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2024-04-19 13:30:25, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_016373 2488 bp mRNA linear PRI 16-JUN-2013
DEFINITION Homo sapiens WW domain containing oxidoreductase (WWOX), transcript
variant 1, mRNA.
ACCESSION NM_016373 NM_004916
VERSION NM_016373.2 GI:333944035
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 2488)
AUTHORS Guo,W., Dong,Z., Dong,Y., Guo,Y., Kuang,G. and Yang,Z.
TITLE Genetic and epigenetic alterations of WWOX in the development of
gastric cardia adenocarcinoma
JOURNAL Environ. Mol. Mutagen. 54 (2), 112-123 (2013)
PUBMED 23197378
REMARK GeneRIF: WWOX may play an important role in gastric cardia
adenocarcinoma especially in individuals with upper
gastrointestinal cancer family history.
REFERENCE 2 (bases 1 to 2488)
AUTHORS Li,Y.P., Wu,C.C., Chen,W.T., Huang,Y.C. and Chai,C.Y.
TITLE The expression and significance of WWOX and beta-catenin in
hepatocellular carcinoma
JOURNAL APMIS 121 (2), 120-126 (2013)
PUBMED 23030478
REMARK GeneRIF: Downregulation of WWOX might lead to accumulation of
cytoplasmic beta-catenin and the subsequent activation of
Wnt/beta-catenin signaling pathway in hepatocellular carcinoma.
REFERENCE 3 (bases 1 to 2488)
AUTHORS Luykx,J.J., Bakker,S.C., Lentjes,E., Neeleman,M., Strengman,E.,
Mentink,L., Deyoung,J., de Jong,S., Sul,J.H., Eskin,E., van
Eijk,K., van Setten,J., Buizer-Voskamp,J.E., Cantor,R.M., Lu,A.,
van Amerongen,M., van Dongen,E.P., Keijzers,P., Kappen,T.,
Borgdorff,P., Bruins,P., Derks,E.M., Kahn,R.S. and Ophoff,R.A.
TITLE Genome-wide association study of monoamine metabolite levels in
human cerebrospinal fluid
JOURNAL Mol. Psychiatry (2013) In press
PUBMED 23319000
REMARK Publication Status: Available-Online prior to print
REFERENCE 4 (bases 1 to 2488)
AUTHORS Hancock,D.B., Artigas,M.S., Gharib,S.A., Henry,A., Manichaikul,A.,
Ramasamy,A., Loth,D.W., Imboden,M., Koch,B., McArdle,W.L.,
Smith,A.V., Smolonska,J., Sood,A., Tang,W., Wilk,J.B., Zhai,G.,
Zhao,J.H., Aschard,H., Burkart,K.M., Curjuric,I., Eijgelsheim,M.,
Elliott,P., Gu,X., Harris,T.B., Janson,C., Homuth,G., Hysi,P.G.,
Liu,J.Z., Loehr,L.R., Lohman,K., Loos,R.J., Manning,A.K.,
Marciante,K.D., Obeidat,M., Postma,D.S., Aldrich,M.C.,
Brusselle,G.G., Chen,T.H., Eiriksdottir,G., Franceschini,N.,
Heinrich,J., Rotter,J.I., Wijmenga,C., Williams,O.D., Bentley,A.R.,
Hofman,A., Laurie,C.C., Lumley,T., Morrison,A.C., Joubert,B.R.,
Rivadeneira,F., Couper,D.J., Kritchevsky,S.B., Liu,Y., Wjst,M.,
Wain,L.V., Vonk,J.M., Uitterlinden,A.G., Rochat,T., Rich,S.S.,
Psaty,B.M., O'Connor,G.T., North,K.E., Mirel,D.B., Meibohm,B.,
Launer,L.J., Khaw,K.T., Hartikainen,A.L., Hammond,C.J., Glaser,S.,
Marchini,J., Kraft,P., Wareham,N.J., Volzke,H., Stricker,B.H.,
Spector,T.D., Probst-Hensch,N.M., Jarvis,D., Jarvelin,M.R.,
Heckbert,S.R., Gudnason,V., Boezen,H.M., Barr,R.G., Cassano,P.A.,
Strachan,D.P., Fornage,M., Hall,I.P., Dupuis,J., Tobin,M.D. and
London,S.J.
