2024-04-26 19:04:41, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_110999 775 bp RNA linear PRI 05-FEB-2022 DEFINITION Homo sapiens family with sequence similarity 74 member A6 (FAM74A6), long non-coding RNA. ACCESSION NR_110999 VERSION NR_110999.1 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AL590491.13. Sequence Note: The RefSeq transcript was derived from the reference genome assembly. The genomic coordinates were determined from alignments. ##Evidence-Data-START## Transcript exon combination :: BC121813.1 [ECO:0000332] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-614 AL590491.13 100261-100874 615-698 AL590491.13 105718-105801 699-775 AL590491.13 106130-106206 FEATURES Location/Qualifiers source 1..775 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="9" /map="9q12" gene 1..775 /gene="FAM74A6" /note="family with sequence similarity 74 member A6" /db_xref="GeneID:653123" /db_xref="HGNC:HGNC:34036" ncRNA 1..775 /ncRNA_class="lncRNA" /gene="FAM74A6" /product="family with sequence similarity 74 member A6" /db_xref="GeneID:653123" /db_xref="HGNC:HGNC:34036" exon 1..614 /gene="FAM74A6" /inference="alignment:Splign:2.1.0" variation 171 /gene="FAM74A6" /replace="a" /replace="c" /db_xref="dbSNP:1554802910" variation 179 /gene="FAM74A6" /replace="a" /replace="g" /db_xref="dbSNP:1554802911" variation 213 /gene="FAM74A6" /replace="g" /replace="t" /db_xref="dbSNP:1554802913" variation 216 /gene="FAM74A6" /replace="c" /replace="g" /db_xref="dbSNP:1554802914" variation 226 /gene="FAM74A6" /replace="c" /replace="t" /db_xref="dbSNP:1554802915" variation 227 /gene="FAM74A6" /replace="a" /replace="t" /db_xref="dbSNP:1554802916" variation 283 /gene="FAM74A6" /replace="c" /replace="g" /db_xref="dbSNP:1554802917" variation 308 /gene="FAM74A6" /replace="a" /replace="g" /db_xref="dbSNP:1554802918" variation 567 /gene="FAM74A6" /replace="g" /replace="t" /db_xref="dbSNP:1825600590" variation 570 /gene="FAM74A6" /replace="a" /replace="g" /db_xref="dbSNP:1825600615" variation 580 /gene="FAM74A6" /replace="a" /replace="t" /db_xref="dbSNP:1198117963" variation 588 /gene="FAM74A6" /replace="c" /replace="t" /db_xref="dbSNP:1312935331" variation 597 /gene="FAM74A6" /replace="a" /replace="g" /db_xref="dbSNP:1825600686" variation 608 /gene="FAM74A6" /replace="a" /replace="c" /db_xref="dbSNP:1554802919" exon 615..698 /gene="FAM74A6" /inference="alignment:Splign:2.1.0" variation 623 /gene="FAM74A6" /replace="a" /replace="t" /db_xref="dbSNP:1825619008" variation 661 /gene="FAM74A6" /replace="a" /replace="g" /db_xref="dbSNP:1825619033" variation 663 /gene="FAM74A6" /replace="c" /replace="t" /db_xref="dbSNP:1825619046" variation 693 /gene="FAM74A6" /replace="a" /replace="g" /db_xref="dbSNP:1825619065" variation 697..698 /gene="FAM74A6" /replace="" /replace="c" /db_xref="dbSNP:1825619094" variation 698 /gene="FAM74A6" /replace="c" /replace="t" /db_xref="dbSNP:1825619110" exon 699..775 /gene="FAM74A6" /inference="alignment:Splign:2.1.0" variation 699 /gene="FAM74A6" /replace="a" /replace="g" /db_xref="dbSNP:1352403093" variation 706 /gene="FAM74A6" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1587527307" variation 712 /gene="FAM74A6" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1825620497" variation 714..715 /gene="FAM74A6" /replace="aa" /replace="aaa" /db_xref="dbSNP:1825620547" variation 714 /gene="FAM74A6" /replace="a" /replace="c" /db_xref="dbSNP:1825620521" variation 716 /gene="FAM74A6" /replace="c" /replace="g" /db_xref="dbSNP:1825620571" variation 717 /gene="FAM74A6" /replace="c" /replace="t" /db_xref="dbSNP:1825620590" variation 718 /gene="FAM74A6" /replace="c" /replace="t" /db_xref="dbSNP:2119027026" variation 719 /gene="FAM74A6" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1327258929" variation 720 /gene="FAM74A6" /replace="c" /replace="t" /db_xref="dbSNP:1825620698" variation 722 /gene="FAM74A6" /replace="c" /replace="t" /db_xref="dbSNP:1376565944" variation 725 /gene="FAM74A6" /replace="g" /replace="t" /db_xref="dbSNP:1825620738" variation 731 /gene="FAM74A6" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1176121678" variation 741 /gene="FAM74A6" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1453150168" variation 753 /gene="FAM74A6" /replace="c" /replace="t" /db_xref="dbSNP:1394504436" variation 754 /gene="FAM74A6" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1177866230" variation 755 /gene="FAM74A6" /replace="a" /replace="t" /db_xref="dbSNP:1825620827" variation 756 /gene="FAM74A6" /replace="c" /replace="t" /db_xref="dbSNP:1331095148" variation 758 /gene="FAM74A6" /replace="c" /replace="t" /db_xref="dbSNP:1825620858" variation 764 /gene="FAM74A6" /replace="c" /replace="t" /db_xref="dbSNP:1471244012" variation 765 /gene="FAM74A6" /replace="a" /replace="g" /db_xref="dbSNP:1231462303" variation 768 /gene="FAM74A6" /replace="a" /replace="c" /db_xref="dbSNP:1203542479" variation 774 /gene="FAM74A6" /replace="c" /replace="t" /db_xref="dbSNP:1825620935" ORIGIN
cagggtagggctccagctaagccacgtaggcactacgatgggcaacagaaaggttggtttctgggcaattcagagaaaccaaggacagctacccccagaactcagagtagccaactgggctgctcacaggagatgccttaactgaaaggtgatcagactccacaggagacccagagaagatgtggagggagctcagaggctgtcctggaggagacgtggagacagctcagaggctgtcccagagaagacgtggaaagagctcagaggctgtcccagagaagacgtggagagctcagaggatgtcccagagaagacgtggagagagttcagaggctgtcccggagaagacgtggaaagagctcagaaactcagagactgtcccggagaagacatggaaacagctcagaggctgtctgcaagaagacgtgcagagagttcagaggctgtcccggagaagacatggagagagctcaaaggctgtccacaagaagatgtggagagagttcagaggctgtcgttactgctgcacttggctgtttttctttggataattattgcaatcaattttagtaattcaggtgttaaatcacagtcaagcacctatttacctagtgtggtctgatgaatttcacttctttgatactttttgagagagctgagagtccatttcctgaggaagaaactcagagaaaacaaatgtaaaatccttaagtaagtcatatttggttgggaagatcaaagaaatcacccagtctcccacatccgaaattgtgca
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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