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2024-04-25 20:54:05, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_018335 3794 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens zinc finger protein 839 (ZNF839), transcript variant
1, mRNA.
ACCESSION NM_018335
VERSION NM_018335.4 GI:392513691
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 3794)
AUTHORS Scanlan,M.J., Gordan,J.D., Williamson,B., Stockert,E., Bander,N.H.,
Jongeneel,V., Gure,A.O., Jager,D., Jager,E., Knuth,A., Chen,Y.T.
and Old,L.J.
TITLE Antigens recognized by autologous antibody in patients with
renal-cell carcinoma
JOURNAL Int. J. Cancer 83 (4), 456-464 (1999)
PUBMED 10508479
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
BX367536.2, DB460089.1, AK093342.1, AK223312.1, AK001994.1,
BQ019232.1 and AL137229.4.
On Jun 22, 2012 this sequence version replaced gi:153251839.
Transcript Variant: This variant (1) represents the longest
transcript and encodes the longer protein (isoform 1).
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
##Evidence-Data-START##
RNAseq introns :: single sample supports all introns ERS025083,
ERS025085 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-8 BX367536.2 1-8
9-476 DB460089.1 1-468
477-1797 AK093342.1 464-1784
1798-2674 AK223312.1 198-1074
2675-3233 AK001994.1 1091-1649
3234-3327 BQ019232.1 19-112 c
3328-3794 AL137229.4 16088-16554
FEATURES Location/Qualifiers
source 1..3794
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="14"
/map="14q32.31"
gene 1..3794
/gene="ZNF839"
/gene_synonym="C14orf131"
/note="zinc finger protein 839"
/db_xref="GeneID:55778"
/db_xref="HGNC:20345"
exon 1..303
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
CDS 16..2799
/gene="ZNF839"
/gene_synonym="C14orf131"
/note="isoform 1 is encoded by transcript variant 1; renal
carcinoma antigen NY-REN-50"
/codon_start=1
/product="zinc finger protein 839 isoform 1"
/protein_id="NP_060805.3"
/db_xref="GI:153251840"
/db_xref="CCDS:CCDS45164.1"
/db_xref="GeneID:55778"
/db_xref="HGNC:20345"
/translation="
MADAEPEAGGGSEDGGGGGGPAPPGQSGSVARVAPLGPEQLRQVLEQVTKAQPPPPPPPFVLRDAARRLRDAAQQAALQRGRGTEPPRLPRLLPPQQLEAICVKVTSGETKGQERPMLLPTTIQPQTARKSQLPRGNSCLVGLHIASPQLLRVQPLVRTEPQSCFLSDLCQPPAQGFVQRPLPALQVVPAKRVPAPKAPDEQGSMLTPLSASDPLAVTSLSSSSAHPFISNLHTRHTEKLKKSLKVKTRSGRVSRPPKYKAKDYKFIKTEDLADGHLSDSDDYSELCVEEDEDQRERHALFDLSSCSLRPKSFKCQTCEKSYIGKGGLARHFKLNPGHGQLDPEMVLSEKASGSTLRGCTEERTLSLTSLGLSMPADPCEGGARSCLVTESARGGLQNGQSVDVEETLPSEPENGALLRSERYQGPRRRACSETLAESRTAVLQQRRAAQLPGGPAAAGEQRASPSKARLKEFLQQCDREDLVELALPQLAQVVTVYEFLLMKVEKDHLAKPFFPAIYKEFEELHKMVKKMCQDYLSSSGLCSQETLEINNDKVAESLGITEFLRKKEIHPDNLGPKHLSRDMDGEQLEGASSEKREREAAEEGLASVKRPRREALSNDTTESLAANSRGREKPRPLHALAAGFSPPVNVTVSPRSEESHTTTVSGGNGSVFQAGPQLQALANLEARRGSIGAALSSRDVSGLPVYAQSGEPRRLTQAQVAAFPGENALEHSSDQDTWDSLRSPGFCSPLSSGGGAESLPPGGPGHAEAGHLGKVCDFHLNHQQPSPTSVLPTEVAAPPLEKILSVDSVAVDCAYRTVPKPGPQPGPHGSLLTEGCLRSLSGDLNRFPCGMEVHSGQRELESVVAVGEAMAFEISNGSHELLSQGQKQIFIQTSDGLILSPPGTIVSQEEDIVTVTDAEGRACGWAR
"
variation 19
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:113722714"
variation 24
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:111952535"
variation 126
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:192593829"
variation 144
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:112795025"
variation 280
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:12890151"
variation 289
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:12890155"
exon 304..1206
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 305
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:199998183"
variation 314
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:371653840"
variation 339
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:376888726"
variation 368
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:7158731"
variation 445
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:371997799"
variation 471
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:7157941"
variation 489
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:369763728"
variation 501
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:372423800"
variation 506
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:376630932"
variation 511
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:200627167"
variation 542
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:372978171"
variation 561
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:375660447"
variation 613
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:7158139"
variation 646
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:372836943"
variation 656
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:185772819"
variation 657
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:371006557"
variation 658
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374612303"
variation 715
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:377448123"
variation 729
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:370243689"
variation 744
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376366454"
variation 833
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:199677123"
variation 834
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:367624048"
variation 835