TITLE Genome-wide joint meta-analysis of SNP and SNP-by-smoking
interaction identifies novel loci for pulmonary function
JOURNAL PLoS Genet. 8 (12), E1003098 (2012)
PUBMED 23284291
REFERENCE 5 (bases 1 to 2488)
AUTHORS Hart,A.B., Engelhardt,B.E., Wardle,M.C., Sokoloff,G., Stephens,M.,
de Wit,H. and Palmer,A.A.
TITLE Genome-wide association study of d-amphetamine response in healthy
volunteers identifies putative associations, including cadherin 13
(CDH13)
JOURNAL PLoS ONE 7 (8), E42646 (2012)
PUBMED 22952603
REFERENCE 6 (bases 1 to 2488)
AUTHORS Bednarek,A.K., Keck-Waggoner,C.L., Daniel,R.L., Laflin,K.J.,
Bergsagel,P.L., Kiguchi,K., Brenner,A.J. and Aldaz,C.M.
TITLE WWOX, the FRA16D gene, behaves as a suppressor of tumor growth
JOURNAL Cancer Res. 61 (22), 8068-8073 (2001)
PUBMED 11719429
REMARK GeneRIF: WWOX, the FRA16D gene, behaves as a suppressor of tumor
growth.
REFERENCE 7 (bases 1 to 2488)
AUTHORS Paige,A.J., Taylor,K.J., Taylor,C., Hillier,S.G., Farrington,S.,
Scott,D., Porteous,D.J., Smyth,J.F., Gabra,H. and Watson,J.E.
TITLE WWOX: a candidate tumor suppressor gene involved in multiple tumor
types
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 98 (20), 11417-11422 (2001)
PUBMED 11572989
REFERENCE 8 (bases 1 to 2488)
AUTHORS Chang,N.S., Pratt,N., Heath,J., Schultz,L., Sleve,D., Carey,G.B.
and Zevotek,N.
TITLE Hyaluronidase induction of a WW domain-containing oxidoreductase
that enhances tumor necrosis factor cytotoxicity
JOURNAL J. Biol. Chem. 276 (5), 3361-3370 (2001)
PUBMED 11058590
REFERENCE 9 (bases 1 to 2488)
AUTHORS Ried,K., Finnis,M., Hobson,L., Mangelsdorf,M., Dayan,S.,
Nancarrow,J.K., Woollatt,E., Kremmidiotis,G., Gardner,A.,
Venter,D., Baker,E. and Richards,R.I.
TITLE Common chromosomal fragile site FRA16D sequence: identification of
the FOR gene spanning FRA16D and homozygous deletions and
translocation breakpoints in cancer cells
JOURNAL Hum. Mol. Genet. 9 (11), 1651-1663 (2000)
PUBMED 10861292
REFERENCE 10 (bases 1 to 2488)
AUTHORS Bednarek,A.K., Laflin,K.J., Daniel,R.L., Liao,Q., Hawkins,K.A. and
Aldaz,C.M.
TITLE WWOX, a novel WW domain-containing protein mapping to human
chromosome 16q23.3-24.1, a region frequently affected in breast
cancer
JOURNAL Cancer Res. 60 (8), 2140-2145 (2000)
PUBMED 10786676
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DB035405.1 and AF211943.1.
This sequence is a reference standard in the RefSeqGene project.
On May 25, 2011 this sequence version replaced gi:7706522.
Summary: WW domain-containing proteins are found in all eukaryotes
and play an important role in the regulation of a wide variety of
cellular functions such as protein degradation, transcription, and
RNA splicing. This gene encodes a protein which contains 2 WW
domains and a short-chain dehydrogenase/reductase domain (SRD). The
highest normal expression of this gene is detected in hormonally
regulated tissues such as testis, ovary, and prostate. This
expression pattern and the presence of an SRD domain suggest a role
for this gene in steroid metabolism. The encoded protein is more
than 90% identical to the mouse protein, which is an essential
mediator of tumor necrosis factor-alpha-induced apoptosis,
suggesting a similar, important role in apoptosis for the human
protein. In addition, there is evidence that this gene behaves as a
suppressor of tumor growth. Alternative splicing of this gene
generates transcript variants that encode different isoforms.
