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2019-03-23 03:29:35, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001013659            7136 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens zinc finger protein 793 (ZNF793), mRNA.
ACCESSION   NM_001013659 XM_372726
VERSION     NM_001013659.2  GI:148727277
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 7136)
  AUTHORS   Kimura,K., Wakamatsu,A., Suzuki,Y., Ota,T., Nishikawa,T.,
            Yamashita,R., Yamamoto,J., Sekine,M., Tsuritani,K., Wakaguri,H.,
            Ishii,S., Sugiyama,T., Saito,K., Isono,Y., Irie,R., Kushida,N.,
            Yoneyama,T., Otsuka,R., Kanda,K., Yokoi,T., Kondo,H., Wagatsuma,M.,
            Murakawa,K., Ishida,S., Ishibashi,T., Takahashi-Fujii,A.,
            Tanase,T., Nagai,K., Kikuchi,H., Nakai,K., Isogai,T. and Sugano,S.
  TITLE     Diversification of transcriptional modulation: large-scale
            identification and characterization of putative alternative
            promoters of human genes
  JOURNAL   Genome Res. 16 (1), 55-65 (2006)
   PUBMED   16344560
REFERENCE   2  (bases 1 to 7136)
  AUTHORS   Bonaldo,M.F., Lennon,G. and Soares,M.B.
  TITLE     Normalization and subtraction: two approaches to facilitate gene
            discovery
  JOURNAL   Genome Res. 6 (9), 791-806 (1996)
   PUBMED   8889548
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AK131417.1, DB180171.1, BX537524.1, AC022148.6, BE219465.1 and
            BU683546.1.
            On Jun 8, 2007 this sequence version replaced gi:61966772.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK131417.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025081, ERS025082 [ECO:0000350]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-575               AK131417.1         1-575
            576-762             DB180171.1         371-557
            763-1365            AK131417.1         763-1365
            1366-1721           BX537524.1         1841-2196
            1722-6167           AC022148.6         126512-130957       c
            6168-6733           BE219465.1         1-566               c
            6734-7136           BU683546.1         1-403               c
FEATURES             Location/Qualifiers
     source          1..7136
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="19"
                     /map="19q13.12"
     gene            1..7136
                     /gene="ZNF793"
                     /note="zinc finger protein 793"
                     /db_xref="GeneID:390927"
                     /db_xref="HGNC:33115"
     exon            1..28
                     /gene="ZNF793"
                     /inference="alignment:Splign:1.39.8"
     exon            29..167
                     /gene="ZNF793"
                     /inference="alignment:Splign:1.39.8"
     variation       94
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:58761658"
     exon            168..296
                     /gene="ZNF793"
                     /inference="alignment:Splign:1.39.8"
     exon            297..412
                     /gene="ZNF793"
                     /inference="alignment:Splign:1.39.8"
     variation       392
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61353573"
     misc_feature    410..412
                     /gene="ZNF793"
                     /note="upstream in-frame stop codon"
     exon            413..457
                     /gene="ZNF793"
                     /inference="alignment:Splign:1.39.8"
     variation       413
                     /gene="ZNF793"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:374475379"
     variation       414
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184271128"
     variation       420
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367691504"
     CDS             443..1663
                     /gene="ZNF793"
                     /codon_start=1
                     /product="zinc finger protein 793"
                     /protein_id="NP_001013681.2"
                     /db_xref="GI:148727278"
                     /db_xref="CCDS:CCDS46062.1"
                     /db_xref="GeneID:390927"
                     /db_xref="HGNC:33115"
                     /translation="
MIEYQIPVSFKDVVVGFTQEEWHRLSPAQRALYRDVMLETYSNLVSVGYEGTKPDVILRLEQEEAPWIGEAACPGCHCWEDIWRVNIQRKRRQDMLLRPGAAISKKTLPKEKSCEYNKFGKISLLSTDLFSSIQSPSNWNPCGKNLNHNLDLIGFKRNCAKKQDECYAYGKLLQRINHGRRPNGEKPRGCSHCEKAFTQNPALMYKPAVSDSLLYKRKRVPPTEKPHVCSECGKAFCYKSEFIRHQRSHTGEKPYGCTDCGKAFSHKSTLIKHQRIHTGVRPFECFFCGKAFTQKSHRTEHQRTHTGERPFVCSECGKSFGEKSYLNVHRKMHTGERPYRCRECGKSFSQKSCLNKHWRTHTGEKPYGCNECGKAFYQKPNLSRHQKIHARKNAYRNENLIIVGNT
"
     misc_feature    464..646
                     /gene="ZNF793"
                     /note="krueppel associated box; Region: KRAB; smart00349"
                     /db_xref="CDD:197671"
     misc_feature    464..580
                     /gene="ZNF793"
                     /note="KRAB (Kruppel-associated box) domain -A box;
                     Region: KRAB_A-box; cd07765"
                     /db_xref="CDD:143639"
     misc_feature    <1115..1597
                     /gene="ZNF793"
                     /note="FOG: Zn-finger [General function prediction only];
                     Region: COG5048"
                     /db_xref="CDD:34653"
     misc_feature    1172..1240
                     /gene="ZNF793"
                     /note="Zinc-finger double domain; Region: zf-H2C2_2;
                     pfam13465"
                     /db_xref="CDD:205643"
     misc_feature    1211..1273
                     /gene="ZNF793"
                     /note="Zinc finger, C2H2 type; Region: zf-C2H2; cl15478"
                     /db_xref="CDD:210117"
     misc_feature    1250..1324
                     /gene="ZNF793"