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:61731137"
variation 844
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:45572332"
variation 854
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:368386323"
variation 905
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:372349522"
variation 909
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:375904596"
variation 910
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:370193621"
variation 915
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:372165787"
variation 918
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374840097"
variation 926
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:368921112"
variation 927
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:200901016"
variation 991
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:201365142"
variation 1000
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:369654865"
variation 1017
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:149249563"
variation 1024
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376706697"
variation 1029
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:75766619"
variation 1072
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:202123139"
variation 1084
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:147318919"
variation 1091
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370145192"
variation 1095
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375280717"
variation 1106
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200171587"
variation 1142
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:199513391"
variation 1149
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375295594"
variation 1166
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:8004621"
variation 1173
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:372355238"
variation 1183
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:370541879"
variation 1193
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375305020"
exon 1207..1431
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1224
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:115710329"
variation 1236
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376599934"
variation 1240
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:192100739"
variation 1270
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374503383"
variation 1300
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:377689182"
variation 1303
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:1543540"
variation 1321
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200649815"
variation 1333
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376102379"
variation 1336
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:201015963"
variation 1385
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:373962634"
variation 1404
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200235026"
variation 1407
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:368513189"
variation 1422
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375163932"
exon 1432..1524
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1437
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:202065904"
variation 1450
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:201839345"
variation 1465
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:201298008"
variation 1474
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:114749589"
variation 1491
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:374064620"
exon 1525..1674
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1534
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:369694092"
variation 1585
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:186815397"
variation 1594
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:189003679"
variation 1602
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:376419486"
variation 1667
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:181795004"
exon 1675..1812
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1709
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:140733581"
variation 1767
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:116469270"
variation 1782
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:201431440"
variation 1794
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:371253844"
variation 1795
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:374849816"
variation 1807
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:199952618"
variation 1808
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:371985656"
exon 1813..1942
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1839
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:201573850"
variation 1904
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:112729291"
variation 1906
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:376304862"
variation 1907
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370674726"
variation 1909
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:375532380"
variation 1919
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:115365685"
variation 1938
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:199523800"