[provided by RefSeq, Jul 2008].
Transcript Variant: This variant (1) encodes the longest isoform.
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 :: AF211943.1, AF227527.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025082, ERS025084 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-224 DB035405.1 18-241
225-2488 AF211943.1 1-2264
FEATURES Location/Qualifiers
source 1..2488
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="16"
/map="16q23.3-q24.1"
gene 1..2488
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/note="WW domain containing oxidoreductase"
/db_xref="GeneID:51741"
/db_xref="HGNC:12799"
/db_xref="HPRD:05501"
/db_xref="MIM:605131"
exon 1..456
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/inference="alignment:Splign:1.39.8"
variation 24
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:117763255"
variation 51
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:188079701"
variation 219
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="g"
/replace="t"
/db_xref="dbSNP:191298606"
variation 298
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:375359239"
variation 311
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="t"
/db_xref="dbSNP:377066400"
misc_feature 320..322
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/note="upstream in-frame stop codon"
variation 334
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368929558"
variation 345
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:11545028"
CDS 350..1594
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/EC_number="1.1.1.-"
/note="isoform 1 is encoded by transcript variant 1; short
chain dehydrogenase/reductase family 41C, member 1; WW
domain-containing protein WWOX; fragile site FRA16D
oxidoreductase"
/codon_start=1
/product="WW domain-containing oxidoreductase isoform 1"
/protein_id="NP_057457.1"
/db_xref="GI:7706523"
/db_xref="CCDS:CCDS42196.1"
/db_xref="GeneID:51741"
/db_xref="HGNC:12799"
/db_xref="HPRD:05501"
/db_xref="MIM:605131"
/translation="
MAALRYAGLDDTDSEDELPPGWEERTTKDGWVYYANHTEEKTQWEHPKTGKRKRVAGDLPYGWEQETDENGQVFFVDHINKRTTYLDPRLAFTVDDNPTKPTTRQRYDGSTTAMEILQGRDFTGKVVVVTGANSGIGFETAKSFALHGAHVILACRNMARASEAVSRILEEWHKAKVEAMTLDLALLRSVQHFAEAFKAKNVPLHVLVCNAATFALPWSLTKDGLETTFQVNHLGHFYLVQLLQDVLCRSAPARVIVVSSESHRFTDINDSLGKLDFSRLSPTKNDYWAMLAYNRSKLCNILFSNELHRRLSPRGVTSNAVHPGNMMYSNIHRSWWVYTLLFTLARPFTKSMQQGAATTVYCAAVPELEGLGGMYFNNCCRCMPSPEAQSEETARTLWALSERLIQERLGSQSG
"
misc_feature 383..385
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (Q9NZC7.1); phosphorylation site"
misc_feature 389..391
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q9NZC7.1); phosphorylation site"
misc_feature 389..391
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 404..493
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/note="Two conserved tryptophans domain; also known as the
WWP or rsp5 domain; around 40 amino acids; functions as an
interaction module in a diverse set of signalling
proteins; binds specific proline-rich sequences but at low
affinities compared to other...; Region: WW; cd00201"
/db_xref="CDD:29258"
misc_feature order(446..448,479..481)
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/note="binding pocket"
/db_xref="CDD:29258"
misc_feature 446..448
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphotyrosine; propagated from
UniProtKB/Swiss-Prot (Q9NZC7.1); phosphorylation site"
misc_feature 446..448
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 446..448
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
/db_xref="HPRD:01819"
misc_feature 497..514
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9NZC7.1);
Region: Nuclear localization signal (By similarity)"
misc_feature 527..616
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/note="Two conserved tryptophans domain; also known as the
WWP or rsp5 domain; around 40 amino acids; functions as an
interaction module in a diverse set of signalling
proteins; binds specific proline-rich sequences but at low
affinities compared to other...; Region: WW; cd00201"
/db_xref="CDD:29258"
misc_feature order(569..571,602..604)
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/note="binding pocket"
/db_xref="CDD:29258"
misc_feature 668..1561
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/note="oxidoreductase; Provisional; Region: PRK06196"
/db_xref="CDD:180460"
misc_feature 719..1570
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/note="human WWOX (WW domain-containing
oxidoreductase)-like, classical (c)-like SDRs; Region:
human_WWOX_like_SDR_c-like; cd09809"
/db_xref="CDD:187669"
misc_feature 722..1591
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9NZC7.1);
Region: Interaction with MAPT (By similarity)"
misc_feature order(740..742,746..757,812..820,893..901,977..985,
1040..1042,1139..1147,1226..1228,1238..1240,1316..1327,
1331..1336)
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/note="putative NAD(P) binding site [chemical binding];
other site"
/db_xref="CDD:187669"
misc_feature 974..1168
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9NZC7.1);
Region: Mediates targeting to the mitochondria (By
similarity)"
misc_feature order(1043..1045,1145..1147,1226..1228,1238..1240)
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/note="active site"
/db_xref="CDD:187669"
misc_feature 1208..1210
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphotyrosine, by TNK2; propagated from
UniProtKB/Swiss-Prot (Q9NZC7.1); phosphorylation site"
variation 368
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371392600"
variation 379
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373146723"
variation 409