                     /note="Zinc-finger double domain; Region: zf-H2C2_2;
                     pfam13465"
                     /db_xref="CDD:205643"
     misc_feature    1331..1402
                     /gene="ZNF793"
                     /note="Zinc-finger double domain; Region: zf-H2C2_2;
                     pfam13465"
                     /db_xref="CDD:205643"
     misc_feature    1415..1492
                     /gene="ZNF793"
                     /note="Zinc-finger double domain; Region: zf-H2C2_2;
                     pfam13465"
                     /db_xref="CDD:205643"
     variation       449
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199878634"
     exon            458..584
                     /gene="ZNF793"
                     /inference="alignment:Splign:1.39.8"
     variation       505
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373921849"
     variation       512
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201422659"
     variation       513
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376870274"
     variation       543
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371262002"
     variation       546
                     /gene="ZNF793"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:374077681"
     variation       552
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:192500733"
     variation       575
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200037315"
     exon            585..680
                     /gene="ZNF793"
                     /inference="alignment:Splign:1.39.8"
     variation       646
                     /gene="ZNF793"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:12977460"
     variation       663
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201416294"
     variation       664
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370904763"
     exon            681..7121
                     /gene="ZNF793"
                     /inference="alignment:Splign:1.39.8"
     variation       692
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376195372"
     variation       701
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368598248"
     variation       716
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200537636"
     variation       719
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377144546"
     variation       754
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:117888549"
     variation       762
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368352700"
     variation       763
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:183189493"
     variation       770
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:186104402"
     variation       839
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:45593644"
     variation       842
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375136979"
     variation       883
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201067882"
     variation       910
                     /gene="ZNF793"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374699540"
     variation       945
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369950802"
     variation       966
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200312043"
     variation       972
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377415105"
     variation       983
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202041227"
     variation       1001
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373385714"
     variation       1004
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376403589"
     variation       1005
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79090159"
     variation       1027
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143852313"
     variation       1042
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374969011"
     variation       1044
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200856065"
     variation       1053
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201677614"
     variation       1054
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190477883"
     variation       1091
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184106216"
     variation       1123
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371897623"
     variation       1146
                     /gene="ZNF793"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374852408"
     variation       1154
                     /gene="ZNF793"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:368150518"
     variation       1216
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:114596628"
     variation       1300
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374828147"
     variation       1320
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368936802"
     variation       1334
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201336836"
     variation       1356
                     /gene="ZNF793"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:375746014"
     variation       1366
                     /gene="ZNF793"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:188659958"
     variation       1376
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373213372"
     variation       1390
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139014237"
     variation       1398
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:192785678"
     variation       1422
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373734998"
     variation       1431
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377400755"
     variation       1453
