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2024-04-20 23:29:18, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001267828 3712 bp mRNA linear PRI 18-APR-2013
DEFINITION Homo sapiens zinc finger protein 839 (ZNF839), transcript variant
3, mRNA.
ACCESSION NM_001267828
VERSION NM_001267828.1 GI:392513697
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 3712)
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
AK289632.1, AL137229.4 and BQ019232.1.
Transcript Variant: This variant (3) differs in the 5' UTR and
lacks an exon in the 5' coding region compared to variant 1, which
results in the use of a downstream translation start codon. The
resulting protein (isoform 2) has a shorter N-terminus compared to
isoform 1. Variants 2 and 3 encode the same protein.
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##
Transcript exon combination :: AK289632.1 [ECO:0000332]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-2530 AK289632.1 1-2530
2531-2856 AL137229.4 15373-15698
2857-3245 BQ019232.1 19-407 c
3246-3712 AL137229.4 16088-16554
FEATURES Location/Qualifiers
source 1..3712
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="14"
/map="14q32.31"
gene 1..3712
/gene="ZNF839"
/gene_synonym="C14orf131"
/note="zinc finger protein 839"
/db_xref="GeneID:55778"
/db_xref="HGNC:20345"
exon 1..221
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 167
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:72635188"
misc_feature 171..173
/gene="ZNF839"
/gene_synonym="C14orf131"
/note="upstream in-frame stop codon"
variation 180
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:189459449"
variation 187
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:138100902"
exon 222..1124
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 223
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:199998183"
variation 232
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:371653840"
variation 257
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:376888726"
CDS 282..2717
/gene="ZNF839"
/gene_synonym="C14orf131"
/note="isoform 2 is encoded by transcript variant 3; renal
carcinoma antigen NY-REN-50"
/codon_start=1
/product="zinc finger protein 839 isoform 2"
/protein_id="NP_001254757.1"
/db_xref="GI:392513698"
/db_xref="CCDS:CCDS58336.1"
/db_xref="GeneID:55778"
/db_xref="HGNC:20345"
/translation="
MLLPTTIQPQTARKSQLPRGNSCLVGLHIASPQLLRVQPLVRTEPQSCFLSDLCQPPAQGFVQRPLPALQVVPAKRVPAPKAPDEQGSMLTPLSASDPLAVTSLSSSSAHPFISNLHTRHTEKLKKSLKVKTRSGRVSRPPKYKAKDYKFIKTEDLADGHLSDSDDYSELCVEEDEDQRERHALFDLSSCSLRPKSFKCQTCEKSYIGKGGLARHFKLNPGHGQLDPEMVLSEKASGSTLRGCTEERTLSLTSLGLSMPADPCEGGARSCLVTESARGGLQNGQSVDVEETLPSEPENGALLRSERYQGPRRRACSETLAESRTAVLQQRRAAQLPGGPAAAGEQRASPSKARLKEFLQQCDREDLVELALPQLAQVVTVYEFLLMKVEKDHLAKPFFPAIYKEFEELHKMVKKMCQDYLSSSGLCSQETLEINNDKVAESLGITEFLRKKEIHPDNLGPKHLSRDMDGEQLEGASSEKREREAAEEGLASVKRPRREALSNDTTESLAANSRGREKPRPLHALAAGFSPPVNVTVSPRSEESHTTTVSGGNGSVFQAGPQLQALANLEARRGSIGAALSSRDVSGLPVYAQSGEPRRLTQAQVAAFPGENALEHSSDQDTWDSLRSPGFCSPLSSGGGAESLPPGGPGHAEAGHLGKVCDFHLNHQQPSPTSVLPTEVAAPPLEKILSVDSVAVDCAYRTVPKPGPQPGPHGSLLTEGCLRSLSGDLNRFPCGMEVHSGQRELESVVAVGEAMAFEISNGSHELLSQGQKQIFIQTSDGLILSPPGTIVSQEEDIVTVTDAEGRACGWAR
"
variation 286
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:7158731"
variation 363
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:371997799"
variation 389
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:7157941"
variation 407
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:369763728"
variation 419
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:372423800"
variation 424
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:376630932"
variation 429
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:200627167"
variation 460
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:372978171"
variation 479
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:375660447"
variation 531
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:7158139"
variation 564
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:372836943"
variation 574
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:185772819"
variation 575
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:371006557"
variation 576
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374612303"
variation 633
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:377448123"
variation 647
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:370243689"
variation 662
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376366454"
variation 751
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:199677123"
variation 752
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:367624048"
variation 753
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:61731137"
variation 762
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:45572332"
variation 772
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:368386323"
variation 823
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:372349522"
variation 827
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:375904596"
variation 828
