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Previous release (v1)
2024-04-29 01:03:17, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_146327 335 bp RNA linear PRI 18-NOV-2023
DEFINITION Homo sapiens ribosomal protein L27 (RPL27), transcript variant 4,
non-coding RNA.
ACCESSION NR_146327
VERSION NR_146327.2
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 335)
AUTHORS Suo L, Gao M, Ma T and Gao Z.
TITLE Effect of RPL27 knockdown on the proliferation and apoptosis of
human liver cancer cells
JOURNAL Biochem Biophys Res Commun 682, 156-162 (2023)
PUBMED 37812860
REMARK GeneRIF: Effect of RPL27 knockdown on the proliferation and
apoptosis of human liver cancer cells.
REFERENCE 2 (bases 1 to 335)
AUTHORS Park SY, Seo D, Jeon EH, Park JY, Jang BC, Kim JI, Im SS, Lee JH,
Kim S, Cho CH and Lee YH.
TITLE RPL27 contributes to colorectal cancer proliferation and stemness
via PLK1 signaling
JOURNAL Int J Oncol 63 (2) (2023)
PUBMED 37387446
REMARK GeneRIF: RPL27 contributes to colorectal cancer proliferation and
stemness via PLK1 signaling.
REFERENCE 3 (bases 1 to 335)
AUTHORS Haenig C, Atias N, Taylor AK, Mazza A, Schaefer MH, Russ J,
Riechers SP, Jain S, Coughlin M, Fontaine JF, Freibaum BD,
Brusendorf L, Zenkner M, Porras P, Stroedicke M, Schnoegl S,
Arnsburg K, Boeddrich A, Pigazzini L, Heutink P, Taylor JP,
Kirstein J, Andrade-Navarro MA, Sharan R and Wanker EE.
TITLE Interactome Mapping Provides a Network of Neurodegenerative Disease
Proteins and Uncovers Widespread Protein Aggregation in Affected
Brains
JOURNAL Cell Rep 32 (7), 108050 (2020)
PUBMED 32814053
REFERENCE 4 (bases 1 to 335)
AUTHORS Liang X, Zuo MQ, Zhang Y, Li N, Ma C, Dong MQ and Gao N.
TITLE Structural snapshots of human pre-60S ribosomal particles before
and after nuclear export
JOURNAL Nat Commun 11 (1), 3542 (2020)
PUBMED 32669547
REMARK Publication Status: Online-Only
REFERENCE 5 (bases 1 to 335)
AUTHORS Zhang Y, You J, Wang X and Weber J.
TITLE The DHX33 RNA Helicase Promotes mRNA Translation Initiation
JOURNAL Mol Cell Biol 35 (17), 2918-2931 (2015)
PUBMED 26100019
REFERENCE 6 (bases 1 to 335)
AUTHORS Harshman K, Bell R, Rosenthal J, Katcher H, Miki Y, Swenson J,
Gholami Z, Frye C, Ding W, Dayananth P et al.
TITLE Comparison of the positional cloning methods used to isolate the
BRCA1 gene
JOURNAL Hum Mol Genet 4 (8), 1259-1266 (1995)
PUBMED 7581362
REFERENCE 7 (bases 1 to 335)
AUTHORS Kato S, Sekine S, Oh SW, Kim NS, Umezawa Y, Abe N,
Yokoyama-Kobayashi M and Aoki T.
TITLE Construction of a human full-length cDNA bank
JOURNAL Gene 150 (2), 243-250 (1994)
PUBMED 7821789
REFERENCE 8 (bases 1 to 335)
AUTHORS Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harshman K,
Tavtigian S, Liu Q, Cochran C, Bennett LM, Ding W et al.
TITLE A strong candidate for the breast and ovarian cancer susceptibility
gene BRCA1
JOURNAL Science 266 (5182), 66-71 (1994)
PUBMED 7545954
REFERENCE 9 (bases 1 to 335)
AUTHORS Gallagher RA, McClean PM and Malik AN.
TITLE Cloning and nucleotide sequence of a full length cDNA encoding
ribosomal protein L27 from human fetal kidney
JOURNAL Biochim Biophys Acta 1217 (3), 329-332 (1994)
PUBMED 8148381
REFERENCE 10 (bases 1 to 335)
AUTHORS Jones KW, Chevrette M, Shapero MH and Fournier RE.
TITLE Generation of region- and species-specific expressed gene probes
from somatic cell hybrids
JOURNAL Nat Genet 1 (4), 278-283 (1992)
PUBMED 1302024
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from BU955518.1, BC098560.1 and
HY108539.1.
On Jul 11, 2019 this sequence version replaced NR_146327.1.