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370145278"
     variation       1455
                     /gene="ZNF793"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375572663"
     variation       1461
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:45505797"
     variation       1513
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200673476"
     variation       1523
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200069012"
     variation       1551
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200604039"
     variation       1571
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371438539"
     variation       1579
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:182541341"
     variation       1585
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374379549"
     variation       1614
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368429968"
     variation       1642
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:187184189"
     variation       1696
                     /gene="ZNF793"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:369737171"
     variation       1698
                     /gene="ZNF793"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:76868510"
     variation       1735
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372339543"
     STS             1737..1839
                     /gene="ZNF793"
                     /standard_name="D11S2921"
                     /db_xref="UniSTS:152074"
     STS             1744..2202
                     /gene="ZNF793"
                     /standard_name="PMC156606P1"
                     /db_xref="UniSTS:271408"
     STS             1744..1833
                     /gene="ZNF793"
                     /standard_name="PMC156606P1"
                     /db_xref="UniSTS:271408"
     variation       1747
                     /gene="ZNF793"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:149389958"
     variation       1756
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144727279"
     variation       1769
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148457624"
     variation       1789
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12972657"
     STS             1791..2261
                     /gene="ZNF793"
                     /standard_name="D8S2278"
                     /db_xref="UniSTS:473906"
     STS             1791..1897
                     /gene="ZNF793"
                     /standard_name="D8S2278"
                     /db_xref="UniSTS:473906"
     STS             1799..2256
                     /gene="ZNF793"
                     /standard_name="D8S2279"
                     /db_xref="UniSTS:473907"
     STS             1799..1892
                     /gene="ZNF793"
                     /standard_name="D8S2279"
                     /db_xref="UniSTS:473907"
     variation       1845
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376366048"
     variation       1852
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368875781"
     variation       1862..1864
                     /gene="ZNF793"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:376288863"
     variation       1863..1865
                     /gene="ZNF793"
                     /replace=""
                     /replace="ttt"
                     /db_xref="dbSNP:369363940"
     variation       1863..1864
                     /gene="ZNF793"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:71177465"
     STS             1874..1976
                     /gene="ZNF793"
                     /standard_name="D11S3114"
                     /db_xref="UniSTS:152207"
     variation       1889
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191696655"
     variation       1890
                     /gene="ZNF793"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:183843667"
     variation       1892
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372115588"
     variation       1900
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189009759"
     variation       1901
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12972887"
     variation       1906
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372744419"
     variation       1934
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:192851002"
     variation       1936..1937
                     /gene="ZNF793"
                     /replace=""
                     /replace="cgt"
                     /db_xref="dbSNP:370077541"
     variation       1941
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185807394"
     variation       1946
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184056548"
     STS             1955..2188
                     /gene="ZNF793"
                     /standard_name="GDB:434012"
                     /db_xref="UniSTS:157204"
     variation       1956
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190314145"
     variation       1979
                     /gene="ZNF793"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:5020265"
     variation       1989
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375011080"
     variation       1994
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113524934"
     variation       2143
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143463991"
     STS             2168..2256
                     /gene="ZNF793"
                     /standard_name="D8S2279"
                     /db_xref="UniSTS:473907"
     variation       2227
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369352759"
     variation       2228
                     /gene="ZNF793"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:181043897"
     variation       2250
