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2024-04-19 18:31:01, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001168479            2924 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens armadillo repeat containing, X-linked 5 (ARMCX5),
            transcript variant 1, mRNA.
ACCESSION   NM_001168479
VERSION     NM_001168479.1  GI:274318366
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 2924)
  AUTHORS   Ross,M.T., Grafham,D.V., Coffey,A.J., Scherer,S., McLay,K.,
            Muzny,D., Platzer,M., Howell,G.R., Burrows,C., Bird,C.P.,
            Frankish,A., Lovell,F.L., Howe,K.L., Ashurst,J.L., Fulton,R.S.,
            Sudbrak,R., Wen,G., Jones,M.C., Hurles,M.E., Andrews,T.D.,
            Scott,C.E., Searle,S., Ramser,J., Whittaker,A., Deadman,R.,
            Carter,N.P., Hunt,S.E., Chen,R., Cree,A., Gunaratne,P., Havlak,P.,
            Hodgson,A., Metzker,M.L., Richards,S., Scott,G., Steffen,D.,
            Sodergren,E., Wheeler,D.A., Worley,K.C., Ainscough,R.,
            Ambrose,K.D., Ansari-Lari,M.A., Aradhya,S., Ashwell,R.I.,
            Babbage,A.K., Bagguley,C.L., Ballabio,A., Banerjee,R., Barker,G.E.,
            Barlow,K.F., Barrett,I.P., Bates,K.N., Beare,D.M., Beasley,H.,
            Beasley,O., Beck,A., Bethel,G., Blechschmidt,K., Brady,N.,
            Bray-Allen,S., Bridgeman,A.M., Brown,A.J., Brown,M.J., Bonnin,D.,
            Bruford,E.A., Buhay,C., Burch,P., Burford,D., Burgess,J.,
            Burrill,W., Burton,J., Bye,J.M., Carder,C., Carrel,L., Chako,J.,
            Chapman,J.C., Chavez,D., Chen,E., Chen,G., Chen,Y., Chen,Z.,
            Chinault,C., Ciccodicola,A., Clark,S.Y., Clarke,G., Clee,C.M.,
            Clegg,S., Clerc-Blankenburg,K., Clifford,K., Cobley,V., Cole,C.G.,
            Conquer,J.S., Corby,N., Connor,R.E., David,R., Davies,J., Davis,C.,
            Davis,J., Delgado,O., Deshazo,D., Dhami,P., Ding,Y., Dinh,H.,
            Dodsworth,S., Draper,H., Dugan-Rocha,S., Dunham,A., Dunn,M.,
            Durbin,K.J., Dutta,I., Eades,T., Ellwood,M., Emery-Cohen,A.,
            Errington,H., Evans,K.L., Faulkner,L., Francis,F., Frankland,J.,
            Fraser,A.E., Galgoczy,P., Gilbert,J., Gill,R., Glockner,G.,
            Gregory,S.G., Gribble,S., Griffiths,C., Grocock,R., Gu,Y.,
            Gwilliam,R., Hamilton,C., Hart,E.A., Hawes,A., Heath,P.D.,
            Heitmann,K., Hennig,S., Hernandez,J., Hinzmann,B., Ho,S., Hoffs,M.,
            Howden,P.J., Huckle,E.J., Hume,J., Hunt,P.J., Hunt,A.R.,
            Isherwood,J., Jacob,L., Johnson,D., Jones,S., de Jong,P.J.,
            Joseph,S.S., Keenan,S., Kelly,S., Kershaw,J.K., Khan,Z.,
            Kioschis,P., Klages,S., Knights,A.J., Kosiura,A., Kovar-Smith,C.,
            Laird,G.K., Langford,C., Lawlor,S., Leversha,M., Lewis,L., Liu,W.,
            Lloyd,C., Lloyd,D.M., Loulseged,H., Loveland,J.E., Lovell,J.D.,
            Lozado,R., Lu,J., Lyne,R., Ma,J., Maheshwari,M., Matthews,L.H.,
            McDowall,J., McLaren,S., McMurray,A., Meidl,P., Meitinger,T.,
            Milne,S., Miner,G., Mistry,S.L., Morgan,M., Morris,S., Muller,I.,
            Mullikin,J.C., Nguyen,N., Nordsiek,G., Nyakatura,G., O'Dell,C.N.,
            Okwuonu,G., Palmer,S., Pandian,R., Parker,D., Parrish,J.,
            Pasternak,S., Patel,D., Pearce,A.V., Pearson,D.M., Pelan,S.E.,
            Perez,L., Porter,K.M., Ramsey,Y., Reichwald,K., Rhodes,S.,
            Ridler,K.A., Schlessinger,D., Schueler,M.G., Sehra,H.K.,
            Shaw-Smith,C., Shen,H., Sheridan,E.M., Shownkeen,R., Skuce,C.D.,
            Smith,M.L., Sotheran,E.C., Steingruber,H.E., Steward,C.A.,
            Storey,R., Swann,R.M., Swarbreck,D., Tabor,P.E., Taudien,S.,
            Taylor,T., Teague,B., Thomas,K., Thorpe,A., Timms,K., Tracey,A.,
            Trevanion,S., Tromans,A.C., d'Urso,M., Verduzco,D., Villasana,D.,
            Waldron,L., Wall,M., Wang,Q., Warren,J., Warry,G.L., Wei,X.,
            West,A., Whitehead,S.L., Whiteley,M.N., Wilkinson,J.E.,
            Willey,D.L., Williams,G., Williams,L., Williamson,A.,
            Williamson,H., Wilming,L., Woodmansey,R.L., Wray,P.W., Yen,J.,
            Zhang,J., Zhou,J., Zoghbi,H., Zorilla,S., Buck,D., Reinhardt,R.,