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:376165565"
exon 457..521
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/inference="alignment:Splign:1.39.8"
variation 463
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372635270"
variation 464
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377106054"
variation 466
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368245025"
variation 484
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="t"
/db_xref="dbSNP:11648112"
exon 522..579
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/inference="alignment:Splign:1.39.8"
variation 563
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201008667"
variation 577
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370579498"
exon 580..758
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/inference="alignment:Splign:1.39.8"
variation 582
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375002918"
variation 610
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368902462"
variation 611
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372362643"
variation 612
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200371768"
variation 642
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144601717"
variation 643
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200208343"
variation 645
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373144603"
variation 660
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199625891"
variation 670
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373306276"
variation 673
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:377442022"
variation 681
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:114755364"
variation 683
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="c"
/db_xref="dbSNP:376308619"
variation 700
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:34944716"
variation 707
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141361080"
variation 741
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374343152"
variation 746
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="c"
/db_xref="dbSNP:376284070"
variation 755
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:193027041"
exon 759..865
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/inference="alignment:Splign:1.39.8"
variation 769
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:374644172"
variation 770
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369907002"
variation 772..773
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace=""
/replace="c"
/db_xref="dbSNP:35771036"
variation 789
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:188859796"
variation 792
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:372660669"
variation 794
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200820063"
variation 802
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375649496"
variation 804
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2303192"
variation 817
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="g"
/replace="t"
/db_xref="dbSNP:140817689"
variation 831
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369055872"
variation 832
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:143067173"
variation 844
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:202215024"
variation 848
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201228765"
variation 849
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377356629"
exon 866..954
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/inference="alignment:Splign:1.39.8"
variation 884
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:11545029"
variation 896
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:74944733"
variation 901
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199715254"
variation 911
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="c"
/db_xref="dbSNP:199511589"
variation 916
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201593515"
variation 935
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370367979"
variation 940
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200847456"
variation 954
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="g"
/replace="t"
/db_xref="dbSNP:112636835"
exon 955..1140
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/inference="alignment:Splign:1.39.8"
variation 962
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="c"
/db_xref="dbSNP:74860463"
variation 967
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376279847"
STS 972..1045
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/standard_name="RH27913"
/db_xref="UniSTS:92030"
variation 980
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370737224"
variation 984
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202006159"
variation 993
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:377191055"
variation 995
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:7201683"
variation 1005
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:367599412"
variation 1018
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:72549408"
variation 1022
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:376040091"
variation 1029
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:368401081"
variation 1038
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="c"
/db_xref="dbSNP:199628364"
variation 1039
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372408512"
variation 1062
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142806268"
variation 1066
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="t"