                     /gene="ZNF793"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:371706598"
     variation       2253
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184324807"
     variation       2323
                     /gene="ZNF793"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372863287"
     variation       2329
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10402827"
     variation       2359
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146673311"
     variation       2380
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140088278"
     variation       2381
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:4803214"
     variation       2382
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2385126"
     variation       2502
                     /gene="ZNF793"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:112601592"
     variation       2520
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188091228"
     variation       2633
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144924173"
     variation       2697
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148987520"
     variation       2742
                     /gene="ZNF793"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:11881806"
     variation       2829
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138465907"
     variation       2885
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:2199644"
     variation       3009
                     /gene="ZNF793"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:77301433"
     variation       3036
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142658313"
     variation       3107
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181304673"
     variation       3111
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185568728"
     variation       3123
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:73632256"
     variation       3136
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:181679208"
     variation       3147
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2385125"
     variation       3169
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115863855"
     variation       3175
                     /gene="ZNF793"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:369100425"
     variation       3184
                     /gene="ZNF793"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:187649798"
     variation       3228..3229
                     /gene="ZNF793"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:34326494"
     variation       3323
                     /gene="ZNF793"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1038085"
     variation       3481
                     /gene="ZNF793"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:74808464"
     variation       3564
                     /gene="ZNF793"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1038084"
     variation       3587
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112070049"
     variation       3602
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12984698"
     variation       3666
                     /gene="ZNF793"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:191955872"
     variation       3667
                     /gene="ZNF793"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:150851670"
     variation       3691
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:183869563"
     variation       3700
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113098429"
     variation       3711
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186696016"
     variation       3747
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:117695292"
     variation       3766
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189593236"
     STS             3795..5467
                     /gene="ZNF793"
                     /standard_name="D11S3316"
                     /db_xref="UniSTS:152558"
     variation       3815
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2126976"
     STS             3876..5377
                     /gene="ZNF793"
                     /standard_name="D8S2279"
                     /db_xref="UniSTS:473907"
     STS             3876..3970
                     /gene="ZNF793"
                     /standard_name="D8S2279"
                     /db_xref="UniSTS:473907"
     variation       3949
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4803215"
     variation       3977
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:62111486"
     variation       4012
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186934939"
     variation       4029
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375620505"
     variation       4030
                     /gene="ZNF793"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368584618"
     variation       4034
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372061490"
     variation       4041
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375146463"
     variation       4049..4050
                     /gene="ZNF793"
                     /replace=""
                     /replace="aa"
                     /db_xref="dbSNP:371729928"
     variation       4049
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:369259817"
     variation       4050..4051
                     /gene="ZNF793"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /replace="aaa"
                     /db_xref="dbSNP:10686444"
     variation       4134
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77317901"
     variation       4148
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374520272"
