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2024-04-26 12:26:46, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001042355 8584 bp mRNA linear PRI 24-JUN-2013
DEFINITION Homo sapiens cylindromatosis (turban tumor syndrome) (CYLD),
transcript variant 2, mRNA.
ACCESSION NM_001042355
VERSION NM_001042355.1 GI:109637773
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 8584)
AUTHORS Yang,W.L., Jin,G., Li,C.F., Jeong,Y.S., Moten,A., Xu,D., Feng,Z.,
Chen,W., Cai,Z., Darnay,B., Gu,W. and Lin,H.K.
TITLE Cycles of ubiquitination and deubiquitination critically regulate
growth factor-mediated activation of Akt signaling
JOURNAL Sci Signal 6 (257), RA3 (2013)
PUBMED 23300340
REMARK GeneRIF: CYLD is a molecular switch for cycles of ubiquitination
and deubiquitination that critically regulate growth
factor-mediated activation of Akt signaling.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 8584)
AUTHORS Ke,H., Augustine,C.K., Gandham,V.D., Jin,J.Y., Tyler,D.S.,
Akiyama,S.K., Hall,R.P. and Zhang,J.Y.
TITLE CYLD inhibits melanoma growth and progression through suppression
of the JNK/AP-1 and beta1-integrin signaling pathways
JOURNAL J. Invest. Dermatol. 133 (1), 221-229 (2013)
PUBMED 22832488
REMARK GeneRIF: these findings demonstrate that the JNK/activator protein
1 signaling pathway underlies the melanoma growth and metastasis
that are associated with CYLD loss of function.
REFERENCE 3 (bases 1 to 8584)
AUTHORS Nagy,N., Farkas,K., Kinyo,A., Nemeth,I.B., Kis,E., Varga,J.,
Bata-Csorgo,Z., Kemeny,L. and Szell,M.
TITLE A novel missense mutation of the CYLD gene identified in a
Hungarian family with Brooke-Spiegler syndrome
JOURNAL Exp. Dermatol. 21 (12), 967-969 (2012)
PUBMED 23171463
REMARK GeneRIF: We investigated a Hungarian Brooke Spiegler syndrome
pedigree with two affected members, demonstrating a novel missense
mutation (c.2613C>G; p.His871Gln) in exon 19 within the
ubiquitin-specific protease domain of the encoded protein.
REFERENCE 4 (bases 1 to 8584)
AUTHORS Chu,Y., Soberon,V., Glockner,L., Beyaert,R., Massoumi,R., van
Loo,G., Krappmann,D. and Schmidt-Supprian,M.
TITLE A20 and CYLD do not share significant overlapping functions during
B cell development and activation
JOURNAL J. Immunol. 189 (9), 4437-4443 (2012)
PUBMED 23002441
REMARK GeneRIF: Lack of both CYLD and A20 do not exacerbate the
developmental defects and hyperresponsive activity of A20-deficient
B cells.
REFERENCE 5 (bases 1 to 8584)
AUTHORS Gomez-Ferreria,M.A., Bashkurov,M., Mullin,M., Gingras,A.C. and
Pelletier,L.
TITLE CEP192 interacts physically and functionally with the
K63-deubiquitinase CYLD to promote mitotic spindle assembly
JOURNAL Cell Cycle 11 (19), 3555-3558 (2012)
PUBMED 22895009
REMARK GeneRIF: CEP192 promotes robust mitotic spindle assembly by
regulating K63-polyubiquitin-mediated signaling through CYLD.
REFERENCE 6 (bases 1 to 8584)
AUTHORS Bignell,G.R., Warren,W., Seal,S., Takahashi,M., Rapley,E.,
Barfoot,R., Green,H., Brown,C., Biggs,P.J., Lakhani,S.R., Jones,C.,
Hansen,J., Blair,E., Hofmann,B., Siebert,R., Turner,G., Evans,D.G.,
Schrander-Stumpel,C., Beemer,F.A., van Den Ouweland,A., Halley,D.,
Delpech,B., Cleveland,M.G., Leigh,I., Leisti,J. and Rasmussen,S.
TITLE Identification of the familial cylindromatosis tumour-suppressor
gene
JOURNAL Nat. Genet. 25 (2), 160-165 (2000)
PUBMED 10835629
REFERENCE 7 (bases 1 to 8584)
AUTHORS Fenske,C., Banerjee,P., Holden,C. and Carter,N.