            Poustka,A., Rosenthal,A., Lehrach,H., Meindl,A., Minx,P.J.,
            Hillier,L.W., Willard,H.F., Wilson,R.K., Waterston,R.H., Rice,C.M.,
            Vaudin,M., Coulson,A., Nelson,D.L., Weinstock,G., Sulston,J.E.,
            Durbin,R., Hubbard,T., Gibbs,R.A., Beck,S., Rogers,J. and
            Bentley,D.R.
  TITLE     The DNA sequence of the human X chromosome
  JOURNAL   Nature 434 (7031), 325-337 (2005)
   PUBMED   15772651
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AK096692.1, BI765968.1 and BC000792.1.
            
            Transcript Variant: This variant (1) represents the longest
            transcript. Variants 1-6 all encode the same protein.
            
            ##Evidence-Data-START##
            Transcript exon combination :: BI765968.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084, ERS025088 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-112               AK096692.1         1-112
            113-510             BI765968.1         65-462
            511-2901            AK096692.1         505-2895
            2902-2924           BC000792.1         1192-1214
FEATURES             Location/Qualifiers
     source          1..2924
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="X"
                     /map="Xq22.1-q22.3"
     gene            1..2924
                     /gene="ARMCX5"
                     /note="armadillo repeat containing, X-linked 5"
                     /db_xref="GeneID:64860"
                     /db_xref="HGNC:25772"
     exon            1..99
                     /gene="ARMCX5"
                     /inference="alignment:Splign:1.39.8"
     variation       95
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186923749"
     exon            100..324
                     /gene="ARMCX5"
                     /inference="alignment:Splign:1.39.8"
     variation       219
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143986897"
     variation       233
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191379211"
     exon            325..466
                     /gene="ARMCX5"
                     /inference="alignment:Splign:1.39.8"
     variation       429
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:113654543"
     exon            467..579
                     /gene="ARMCX5"
                     /inference="alignment:Splign:1.39.8"
     exon            580..625
                     /gene="ARMCX5"
                     /inference="alignment:Splign:1.39.8"
     exon            626..2905
                     /gene="ARMCX5"
                     /inference="alignment:Splign:1.39.8"
     variation       665
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:180686160"
     variation       748
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187431863"
     variation       754
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150456888"
     variation       846
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371888083"
     misc_feature    876..878
                     /gene="ARMCX5"
                     /note="upstream in-frame stop codon"
     CDS             888..2564
                     /gene="ARMCX5"
                     /codon_start=1
                     /product="armadillo repeat-containing X-linked protein 5"
                     /protein_id="NP_001161951.1"
                     /db_xref="GI:274318367"
                     /db_xref="CCDS:CCDS14500.1"
                     /db_xref="GeneID:64860"
                     /db_xref="HGNC:25772"
                     /translation="
MVDSGTEARARGKAEAGLQDGISGPATARVNGKTQAEAVAEAELKTESVTQAKAGDGAMTRTHTVTYREAMAVTREVIKVEDTTKTRVMVETKTKPLAERSIVPQTKSKAMPMSRVSTVTKSEVKVVAVIEANIRSYAKSHDKANTGSRPDRREETSIGMKSSDEDEENICSWFWTGEEPSVGSWFWPEEETSLQVYKPLPKIQEKPKPTHKPTLTIKQKVIAWSRARYIVLVPVEGGEQSLPPEGNWTLVETLIETPLGIRPLTKIPPYHGPYYQTLAEIKKQIRQREKYGPNPKACHCKSRGFSLEPKEFDKLVALLKLTKDPFIHEIATMIMGISPAYPFTQDIIHDVGITVMIENLVNNPNVKEHPGALSMVDDSSESSEEPKSGESYIHQVCKGIISCPLNSPVQLAGLKLLGHLSIKFEDHYVITSYIPDFLTLLNKGSVKTKFYVLKVFSCLSKNHANTRELISAKVLSSLVAPFNKNESKANILNIIEIFENINFQFKTKAKLFTKEKFTKSELISIFQEAKQFGQKLQDLAEHSDPEVRDKVIRLILKL
"
     misc_feature    1779..2543