Summary: Ribosomes, the organelles that catalyze protein synthesis,
consist of a small 40S subunit and a large 60S subunit. Together
these subunits are composed of four RNA species and approximately
80 structurally distinct proteins. This gene encodes a member of
the L27e family of ribosomal proteins and a component of the 60S
subunit. A splice site mutation in this gene has been identified in
a Diamond-Blackfan anemia (DBA) patient. As is typical for genes
encoding ribosomal proteins, there are multiple processed
pseudogenes of this gene dispersed through the genome. [provided by
RefSeq, Mar 2017].
Transcript Variant: This variant (4) lacks an alternate internal
exon compared to variant 1. This variant is represented as
non-coding because the use of the 5'-most expected translational
start codon renders the transcript a candidate for
nonsense-mediated mRNA decay (NMD).
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: HY108539.1, HY302747.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1965299, SAMEA1966682
[ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-30 BU955518.1 27-56
31-36 BC098560.1 16-21
37-334 HY108539.1 15-312
335-335 BC098560.1 490-490
FEATURES Location/Qualifiers
source 1..335
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="17"
/map="17q21.31"
gene 1..335
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/note="ribosomal protein L27"
/db_xref="GeneID:6155"
/db_xref="HGNC:HGNC:10328"
/db_xref="MIM:607526"
misc_RNA 1..335
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/product="ribosomal protein L27, transcript variant 4"
/db_xref="GeneID:6155"
/db_xref="HGNC:HGNC:10328"
/db_xref="MIM:607526"
exon 1..53
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/inference="alignment:Splign:2.1.0"
variation 3
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1000185672"
variation 8
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:2050321520"
variation 9
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1033468332"
variation 10
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446973371"
variation 11
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354959777"
variation 12
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1597768923"
variation 13..18
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="ctt"
/replace="cttctt"
/db_xref="dbSNP:201231264"
variation 14
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="g"
/replace="t"
/db_xref="dbSNP:2050321715"
variation 15..17
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="tct"
/replace="tctct"
/db_xref="dbSNP:869200406"
variation 15
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:774786980"
variation 16
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:890850564"
variation 17..19
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1555569933"
variation 17
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:2050321877"
variation 19
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1445413601"
variation 20
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1387288412"
variation 21
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:145515343"
variation 28
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace=""
/replace="c"
/db_xref="dbSNP:1255247844"
variation 29
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace=""
/replace="t"
/db_xref="dbSNP:542792131"
variation 29
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:2151964307"
variation 30..31
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace=""
/replace="gg"
/db_xref="dbSNP:2050322233"
variation 30..31
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="g"
/replace="gg"
/db_xref="dbSNP:11305686"
variation 30
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201144020"
variation 31..32
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace=""
/replace="gt"
/db_xref="dbSNP:2050322295"
variation 31
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:2050322263"
variation 32
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1474497759"
variation 33
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace=""
/replace="a"
/db_xref="dbSNP:2050322407"
variation 33
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:538377203"
variation 34..36
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:2050322466"
variation 34
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/db_xref="dbSNP:2050322425"
variation 36
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:9899458"
variation 37
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:950748325"
variation 38..39
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace=""
/replace="t"
/db_xref="dbSNP:2050322666"
variation 38
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:578236915"
variation 39
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1439889683"
variation 40
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:545276486"
variation 41
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="g"
/replace="t"
/db_xref="dbSNP:560698130"
variation 43
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1303739710"
variation 47
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/db_xref="dbSNP:2050322843"
variation 48
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:572667986"
variation 50
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:58834964"
variation 50
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2050322969"
variation 51
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:913824221"
variation 52
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1940487923"
variation 53
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:954504806"
exon 54..136
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/inference="alignment:Splign:2.1.0"
variation 54
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:2050326737"
misc_feature 56..178
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/inference="COORDINATES:
alignment:Blast2seq::RefSeq|NM_001349922.2"
/note="primary ORF has stop codon >50 nucleotides from the
terminal splice site; nonsense-mediated decay (NMD)
candidate"
variation 63
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:2050326768"
variation 68
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/db_xref="dbSNP:2050326806"
variation 70
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:2050326842"
variation 74
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:2050326890"
variation 77
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="g"
/replace="t"
/db_xref="dbSNP:776825853"
variation 88
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:149080883"
variation 92
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/db_xref="dbSNP:1289898955"
variation 94
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/db_xref="dbSNP:770107343"
variation 95
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/db_xref="dbSNP:2050327081"
variation 96
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="t"
/db_xref="dbSNP:143145441"
variation 98
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="g"
/replace="t"
/db_xref="dbSNP:376971321"
variation 104
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/db_xref="dbSNP:764058005"
variation 106
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1804328"
variation 107
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:2050327298"
variation 108
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:116316268"
variation 109
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285078333"
variation 111
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/db_xref="dbSNP:1195159309"
variation 113
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481595913"
variation 114
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:2151964508"
variation 117
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="g"
/replace="t"
/db_xref="dbSNP:761868372"
variation 118
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:766933649"
variation 122
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:749989076"
variation 128
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="t"
/db_xref="dbSNP:766040122"
variation 130
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:148271218"
exon 137..247