variation 1939
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:373766097"
exon 1943..3794
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1948
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="tc"
/db_xref="dbSNP:58660213"
variation 1954
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:9464"
variation 1968
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:371906391"
STS 1987..2114
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="RH47332"
/db_xref="UniSTS:41544"
variation 1987
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200026357"
variation 2000
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:187162307"
variation 2018
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:369990834"
variation 2020
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:201911497"
variation 2036
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:201952805"
variation 2037
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:374840960"
variation 2043
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:368919341"
variation 2107
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:35472059"
variation 2124
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375836612"
variation 2137
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200735310"
variation 2150
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:71415891"
variation 2175
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:373049928"
variation 2181
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:202001193"
variation 2224
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:184177701"
variation 2227
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:371235481"
variation 2246
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200152705"
variation 2272
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376081264"
variation 2332
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:377410566"
variation 2367
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:140180484"
variation 2383
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370117834"
variation 2412
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375324501"
variation 2440
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:28646161"
variation 2453
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:145520632"
variation 2460
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200007235"
variation 2487
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370680612"
variation 2488
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374364651"
variation 2501
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:201782124"
variation 2529
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200933608"
variation 2551
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200295748"
variation 2556
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:1053019"
variation 2579
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:375304978"
variation 2601
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:367718180"
variation 2613
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:12590618"
variation 2674
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:201197821"
variation 2676
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200165854"
variation 2698
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:199645167"
variation 2767
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:188964576"
variation 2794
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:201035007"
variation 2795
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:373342974"
variation 2832
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375672028"
variation 2838..2841
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="gtgga"
/db_xref="dbSNP:34220197"
variation 2839..2842
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="tggag"
/db_xref="dbSNP:57469946"
variation 2839
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:115640468"
variation 2845
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:56144634"
variation 2923
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:148816192"
variation 2938
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:11704"
variation 3061
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:79599148"
variation 3063
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:114001492"
variation 3070
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370351735"
variation 3089
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:142497784"
variation 3091
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:146433857"
variation 3109
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374073075"
variation 3126
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:182242624"
variation 3271
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:140712552"
variation 3295
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:79512799"
variation 3299
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:138374403"
variation 3312..3315
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="aatt"
/db_xref="dbSNP:201915133"
variation 3313
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:1056745"
variation 3314..3318