TITLE Brooke-Spiegler syndrome locus assigned to 16q12-q13
JOURNAL J. Invest. Dermatol. 114 (5), 1057-1058 (2000)
PUBMED 10792569
REFERENCE 8 (bases 1 to 8584)
AUTHORS Thomson,S.A., Rasmussen,S.A., Zhang,J. and Wallace,M.R.
TITLE A new hereditary cylindromatosis family associated with CYLD1 on
chromosome 16
JOURNAL Hum. Genet. 105 (1-2), 171-173 (1999)
PUBMED 10480375
REFERENCE 9 (bases 1 to 8584)
AUTHORS Biggs,P.J., Chapman,P., Lakhani,S.R., Burn,J. and Stratton,M.R.
TITLE The cylindromatosis gene (cyld1) on chromosome 16q may be the only
tumour suppressor gene involved in the development of cylindromas
JOURNAL Oncogene 12 (6), 1375-1377 (1996)
PUBMED 8649842
REFERENCE 10 (bases 1 to 8584)
AUTHORS Biggs,P.J., Wooster,R., Ford,D., Chapman,P., Mangion,J., Quirk,Y.,
Easton,D.F., Burn,J. and Stratton,M.R.
TITLE Familial cylindromatosis (turban tumour syndrome) gene localised to
chromosome 16q12-q13: evidence for its role as a tumour suppressor
gene
JOURNAL Nat. Genet. 11 (4), 441-443 (1995)
PUBMED 7493027
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DA785459.1, BI458962.1,
AK056226.1, AJ250014.1, BX642061.1, DA157717.1, DA940312.1 and
AL050166.1.
Summary: This gene is encodes a cytoplasmic protein with three
cytoskeletal-associated protein-glycine-conserved (CAP-GLY) domains
that functions as a deubiquitinating enzyme. Mutations in this gene
have been associated with cylindromatosis, multiple familial
trichoepithelioma, and Brooke-Spiegler syndrome. Alternate
transcriptional splice variants, encoding different isoforms, have
been characterized. [provided by RefSeq, Jul 2008].
Transcript Variant: This variant (2) lacks one exon in the 5' UTR
and a second in-frame exon in the coding region, compared to
variant 1, resulting in a shorter protein (isoform 2), compared to
isoform 1. Variants 2 and 3 encode the same 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 :: AK292975.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025082, ERS025083 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-39 DA785459.1 1-39
40-45 BI458962.1 36-41
46-1999 AK056226.1 1-1954
2000-5107 AJ250014.1 2122-5229
5108-5120 BX642061.1 146-158 c
5121-5249 AJ250014.1 5243-5371
5250-5640 DA157717.1 182-572
5641-6227 DA940312.1 9-595
6228-8584 AL050166.1 315-2671
FEATURES Location/Qualifiers
source 1..8584
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="16"
/map="16q12.1"
gene 1..8584
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/note="cylindromatosis (turban tumor syndrome)"
/db_xref="GeneID:1540"
/db_xref="HGNC:2584"
/db_xref="MIM:605018"
exon 1..75
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 8
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373031484"
exon 76..155
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
exon 156..782
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 179..180
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace=""
/replace="a"
/db_xref="dbSNP:67190903"
variation 188
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369755094"
misc_feature 255..257
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/note="upstream in-frame stop codon"
variation 259
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:190977024"
CDS 279..3140
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/EC_number="3.4.19.12"
/note="isoform 2 is encoded by transcript variant 2;
ubiquitin specific peptidase like 2; ubiquitin
thiolesterase CYLD; probable ubiquitin carboxyl-terminal
hydrolase CYLD; ubiquitin-specific-processing protease
CYLD; deubiquitinating enzyme CYLD; ubiquitin thioesterase
CYLD"
/codon_start=1
/product="ubiquitin carboxyl-terminal hydrolase CYLD
isoform 2"
/protein_id="NP_001035814.1"
/db_xref="GI:109637774"
/db_xref="CCDS:CCDS42164.1"
/db_xref="GeneID:1540"
/db_xref="HGNC:2584"
/db_xref="MIM:605018"
/translation="
MSSGLWSQEKVTSPYWEERIFYLLLQECSVTDKQTQKLLKVPKGSIGQYIQDRSVGHSRIPSAKGKKNQIGLKILEQPHAVLFVDEKDVVEINEKFTELLLAITNCEERFSLFKNRNRLSKGLQIDVGCPVKVQLRSGEEKFPGVVRFRGPLLAERTVSGIFFGVELLEEGRGQGFTDGVYQGKQLFQCDEDCGVFVALDKLELIEDDDTALESDYAGPGDTMQVELPPLEINSRVSLKVGETIESGTVIFCDVLPGKESLGYFVGVDMDNPIGNWDGRFDGVQLCSFACVESTILLHINDIIPESVTQERRPPKLAFMSRGVGDKGSSSHNKPKATGSTSDPGNRNRSELFYTLNGSSVDSQPQSKSKNTWYIDEVAEDPAKSLTEISTDFDRSSPPLQPPPVNSLTTENRFHSLPFSLTKMPNTNGSIGHSPLSLSAQSVMEELNTAPVQESPPLAMPPGNSHGLEVGSLAEVKENPPFYGVIRWIGQPPGLNEVLAGLELEDECAGCTDGTFRGTRYFTCALKKALFVKLKSCRPDSRFASLQPVSNQIERCNSLAFGGYLSEVVEENTPPKMEKEGLEIMIGKKKGIQGHYNSCYLDSTLFCLFAFSSVLDTVLLRPKEKNDVEYYSETQELLRTEIVNPLRIYGYVCATKIMKLRKILEKVEAASGFTSEEKDPEEFLNILFHHILRVEPLLKIRSAGQKVQDCYFYQIFMEKNEKVGVPTIQQLLEWSFINSNLKFAEAPSCLIIQMPRFGKDFKLFKKIFPSLELNITDLLEDTPRQCRICGGLAMYECRECYDDPDISAGKIKQFCKTCNTQVHLHPKRLNHKYNPVSLPKDLPDWDWRHGCIPCQNMELFAVLCIETSHYVAFVKYGKDDSAWLFFDSMADRDGGQNGFNIPQVTPCPEVGEYLKMSLEDLHSLDSRRIQGCARRLLCDAYMCMYQSPTMSLYK
