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2024-04-20 17:58:11, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001267827 3781 bp mRNA linear PRI 18-APR-2013
DEFINITION Homo sapiens zinc finger protein 839 (ZNF839), transcript variant
2, mRNA.
ACCESSION NM_001267827
VERSION NM_001267827.1 GI:392513695
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 3781)
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
AK093342.1, AL137229.4 and BQ019232.1.
Transcript Variant: This variant (2) 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 :: AK093342.1 [ECO:0000332]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-1784 AK093342.1 1-1784
1785-1785 AL137229.4 12319-12319
1786-2599 AK093342.1 1786-2599
2600-2925 AL137229.4 15373-15698
2926-3314 BQ019232.1 19-407 c
3315-3781 AL137229.4 16088-16554
FEATURES Location/Qualifiers
source 1..3781
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="14"
/map="14q32.31"
gene 1..3781
/gene="ZNF839"
/gene_synonym="C14orf131"
/note="zinc finger protein 839"
/db_xref="GeneID:55778"
/db_xref="HGNC:20345"
exon 1..290
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 167..168
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="c"
/db_xref="dbSNP:35476513"
variation 184
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="g"
/db_xref="dbSNP:58716954"
variation 268
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:9324046"
misc_feature 273..275
/gene="ZNF839"
/gene_synonym="C14orf131"
/note="upstream in-frame stop codon"
variation 288
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:1278128"
exon 291..1193
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 292
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:199998183"
variation 301
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:371653840"
variation 326
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:376888726"
CDS 351..2786
/gene="ZNF839"
/gene_synonym="C14orf131"
/note="isoform 2 is encoded by transcript variant 2; renal
carcinoma antigen NY-REN-50"
/codon_start=1
/product="zinc finger protein 839 isoform 2"
/protein_id="NP_001254756.1"
/db_xref="GI:392513696"
/db_xref="CCDS:CCDS58336.1"
/db_xref="GeneID:55778"
/db_xref="HGNC:20345"
/translation="
MLLPTTIQPQTARKSQLPRGNSCLVGLHIASPQLLRVQPLVRTEPQSCFLSDLCQPPAQGFVQRPLPALQVVPAKRVPAPKAPDEQGSMLTPLSASDPLAVTSLSSSSAHPFISNLHTRHTEKLKKSLKVKTRSGRVSRPPKYKAKDYKFIKTEDLADGHLSDSDDYSELCVEEDEDQRERHALFDLSSCSLRPKSFKCQTCEKSYIGKGGLARHFKLNPGHGQLDPEMVLSEKASGSTLRGCTEERTLSLTSLGLSMPADPCEGGARSCLVTESARGGLQNGQSVDVEETLPSEPENGALLRSERYQGPRRRACSETLAESRTAVLQQRRAAQLPGGPAAAGEQRASPSKARLKEFLQQCDREDLVELALPQLAQVVTVYEFLLMKVEKDHLAKPFFPAIYKEFEELHKMVKKMCQDYLSSSGLCSQETLEINNDKVAESLGITEFLRKKEIHPDNLGPKHLSRDMDGEQLEGASSEKREREAAEEGLASVKRPRREALSNDTTESLAANSRGREKPRPLHALAAGFSPPVNVTVSPRSEESHTTTVSGGNGSVFQAGPQLQALANLEARRGSIGAALSSRDVSGLPVYAQSGEPRRLTQAQVAAFPGENALEHSSDQDTWDSLRSPGFCSPLSSGGGAESLPPGGPGHAEAGHLGKVCDFHLNHQQPSPTSVLPTEVAAPPLEKILSVDSVAVDCAYRTVPKPGPQPGPHGSLLTEGCLRSLSGDLNRFPCGMEVHSGQRELESVVAVGEAMAFEISNGSHELLSQGQKQIFIQTSDGLILSPPGTIVSQEEDIVTVTDAEGRACGWAR
"
variation 355
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:7158731"
variation 432
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:371997799"
variation 458
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:7157941"
variation 476
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:369763728"
variation 488
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:372423800"
variation 493
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:376630932"
variation 498
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:200627167"
variation 529
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:372978171"
variation 548
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:375660447"
variation 600
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:7158139"
variation 633
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:372836943"
variation 643
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:185772819"
variation 644
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:371006557"
variation 645
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374612303"
variation 702
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:377448123"
variation 716
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:370243689"
variation 731
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376366454"
variation 820
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:199677123"
variation 821
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:367624048"
variation 822
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:61731137"
variation 831
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:45572332"
variation 841
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:368386323"
variation 892
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:372349522"
variation 896
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:375904596"
variation 897
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:370193621"
variation 902
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:372165787"
variation 905
