSGKMITPEYLQSVCVRLFSNQMRQSLAHSVDFTRPGTASTMLRASLAPVKLKDVPLLPSLDYEKLKKDLILGSDRLKAFLLQALRWRLTTSHPGEQRETVLQAYISNDLLDCYSHNQRSVLQLLHSTSDVVRQYMARLINAFASLAEGRLYLAQNTKVLQMLEGRLKEEDKDIITRENVLGALQKFSLRRPLQTAMIQDGLIFWLVDVLKDPDCLSDYTLEYSVALLMNLCLRSTGKNMCAKVAGLVLKVLSDLLGHENHEIQPYVNGALYSILSVPSIREEARAMGMEDILRCFIKEGNAEMIRQIEFIIKQLNSEELPDGVLESDDDEDEDDEEDHDIMEADLDKDELIQPQLGELSGEKLLTTEYLGIMTNTGKTRRKGLANVQWSGDEPLQRPVTPGGHRNGYPV
"
misc_feature 179..274
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/note="LisH; Region: LisH; cl11662"
/db_xref="CDD:199226"
misc_feature 1511..1876
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/note="Armadillo/beta-catenin-like repeats. An
approximately 40 amino acid long tandemly repeated
sequence motif first identified in the Drosophila segment
polarity gene armadillo; these repeats were also found in
the mammalian armadillo homolog beta-catenin; Region: ARM;
cl02500"
/db_xref="CDD:207616"
misc_feature order(1589..1591,1601..1603,1613..1615,1709..1711,
1721..1723,1730..1732,1742..1744,1844..1846,1853..1855,
1862..1867,1874..1876)
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/note="protein binding surface [polypeptide binding];
other site"
/db_xref="CDD:28904"
misc_feature 1904..1906
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q7Z3E5.2); phosphorylation site"
variation 170
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:61753914"
variation 173
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="g"
/db_xref="dbSNP:376958829"
variation 179
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200925709"
exon 212..337
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 263
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:367894831"
variation 270
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200364288"
variation 284
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:11558174"
variation 301
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:35643982"
exon 338..508
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 349
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200269213"
variation 350
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144388331"
variation 351
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368431189"
variation 364
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:143756333"
variation 414
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140272259"
variation 415
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201455171"
variation 419
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="c"
/db_xref="dbSNP:372770167"
variation 424
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="g"
/replace="t"
/db_xref="dbSNP:7426058"
variation 441
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376271713"
variation 476
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199768804"
variation 482
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:11558175"
exon 509..664
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 520
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="g"
/db_xref="dbSNP:371282155"
variation 527
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201901213"
variation 606
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369095745"
exon 665..757
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 668
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="g"
/replace="t"
/db_xref="dbSNP:138398575"
variation 698
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1626450"
variation 699
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1626451"
variation 709
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199882687"
variation 741
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:78600608"
variation 754
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373903250"
exon 758..782
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
exon 783..940
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 786
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:16827883"
variation 796
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201590882"
variation 823
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="c"
/db_xref="dbSNP:374113705"
variation 825
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:3752780"
variation 855
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:184314019"
variation 862
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="g"
/db_xref="dbSNP:148694421"
variation 879
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149062293"
variation 885
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147777576"
variation 905
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147006089"
variation 914
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace=""
/replace="c"
/db_xref="dbSNP:370477312"
variation 931
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370669179"
exon 941..1039
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 955
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372815655"
variation 963
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376477328"
variation 965
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140828136"
variation 983
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="c"
/db_xref="dbSNP:201015764"
variation 1009
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138186372"
variation 1024
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149589070"
exon 1040..1074
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
exon 1075..1186
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 1096
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="t"
/db_xref="dbSNP:201981676"
variation 1109
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="g"
/replace="t"
/db_xref="dbSNP:141984986"
variation 1129
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146386454"
variation 1139
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:35322543"
variation 1151
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376952620"
variation 1165
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="g"
/db_xref="dbSNP:369454946"
exon 1187..1279
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 1239
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369080231"
variation 1249
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372539616"
variation 1257
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376382781"
exon 1280..1370
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 1280
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149697104"
variation 1313
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141090328"
variation 1316
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147807280"
variation 1322
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200265998"
variation 1323
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201100561"
variation 1327
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146934178"
variation 1335
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377378221"
variation 1347
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:186036637"
variation 1356
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200495416"