"
misc_feature 657..887
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/note="Cytoskeleton-associated proteins (CAPs) are
involved in the organisation of microtubules and
transportation of vesicles and organelles along the
cytoskeletal network; Region: CAP_GLY; smart01052"
/db_xref="CDD:198120"
misc_feature 972..1187
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/note="CAP-Gly domain; Region: CAP_GLY; pfam01302"
/db_xref="CDD:201721"
misc_feature 1449..1676
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9NQC7.1);
Region: Interaction with TRAF2"
misc_feature 1464..1466
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1521..1523
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q9NQC7.1); phosphorylation site"
misc_feature 1677..1931
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9NQC7.1);
Region: Interaction with IKBKG/NEMO"
misc_feature 1683..1889
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/note="Cytoskeleton-associated proteins (CAPs) are
involved in the organisation of microtubules and
transportation of vesicles and organelles along the
cytoskeletal network; Region: CAP_GLY; smart01052"
/db_xref="CDD:198120"
misc_feature 2298..3113
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/note="A subfamily of Peptidase C19. Peptidase C19
contains ubiquitinyl hydrolases. They are intracellular
peptidases that remove ubiquitin molecules from
polyubiquinated peptides by cleavage of isopeptide bonds.
They hydrolyze bonds involving the carboxyl...; Region:
Peptidase_C19N; cd02670"
/db_xref="CDD:73076"
misc_feature order(2880..2882,2937..2939)
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/note="active site"
/db_xref="CDD:73076"
variation 334
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374624194"
variation 348
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368114885"
variation 365
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:34564491"
variation 404
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:202119806"
variation 436
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375455772"
variation 486
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369619557"
variation 491
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373198684"
variation 517
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201666656"
variation 522
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376006417"
variation 656
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369238843"
variation 779
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:373896011"
exon 783..1085
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 792
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201836260"
variation 796
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:12599808"
variation 812
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:377383082"
variation 816
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:370450747"
variation 847
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="t"
/db_xref="dbSNP:374118770"
variation 860
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201431389"
variation 872
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:367580462"
variation 896
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371338061"
variation 913
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375434282"
variation 950
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:372885659"
variation 953
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:184354524"
variation 974
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="c"
/db_xref="dbSNP:375486280"
variation 1037
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:372020998"
exon 1086..1191
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 1169
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:140033230"
variation 1176
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:377066412"
variation 1187
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:202154956"
exon 1192..1290
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 1201
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200271412"
variation 1229
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:369147527"
variation 1252
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372199798"
variation 1274
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374929114"
exon 1291..1407
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 1310
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="c"
/db_xref="dbSNP:369452792"
variation 1314
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373172148"