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:370193621"
variation 833
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:372165787"
variation 836
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374840097"
variation 844
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:368921112"
variation 845
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:200901016"
variation 909
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:201365142"
variation 918
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:369654865"
variation 935
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:149249563"
variation 942
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376706697"
variation 947
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:75766619"
variation 990
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:202123139"
variation 1002
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:147318919"
variation 1009
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370145192"
variation 1013
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375280717"
variation 1024
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200171587"
variation 1060
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:199513391"
variation 1067
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375295594"
variation 1084
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:8004621"
variation 1091
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:372355238"
variation 1101
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:370541879"
variation 1111
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375305020"
exon 1125..1349
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1142
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:115710329"
variation 1154
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376599934"
variation 1158
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:192100739"
variation 1188
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374503383"
variation 1218
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:377689182"
variation 1221
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:1543540"
variation 1239
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200649815"
variation 1251
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376102379"
variation 1254
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:201015963"
variation 1303
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:373962634"
variation 1322
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200235026"
variation 1325
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:368513189"
variation 1340
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375163932"
exon 1350..1442
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1355
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:202065904"
variation 1368
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:201839345"
variation 1383
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:201298008"
variation 1392
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:114749589"
variation 1409
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:374064620"
exon 1443..1592
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1452
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:369694092"
variation 1503
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:186815397"
variation 1512
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:189003679"
variation 1520
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:376419486"
variation 1585
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:181795004"
exon 1593..1730
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1627
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:140733581"
variation 1685
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:116469270"
variation 1700
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:201431440"
variation 1712
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:371253844"
variation 1713
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:374849816"
variation 1725
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:199952618"
variation 1726
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:371985656"
exon 1731..1860
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1757
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:201573850"
variation 1822
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:112729291"
variation 1824
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:376304862"
variation 1825
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370674726"
variation 1827
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:375532380"
variation 1837
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:115365685"
variation 1856
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:199523800"
variation 1857
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:373766097"
exon 1861..3712
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1866