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374840097"
variation 913
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:368921112"
variation 914
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:200901016"
variation 978
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:201365142"
variation 987
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:369654865"
variation 1004
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:149249563"
variation 1011
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376706697"
variation 1016
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:75766619"
variation 1059
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:202123139"
variation 1071
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:147318919"
variation 1078
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370145192"
variation 1082
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375280717"
variation 1093
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200171587"
variation 1129
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:199513391"
variation 1136
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375295594"
variation 1153
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:8004621"
variation 1160
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:372355238"
variation 1170
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:370541879"
variation 1180
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375305020"
exon 1194..1418
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1211
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:115710329"
variation 1223
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376599934"
variation 1227
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:192100739"
variation 1257
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374503383"
variation 1287
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:377689182"
variation 1290
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:1543540"
variation 1308
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200649815"
variation 1320
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376102379"
variation 1323
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:201015963"
variation 1372
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:373962634"
variation 1391
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200235026"
variation 1394
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:368513189"
variation 1409
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375163932"
exon 1419..1511
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1424
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:202065904"
variation 1437
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:201839345"
variation 1452
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:201298008"
variation 1461
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:114749589"
variation 1478
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:374064620"
exon 1512..1661
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1521
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:369694092"
variation 1572
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:186815397"
variation 1581
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:189003679"
variation 1589
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:376419486"
variation 1654
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:181795004"
exon 1662..1799
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1696
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:140733581"
variation 1754
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:116469270"
variation 1769
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:201431440"
variation 1781
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:371253844"
variation 1782
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:374849816"
variation 1794
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:199952618"
variation 1795
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:371985656"
exon 1800..1929
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1826
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:201573850"
variation 1891
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:112729291"
variation 1893
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:376304862"
variation 1894
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370674726"
variation 1896
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:375532380"
variation 1906
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:115365685"
variation 1925
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:199523800"
variation 1926
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:373766097"
exon 1930..3781
/gene="ZNF839"
/gene_synonym="C14orf131"
/inference="alignment:Splign:1.39.8"
variation 1935
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="tc"
/db_xref="dbSNP:58660213"
variation 1941
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:9464"
variation 1955