     variation       4191
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:193186763"
     variation       4242
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:55731325"
     variation       4254
                     /gene="ZNF793"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:185124442"
     variation       4332
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368745575"
     variation       4342..4349
                     /gene="ZNF793"
                     /replace=""
                     /replace="aaaaaaaa"
                     /db_xref="dbSNP:374754813"
     variation       4359
                     /gene="ZNF793"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:189233806"
     variation       4550
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:114899421"
     variation       4686
                     /gene="ZNF793"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:372343945"
     variation       4711
                     /gene="ZNF793"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:193097727"
     variation       4734..4736
                     /gene="ZNF793"
                     /replace=""
                     /replace="aca"
                     /db_xref="dbSNP:200556445"
     variation       4764
                     /gene="ZNF793"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:955476"
     variation       4866
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73031309"
     variation       4922
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146009576"
     variation       4937
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:111689603"
     variation       4979
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:367927459"
     variation       4981
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201114648"
     variation       4982
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375013937"
     variation       5051
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:368947963"
     variation       5183
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:188345569"
     variation       5206
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:180755559"
     variation       5292
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12608477"
     STS             5335..6131
                     /gene="ZNF793"
                     /standard_name="L18426"
                     /db_xref="UniSTS:34648"
     STS             5339..6122
                     /gene="ZNF793"
                     /standard_name="D1S1423"
                     /db_xref="UniSTS:149619"
     STS             5438..5930
                     /gene="ZNF793"
                     /standard_name="L18506"
                     /db_xref="UniSTS:54024"
     variation       5638
                     /gene="ZNF793"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:146269324"
     variation       5640
                     /gene="ZNF793"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148404230"
     variation       5656
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375087932"
     variation       5693
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:142496473"
     variation       5795
                     /gene="ZNF793"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:77771184"
     variation       5799
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12608818"
     variation       5966
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184273015"
     STS             6003..6091
                     /gene="ZNF793"
                     /standard_name="D8S2279"
                     /db_xref="UniSTS:473907"
     variation       6011
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187631963"
     variation       6012
                     /gene="ZNF793"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:375028323"
     STS             6022..6132
                     /gene="ZNF793"
                     /standard_name="D10S275"
                     /db_xref="UniSTS:147992"
     variation       6070
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:59411835"
     variation       6133
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:9797618"
     variation       6333
                     /gene="ZNF793"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:188644740"
     variation       6386
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:58208767"
     variation       6533
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139536262"
     variation       6556
                     /gene="ZNF793"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:4803216"
     variation       6568
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73931002"
     variation       6646
                     /gene="ZNF793"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144283741"
     variation       6755
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373508875"
     variation       6808
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2291002"
     variation       6830
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182189610"
     variation       6964
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147731631"
     variation       6971
                     /gene="ZNF793"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:4803220"
     variation       6972
                     /gene="ZNF793"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:369536506"
     STS             6980..7101
                     /gene="ZNF793"
                     /standard_name="RH92678"
                     /db_xref="UniSTS:92408"
     variation       7047
                     /gene="ZNF793"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:142529330"