/db_xref="dbSNP:368070977"
variation 1072
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:191029309"
variation 1086
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200966505"
variation 1096
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375934868"
variation 1098
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:368928190"
variation 1103
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:75559202"
variation 1109
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369715848"
variation 1135
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376709568"
exon 1141..1405
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/inference="alignment:Splign:1.39.8"
variation 1147
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="c"
/db_xref="dbSNP:377727422"
variation 1156
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:62034095"
variation 1165
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="g"
/replace="t"
/db_xref="dbSNP:186745328"
variation 1177
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:372225190"
variation 1179
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200278119"
variation 1184
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:77314072"
variation 1192
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="t"
/db_xref="dbSNP:367855242"
variation 1193
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:3764340"
variation 1205
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="g"
/replace="t"
/db_xref="dbSNP:374658336"
variation 1209
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369890118"
variation 1219
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199809390"
variation 1221
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:119487098"
variation 1222
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372210893"
variation 1223
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="g"
/replace="t"
/db_xref="dbSNP:376560613"
variation 1225
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:74030232"
variation 1227
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="t"
/db_xref="dbSNP:376488280"
variation 1233
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201417061"
variation 1234
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:79771882"
variation 1237
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:3764341"
variation 1241
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371364838"
variation 1247
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374541202"
variation 1255
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377404672"
variation 1264
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201818301"
variation 1268
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200320711"
variation 1275
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370792938"
variation 1277
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:193001955"
variation 1284
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="c"
/db_xref="dbSNP:79399971"
variation 1286
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:370345936"
variation 1290
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:73572838"
variation 1295
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201941494"
variation 1297
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201986739"
variation 1306
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144417100"
variation 1307
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368670215"
variation 1326
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371996496"
variation 1339
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:117209694"
variation 1346
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369281766"
variation 1347
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:184773837"
variation 1365
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376672888"
variation 1370
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="c"
/db_xref="dbSNP:201616456"
variation 1384
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:189695070"
variation 1388
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="c"
/db_xref="dbSNP:200699154"
exon 1406..2465
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/inference="alignment:Splign:1.39.8"
variation 1426
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150912992"
variation 1427
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200019508"
variation 1432
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368680750"
variation 1456
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369673368"
variation 1474
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372703745"
variation 1480
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="c"
/db_xref="dbSNP:377129275"
variation 1481
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="t"
/db_xref="dbSNP:201970084"
variation 1482
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201901491"
variation 1483
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201088847"
variation 1490
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200461412"
variation 1491
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:202002431"
variation 1494
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199585408"
variation 1519
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372635911"
variation 1520
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:375757102"
variation 1521
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369959670"
variation 1527
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139253468"
variation 1528
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376293017"