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="tc"
/db_xref="dbSNP:58660213"
variation 1872
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:9464"
variation 1886
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:371906391"
STS 1905..2032
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="RH47332"
/db_xref="UniSTS:41544"
variation 1905
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200026357"
variation 1918
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:187162307"
variation 1936
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:369990834"
variation 1938
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:201911497"
variation 1954
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:201952805"
variation 1955
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:374840960"
variation 1961
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:368919341"
variation 2025
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:35472059"
variation 2042
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375836612"
variation 2055
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200735310"
variation 2068
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:71415891"
variation 2093
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:373049928"
variation 2099
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:202001193"
variation 2142
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:184177701"
variation 2145
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:371235481"
variation 2164
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200152705"
variation 2190
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376081264"
variation 2250
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:377410566"
variation 2285
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:140180484"
variation 2301
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370117834"
variation 2330
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375324501"
variation 2358
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:28646161"
variation 2371
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:145520632"
variation 2378
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200007235"
variation 2405
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370680612"
variation 2406
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374364651"
variation 2419
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:201782124"
variation 2447
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200933608"
variation 2469
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200295748"
variation 2474
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:1053019"
variation 2497
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:375304978"
variation 2519
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:367718180"
variation 2531
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:12590618"
variation 2592
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:201197821"
variation 2594
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200165854"
variation 2616
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:199645167"
variation 2685
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:188964576"
variation 2712
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:201035007"
variation 2713
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:373342974"
variation 2750
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375672028"
variation 2756..2759
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="gtgga"
/db_xref="dbSNP:34220197"
variation 2757..2760
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="tggag"
/db_xref="dbSNP:57469946"
variation 2757
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:115640468"
variation 2763
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:56144634"
variation 2841
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:148816192"
variation 2856
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:11704"
variation 2979
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:79599148"
variation 2981
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:114001492"
variation 2988
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370351735"
variation 3007
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:142497784"
variation 3009
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:146433857"
variation 3027
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374073075"
variation 3044
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:182242624"
variation 3189
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:140712552"
variation 3213
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:79512799"
variation 3217
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:138374403"
variation 3230..3233
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="aatt"
/db_xref="dbSNP:201915133"
variation 3231
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:1056745"
variation 3232..3236
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="ttaat"