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:371906391"
STS 1974..2101
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="RH47332"
/db_xref="UniSTS:41544"
variation 1974
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200026357"
variation 1987
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:187162307"
variation 2005
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:369990834"
variation 2007
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:201911497"
variation 2023
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:201952805"
variation 2024
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:374840960"
variation 2030
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:368919341"
variation 2094
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:35472059"
variation 2111
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375836612"
variation 2124
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200735310"
variation 2137
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:71415891"
variation 2162
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:373049928"
variation 2168
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:202001193"
variation 2211
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:184177701"
variation 2214
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:371235481"
variation 2233
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200152705"
variation 2259
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:376081264"
variation 2319
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:377410566"
variation 2354
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:140180484"
variation 2370
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370117834"
variation 2399
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375324501"
variation 2427
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:28646161"
variation 2440
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:145520632"
variation 2447
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200007235"
variation 2474
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370680612"
variation 2475
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374364651"
variation 2488
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:201782124"
variation 2516
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200933608"
variation 2538
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:200295748"
variation 2543
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:1053019"
variation 2566
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:375304978"
variation 2588
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:367718180"
variation 2600
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:12590618"
variation 2661
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:201197821"
variation 2663
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:200165854"
variation 2685
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:199645167"
variation 2754
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:188964576"
variation 2781
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:201035007"
variation 2782
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:373342974"
variation 2819
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:375672028"
variation 2825..2828
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="gtgga"
/db_xref="dbSNP:34220197"
variation 2826..2829
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="tggag"
/db_xref="dbSNP:57469946"
variation 2826
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:115640468"
variation 2832
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:56144634"
variation 2910
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:148816192"
variation 2925
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="g"
/db_xref="dbSNP:11704"
variation 3048
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:79599148"
variation 3050
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:114001492"
variation 3057
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:370351735"
variation 3076
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:142497784"
variation 3078
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:146433857"
variation 3096
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:374073075"
variation 3113
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="g"
/replace="t"
/db_xref="dbSNP:182242624"
variation 3258
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:140712552"
variation 3282
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:79512799"
variation 3286
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:138374403"
variation 3299..3302
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="aatt"
/db_xref="dbSNP:201915133"
variation 3300
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:1056745"
variation 3301..3305
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="ttaat"
/db_xref="dbSNP:200011760"
variation 3305
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="t"
/db_xref="dbSNP:76612776"