variation 1533
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373148311"
variation 1544
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375970162"
variation 1545
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200815431"
variation 1546
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376935572"
variation 1552
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201428060"
variation 1553
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200839945"
variation 1571
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144234059"
variation 1575
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368397011"
variation 1577
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="g"
/replace="t"
/db_xref="dbSNP:76204496"
variation 1587
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="c"
/db_xref="dbSNP:117065412"
variation 1588
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199576434"
variation 1589
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201606637"
variation 1597
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="g"
/replace="t"
/db_xref="dbSNP:140060332"
variation 1608
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375034238"
variation 1612
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369101141"
variation 1615
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372346879"
variation 1627
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:11545030"
variation 1628
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373152257"
variation 1638
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="g"
/replace="t"
/db_xref="dbSNP:200566063"
variation 1640
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369379648"
variation 1647
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="c"
/db_xref="dbSNP:146481440"
variation 1666
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:73569323"
variation 1682
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:139933122"
variation 1687
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:77897021"
variation 1691
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142218559"
variation 1718
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200371035"
variation 1721
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="g"
/replace="t"
/db_xref="dbSNP:383362"
variation 1756
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:183921789"
variation 1769
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:151232564"
variation 1774..1775
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace=""
/replace="gtaaa"
/db_xref="dbSNP:138002331"
variation 1775..1776
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace=""
/replace="gtaaa"
/db_xref="dbSNP:372153781"
variation 1777..1778
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace=""
/replace="aagta"
/db_xref="dbSNP:199719257"
variation 1794..1798
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace=""
/replace="gggct"
/db_xref="dbSNP:144412859"
variation 1805
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:78687618"
variation 1831
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2288035"
variation 1857
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2288034"
variation 1862
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2288033"
variation 1873
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140398425"
variation 1878
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373427613"
variation 1887
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:117863142"
STS 1922..2041
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/standard_name="RH11464"
/db_xref="UniSTS:42517"
variation 1956
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:187870156"
variation 1964..1972
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace=""
/replace="gccaccact"
/db_xref="dbSNP:143553940"
variation 1964
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1139446"
variation 1966..1974
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace=""
/replace="caccactgc"
/db_xref="dbSNP:369295302"
variation 1979
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2288032"
variation 2061
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:150285033"
variation 2091
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1126520"
variation 2171
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:116830872"
variation 2201
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147568401"
variation 2224
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:12828"
variation 2237..2238
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace=""
/replace="agag"
/db_xref="dbSNP:200479792"
variation 2238..2239
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace=""
/replace="gaga"
/db_xref="dbSNP:377694307"
variation 2280
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:371613343"
variation 2298
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:192942549"
variation 2299..2300
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace=""
/replace="gt"
/db_xref="dbSNP:376803237"
STS 2330..2426
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/standard_name="D16S3307"
/db_xref="UniSTS:14859"
variation 2337
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375637168"
variation 2347..2348
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace=""
/replace="cgtt"
/db_xref="dbSNP:369721192"
variation 2347
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:57224164"
variation 2348..2351
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace=""
/replace="gtta"
/db_xref="dbSNP:145925570"
variation 2358
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:184137904"