                     /gene="ARMCX5"
                     /note="Armadillo-like; Region: Arm_2; pfam04826"
                     /db_xref="CDD:191105"
     misc_feature    1785..1904
                     /gene="ARMCX5"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q6P1M9.1);
                     Region: ARM 1"
     misc_feature    2151..2270
                     /gene="ARMCX5"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q6P1M9.1);
                     Region: ARM 2"
     misc_feature    2274..2396
                     /gene="ARMCX5"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q6P1M9.1);
                     Region: ARM 3"
     variation       897
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376521671"
     variation       913
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147081834"
     variation       1043
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:17854978"
     variation       1082
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369765869"
     variation       1138
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138502487"
     variation       1145
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142005126"
     variation       1185
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12013441"
     variation       1186
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112989637"
     variation       1192
                     /gene="ARMCX5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:374726828"
     variation       1196
                     /gene="ARMCX5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:191839863"
     variation       1236
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112318694"
     variation       1242
                     /gene="ARMCX5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:41307379"
     variation       1343
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150705414"
     variation       1353
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:35450554"
     variation       1359
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369047406"
     variation       1364
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149447145"
     variation       1376
                     /gene="ARMCX5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201641747"
     variation       1395
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:375887903"
     variation       1477
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370774795"
     variation       1496
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:55673173"
     variation       1568
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:146343503"
     variation       1576
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373013040"
     variation       1615
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139851001"
     variation       1633
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377411016"
     variation       1641
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375842205"
     variation       1664
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371062313"
     variation       1686
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:143305512"
     variation       1716
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139067925"
     variation       1771
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376270648"
     variation       1804
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377359903"
     variation       1819
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113918916"
     variation       1885
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370182133"
     variation       2021
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200145435"
     variation       2036
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374899022"
     variation       2057
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149355875"
     variation       2072
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148467545"
     variation       2113
                     /gene="ARMCX5"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:142617709"