variation 1357
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376296930"
variation 1369
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145076596"
exon 1371..1494
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 1396
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144180870"
variation 1405
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:140970478"
variation 1423
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="g"
/replace="t"
/db_xref="dbSNP:372199720"
variation 1474
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="g"
/db_xref="dbSNP:114966997"
variation 1476
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="g"
/replace="t"
/db_xref="dbSNP:202134961"
exon 1495..1634
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 1501
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:59475942"
variation 1506
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113569367"
variation 1526
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144320508"
variation 1573
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369877851"
variation 1584
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:116712981"
variation 1585
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147377923"
variation 1597
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141707678"
exon 1635..1711
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 1642
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139607491"
variation 1650
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150092118"
variation 1674
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144120568"
variation 1681
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371100186"
variation 1699
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375669516"
exon 1712..1786
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 1720
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:34385474"
variation 1742
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202200847"
variation 1766
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201558091"
exon 1787..1877
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 1804
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146650763"
variation 1805
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148296188"
variation 1877
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201888838"
exon 1878..1933
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 1889
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369223097"
variation 1927
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200267481"
exon 1934..2038
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 1958
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143200464"
variation 1967
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:367927015"
variation 1971
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:137962185"
variation 1972
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199727070"
variation 1978
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="g"
/replace="t"
/db_xref="dbSNP:148607124"
variation 1993
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1669083"
variation 1999
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:76068318"
variation 2018
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144278301"
variation 2026
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1669084"
variation 2032
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370520160"
exon 2039..2263
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/inference="alignment:Splign:1.39.8"
variation 2041
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="g"
/db_xref="dbSNP:148366086"
variation 2052
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147080561"
variation 2053
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201586626"
variation 2066
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144026971"
variation 2099
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="g"
/replace="t"
/db_xref="dbSNP:138555701"
variation 2100
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:149241883"
variation 2110
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371676530"
variation 2124
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202164814"
variation 2129
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199869743"
variation 2139
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201289966"
variation 2176
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202091151"
variation 2190
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200117043"
variation 2233
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="t"
/db_xref="dbSNP:145038049"
variation 2262
/gene="ARMC9"
/gene_synonym="ARM; KU-MEL-1"
/replace="a"
/replace="g"
/db_xref="dbSNP:116552131"
ORIGIN
gcgcgattggctgcgccgcccccacgtgacgccggggtggcggcggcggttgcccgggtgacggctgcggaggtggcggccgggctgggatagcgcgagtgtccgcggccgagcagcagagatttttgctgtgagaattaattaccagtaacagttcaatatgggggacattctggctcatgaatctgaattacttggactagtgaaagagtatttagattttgctgaatttgaagacaccttgaaaacattttcaaaagaatgcaaaataaaaggaaaaccattgtgtaaaacagtaggcggatctttcagagactccaaatcattgacaattcagaaggatcttgtcgctgcatttgacaacggagaccagaaggtgttcttcgatctgtgggaggagcacatttcaagttccatccgagatggggactcctttgcccagaagctggaattctatctccacatccattttgccatctatcttttgaagtactctgtggggagaccggacaaagaggagctggatgaaaagatttcctacttcaaaacctacctggagaccaaaggggcagccttgagccagaccacagagtttcttcctttctatgcccttccttttgttcccaaccctatggtgcacccctcatttaaagaactcttccaggattcctggactccagagttaaagttgaagttggaaaagtttctagctttaatatctaaagccagcaacacgccaaagcttttaacaatatataaggagaatggacaaagtaacaaagaaatcttgcagcagctccaccagcagctggttgaagctgaacgtaggtcagtgacatacctcaaacggtacaataagatccaggccgactaccacaatctcattggagtcacagcagagctggtggattctctagaggccacagtcagcggcaagatgatcacccctgagtacctccagagcgtctgtgtccgcctgttcagtaaccagatgcggcagagcctggcgcatagtgtggacttcacgaggcctgggacggcatccaccatgttacgagcctccttggcacccgtgaaattgaaggatgtcccattactgccctccttggattatgagaaactgaagaaggatttgattttggggagtgaccgcttgaaagccttcttgttgcaggctctgcgctggcgcttgaccacatcccatcctggagagcagagggagaccgttctgcaagcctacatcagcaatgacctcttggactgttatagccacaaccagaggagtgtgcttcagttgctgcactccacgagcgacgtggtgcggcagtacatggccaggctcatcaatgcttttgcgtcactggcagaaggtcgcctctaccttgcccagaacacaaaggtgctgcagatgctggagggaaggctgaaggaggaggacaaggatatcatcaccagggagaatgttcttggggccctgcagaagttcagtctcaggcgcccgctgcagacagcgatgattcaagacggcctcatcttctggctggttgatgttctgaaggaccctgactgcctgtctgactacacgctggagtactcggtggctttgctcatgaacctctgcctccgcagcacagggaagaacatgtgtgccaaggtggcaggcctcgtgctcaaagtcctttcggatcttcttggccatgaaaaccatgagatacagccgtatgtgaatggagctctgtacagcatcctttctgttccatccattcgtgaggaagcaagagcaatgggaatggaagacatcctacgctgcttcatcaaagaaggcaatgctgaaatgatccgccagatagaattcatcatcaagcagctaaattccgaagagctaccagatggtgttcttgaatctgatgatgatgaagatgaagatgatgaagaggaccatgacatcatggaagccgatctggacaaagacgaactgatccagccccagctcggagaactctcaggagagaagcttctgaccacggagtacctggggatcatgaccaacacggggaagacaaggcggaaggggctggctaatgtgcagtggagcggggatgagcccctgcaaaggcccgtcacccccggcggccacagaaacgggtacccagtgtaagtcagggctaaaggaagcgggaattgactttcttaagctttgttttgattacagtgtaagatgtatgtatttttaaaattcaaaataaagcattcattttgaaaaaaaaaaaaaaaaaaa
//
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.