variation 2360
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:145901191"
variation 2368
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139222337"
variation 2370
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="g"
/db_xref="dbSNP:76642212"
variation 2375
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="t"
/db_xref="dbSNP:118128947"
variation 2427
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369316900"
variation 2436
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="a"
/replace="g"
/db_xref="dbSNP:391870"
variation 2451
/gene="WWOX"
/gene_synonym="D16S432E; FOR; FRA16D; HHCMA56; PRO0128;
SDR41C1; WOX1"
/replace="c"
/replace="t"
/db_xref="dbSNP:189463977"
ORIGIN
gatgcgcacgccccttccctgcggcggggaggctgacaaggctccgctctatctctagcgcctcggagcgctctccggctttgctgtctagcccggcggcagcgcgatctcttaggcactttcaccgccttcctctccaggccctgcccctttgacgccggccgtcgcgatattgcggagactggatttcagcttcgtggtcggcggagcggcccctggagggcgcagtgcgcaggcgtgagcggtcgggccccgacgcgcgcgggtctcgtttggagcgggagtgagttcctgagcgagtggacccggcagcgggcgataggggggccaggtgcctccacagtcagccatggcagcgctgcgctacgcggggctggacgacacggacagtgaggacgagctgcctccgggctgggaggagagaaccaccaaggacggctgggtttactacgccaatcacaccgaggagaagactcagtgggaacatccaaaaactggaaaaagaaaacgagtggcaggagatttgccatacggatgggaacaagaaactgatgagaacggacaagtgttttttgttgaccatataaataaaagaaccacctacttggacccaagactggcgtttactgtggatgataatccgaccaagccaaccacccggcaaagatacgacggcagcaccactgccatggaaattctccagggccgggatttcactggcaaagtggttgtggtcactggagctaattcaggaatagggttcgaaaccgccaagtcttttgccctccatggtgcacatgtgatcttggcctgcaggaacatggcaagggcgagtgaagcagtgtcacgcattttagaagaatggcataaagccaaggtagaagcaatgaccctggacctcgctctgctccgtagcgtgcagcattttgctgaagcattcaaggccaagaatgtgcctcttcatgtgcttgtgtgcaacgcagcaacttttgctctaccctggagtctcaccaaagatggcctggagaccacctttcaagtgaatcatctggggcacttctaccttgtccagctcctccaggatgttttgtgccgctcagctcctgcccgtgtcattgtggtctcctcagagtcccatcgatttacagatattaacgactccttgggaaaactggacttcagtcgcctctctccaacaaaaaacgactattgggcgatgctggcttataacaggtccaagctctgcaacatcctcttctccaacgagctgcaccgtcgcctctccccacgcggggtcacgtcgaacgcagtgcatcctggaaatatgatgtactccaacattcatcgcagctggtgggtgtacacactgctgtttaccttggcgaggcctttcaccaagtccatgcaacagggagctgccaccaccgtgtactgtgctgctgtcccagaactggagggtctgggagggatgtacttcaacaactgctgccgctgcatgccctcaccagaagctcagagcgaagagacggcccggaccctgtgggcgctcagcgagaggctgatccaagaacggcttggcagccagtccggctaagtggagctcagagcggatgggcacacacacccgccctgtgtgtgtcccctcacgcaagtgccagggctgggccccttccaaatgtccctccaacacagatccgcaagagtaaaggaaataagagcagtcacaacagagtgaaaaatcttaagtaccaatgggaagcagggaattcctggggtaaagtatcacttttctggggctgggctaggcataggtctctttgctttctggtggtggcctgtttgaaagtaaaaacctgcttggtgtgtaggttccgtatctccctggagaagcaccagcaattctctttcttttactgttatagaatagcctgaggtcccctcgtcccatccagctaccaccacggccaccactgcagccgggggctggccttctcctacttagggaagaaaaagcaagtgttcactgctccttgctgcattgatccaggagataattgtttcattcatcctgaccaagactgagccagcttagcaactgctggggagacaaatctcagaaccttgtcccagccagtgaggatgacagtgacacccagagggagtagaatacgcagaactaccaggtggcaaagtacttgtcatagactcctttgctaatgctatgcaaaaaattctttagagattataacaaatttttcaaatcattccttagataccttgaaaggcaggaagggaagcgtatatacttaagaatacacaggatattttggggggcagagaataaaacgttagttaatccctttgtctgtcaatcacagtctcagttctcttgctttcacattgtacttaaacctcctgctgtgcctcgcatcctatgcttaataaaagaacatgcttgaatatcaaaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:51741 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:51741 -> Molecular function: GO:0016491 [oxidoreductase activity] evidence: NAS
GeneID:51741 -> Molecular function: GO:0016491 [oxidoreductase activity] evidence: TAS
GeneID:51741 -> Molecular function: GO:0019899 [enzyme binding] evidence: IPI
GeneID:51741 -> Molecular function: GO:0046983 [protein dimerization activity] evidence: TAS
GeneID:51741 -> Molecular function: GO:0048037 [cofactor binding] evidence: TAS
GeneID:51741 -> Molecular function: GO:0050662 [coenzyme binding] evidence: TAS
GeneID:51741 -> Biological process: GO:0001649 [osteoblast differentiation] evidence: IEA
GeneID:51741 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA
GeneID:51741 -> Biological process: GO:0006917 [induction of apoptosis] evidence: IEA
GeneID:51741 -> Biological process: GO:0008202 [steroid metabolic process] evidence: TAS
GeneID:51741 -> Biological process: GO:0016055 [Wnt receptor signaling pathway] evidence: IEA
GeneID:51741 -> Biological process: GO:0030178 [negative regulation of Wnt receptor signaling pathway] evidence: IDA
GeneID:51741 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: ISS
GeneID:51741 -> Biological process: GO:0048705 [skeletal system morphogenesis] evidence: ISS
GeneID:51741 -> Biological process: GO:0055114 [oxidation-reduction process] evidence: TAS
GeneID:51741 -> Biological process: GO:0071560 [cellular response to transforming growth factor beta stimulus] evidence: IDA
GeneID:51741 -> Biological process: GO:2001238 [positive regulation of extrinsic apoptotic signaling pathway] evidence: ISS
GeneID:51741 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:51741 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
GeneID:51741 -> Cellular component: GO:0005737 [cytoplasm] evidence: TAS
GeneID:51741 -> Cellular component: GO:0005739 [mitochondrion] evidence: ISS
GeneID:51741 -> Cellular component: GO:0005794 [Golgi apparatus] evidence: IDA
GeneID:51741 -> Cellular component: GO:0005829 [cytosol] evidence: IDA
GeneID:51741 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
GeneID:51741 -> Cellular component: GO:0005886 [plasma membrane] evidence: IDA
GeneID:51741 -> Cellular component: GO:0005902 [microvillus] evidence: IDA
ANNOTATIONS from NCBI Entrez Gene (20130726):
NP_057457 -> EC 1.1.1.-
by
@meso_cacase at
DBCLS
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