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/inference="alignment:Splign:2.1.0"
variation 139
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:1423049747"
variation 143
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1420459977"
variation 146
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:2050377720"
variation 149..151
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="tat"
/replace="tattat"
/db_xref="dbSNP:2050377759"
variation 150
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:1189541438"
variation 151
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:2151966289"
variation 153
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:199713340"
variation 154
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:376827420"
variation 155
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:544770646"
variation 156
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:766924583"
variation 159
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="g"
/replace="t"
/db_xref="dbSNP:2050378016"
variation 161
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:2050378048"
variation 165
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/db_xref="dbSNP:777290039"
variation 166
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/db_xref="dbSNP:1567739202"
variation 167
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:760178247"
variation 168
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:765351338"
variation 170
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:752755283"
variation 171
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:753830462"
variation 175
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:976153783"
variation 182
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1360778930"
variation 184
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:764241143"
variation 186
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="g"
/replace="t"
/db_xref="dbSNP:2050378434"
variation 187
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:2050378470"
variation 188
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:144939879"
variation 189
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:1567739239"
variation 195
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:191256004"
variation 196
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203028295"
variation 197
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:2050378675"
variation 199
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1052516238"
variation 201
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/db_xref="dbSNP:931971715"
variation 203
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261158093"
variation 204
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:1597773044"
variation 207
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:138826063"
variation 208
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:533615868"
variation 210
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:2050378994"
variation 215
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1242939580"
variation 216
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/db_xref="dbSNP:2050379072"
variation 217
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:368506285"
variation 219
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:774149621"
variation 220
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:747319203"
variation 221
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:142006401"
variation 222..227
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="gaggcc"
/replace="gaggccgaggcc"
/db_xref="dbSNP:2050379261"
variation 227
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176387199"
variation 230
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:1427764880"
variation 232
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="t"
/db_xref="dbSNP:777199664"
variation 233
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="g"
/db_xref="dbSNP:760084490"
variation 234
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/db_xref="dbSNP:1175285462"
variation 237
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:2050379518"
variation 238
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:372454661"
variation 239
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775586874"
variation 244
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:762950023"
variation 245
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:2050379647"
variation 246
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/db_xref="dbSNP:1419088568"
exon 248..335
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/inference="alignment:Splign:2.1.0"
variation 249
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:201969823"
variation 251
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:531503727"
variation 258
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="g"
/replace="t"
/db_xref="dbSNP:1247844188"
variation 259
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="g"
/replace="t"
/db_xref="dbSNP:1402434667"
variation 260
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/db_xref="dbSNP:1294246436"
variation 262
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:762000722"
variation 263
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:1221844469"
variation 265
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:2050381293"
variation 275
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1265436384"
variation 278
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1439617239"
variation 284
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:2050381460"
variation 285
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:1372663547"
variation 287
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1804329"
variation 288
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:146328911"
variation 289
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:760389648"
variation 290
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:369125440"
variation 293
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:753705175"
variation 297
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:755008755"
variation 302
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:2050381790"
variation 307
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="c"
/replace="t"
/db_xref="dbSNP:2050381822"
variation 311
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="t"
/db_xref="dbSNP:979078268"
variation 319
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/db_xref="dbSNP:201223440"
variation 320
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/db_xref="dbSNP:199869182"
variation 321
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:925310997"
variation 323..329
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="ataaaga"
/db_xref="dbSNP:776719048"
variation 323
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:758073004"
variation 324
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1567739439"
variation 325..331
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="aaa"
/replace="aaagaaa"
/db_xref="dbSNP:761897795"
variation 325
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:2050382138"
variation 328
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:1555570473"
variation 329..335
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="aaaa"
/replace="aaaaaa"
/replace="aaaaaaa"
/db_xref="dbSNP:765073347"
variation 329
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1333857275"
variation 330
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454389562"
variation 332
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:2050382352"
variation 334
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="g"
/db_xref="dbSNP:777596481"
variation 335
/gene="RPL27"
/gene_synonym="DBA16; eL27; L27"
/replace="a"
/replace="t"
/db_xref="dbSNP:1381758157"
ORIGIN
agcggaagtgtccttctttcctttttgctggtagggccgggtggttgctgccgaaatgggcaagttcatgaaacctgggaaggtggtgcttgtcctggctggacgctactccggacgcaaagctgtcatcgtgaaggtactctgtggatatccccttggacaaaactgtcgtcaataaggatgtcttcagagatcctgctcttaaacgcaaggcccgacgggaggccaaggtcaagtttgaagagagatacaagacaggcaagaacaagtggttcttccagaaactgcggttttagatgctttgttttgatcattaaaaattataaagaaaaaaa
//
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.
[Full Text]