     variation       2126
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:35168882"
     variation       2235
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201473675"
     variation       2250
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186882890"
     variation       2275
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140890801"
     variation       2288
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148274740"
     variation       2443
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367941873"
     variation       2466
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200184974"
     variation       2522
                     /gene="ARMCX5"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35897621"
     variation       2576
                     /gene="ARMCX5"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374272924"
     STS             2689..2832
                     /gene="ARMCX5"
                     /standard_name="A002R08"
                     /db_xref="UniSTS:60223"
     polyA_signal    2876..2881
                     /gene="ARMCX5"
     polyA_site      2905
                     /gene="ARMCX5"
ORIGIN      
gaacttcgaaagactggaacacttccgcctgtcaggccagaagagatttcctgacaccacagctggaaacccatgtgcatttcagttcaggaaagaatgcgccgttttccctatatccggaattcgtccctgcgcattccaatacctgaagcggccacagggtacaggacagggagccctccgacagaaaagagtcgcggcgctaaacaaagcctgatatcactccgcttccataagccggatccccataaactacgctctagctcctcccactgccgttgtgggtaacgcggacgtggaagaacctcgtctgcggaggaaaagtcccaggtgccgagtcaatccccatacacagccgccgccattgcctcgagtccttgtgtctgactgtctgttcctgctgctgtatgacacagcacctcgaggcaaggaaataagaaaactgcctctgatccaagcagagaaggtagatctgtccccaggtctgtggaactgtcagttgtgaagttttgtaaaatggtcacccaacttaaaactaggaaattacgaagaagagaaaattgccctgtatctgttaaggtctgcctgtagatctgctgtagggcttgtcaccattggaagcaaggtcctacttcagtggcagatctggtggccttggagtggctgaagaccaccaccctccacagggctgggcccatgcacagccatccttccctaccttgagtgagcttcctctgcatgttttctatatcactggcagagcctgtagttggaaaggggacagagtgactactggactttgtgtgaaaacaccaaccgggacaaaacttcagtcaaggctgagacgggtgggggtatataacttgtccttacgttaaacttggaacatggttgactctgggacagaagcaagggctagaggaaaggctgaggctggcctgcaagatggaatcagtggtcctgccactgctagagtgaatggtaaaacccaggccgaggcagtggctgaggcagaactgaaaacagaatcagtgacccaggccaaagctggtgatggagcaatgaccaggacacatacagtgacctacagggaggctatggctgtgacaagggaagtgatcaaggtggaagatacaactaagactagagtcatggttgagactaagacaaaacccctggcagaacgcagtatagtgccacaaaccaagtcaaaggccatgcctatgtctagggtcagtactgtaaccaagtctgaagtcaaggttgttgctgtcattgaggcaaatattaggtcctatgccaagtcacatgataaggccaatactgggtccagacctgacagaagggaagagaccagcattgggatgaaatccagtgatgaggatgaagaaaatatatgctcctggttctggactggagaagagcctagtgtagggtcctggttctggcctgaagaagagacctctcttcaagtttataagcccctacctaagatccaggaaaagcccaagcccacacacaaacccacacttactataaaacaaaaggtaatagcatggtcaagggccaggtatattgtcctagttccagttgaaggaggggagcaatccttgcctccagaaggaaactggaccctggttgagaccttgattgaaactcctctggggattcgacctttgaccaagatcccaccttatcatgggccttattaccagaccttagctgagatcaaaaaacagattaggcaaagggaaaagtatgggcctaatccgaaggcctgccactgcaaatcacgtggctttagtttagagcctaaagagtttgataaacttgttgccctccttaagttaactaaggatcctttcattcatgaaatagctacaatgataatgggcatcagtcctgcttatccatttactcaagatataattcatgatgtaggtattactgttatgattgaaaacttggtcaataatcccaatgttaaagaacaccctggagctttaagtatggtggatgacagctctgagtcttccgaagaaccaaaatcaggggagtcatatatacatcaagtttgtaaaggcataatctcttgccccttgaactcccctgtgcagctggctggactgaaattactagggcacttgagtataaaatttgaagatcactatgtgattaccagttatattccagatttcctcaccttgttaaacaagggaagtgtcaaaaccaagttttatgttttaaaagtgttttcgtgtttgtctaaaaatcacgccaatacaagagaattgatcagtgccaaagtactgtcatcattggttgcaccctttaacaagaatgagtcaaaggccaatattcttaatattattgaaatatttgagaatataaattttcagttcaaaacaaaggcaaagctatttaccaaggaaaagttcactaaatctgagcttatttcaatattccaggaagcaaaacagtttggtcagaaactccaagacttagcagagcacagtgatcccgaagtgagagataaagtcatacgattaatactaaaactctgaatacccctctgttctcataaagcctcaaacagttttttggagttgcaatatgaaaccaatgcatattgtaattataaattcaatacttatgttttccatgttgattgagggaggcaattttatggataccaattaatcttgagatcctgaacatgtgctgatttttattgtgctatatagtatataaattgagatatttttggtatttctgcaacgtgacctgataatgaatctattcatcctgagtaagctatacttctgtgctttatattgatatgtgtattcttttgagattttatttacatgttgttaataaagttgcatgctaaaactggtgaaaaaaaaaaaaaaaaaaaaaaa
//

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