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2025-05-09 18:44:54, 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
attcaggatgggacgaccttataccgcggctctttctggcaaaggtaatgacatacgcatctgtgccagcatcccaagagtgaggctggtttctggaaatccattctgactctgtgacagcggggatggatgtgaccttgcccgtggttagaaaacaaatttactgagttctctgggtgccctgcagacctttggatcctgccaccttgctggacgggagggctctctagctcctgccagcccttagagccacaggaccttggtcacaacatctacagaaggccctgcagctaagtgatctaatccaggatcatatgctgcctttaggtgacacatccctttagtctcctttaatcaggagcagtttctcagtgttcatcttccatgaagtcgacatttttgaagagtataggtgtcagatctttttcaagaacagcagaaaatgatcgaataccagatacctgtgtcattcaaagatgtggttgtgggcttcacccaagaggagtggcaccggctgagtcctgctcagagggccctgtaccgggatgtgatgctggaaacctatagcaacctcgtctcagtgggttatgaaggcaccaaaccagatgtgatcctcagactggagcaggaagaagcaccatggattggtgaggcagcatgcccgggctgccactgttgggaagacatctggcgagttaatatccagaggaaaagacggcaagacatgcttttgaggccaggcgcagccataagcaagaaaacattgcccaaggagaaaagctgtgaatataataagtttgggaaaatatcacttctgagcactgatcttttttcttcaatccagagccctagtaactggaacccttgtggaaagaatttgaaccataatttagacttgattggttttaagagaaactgtgcaaaaaagcaagatgagtgttatgcttatgggaaattgcttcagcgtataaatcatggtagacgacctaatggagaaaagccccggggttgcagtcactgtgagaaagctttcacccagaacccggcacttatgtataaaccagcagtaagtgattctctcttgtacaaacggaagagggttccacctacagaaaaaccccacgtctgtagtgagtgtgggaaagccttctgctacaagtctgaattcattaggcatcagagaagtcacactggggagaagccttatggctgcactgactgtgggaaagccttttcacataagtcaaccctcatcaaacaccagagaattcacactggggtaagaccctttgaatgttttttttgtgggaaagcctttacccagaagtcacaccgcacagaacatcagagaacacacacaggagagagaccctttgtctgcagtgaatgcgggaaatcgtttggtgagaagtcatacctcaatgtacatcgaaaaatgcacacaggagaaagaccgtatcgttgcagagaatgtggaaaatccttcagccagaagtcatgcctcaataaacattggagaactcacacaggagagaagccctatgggtgcaatgaatgtgggaaagctttctaccagaagccaaacctcagcagacatcagaaaattcatgctcggaagaatgcctacaggaatgaaaacttaataattgtgggaaatacttgagcaaaatatctggtttcatggtatgtagggaattttttttttttttttttgagttggaatctcactttgtcacccaggctggagtgcagtggcgcgatctcggcttactgcaagctctgcctcccgggttcacgccattctcctgcctcagcctcccgagtagctgggactacaggtgcccaccaccatgcccggctaattttttttttgtatttttagtagagacggggtttcaccgtgttagccaggatggtctcgatctcctgaccttgtgatctgcccgccttgtcctcccaaagtgctgggattacaggcgtgagccaccgcgcctggccggtatgtagggaatttatccttaggagaaatcttatcattttaatgaatttgaacagtgtgtttttattttatttatttatttattttgagttgtattctctgtttcccaggctggagtgcaatggcactatctcggctcactgtaacctcagcctcccaggttcaagcagttctcctgcctcagcctcccaagtagctgggattacaggcacctgccaccacgcctggctaatttttgtatttttagtagagatggggtttcaccatgttggtcaggctggtctctttggctaggctggtctcgaactcctgacctcgtgataccccccaaccccccgcccttggcctcccaaagtgttgggattacaggcatgagccaacgcgcccaaccgacagtgttgtatcataatggaaatcatgatctaattgtgatacaaacttttctagaaaatactttctcaaacataagcatggacaccctggcatgtaaacgtttaaaaatgtattaaatggaataacagcagaatacaaaatatctgtgaagagacttaaaggcatactctggtatattccacagtgagccatacaatcagcattatttgtattttggagttgtaaatgtgaaattaacataaaatgtgaatatcagacacatgtcacacaacatatagaatgccattcagaaaacttttccactttaaatatcatcattgtcttttgatgtcttaacaatacaaaaaaataacaacaacatggcccactattgttaaaagaactttattataccagctacatttttccacctttttgtaatacatgtaaatggctatagaggttgttactgtcctctgcagaaataataaagcagtgtttttaaatgtatttggataatttggccaaaaattttactaaaatgtagttatttatattaaaaatgcaagctaaggaatagtttaagaacctgatactgggtaaatgaaacactgtaaactatttgacaaaatgtagtgtcaccctggtgtacagtacactgttcatattttcttagtcttgcttaaaatatcttgtagcaaattagtagcattgctacactattctagatacactattctatatacaggttgtataactcagaaatgtttcatgcgtagaccactgaaggagaatttcttttctctctatccctctgcaaattaattcaagaatattcatttttttcatataaatttccttgcaagtgtcctagacactaaatcccaaggttttaattatttcaatgtttggaaagaagtctgcttccctgagttgctatgtcatccatattagaaaataaatggccatgtggaatctacatttttcaagatttccctccatgtaagactgcctgatccagaatgagaaaggagacataaccacagatatcaatatgattttttaagtgataaaaagatacctcatacaactctaatcaacatattttttaaaaagaggaggtggatgcttttctaataaacttaagttatgaaaactgcaataagaagtagaaaacttggtaggatagttaacattgaaaaactcaaaaaagctattaaagatctataatgggaaaatgctccaggctcagaagagttcatgcttagttctatcttttaaagaaagagtaataccagtgttatttattatatggatgtaatacaatccatgaactgtactcatttattttattaagtcagaataaattttaacaccaaaatcaaatacagatagttgaaaaaagaaaacttctgctgggtgcggtggctcacgcctgtaatcccaacactttgggaggccgaggcaggtggatcatgaggtcagaagttcgagatggtgaaaccccatctctactaaaaatacaaaaattagccgggtgtggtggcacacacctgtagtcccagctacttgggaggttgaggcatgaggcaggagaattgcttgtacccaggaggtagaggttgcggtgagccaagatcgtgccatccagcctgggtgacaagagcgaaactccgtcaaaaaaaaaaaaaaaaaaagaaaacttcagaccagtcttactcatgaatatagaaacaaaaattatagttaaaatactagcaaatagaattcagccatatacccaaagagtgacatagtaagagtcatcccaagaatgccaaaccagttcagttaataggaaatgcatcaatcaaattaacagtttaaaggagaagaatcatatgaactctcaacagatactgagaaggcatttcatagaatgtgttaatttacattgtaatagatgggaaccacttaaagcggtttttcttaaaaaaaattttttttaacccaaaccccaaagcatatattatgccaaagccattttttaaaatcaggaattcaatattggcttagagattccagtgaaggcaataaaaagaaatgaattggtataaacagcagaaaaggtaaaactatccatttttactgatgatatggttgtacaccaataaatgaaaagactattttttgagttaacttttctaagaagacagggtaccaaaatcaagagctgttctccatactgacaagaaaacataatttatatgtacttcttttggaattacactaaatctcaatgattttttgacaatcattgaaaaaaatatatgaaaaaaatcataccatgtataaaaacatcacatgtacccaataaatatatacaacaattatatatctataataattaaaaatttttaaaatgccatgctagataccagaagataacatgaagccattctaatgaaattaatattgtattggcaaaggaacaggtaaatacatcattagaacacagtagaaaattcagaaatagacttcgatatatatgaactttttcatatgtgaaaaaggtgaaatctgaaaccacaggggaaaagagtagtttacttaaaaagaattctggaacagaaccttttaatcttaaaggaagaaaatttggattaacagcacaaaaataaattctgggtggctttaagacgtaaaattttaaagcaacagaattcttaaaagaaaatcaaaggagcctatgtgtacaatctaggagttgggagatattaactttaccaacacaggacactcagaagctatttagaaataagcagttgaaggctgggtgcagtggctcatgcctgtaatcccaacactttgggaggctgaggcaggaggatcacctgaggttaggagttcaagactagtctggtcaacatggtgaaaccccatctccactaaaaatacaaaaattagctgggtgtggtggcacatgcctgtagtcccagctacttgggaggctgaggcaggagaatcacttgaacctggaaggcaggggttgaagtgagctgagattgcaccactgcactccagcctgggcaacagagcaagactccatctcagaaaaaaagaaaaagaaaaaaaaaaggaaacaaacatttgactacgtagaatcttttggtacaatcttttgggtgacaaaagatgccatcagcaaactcaagagataatagattgtggggaaatatttgtaaagctgatcagagagaaggcattcatgaaatggacaggaaaaaaacccaatagcaaaatgtggcaaagaatatgagttgacagttgtgagaagagcaaatctaagtggccaatggacctgtccaaaaatgtttatcctcagtagtcactgggggatgcagatttaaagttaaaatcaaataacactgtgtaacagcatttttagctatcagaacaaaagatgttacacactgctggtggagaaataaattttgaaaaacaatgcaaattactgttttggaaagaaatctggtaatatttaggctgggcgtggtggctcacacctgtaatcctagcactttgggaggccgaggcaggcaaattgtctgaggtcgggagttcgagaacagcctggccagcatggtgaaaccccgtctctactaaaaatacaaaaattagctgggcatggtggcaggcacctgtgatcccagctactcgggaggctgaggcaggagaatcacttgaacccaggaggcagaggttgcagtgagccaagatcgcgccattgcactccaacctgggcaacagagcaaaaagattccatctcaaaagaaaagaaaagaaatctgttaatattattaaaatatttatgtcactttggagaatcttcccttagaagtaaaagctccaatacataaaagacagatgaacatgtgaacatggacatttattgtaaaaattgttcttaatggcaaaaaaacccccaaaaccaaagcaaacactagaatcaaagtaaatacccatcaactgggaaattgtagaaaggaaaaaactatagtgtatccattccatagaatgttaatatagccattaaggtggacaaattaaaactatgctagtggacttgagtggaattccacaatgttctcttgagtgaaaaatgcaaggtagatattaagtatgttaaatatgactccatttttttaaatcattaacaaaatgtctctaggtgtttgtcagcaataaacggtatctatatatgtttatttgattttatgtgcatgaagaaaagtatagaagagtatgcattgacttggagggaggtgggtaatgcaggtaggttatgggggagtcaggggtgtagggaaaaggaaaaccaaaaaagaaaaatacataaatgactgaatcacgggtgataccacaaatgtgtgagttagtaaatttggctggggatgggggagctagaattttgctaatttgtggggatgttcatggtatatattgtaaaaagggaaaatttcataataatgtatacgattctatttttaaaaaaagtaaaaactcctgtgtgtgtatatatgcatgtggatgtttatatgaacatagaaaagtgtagaagaatacacacgaaggtgttaacattcattggttaccttggtggagaagggtaataagttttctgaatacctttgcattgtcttgttcacatatattgcttttgtaatttgaaaaacaaaataaagggggaaaacatttcaaactgaatgaaaaaaaaaaaaaaaaa
//
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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