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2024-04-20 14:32:11, GGRNA : RefSeq release 60 (20130726)
LOCUS NR_051988 3494 bp RNA linear PRI 17-JUL-2013
DEFINITION Homo sapiens F-box and WD repeat domain containing 10 (FBXW10),
transcript variant 3, non-coding RNA.
ACCESSION NR_051988
VERSION NR_051988.1 GI:389885062
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 3494)
AUTHORS Chaturvedi,P. and Parnaik,V.K.
TITLE Lamin A rod domain mutants target heterochromatin protein 1alpha
and beta for proteasomal degradation by activation of F-box
protein, FBXW10
JOURNAL PLoS ONE 5 (5), E10620 (2010)
PUBMED 20498703
REMARK GeneRIF: Mislocalized lamins can induce ubiquitin-mediated
proteasomal degradation of certain HP1 isoforms by activation of
FBXW10, a member of the F-box family of proteins that is involved
in E3 ubiquitin ligase activity.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 3494)
AUTHORS Jin,J., Cardozo,T., Lovering,R.C., Elledge,S.J., Pagano,M. and
Harper,J.W.
TITLE Systematic analysis and nomenclature of mammalian F-box proteins
JOURNAL Genes Dev. 18 (21), 2573-2580 (2004)
PUBMED 15520277
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
DB055860.1, AK310383.1, AC107982.6 and AL136822.1.
Summary: Members of the F-box protein family, such as FBXW10, are
characterized by an approximately 40-amino acid F-box motif. SCF
complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM
603134), and F-box proteins, act as protein-ubiquitin ligases.
F-box proteins interact with SKP1 through the F box, and they
interact with ubiquitination targets through other protein
interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied
by OMIM, Mar 2008].
Transcript Variant: This variant (3) uses alternate 5' and 3'
terminal exons, compared to variant 1. This variant is represented
as non-coding because use of the expected translational start
codon, as used in variant 1, renders the transcript a candidate for
nonsense-mediated mRNA decay (NMD).
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-300 DB055860.1 1-300
301-1062 AK310383.1 242-1003
1063-1190 AC107982.6 128467-128594 c
1191-1583 AK310383.1 1130-1522
1584-1584 AC107982.6 123912-123912 c
1585-2961 AK310383.1 1524-2900
2962-2962 AC107982.6 101180-101180 c
2963-3220 AK310383.1 2902-3159
3221-3494 AL136822.1 2958-3231
FEATURES Location/Qualifiers
source 1..3494
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="17"
/map="17p12"
gene 1..3494
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/note="F-box and WD repeat domain containing 10"
/db_xref="GeneID:10517"
/db_xref="HGNC:1211"
/db_xref="MIM:611679"
misc_RNA 1..3494
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/product="F-box and WD repeat domain containing 10,
transcript variant 3"
/db_xref="GeneID:10517"
/db_xref="HGNC:1211"
/db_xref="MIM:611679"
exon 1..1383
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 3
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371194302"
variation 25
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="g"
/db_xref="dbSNP:367810251"
variation 138
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:150230158"
variation 183
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369742505"
variation 198
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:186119518"
variation 214
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:116483657"
misc_feature 233..823
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="COORDINATES:
alignment:Blast2seq::RefSeq|NM_001267585.1"
/note="primary ORF has stop codon >50 nucleotides from the
terminal splice site; nonsense-mediated mRNA decay (NMD)
candidate"
variation 300
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="t"
/db_xref="dbSNP:74502778"
variation 312
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200553727"
variation 326
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="g"
/replace="t"
/db_xref="dbSNP:143662391"
variation 338
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138647311"
variation 397
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="g"
/replace="t"
/db_xref="dbSNP:200806553"
variation 441
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:149323817"
variation 464
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:143573197"
variation 477
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201935353"
variation 500
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="g"
/replace="t"
/db_xref="dbSNP:148027955"
variation 536
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:377476079"
variation 575
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142528410"
variation 640
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145973790"
variation 746
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="g"
/replace="t"
/db_xref="dbSNP:370104676"
variation 786
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370158560"
variation 853
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="t"
/db_xref="dbSNP:114381083"
variation 861
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:149324181"
variation 1063
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:112087876"
variation 1216
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:191912090"
variation 1365
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:114067349"
exon 1384..1548
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 1388
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376114266"
variation 1399
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="t"
/db_xref="dbSNP:370476175"
variation 1500
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376241364"
variation 1526
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="g"
/db_xref="dbSNP:370045217"
variation 1537
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370320215"
exon 1549..1749
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 1572
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375699839"
variation 1582