STS 3348..3752
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="PMC156606P1"
/db_xref="UniSTS:271408"
STS 3362..3472
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="D10S275"
/db_xref="UniSTS:147992"
STS 3403..3498
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="D8S2279"
/db_xref="UniSTS:473907"
variation 3403
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:141050487"
STS 3438..3560
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="D13S116"
/db_xref="UniSTS:147007"
variation 3494
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="c"
/replace="t"
/db_xref="dbSNP:188689300"
STS 3562..3738
/gene="ZNF839"
/gene_synonym="C14orf131"
/standard_name="GDB:434012"
/db_xref="UniSTS:157204"
variation 3616
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace=""
/replace="t"
/db_xref="dbSNP:199844270"
variation 3667
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:185631319"
variation 3714
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:377096853"
variation 3715
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="g"
/db_xref="dbSNP:150210883"
variation 3770
/gene="ZNF839"
/gene_synonym="C14orf131"
/replace="a"
/replace="c"
/db_xref="dbSNP:80178328"
ORIGIN
agaatgccattggttaggccttttacttttgtcgttttaaaggacactctggacatccaaccgatgcacatcccacgcccccaccccccacgtttcctgaggctgcgtctggcctggaggaaccgcccagtgaagacaggtgctcgcagatatcaccgcctagtgttccctgggcccacttgcggggaagtcttggaggtgaaaatccaggtctggaatgaatgcattccacagatgcatatggagagctactgcatgcccagcaccattcctaggctgggagcaaaacgcaactagaagccatttgtgtcaaggtaacgtctggagaaacaaaaggtcaggaaaggccaatgctcctaccgaccacaatccagccccaaactgcaagaaagagccagctgccccgggggaattcctgcctggtggggctccatatcgccagccctcagctgctcagggtacagccgcttgtgagaaccgagccacagtcctgcttcctaagtgacttatgccaacctcctgctcaggggtttgtacagagaccactgccagccctccaggtggtccctgcaaagagagtcccagcccccaaggctccagatgaacagggctccatgttgacccctttgtctgcctctgacccgctggcagtaacatctctttcatccagttcagcacatccatttatttccaacttgcatacaagacatactgagaaactaaaaaaatcgttaaaagtaaagacacgttctggacgggtatctcgacctcccaaatataaagctaaagattataagttcataaaaacagaggatctggcggatggtcatctgtcagattctgatgattactcagaactctgtgtggaagaagatgaagatcagagggagaggcacgcactctttgacttatcgagctgctccctgaggcccaaaagctttaagtgtcagacttgtgaaaagtcatatatagggaaggggggactggcccgacattttaaacttaacccaggccacggccagttggaccccgagatggtgctgtctgagaaagccagtggaagcaccctccgggggtgcacggaggaaaggacgctcagcctgacctccctggggctgtccatgccagcggatccatgtgagggaggggcccgctcctgcttggtgacagagtcagcacgcggtggcctgcagaatggtcagtctgtagacgttgaagagacattgccatctgaaccagaaaatggagctcttttgcgatcagagagataccaaggacctagaagacgcgcatgctcagagacccttgcagagtcccgcacagctgtcctccagcagagaagagctgctcagctacctggtggccctgctgcggcaggggagcagagggcgtcgccaagcaaagccaggctcaaggagttcctccagcagtgtgaccgggaggatctggtggaattggctctgcctcagctggctcaggttgtgaccgtgtatgagtttcttctgatgaaggttgaaaaagatcatctagcaaagccttttttcccagctatatataaggaatttgaagagttgcataaaatggttaagaaaatgtgccaagattacctcagtagttctggtctgtgttcccaggagaccctggaaataaacaatgataaggttgctgagtcattaggaatcacagaattcctacggaagaaagaaatacacccagacaaccttggacccaagcacctcagccgagacatggatggggagcagctagagggagctagcagcgagaagagggaacgtgaggctgcggaggagggactggcctcagtgaaaaggcccagaagagaagccctgtccaacgataccactgaatctcttgctgccaacagcagaggccgggagaagcccaggcccttgcatgctttggccgctggtttttcccctccagtaaatgtgactgtctctccccgttctgaagaaagccatacaacgacggtttctggtggcaatgggagcgtgttccaggcgggcccgcagcttcaggcactggctaacttagaagccaggagggggtctataggtgctgctctctcatcccgggatgtcagtgggctgcctgtttatgctcagtcaggagagcctaggaggctgacccaggcacaggtggcagcgtttcctggagagaatgctttggaacactcttcagaccaggacacctgggacagcctgaggagcccgggtttctgcagccctttgtcatctggtggtggagcagagtccctgccgcctggggggcctggacatgcagaggcaggacacctcggcaaggtttgtgacttccacctgaaccaccagcagcccagccccaccagcgtcctgcctacagaggtggcagcccctccgcttgagaaaattttgtctgtggatagcgtggcagtggactgtgcctacaggactgtgcccaagccagggcctcagcctggcccacatggatcactattgactgaagggtgtctcagaagcctttcgggggacttgaaccggttcccctgtgggatggaggtgcactctggccagagagaactggagagcgtggttgctgtcggcgaagccatggcttttgaaatttccaatgggagccatgagttactgtctcagggacagaagcagatttttattcagacttccgatgggcttatcttgtcccctccaggtacaatagtgtctcaggaggaggacattgtcacagtgactgatgcagaggggcgtgcctgcggatgggcccgctagaaggagttcctctagaagctgtggagtcggtcgtcaccgtggagccagagccctcacagtgaagtggagtcagatcctagattcgtctgattttatccagagaaggtctatggcaagcaatgtatatttttctaatgtgaatattgcacagatgaaccttttatttataaagaataatgtctttctgccctgctgtctacatttttctatggagcttgtcataataatagcagatattacctgatcaggaatccctgtggcgcgtctgacgctcatgagtttttcatgatggtgatgagtagcactgcactgtcacctgatgattggccctgctccgtttcccttctctcctgggagatatgctgcttttccaccagacttgctccatactagaagcttcttttgggttcaattaaaaagaaaataagctagtcattctgggcagcattttattgatagaagggggaaaaagtcatttctacttgcatgattttttaaattaaattaaattaaattaatttaattatttttgagaccaagtcttactctgtagcccaagctggagtgcagtggcgcgatcttggctcactgcaacctctgccgcctgggctcaagcgattctcgtgcctcagcctcctgagtagctgtgactacaggagcatgccaccatgcccagctaattttttttttttgtattttagtagatacggggtttcaccatgttgcccagggtggtctcaaactcttgagctcaggcaatccgcccacctcagcttcccaaagtgctgggattacagtacaggcatgagccactgcacctggccaatgatttttttttttttttttgagatggagttttggtcttgttgcccaagctggagtgcaatggctcgatcttggctcaccgcaacctccaccacagggttcaagcaattctcctgcctcagcctcccaagtagctgggattacaggcatgtgccatcacacctggatca
//
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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