exon 1408..1787
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 1432
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:199606039"
variation 1435
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:200759332"
variation 1441
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138976689"
variation 1458
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:149427272"
variation 1459
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370428449"
variation 1461
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:202120212"
variation 1478
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371382898"
variation 1494
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375579250"
variation 1561
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200494719"
variation 1592
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="t"
/db_xref="dbSNP:368393884"
variation 1600
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:371683706"
variation 1625
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200886685"
variation 1629
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200451975"
variation 1634
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371867434"
variation 1742
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:75757530"
variation 1751
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369789110"
exon 1788..1953
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 1819
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:201523761"
exon 1954..2095
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 1994
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373031051"
exon 2096..2218
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 2189
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:182210792"
exon 2219..2310
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 2288
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373899187"
exon 2311..2377
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
exon 2378..2510
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 2414
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200905032"
variation 2441
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="c"
/db_xref="dbSNP:373971257"
variation 2509
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:121908389"
exon 2511..2619
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 2513
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370702435"
variation 2541
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:121908388"
variation 2588
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199912760"
exon 2620..2738
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 2655
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374104988"
variation 2659
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199624138"
variation 2681
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2066852"
variation 2703
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371330250"
exon 2739..2955
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 2807
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="c"
/db_xref="dbSNP:376293566"
variation 2822
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370020837"
variation 2858
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201868355"
variation 2867
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="c"
/db_xref="dbSNP:200765362"
variation 2875
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="c"
/db_xref="dbSNP:200154154"
variation 2888
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:373541485"
exon 2956..8567
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/inference="alignment:Splign:1.39.8"
variation 3075
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:121908390"
variation 3083
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199632232"
variation 3151
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373881703"
variation 3174
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:376027595"
variation 3187
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:116979331"
STS 3197..3486
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/standard_name="SHGC-60837"
/db_xref="UniSTS:67819"
variation 3279
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:148107725"
STS 3285..3473
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/standard_name="RH64884"
/db_xref="UniSTS:83726"
polyA_signal 3492..3497
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
polyA_site 3521
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
variation 3522
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:142580891"
variation 3919