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374206318"
variation 1584
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:9895749"
variation 1649
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:139842854"
variation 1659
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="g"
/db_xref="dbSNP:200535885"
variation 1702
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="g"
/replace="t"
/db_xref="dbSNP:139431164"
variation 1713
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368213609"
exon 1750..1877
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 1821
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="g"
/replace="t"
/db_xref="dbSNP:372345142"
variation 1830
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150057313"
variation 1845
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:145368701"
variation 1853
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200034399"
exon 1878..2000
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 1910
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="g"
/replace="t"
/db_xref="dbSNP:372134223"
variation 1952
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376056941"
variation 1953
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:140944543"
variation 1978
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371774794"
variation 1979
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376006877"
variation 1989
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:149924362"
variation 1992
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:7209610"
exon 2001..2110
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 2010
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201169182"
variation 2022
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="g"
/replace="t"
/db_xref="dbSNP:147905984"
variation 2033
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200851525"
variation 2038
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144179290"
variation 2041
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373122324"
variation 2110
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="g"
/db_xref="dbSNP:142047019"
exon 2111..2311
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 2116
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="t"
/db_xref="dbSNP:200464103"
variation 2124
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201657571"
variation 2125
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376791823"
variation 2173
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199572430"
variation 2210
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="g"
/db_xref="dbSNP:373654877"
variation 2233
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376635428"
variation 2247
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370583951"
variation 2288
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:151034607"
variation 2289
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:140412541"
variation 2295
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:150381644"
variation 2297
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138093156"
exon 2312..2433
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 2366
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="g"
/db_xref="dbSNP:376019829"
exon 2434..2582
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 2435
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144567782"
variation 2460
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="g"
/db_xref="dbSNP:368003711"
variation 2467
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:142568223"
variation 2474
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="c"
/db_xref="dbSNP:182760245"
variation 2486
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:144724584"
variation 2535
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138625739"
variation 2536
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:141626132"
variation 2550
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144460161"
variation 2576
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="g"
/db_xref="dbSNP:368262323"
variation 2577
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="g"
/replace="t"
/db_xref="dbSNP:372082761"
exon 2583..2725
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 2589
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="c"
/db_xref="dbSNP:148396663"
variation 2651
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:149882032"
variation 2662
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="g"
/replace="t"
/db_xref="dbSNP:375390149"
variation 2668
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:150697158"
variation 2679
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:140982768"
variation 2694
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:147930073"
variation 2697
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:79757327"
variation 2697
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:144931466"
exon 2726..2884
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 2729
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370227023"
variation 2735
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200519240"
variation 2738
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:150006059"
variation 2739
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:145231603"
variation 2747
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:17852530"
variation 2748
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="g"
/db_xref="dbSNP:149142028"
variation 2753
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374611444"
variation 2769
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:371753550"
variation 2791
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143215236"
variation 2817
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146517457"
variation 2831
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:117585894"
variation 2847