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="ttaat"
/db_xref="dbSNP:200011760"
variation 3318
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:76612776"
STS 3361..3765
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="PMC156606P1"
/db_xref="UniSTS:271408"
STS 3375..3485
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="D10S275"
/db_xref="UniSTS:147992"
STS 3416..3511
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="D8S2279"
/db_xref="UniSTS:473907"
variation 3416
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:141050487"
STS 3451..3573
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="D13S116"
/db_xref="UniSTS:147007"
variation 3507
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:188689300"
STS 3575..3751
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="GDB:434012"
/db_xref="UniSTS:157204"
variation 3629
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="t"
/db_xref="dbSNP:199844270"
variation 3680
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:185631319"
variation 3727
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:377096853"
variation 3728
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:150210883"
variation 3783
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:80178328"
ORIGIN
cccgcctcggccgccatggcggatgcggagccggaggctgggggcggcagcgaggatggcggcggcggcggcggcccggctcctccgggccagagcggcagcgtcgcacgtgtggccccgctgggccccgagcagctgcggcaggtcctggagcaggtgacgaaggcgcagccgccgccgccgccgccccccttcgtgctgcgggacgcggcgcggcggctgcgggacgcggcccaacaggccgccctgcagcggggccggggcaccgagcccccgcgcctgccgcgcctgctcccgccccagcaactagaagccatttgtgtcaaggtaacgtctggagaaacaaaaggtcaggaaaggccaatgctcctaccgaccacaatccagccccaaactgcaagaaagagccagctgccccgggggaattcctgcctggtggggctccatatcgccagccctcagctgctcagggtacagccgcttgtgagaaccgagccacagtcctgcttcctaagtgacttatgccaacctcctgctcaggggtttgtacagagaccactgccagccctccaggtggtccctgcaaagagagtcccagcccccaaggctccagatgaacagggctccatgttgacccctttgtctgcctctgacccgctggcagtaacatctctttcatccagttcagcacatccatttatttccaacttgcatacaagacatactgagaaactaaaaaaatcgttaaaagtaaagacacgttctggacgggtatctcgacctcccaaatataaagctaaagattataagttcataaaaacagaggatctggcggatggtcatctgtcagattctgatgattactcagaactctgtgtggaagaagatgaagatcagagggagaggcacgcactctttgacttatcgagctgctccctgaggcccaaaagctttaagtgtcagacttgtgaaaagtcatatatagggaaggggggactggcccgacattttaaacttaacccaggccacggccagttggaccccgagatggtgctgtctgagaaagccagtggaagcaccctccgggggtgcacggaggaaaggacgctcagcctgacctccctggggctgtccatgccagcggatccatgtgagggaggggcccgctcctgcttggtgacagagtcagcacgcggtggcctgcagaatggtcagtctgtagacgttgaagagacattgccatctgaaccagaaaatggagctcttttgcgatcagagagataccaaggacctagaagacgcgcatgctcagagacccttgcagagtcccgcacagctgtcctccagcagagaagagctgctcagctacctggtggccctgctgcggcaggggagcagagggcgtcgccaagcaaagccaggctcaaggagttcctccagcagtgtgaccgggaggatctggtggaattggctctgcctcagctggctcaggttgtgaccgtgtatgagtttcttctgatgaaggttgaaaaagatcatctagcaaagccttttttcccagctatatataaggaatttgaagagttgcataaaatggttaagaaaatgtgccaagattacctcagtagttctggtctgtgttcccaggagaccctggaaataaacaatgataaggttgctgagtcattaggaatcacagaattcctacggaagaaagaaatacacccagacaaccttggacccaagcacctcagccgagacatggatggggagcagctagagggagctagcagcgagaagagggaacgtgaggctgcggaggagggactggcctcagtgaaaaggcccagaagagaagccctgtccaacgataccactgaatctcttgctgccaacagcagaggccgggagaagcccaggcccttgcatgctttggccgctggtttttcccctccagtaaatgtgactgtctctccccgttctgaagaaagccatacaacgacggtttctggtggcaatgggagcgtgttccaggcgggcccgcagcttcaggcactggctaacttagaagccaggagggggtctataggtgctgctctctcatcccgggatgtcagtgggctgcctgtttatgctcagtcaggagagcctaggaggctgacccaggcacaggtggcagcgtttcctggagagaatgctttggaacactcttcagaccaggacacctgggacagcctgaggagcccgggtttctgcagccctttgtcatctggtggtggagcagagtccctgccgcctggggggcctggacatgcagaggcaggacacctcggcaaggtttgtgacttccacctgaaccaccagcagcccagccccaccagcgtcctgcctacagaggtggcagcccctccgcttgagaaaattttgtctgtggatagcgtggcagtggactgtgcctacaggactgtgcccaagccagggcctcagcctggcccacatggatcactattgactgaagggtgtctcagaagcctttcgggggacttgaaccggttcccctgtgggatggaggtgcactctggccagagagaactggagagcgtggttgctgtcggcgaagccatggcttttgaaatttccaatgggagccatgagttactgtctcagggacagaagcagatttttattcagacttccgatgggcttatcttgtcccctccaggtacaatagtgtctcaggaggaggacattgtcacagtgactgatgcagaggggcgtgcctgcggatgggcccgctagaaggagttcctctagaagctgtggagtcggtcgtcaccgtggagccagagccctcacagtgaagtggagtcagatcctagattcgtctgattttatccagagaaggtctatggcaagcaatgtatatttttctaatgtgaatattgcacagatgaaccttttatttataaagaataatgtctttctgccctgctgtctacatttttctatggagcttgtcataataatagcagatattacctgatcaggaatccctgtggcgcgtctgacgctcatgagtttttcatgatggtgatgagtagcactgcactgtcacctgatgattggccctgctccgtttcccttctctcctgggagatatgctgcttttccaccagacttgctccatactagaagcttcttttgggttcaattaaaaagaaaataagctagtcattctgggcagcattttattgatagaagggggaaaaagtcatttctacttgcatgattttttaaattaaattaaattaaattaatttaattatttttgagaccaagtcttactctgtagcccaagctggagtgcagtggcgcgatcttggctcactgcaacctctgccgcctgggctcaagcgattctcgtgcctcagcctcctgagtagctgtgactacaggagcatgccaccatgcccagctaattttttttttttgtattttagtagatacggggtttcaccatgttgcccagggtggtctcaaactcttgagctcaggcaatccgcccacctcagcttcccaaagtgctgggattacagtacaggcatgagccactgcacctggccaatgatttttttttttttttttgagatggagttttggtcttgttgcccaagctggagtgcaatggctcgatcttggctcaccgcaacctccaccacagggttcaagcaattctcctgcctcagcctcccaagtagctgggattacaggcatgtgccatcacacctggatca
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:55778 -> Molecular function: GO:0046872 [metal ion binding] evidence: IEA
by
@meso_cacase at
DBCLS
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