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:190787930"
variation 3971
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:144877731"
variation 3977
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:3743781"
variation 3981
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:117537927"
variation 4062
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375222421"
variation 4115
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:369791294"
STS 4157..4298
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/standard_name="RH94254"
/db_xref="UniSTS:88351"
variation 4193
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="t"
/db_xref="dbSNP:147959249"
variation 4242
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:141088048"
variation 4262
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:114552144"
variation 4331
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:146935881"
variation 4382
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="c"
/db_xref="dbSNP:150937990"
variation 4385
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:192470603"
variation 4481
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:140767609"
variation 4567
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150124371"
STS 4597..5297
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/standard_name="CYLD__4662"
/db_xref="UniSTS:471409"
variation 4715
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:184344245"
variation 4789
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:188778402"
variation 4939
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138586985"
variation 4971
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:181246559"
variation 5062
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="t"
/db_xref="dbSNP:141752920"
variation 5124
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="c"
/db_xref="dbSNP:145519346"
variation 5245..5247
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace=""
/replace="gga"
/db_xref="dbSNP:75414200"
variation 5247
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace=""
/replace="a"
/db_xref="dbSNP:111804189"
variation 5248
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:79868875"
variation 5260..5262
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace=""
/replace="aaa"
/db_xref="dbSNP:74757288"
variation 5264
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:199826833"
variation 5302
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="c"
/db_xref="dbSNP:138143910"
variation 5376
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:57638820"
variation 5411
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:185590115"
variation 5451..5453
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace=""
/replace="ttc"
/db_xref="dbSNP:370824949"
variation 5475
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:9646285"
variation 5509
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:16948829"
variation 5522
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:189512578"
variation 5591
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368296872"
variation 5673
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:371051271"
STS 5698..5866
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/standard_name="RH48312"
/db_xref="UniSTS:65489"
variation 5746
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace=""
/replace="t"
/db_xref="dbSNP:371917388"
variation 5755
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:181056407"
variation 5816
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="c"
/db_xref="dbSNP:76888453"
variation 5850
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141928186"
polyA_signal 5910..5915
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
variation 5928..5929
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace=""
/replace="tg"
/db_xref="dbSNP:375257369"
polyA_site 5931
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
variation 6210
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144667145"
variation 6223
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:185943382"
variation 6252
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace=""
/replace="t"
/db_xref="dbSNP:149875014"
variation 6275
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:374305356"
variation 6379
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:34088926"
variation 6392
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:375925980"
variation 6449
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:192317768"
variation 6563
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:183255879"
variation 6595
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:186163821"