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="g"
/db_xref="dbSNP:144820718"
exon 2885..3156
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 2903
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368827263"
variation 2933
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:372149006"
variation 2936
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:138657360"
variation 2945
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369517876"
variation 2952
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:78640521"
variation 2962
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:150329747"
variation 2971
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="c"
/db_xref="dbSNP:137965030"
variation 3000
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="g"
/replace="t"
/db_xref="dbSNP:372209815"
variation 3011
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200658685"
variation 3023..3026
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace=""
/replace="tctc"
/db_xref="dbSNP:377314029"
variation 3098
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:139177136"
variation 3107
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="g"
/db_xref="dbSNP:149546887"
variation 3124
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376804860"
variation 3125
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:147138981"
exon 3157..3213
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 3204
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:372890959"
variation 3205
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375352795"
exon 3214..3484
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/inference="alignment:Splign:1.39.8"
variation 3221
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318979"
variation 3221
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:147994056"
variation 3231
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:77817142"
variation 3312
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373632534"
variation 3327
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1024657"
variation 3327
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="c"
/replace="t"
/db_xref="dbSNP:117160613"
variation 3454
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2014354"
variation 3454
/gene="FBXW10"
/gene_synonym="Fbw10; HREP; SM25H2; SM2SH2"
/replace="a"
/replace="g"
/db_xref="dbSNP:28690836"
ORIGIN
acggtaaagccatgtttccaaggaggtctgtacaaaaagccagacttctgctggcagttactgagagagataggctttccatccatggcagccatttacttttgctctgggagacgtttgtaatagaaaaggcacaactggggtatttattcattccccccgttcctctagtgtttggtggcgttgccgttgcaagtgcgcagggctaaaatggactggttatcttaggatcatggaaaacctggaatcaaggctcaagaatgccccctattttcgttgtgagaagggaaccgattccatccctctatgccggaagtgtgagacgtgtgtcttagcctggaagatcttctctaccaaagagtggttctgcaggatcaatgacatatcacagaggaggtttctagttggcattctgaagcagttaaatagcttatatttgttacactatttccaaaatatccttcagaccacacagggaaaggatttcatctataacaggtcccggatcaacctcagcaagaaagaggggaaagttgtgaagtcctccttgaaccaaatgttggataaaacagtagaacagaagatgaaagagatcttgtactggtttgcgaacagcacccagtggaccaaggcgaattatactctcttactgctgcagatgtgcaaccccaaattactgctcactgctgccaatgtgatcagagtcctgtttctgagagaggagaacaatatctcaggtaaacaaggccacaggcagagactagagggcccccgaagaccagaaggcaaggcttcagaaatctgtaaggaactgcagttgtagacaacataggtagacagagattgcacagaactcagcataggttttttgaactgacaccttgtcctgacacccgatcctgtttaccaaaggagaaatgactgagtgtaacttccttcttgaaaatgatcaatgcaggaggaagtacacaacttttaactcacaagcatttatcatggatttctgcatctcataggcccagaaatggctggtccctgcccctgaccccttaatgctggtgtcgttcctgctttagggattggactgagctcgagagggttgtaaaggggaagcttttgtttttctcttcagctgccctgcacagaaaccagaccaagaagtcaaaacttagggctttttttttttttttcattcactctaccatgctccttgcttatccatgaaatgaaaccttaaagtagagtttctccaaggctggagatagcttaagggccaaataagtctagggtggtagttctccagctgtggcttgtatcaggatctccagcaggacctgttaaaacaagctcctcccccagaacttcggactcagcaggtctgagggctcaatcaagacatcacagatgtgtgtttttcccctgagaaagaccacagctccaagtctgcgacctcacaagtctattggacagccaaaactcagcacacatcccttcctttgtccaaagccccagaaaatgaacacttgcttggggcagcatctaaccctgaggaaccatggaggaattcactccggtgtatatccgaaatgaataggctgttttctggaaaaggagacataaccaagccagggtacgatccctgcaatctattggttgacctggatgacatcagagacctgtcttctgggttcagcaaataccgagacttcatccgttacctgcccatccacctctccaagtacattctaagaatgctggatagacacaccctgaacaagtgcgcctctgtgagccagcactgggccgccatggctcaacaggtcaagatggacttgtcagcgcacggcttcattcagaaccagattaccttcttgcaggggtcctacacaagaggaattgatcctaattatgccaataaggtttctatcccagttcctaaaatggtagatgacgggaagagcatgcgtgtgaaacatccgaagtggaagctgagaacgaagaatgagtacaacctgtggactgcataccagaacgaggaaacgcagcaggtcctgatagaggagagaaatgttttctgtgggacctacaatgttcgcattctctctgacacgtgggatcaaaaccgagtcatccactattccgggggagatctgatagctgtgtcatctaatcgaaagatccatcttctggacatcatacaagtgaaagcgatacccgttgaattccgaggccatgctgggagtgtccgggccctcttcctgtgtgaggaggaaaactttctcctaagcgggagctatgacctaagtatcagatactgggatctgaaaagtggggtttgcacacgaatcttcggtggtcaccaggggactatcacttgcatggacttgtgtaagaacaggctcgtatctggaggaagagattgccaggtaaaagtatgggatgtagacacagggaagtgcctgaagacgtttagacacaaagaccccatcttggccaccaggatcaatgatacctacattgtgagcagctgtgagcgagggctggtgaaagtgtggcacattgccatggcccagttggtaaagactctcagtggccatgagggagccgtgaaatgcctgttctttgaccagtggcatctcctctcaggaagtactgatggcctggtcatggcctggagcatggtggggaagtacgagcgctgcctgatggccttcaagcatcccaaggaggtgctcgacgtgtcccttctcttcctccgggtcatcagcgcctgtgcagatggcaagatccgaatttacaatttcctcaacgggaactgtatgaaggtgttaaaagccaatggcagaggtgatcctgtgctgtccttctttattcagggcaacaggatggtggtcaacacagagagcaatgttctcatgttccagtttgagcacataaagtggcagtatgccgtggaaaaaacgaaacaaaagaagaataaggagaaagaggaggaaaaagaagaaaatagtctcatggaaattctctctaagtgtaatattcaggttcacagcccaagagagtctgtatccagtaaacaaactgtgatccaagagctcctaccaggcaaacctcccaagtcccgagtactcctgaagccggccaagttctcttcagcagtgttaatagaggaacttcaaagtcaaggaaagtcaaaatcaccccgaagagatgagtgaacactgagttcgtgctgttgaccgtgaaggaggagaaggagcaccaggaagccaagatgaaggaatatcaggccagggagtccactggagtggttgatccaggaaaagtcagcaaagctgcatggatcaggaagatcaaaggcctgcctattgataatttcacgaagcaagggaaaacagcggcccctgaacttggacaaaatgtatttatctaaaccagccttgggaaattacaatgttttacaataaacagaaagccaagcggaaaaaaaaaaa
//
by
@meso_cacase at
DBCLS
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