     variation       7077
                     /gene="ZNF793"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186769987"
ORIGIN      
attcaggatgggacgaccttataccgcggctctttctggcaaaggtaatgacatacgcatctgtgccagcatcccaagagtgaggctggtttctggaaatccattctgactctgtgacagcggggatggatgtgaccttgcccgtggttagaaaacaaatttactgagttctctgggtgccctgcagacctttggatcctgccaccttgctggacgggagggctctctagctcctgccagcccttagagccacaggaccttggtcacaacatctacagaaggccctgcagctaagtgatctaatccaggatcatatgctgcctttaggtgacacatccctttagtctcctttaatcaggagcagtttctcagtgttcatcttccatgaagtcgacatttttgaagagtataggtgtcagatctttttcaagaacagcagaaaatgatcgaataccagatacctgtgtcattcaaagatgtggttgtgggcttcacccaagaggagtggcaccggctgagtcctgctcagagggccctgtaccgggatgtgatgctggaaacctatagcaacctcgtctcagtgggttatgaaggcaccaaaccagatgtgatcctcagactggagcaggaagaagcaccatggattggtgaggcagcatgcccgggctgccactgttgggaagacatctggcgagttaatatccagaggaaaagacggcaagacatgcttttgaggccaggcgcagccataagcaagaaaacattgcccaaggagaaaagctgtgaatataataagtttgggaaaatatcacttctgagcactgatcttttttcttcaatccagagccctagtaactggaacccttgtggaaagaatttgaaccataatttagacttgattggttttaagagaaactgtgcaaaaaagcaagatgagtgttatgcttatgggaaattgcttcagcgtataaatcatggtagacgacctaatggagaaaagccccggggttgcagtcactgtgagaaagctttcacccagaacccggcacttatgtataaaccagcagtaagtgattctctcttgtacaaacggaagagggttccacctacagaaaaaccccacgtctgtagtgagtgtgggaaagccttctgctacaagtctgaattcattaggcatcagagaagtcacactggggagaagccttatggctgcactgactgtgggaaagccttttcacataagtcaaccctcatcaaacaccagagaattcacactggggtaagaccctttgaatgttttttttgtgggaaagcctttacccagaagtcacaccgcacagaacatcagagaacacacacaggagagagaccctttgtctgcagtgaatgcgggaaatcgtttggtgagaagtcatacctcaatgtacatcgaaaaatgcacacaggagaaagaccgtatcgttgcagagaatgtggaaaatccttcagccagaagtcatgcctcaataaacattggagaactcacacaggagagaagccctatgggtgcaatgaatgtgggaaagctttctaccagaagccaaacctcagcagacatcagaaaattcatgctcggaagaatgcctacaggaatgaaaacttaataattgtgggaaatacttgagcaaaatatctggtttcatggtatgtagggaattttttttttttttttttgagttggaatctcactttgtcacccaggctggagtgcagtggcgcgatctcggcttactgcaagctctgcctcccgggttcacgccattctcctgcctcagcctcccgagtagctgggactacaggtgcccaccaccatgcccggctaattttttttttgtatttttagtagagacggggtttcaccgtgttagccaggatggtctcgatctcctgaccttgtgatctgcccgccttgtcctcccaaagtgctgggattacaggcgtgagccaccgcgcctggccggtatgtagggaatttatccttaggagaaatcttatcattttaatgaatttgaacagtgtgtttttattttatttatttatttattttgagttgtattctctgtttcccaggctggagtgcaatggcactatctcggctcactgtaacctcagcctcccaggttcaagcagttctcctgcctcagcctcccaagtagctgggattacaggcacctgccaccacgcctggctaatttttgtatttttagtagagatggggtttcaccatgttggtcaggctggtctctttggctaggctggtctcgaactcctgacctcgtgataccccccaaccccccgcccttggcctcccaaagtgttgggattacaggcatgagccaacgcgcccaaccgacagtgttgtatcataatggaaatcatgatctaattgtgatacaaacttttctagaaaatactttctcaaacataagcatggacaccctggcatgtaaacgtttaaaaatgtattaaatggaataacagcagaatacaaaatatctgtgaagagacttaaaggcatactctggtatattccacagtgagccatacaatcagcattatttgtattttggagttgtaaatgtgaaattaacataaaatgtgaatatcagacacatgtcacacaacatatagaatgccattcagaaaacttttccactttaaatatcatcattgtcttttgatgtcttaacaatacaaaaaaataacaacaacatggcccactattgttaaaagaactttattataccagctacatttttccacctttttgtaatacatgtaaatggctatagaggttgttactgtcctctgcagaaataataaagcagtgtttttaaatgtatttggataatttggccaaaaattttactaaaatgtagttatttatattaaaaatgcaagctaaggaatagtttaagaacctgatactgggtaaatgaaacactgtaaactatttgacaaaatgtagtgtcaccctggtgtacagtacactgttcatattttcttagtcttgcttaaaatatcttgtagcaaattagtagcattgctacactattctagatacactattctatatacaggttgtataactcagaaatgtttcatgcgtagaccactgaaggagaatttcttttctctctatccctctgcaaattaattcaagaatattcatttttttcatataaatttccttgcaagtgtcctagacactaaatcccaaggttttaattatttcaatgtttggaaagaagtctgcttccctgagttgctatgtcatccatattagaaaataaatggccatgtggaatctacatttttcaagatttccctccatgtaagactgcctgatccagaatgagaaaggagacataaccacagatatcaatatgattttttaagtgataaaaagatacctcatacaactctaatcaacatattttttaaaaagaggaggtggatgcttttctaataaacttaagttatgaaaactgcaataagaagtagaaaacttggtaggatagttaacattgaaaaactcaaaaaagctattaaagatctataatgggaaaatgctccaggctcagaagagttcatgcttagttctatcttttaaagaaagagtaataccagtgttatttattatatggatgtaatacaatccatgaactgtactcatttattttattaagtcagaataaattttaacaccaaaatcaaatacagatagttgaaaaaagaaaacttctgctgggtgcggtggctcacgcctgtaatcccaacactttgggaggccgaggcaggtggatcatgaggtcagaagttcgagatggtgaaaccccatctctactaaaaatacaaaaattagccgggtgtggtggcacacacctgtagtcccagctacttgggaggttgaggcatgaggcaggagaattgcttgtacccaggaggtagaggttgcggtgagccaagatcgtgccatccagcctgggtgacaagagcgaaactccgtcaaaaaaaaaaaaaaaaaaagaaaacttcagaccagtcttactcatgaatatagaaacaaaaattatagttaaaatactagcaaatagaattcagccatatacccaaagagtgacatagtaagagtcatcccaagaatgccaaaccagttcagttaataggaaatgcatcaatcaaattaacagtttaaaggagaagaatcatatgaactctcaacagatactgagaaggcatttcatagaatgtgttaatttacattgtaatagatgggaaccacttaaagcggtttttcttaaaaaaaattttttttaacccaaaccccaaagcatatattatgccaaagccattttttaaaatcaggaattcaatattggcttagagattccagtgaaggcaataaaaagaaatgaattggtataaacagcagaaaaggtaaaactatccatttttactgatgatatggttgtacaccaataaatgaaaagactattttttgagttaacttttctaagaagacagggtaccaaaatcaagagctgttctccatactgacaagaaaacataatttatatgtacttcttttggaattacactaaatctcaatgattttttgacaatcattgaaaaaaatatatgaaaaaaatcataccatgtataaaaacatcacatgtacccaataaatatatacaacaattatatatctataataattaaaaatttttaaaatgccatgctagataccagaagataacatgaagccattctaatgaaattaatattgtattggcaaaggaacaggtaaatacatcattagaacacagtagaaaattcagaaatagacttcgatatatatgaactttttcatatgtgaaaaaggtgaaatctgaaaccacaggggaaaagagtagtttacttaaaaagaattctggaacagaaccttttaatcttaaagg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//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:390927 -> Molecular function: GO:0003677 [DNA binding] evidence: IEA
            GeneID:390927 -> Molecular function: GO:0046872 [metal ion binding] evidence: IEA
            GeneID:390927 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
            GeneID:390927 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: IEA
            GeneID:390927 -> Cellular component: GO:0005634 [nucleus] evidence: IEA

by @meso_cacase at DBCLS
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