variation 6609
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:111951225"
variation 6703
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:190533095"
variation 6733
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368698335"
variation 6737
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:372708124"
variation 6754
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="c"
/db_xref="dbSNP:372370285"
variation 6819
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141888517"
variation 6820
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:374723746"
variation 6836
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:182950511"
variation 6879
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:16948836"
variation 6896
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:188392607"
variation 7013
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:192669779"
variation 7086
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:367816704"
variation 7095
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371569379"
variation 7220
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:183024011"
variation 7294
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376037772"
variation 7421
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:187441896"
variation 7701
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:17314948"
variation 7707
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:113748745"
variation 7716
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373507820"
variation 7755..7756
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace=""
/replace="g"
/db_xref="dbSNP:34262697"
variation 7849
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:192535029"
variation 7980
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150641352"
variation 8025
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="a"
/replace="t"
/db_xref="dbSNP:184571054"
variation 8028..8029
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace=""
/replace="at"
/db_xref="dbSNP:143814807"
variation 8189
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:187446083"
variation 8377
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:192242759"
variation 8412
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:140875917"
STS 8419..8522
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
/standard_name="SGC32374"
/db_xref="UniSTS:28941"
polyA_signal 8544..8549
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
polyA_site 8567
/gene="CYLD"
/gene_synonym="BRSS; CDMT; CYLD1; CYLDI; EAC; MFT; MFT1;
SBS; TEM; USPL2"
ORIGIN
gtgcggttcggaggcggggcaggtgggggcgggcccaggtagcaggtttggctgcgcgggggccgcgcgtcggagtttccccctttctagggtgaggatggttctacacagccacccggagttccttagttgaaaggtgcgccctgctgtgacagcatggacaccacgttgctgaaaacatgctttgggactgccactgaatttatcttttgcggttttatgacaaagttattagtagtttcccttttttgaattagtattttgaagttaatatcacaatgagttcaggcttatggagccaagaaaaagtcacttcaccctactgggaagagcggattttttacttgcttcttcaagaatgcagcgttacagacaaacaaacacaaaagctccttaaagtaccgaagggaagtataggacagtatattcaagatcgttctgtggggcattcaaggattccttctgcaaaaggcaagaaaaatcagattggattaaaaattctagagcaacctcatgcagttctctttgttgatgaaaaggatgttgtagagataaatgaaaagttcacagagttacttttggcaattaccaattgtgaggagaggttcagcctgtttaaaaacagaaacagactaagtaaaggcctccaaatagacgtgggctgtcctgtgaaagtacagctgagatctggggaagaaaaatttcctggagttgtacgcttcagaggacccctgttagcagagaggacagtctccggaatattctttggagttgaattgctggaagaaggtcgtggtcaaggtttcactgacggggtgtaccaagggaaacagctttttcagtgtgatgaagattgtggcgtgtttgttgcattggacaagctagaactcatagaagatgatgacactgcattggaaagtgattacgcaggtcctggggacacaatgcaggtcgaacttcctcctttggaaataaactccagagtttctttgaaggttggagaaacaatagaatctggaacagttatattctgtgatgttttgccaggaaaagaaagcttaggatattttgttggtgtggacatggataaccctattggcaactgggatggaagatttgatggagtgcagctttgtagttttgcgtgtgttgaaagtacaattctattgcacatcaatgatatcatcccagagagtgtgacgcaggaaaggaggcctcccaaacttgcctttatgtcaagaggtgttggggacaaaggttcatccagtcataataaaccaaaggctacaggatctacctcagaccctggaaatagaaacagatctgaattattttataccttaaatgggtcttctgttgactcacaaccacaatccaaatcaaaaaatacatggtacattgatgaagttgcagaagaccctgcaaaatctcttacagagatatctacagactttgaccgttcttcaccaccactccagcctcctcctgtgaactcactgaccaccgagaacagattccactctttaccattcagtctcaccaagatgcccaataccaatggaagtattggccacagtccactttctctgtcagcccagtctgtaatggaagagctaaacactgcacccgtccaagagagtccacccttggccatgcctcctgggaactcacatggtctagaagtgggctcattggctgaagttaaggagaaccctcctttctatggggtaatccgttggatcggtcagccaccaggactgaatgaagtgctcgctggactggaactggaagatgagtgtgcaggctgtacggatggaaccttcagaggcactcggtatttcacctgtgccctgaagaaggcgctgtttgtgaaactgaagagctgcaggcctgactctaggtttgcatcattgcagccggtttccaatcagattgagcgctgtaactctttagcatttggaggctacttaagtgaagtagtagaagaaaatactccaccaaaaatggaaaaagaaggcttggagataatgattgggaagaagaaaggcatccagggtcattacaattcttgttacttagactcaaccttattctgcttatttgcttttagttctgttctggacactgtgttacttagacccaaagaaaagaacgatgtagaatattatagtgaaacccaagagctactgaggacagaaattgttaatcctctgagaatatatggatatgtgtgtgccacaaaaattatgaaactgaggaaaatacttgaaaaggtggaggctgcatcaggatttacctctgaagaaaaagatcctgaggaattcttgaatattctgtttcatcatattttaagggtagaacctttgctaaaaataagatcagcaggtcaaaaggtacaagattgttacttctatcaaatttttatggaaaaaaatgagaaagttggcgttcccacaattcagcagttgttagaatggtcttttatcaacagtaacctgaaatttgcagaggcaccatcatgtctgattattcagatgcctcgatttggaaaagactttaaactatttaaaaaaatttttccttctctggaattaaatataacagatttacttgaagacactcccagacagtgccggatatgtggagggcttgcaatgtatgagtgtagagaatgctacgacgatccggacatctcagctggaaaaatcaagcagttttgtaaaacctgcaacactcaagtccaccttcatccgaagaggctgaatcataaatataacccagtgtcacttcccaaagacttacccgactgggactggagacacggctgcatcccttgccagaatatggagttatttgctgttctctgcatagaaacaagccactatgttgcttttgtgaagtatgggaaggacgattctgcctggctcttctttgacagcatggccgatcgggatggtggtcagaatggcttcaacattcctcaagtcaccccatgcccagaagtaggagagtacttgaagatgtctctggaagacctgcattccttggactccaggagaatccaaggctgtgcacgaagactgctttgtgatgcatatatgtgcatgtaccagagtccaacaatgagtttgtacaaataactggggtcatcgggaaaggcaaagaaactgaaggcagagtcctaacgttgcatcttattcgagctggcagttctgttcacgtccattgccggcaatggatgtctttgtggtgatgatccttcagaaaaggatgcctctgtttaaaaacaaattgcttttgtgtccctgaagtatttaataagaagcattttgcactctagaaagtatgtttgtgttggttttttaagaagtctaaatgaagttattaatacctgaagctttaagttaagtgcattgatcatatgatatttttggaagcatacaattttaattgtggaagtttaaagcctcttttagtccattgagaatgtaaataaatgtgtcttctttatggaccaaggatatgaaatcatttttcttttgtagctaacggttgccttgaggaagaaataatttggttttattaagagtctactctcaatccagttattagagatgtactgagtttgatttgttaatcctttctatatactgctgatcttgcatgtctacaatctgctcagtttttctgtgtttctgcaatagtggtcagaaaaatacttaaattcccttaatggtgttgttttctatttgttctggttttgagataaatgagtgattctgtccccaaatgtccatttttgaagtgattttcctggaggattagggtatttagcagttgaagctcttcattcatagtagttactgtcagctaacaggttttttaaggcttttaactattaatattttatggaatggggcaaagtaaattgatgaaagaattggagtgataatagtcctttacaaacatacagtccataagaaaatgaatttggcatatagaattattacaatttcctgggagagatggatatttaaacctctattattttagacaagactgtctagaacttaagtttgatctgtcagccagtactcccattaaattcagtgtagtttcacttgatagaatcagatatgttatcgaaatgttagcagcagcttcatcctccttctgattaaagtaagtagaaatgggatgttttgtttaataacagccatagtgtgtgtttagaccacagcggatgttgtagaccaggaccatagatgatacatgtcagtgctgtggaatgtgcattctctgagtgttgttttgtggtatcattgtctttcctgaatgactttctaactgtgcagaaaggcagaaaagtcatcatatgtatatgtcatatgactttataaaatatttaatgtgacaaaaagtggaaagaatctttacaaaccctgcaattacttttttaaaggcacttttactctttggttttatcattccattttgctaatatttactagctttataaattacagtaaggtacaaaaactcatcttgtaatattttcatttttgaagtgaaaaagtacatatattttgcacaaggttttatactgctaagtgcttggttggggtggtgagatgatgattagatcaggggtgaggctgagagactctgggtttagggctagccctgcctccatctcccttgggtaaaatgaagggtgtggggtaaaagatgcataaggccttttctagctctgacagcctagaagtccaatcaccctgtaataaatatgtgttgaatgaagaaatgggtgaatgagcttgtcaatgtgattttaaaaaattgactacctggaggaatgattaggaatctaaatgaagccagccctcggtatctgcaggtttctcatccatggattcaaccaactgcaaatggaaaatacgattttttttaaaaaaaggatggttacatccgtattgaacatgtacagacttttttcttgtcattattctctgaacaatacaagaactctttatgtagcatttacatttattaggtattataagtaatctagagattatttaattaaaatatacaggaggatgtgtgtcagttatatgcaaattctgtaccattttgtatcagggaattgagcatcttcagatgttggtatctgcagggatcctggaaccaaacccctgcagatactaagggctgacgatctaggtaagactggatttaacagttggaaaaaaaaaaaaaaaaggagagagaagacagttcctttcctgtagaaattaaaacaaaatacaaattgaggaagctctgctacccaggctgtcatggtagagaacttgaagaagacctgtttggatggacacctggtttcaaaagtcaggtgtggagactgttaaatgggagggcctcatccataaatgatttctggcaacgtcttcttcaggtggagcttgacgtctttttaatgttacttggggagggagtgctcattaagggatgccagggccagctctggtggttcctggggaggctgcgtccttccctgcttctgcatgtcatgaggcagcaggaaggtttcccctgcacctgtctgtcctggctccctctgggtagccccctactgttctgtgcttcagcacagcctggtttgtcaagaggcacatagttggggctgggctgcatggcacaggggcttatgtgcctgctggttatttaattttcagccttaagttttctttaatattttcctgttggctatttaaaggttttggttatcttttattccttatctacaatcaagatgacaatgtaattgaattatcttatttataacacggttcgtgattcatgattcatgattacaagtagaaaatatgtcatgttcctcacctccaaataaatatgtgtgtgtctgtgtgtgtgtatatatgtatgtggcggagagggagagagtggggaaggagagcagtgttatcatacatagagaggctaaatgtgtcccatccctcactgtcagctttataaaggagtttgactccatccacagaagaatgttttataagactaggaaaacacgttgaaaactaggataaacagcaacaaaaatcaactaaatatgttgttactgttgctaaggattttctccttagaataatttaggatttttaaaaatttctgtttgccaaatgctgtagataaatggccagattcttcctatccctaggattcctttattattttttttcacagattttgagaacaagggggagagatagtatggaagattaagattccattaatcttatagaactgtgttgtcacccaaattcctgcttgtttgaacatggcatcttcatagattcaggattcactaccctctatagctggatcttgaaaattatctggccagataattttgcatctgcttggatgattgtagactgagatgtgagtggaggataaagtattagacttttgctgagtaactgccaaccaagaagtatttatcggacacttactaggtgcctaggattgtatcagagggaatatgaaatgtgtccctgccctacctagttttaacgacagaatatctattaaaggctacttagctgaagggtaagggtgacaggtctaggggaagctttgggaggtggtgtgctgtgacagaaaaagtggcagagtagggacgagagacctgcattctagccctgtttctgtcacttgctctgtacacttagacaacagcttgacctcttgagctttagtttcctcctctgcataatgagagggttagactactgaattgtatgggaaaaaaatacaaattcctgggtcctaggccatgcctgctgaatccgactgttcaggaagaggcctaggaaatctgtgagggaatccccaggggaatctcgtgaccagccaggtgtgaaatctgctaactggaagatctcaaagcttccttcactttttgtgattttgtggtcatgtaacgttactgtattattctacgtaaatgtgggtacttggatgtttatcatactgtttctctgtgtttacatactaatttgtgtaagaaatgcattttagtctgtgtacctcaacctgctgtttgtttcctagaggtgttagtagtctttaaatacaagtaagacttaagaggatatttgatgttatttacctggatattttcttccccttttatttatttagaggaaattgagattctaggagccaaaaaaatgaaaacaaaattctaaggcaaagttaaagaaaaaaattacattatttcttaccatttgctactttataatgaaaatttaaaaattatatgggaagatttttctctgggataacaaatccttgtcataaagtaagaggtctttttaaagtaggtaggctataaggcctgtaatttaaaataatactcctttctctagggtttggtgcaattctccattaatgaagataacatttgaattccccaaagcaggtgaggagtcggggaggagaaagcgatgttaaaatgaaaactcactgcaaaagaggaggcagaggaagaaggaatgtaaaccccttaaagcagatgtgtgtggggccttatgaagaccaggattctgcgggtgtcaggggattgcccctcttgacagagactagggttttagactgaggcttcctgcagggtgttcgcattgcccttctccgttccccttcagacctttctggggagaagaggtgggaggaggggagaaagactgttcatcttattctgaatcctggagcagctgaaggttttctcttgagtcaggatgcagtggtaatgcattaaccagcaagtgtggccaaggataatgaaaaagtgggaaaggaaggtcctcctcctccctgattgtagcatccagcagtctctgtagccaggttactcaagaaccacatttgatttcctggccctttgccttggcagtgatggcatttttatttcactgtgttttaaagtcttcatttatttttataacatgggttagggagaagggccacaaatggagggattgtcctttcaagcaccacagcttcagataaaattagtactttcaaatattgtccactttaacttaaaaaattctagagggattatattggagactcaactgcccttggttttagtttataaaatggcctagtactgtggaattttaattttagaaagtcttagcatcagatcataaacattcattaaaagaactcacatcccatctgaaacttcccaggggagttgggattcttagtagattggtagaaaggggctcattttctactgcatttcccatttttggtatcttgttcagcatgttttatttttatttcttgtctgcagaacatcctatatttatgagaacattctttaagaagaccaccacatagaataccccttcctatcagctcgctctgatttagccttaattttgttaaattttttagagatgaatgaagtgctgctgtggaaagaaatgtacatatactatttctgtatcattaaaattacatttttatggttcaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:1540 -> Molecular function: GO:0004221 [ubiquitin thiolesterase activity] evidence: IEA
GeneID:1540 -> Molecular function: GO:0004843 [ubiquitin-specific protease activity] evidence: IDA
GeneID:1540 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:1540 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IDA
GeneID:1540 -> Molecular function: GO:0019901 [protein kinase binding] evidence: IPI
GeneID:1540 -> Molecular function: GO:0070064 [proline-rich region binding] evidence: IPI
GeneID:1540 -> Biological process: GO:0006511 [ubiquitin-dependent protein catabolic process] evidence: IEA
GeneID:1540 -> Biological process: GO:0006917 [induction of apoptosis] evidence: IDA
GeneID:1540 -> Biological process: GO:0007049 [cell cycle] evidence: IEA
GeneID:1540 -> Biological process: GO:0007346 [regulation of mitotic cell cycle] evidence: IMP
GeneID:1540 -> Biological process: GO:0016055 [Wnt receptor signaling pathway] evidence: IEA
GeneID:1540 -> Biological process: GO:0032088 [negative regulation of NF-kappaB transcription factor activity] evidence: IDA
GeneID:1540 -> Biological process: GO:0032480 [negative regulation of type I interferon production] evidence: TAS
GeneID:1540 -> Biological process: GO:0035872 [nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway] evidence: TAS
GeneID:1540 -> Biological process: GO:0042347 [negative regulation of NF-kappaB import into nucleus] evidence: IDA
GeneID:1540 -> Biological process: GO:0045087 [innate immune response] evidence: TAS
GeneID:1540 -> Biological process: GO:0070423 [nucleotide-binding oligomerization domain containing signaling pathway] evidence: TAS
GeneID:1540 -> Biological process: GO:0070507 [regulation of microtubule cytoskeleton organization] evidence: IMP
GeneID:1540 -> Biological process: GO:0070536 [protein K63-linked deubiquitination] evidence: IDA
GeneID:1540 -> Biological process: GO:0090090 [negative regulation of canonical Wnt receptor signaling pathway] evidence: IMP
GeneID:1540 -> Biological process: GO:2001238 [positive regulation of extrinsic apoptotic signaling pathway] evidence: IMP
GeneID:1540 -> Cellular component: GO:0005829 [cytosol] evidence: IDA
GeneID:1540 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
GeneID:1540 -> Cellular component: GO:0005881 [cytoplasmic microtubule] evidence: IDA
GeneID:1540 -> Cellular component: GO:0030496 [midbody] evidence: IDA
GeneID:1540 -> Cellular component: GO:0031234 [extrinsic to internal side of plasma membrane] evidence: IDA
GeneID:1540 -> Cellular component: GO:0048471 [perinuclear region of cytoplasm] evidence: IEA
ANNOTATIONS from NCBI Entrez Gene (20130726):
NP_001035814 -> EC 3.4.19.12
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@meso_cacase at
DBCLS
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