/db_xref="dbSNP:200011760"
variation 3236
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:76612776"
STS 3279..3683
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="PMC156606P1"
/db_xref="UniSTS:271408"
STS 3293..3403
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="D10S275"
/db_xref="UniSTS:147992"
STS 3334..3429
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="D8S2279"
/db_xref="UniSTS:473907"
variation 3334
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:141050487"
STS 3369..3491
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="D13S116"
/db_xref="UniSTS:147007"
variation 3425
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:188689300"
STS 3493..3669
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="GDB:434012"
/db_xref="UniSTS:157204"
variation 3547
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="t"
/db_xref="dbSNP:199844270"
variation 3598
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:185631319"
variation 3645
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:377096853"
variation 3646
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:150210883"
variation 3701
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:80178328"
ORIGIN
gaaacactctcgttaacaattcaaactgtggtcccctcccagatgtataaatccaaatgtttaggggtgggcacagtactctgcatctccagacagcatcctccgctgattcggatgcatgatgacgtcagaacacttggatattgtggtaacttttgggccaggggctctgaaaccccgaagacctccccctgggagatccgggacagctcccagagaagcaactagaagccatttgtgtcaaggtaacgtctggagaaacaaaaggtcaggaaaggccaatgctcctaccgaccacaatccagccccaaactgcaagaaagagccagctgccccgggggaattcctgcctggtggggctccatatcgccagccctcagctgctcagggtacagccgcttgtgagaaccgagccacagtcctgcttcctaagtgacttatgccaacctcctgctcaggggtttgtacagagaccactgccagccctccaggtggtccctgcaaagagagtcccagcccccaaggctccagatgaacagggctccatgttgacccctttgtctgcctctgacccgctggcagtaacatctctttcatccagttcagcacatccatttatttccaacttgcatacaagacatactgagaaactaaaaaaatcgttaaaagtaaagacacgttctggacgggtatctcgacctcccaaatataaagctaaagattataagttcataaaaacagaggatctggcggatggtcatctgtcagattctgatgattactcagaactctgtgtggaagaagatgaagatcagagggagaggcacgcactctttgacttatcgagctgctccctgaggcccaaaagctttaagtgtcagacttgtgaaaagtcatatatagggaaggggggactggcccgacattttaaacttaacccaggccacggccagttggaccccgagatggtgctgtctgagaaagccagtggaagcaccctccgggggtgcacggaggaaaggacgctcagcctgacctccctggggctgtccatgccagcggatccatgtgagggaggggcccgctcctgcttggtgacagagtcagcacgcggtggcctgcagaatggtcagtctgtagacgttgaagagacattgccatctgaaccagaaaatggagctcttttgcgatcagagagataccaaggacctagaagacgcgcatgctcagagacccttgcagagtcccgcacagctgtcctccagcagagaagagctgctcagctacctggtggccctgctgcggcaggggagcagagggcgtcgccaagcaaagccaggctcaaggagttcctccagcagtgtgaccgggaggatctggtggaattggctctgcctcagctggctcaggttgtgaccgtgtatgagtttcttctgatgaaggttgaaaaagatcatctagcaaagccttttttcccagctatatataaggaatttgaagagttgcataaaatggttaagaaaatgtgccaagattacctcagtagttctggtctgtgttcccaggagaccctggaaataaacaatgataaggttgctgagtcattaggaatcacagaattcctacggaagaaagaaatacacccagacaaccttggacccaagcacctcagccgagacatggatggggagcagctagagggagctagcagcgagaagagggaacgtgaggctgcggaggagggactggcctcagtgaaaaggcccagaagagaagccctgtccaacgataccactgaatctcttgctgccaacagcagaggccgggagaagcccaggcccttgcatgctttggccgctggtttttcccctccagtaaatgtgactgtctctccccgttctgaagaaagccatacaacgacggtttctggtggcaatgggagcgtgttccaggcgggcccgcagcttcaggcactggctaacttagaagccaggagggggtctataggtgctgctctctcatcccgggatgtcagtgggctgcctgtttatgctcagtcaggagagcctaggaggctgacccaggcacaggtggcagcgtttcctggagagaatgctttggaacactcttcagaccaggacacctgggacagcctgaggagcccgggtttctgcagccctttgtcatctggtggtggagcagagtccctgccgcctggggggcctggacatgcagaggcaggacacctcggcaaggtttgtgacttccacctgaaccaccagcagcccagccccaccagcgtcctgcctacagaggtggcagcccctccgcttgagaaaattttgtctgtggatagcgtggcagtggactgtgcctacaggactgtgcccaagccagggcctcagcctggcccacatggatcactattgactgaagggtgtctcagaagcctttcgggggacttgaaccggttcccctgtgggatggaggtgcactctggccagagagaactggagagcgtggttgctgtcggcgaagccatggcttttgaaatttccaatgggagccatgagttactgtctcagggacagaagcagatttttattcagacttccgatgggcttatcttgtcccctccaggtacaatagtgtctcaggaggaggacattgtcacagtgactgatgcagaggggcgtgcctgcggatgggcccgctagaaggagttcctctagaagctgtggagtcggtcgtcaccgtggagccagagccctcacagtgaagtggagtcagatcctagattcgtctgattttatccagagaaggtctatggcaagcaatgtatatttttctaatgtgaatattgcacagatgaaccttttatttataaagaataatgtctttctgccctgctgtctacatttttctatggagcttgtcataataatagcagatattacctgatcaggaatccctgtggcgcgtctgacgctcatgagtttttcatgatggtgatgagtagcactgcactgtcacctgatgattggccctgctccgtttcccttctctcctgggagatatgctgcttttccaccagacttgctccatactagaagcttcttttgggttcaattaaaaagaaaataagctagtcattctgggcagcattttattgatagaagggggaaaaagtcatttctacttgcatgattttttaaattaaattaaattaaattaatttaattatttttgagaccaagtcttactctgtagcccaagctggagtgcagtggcgcgatcttggctcactgcaacctctgccgcctgggctcaagcgattctcgtgcctcagcctcctgagtagctgtgactacaggagcatgccaccatgcccagctaattttttttttttgtattttagtagatacggggtttcaccatgttgcccagggtggtctcaaactcttgagctcaggcaatccgcccacctcagcttcccaaagtgctgggattacagtacaggcatgagccactgcacctggccaatgatttttttttttttttttgagatggagttttggtcttgttgcccaagctggagtgcaatggctcgatcttggctcaccgcaacctccaccacagggttcaagcaattctcctgcctcagcctcccaagtagctgggattacaggcatgtgccatcacacctggatca
//
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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