2024-04-26 00:54:25, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_144687 3880 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens NLR family, pyrin domain containing 12 (NLRP12), transcript variant 2, mRNA. ACCESSION NM_144687 VERSION NM_144687.3 GI:459683879 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 3880) AUTHORS Zambetti,L.P., Laudisi,F., Licandro,G., Ricciardi-Castagnoli,P. and Mortellaro,A. TITLE The rhapsody of NLRPs: master players of inflammation...and a lot more JOURNAL Immunol. Res. 53 (1-3), 78-90 (2012) PUBMED 22427013 REMARK Review article REFERENCE 2 (bases 1 to 3880) AUTHORS Pinheiro,A.S., Eibl,C., Ekman-Vural,Z., Schwarzenbacher,R. and Peti,W. TITLE The NLRP12 pyrin domain: structure, dynamics, and functional insights JOURNAL J. Mol. Biol. 413 (4), 790-803 (2011) PUBMED 21978668 REMARK GeneRIF: The authors report the first in vitro confirmed non-homotypic interaction between NLRP12 pyrin domain and the pro-apoptotic protein Fas-associated factor 1 (FAF-1), which links the innate immune system to apoptotic signaling. REFERENCE 3 (bases 1 to 3880) AUTHORS Jeru,I., Le Borgne,G., Cochet,E., Hayrapetyan,H., Duquesnoy,P., Grateau,G., Morali,A., Sarkisian,T. and Amselem,S. TITLE Identification and functional consequences of a recurrent NLRP12 missense mutation in periodic fever syndromes JOURNAL Arthritis Rheum. 63 (5), 1459-1464 (2011) PUBMED 21538323 REMARK GeneRIF: NLRP12 missense mutation in periodic fever syndromes; study provides evidence of deleterious effect of an NLRP12 missense mutation; this newly identified molecular defect emphasizes the crucial role played by NLRP12 in autoinflammation REFERENCE 4 (bases 1 to 3880) AUTHORS Borghini,S., Tassi,S., Chiesa,S., Caroli,F., Carta,S., Caorsi,R., Fiore,M., Delfino,L., Lasiglie,D., Ferraris,C., Traggiai,E., Di Duca,M., Santamaria,G., D'Osualdo,A., Tosca,M., Martini,A., Ceccherini,I., Rubartelli,A. and Gattorno,M. TITLE Clinical presentation and pathogenesis of cold-induced autoinflammatory disease in a family with recurrence of an NLRP12 mutation JOURNAL Arthritis Rheum. 63 (3), 830-839 (2011) PUBMED 21360512 REMARK GeneRIF: Even with a variable range of associated manifestations, the extreme sensitivity to cold represents the main clinical hallmark in an individual carrying the p.D294E mutation of the NLRP12 gene. REFERENCE 5 (bases 1 to 3880) AUTHORS Lich,J.D., Williams,K.L., Moore,C.B., Arthur,J.C., Davis,B.K., Taxman,D.J. and Ting,J.P. TITLE Monarch-1 suppresses non-canonical NF-kappaB activation and p52-dependent chemokine expression in monocytes JOURNAL J. Immunol. 178 (3), 1256-1260 (2007) PUBMED 17237370 REMARK GeneRIF: Monarch-1 inhibits CD40-mediated activation of NF-kappaB via the non-canonical pathway in human monocytes. This inhibition stems from the ability of Monarch-1 to associate with and induce proteasome-mediated degradation of NF-kappaB inducing kinase REFERENCE 6 (bases 1 to 3880) AUTHORS Williams,K.L., Lich,J.D., Duncan,J.A., Reed,W., Rallabhandi,P., Moore,C., Kurtz,S., Coffield,V.M., Accavitti-Loper,M.A., Su,L., Vogel,S.N., Braunstein,M. and Ting,J.P. TITLE The CATERPILLER protein monarch-1 is an antagonist of toll-like receptor-, tumor necrosis factor alpha-, and Mycobacterium tuberculosis-induced pro-inflammatory signals JOURNAL J. Biol. Chem. 280 (48), 39914-39924 (2005) PUBMED 16203735 REMARK GeneRIF: Monarch-1 associates with IRAK-1 but not MyD88, resulting in the blockage of IRAK-1 hyperphosphorylation REFERENCE 7 (bases 1 to 3880) AUTHORS Williams,K.L., Taxman,D.J., Linhoff,M.W., Reed,W. and Ting,J.P. TITLE Cutting edge: Monarch-1: a pyrin/nucleotide-binding domain/leucine-rich repeat protein that controls classical and nonclassical MHC class I genes JOURNAL J. Immunol. 170 (11), 5354-5358 (2003) PUBMED 12759408 REMARK GeneRIF: Monarch-1 enhances nonclassical and classical major histocompatibility complex class I expression at the level of the promoter, RNA, and protein expression. REFERENCE 8 (bases 1 to 3880) AUTHORS Tschopp,J., Martinon,F. and Burns,K. TITLE NALPs: a novel protein family involved in inflammation JOURNAL Nat. Rev. Mol. Cell Biol. 4 (2), 95-104 (2003) PUBMED 12563287 REMARK Review article REFERENCE 9 (bases 1 to 3880) AUTHORS Wang,L., Manji,G.A., Grenier,J.M., Al-Garawi,A., Merriam,S., Lora,J.M., Geddes,B.J., Briskin,M., DiStefano,P.S. and Bertin,J. TITLE PYPAF7, a novel PYRIN-containing Apaf1-like protein that regulates activation of NF-kappa B and caspase-1-dependent cytokine processing JOURNAL J. Biol. Chem. 277 (33), 29874-29880 (2002) PUBMED 12019269 REMARK GeneRIF: regulates activation of NF-kappa B and caspase-1-dependent cytokine processing REFERENCE 10 (bases 1 to 3880) AUTHORS Shami,P.J., Kanai,N., Wang,L.Y., Vreeke,T.M. and Parker,C.H. TITLE Identification and characterization of a novel gene that is upregulated in leukaemia cells by nitric oxide JOURNAL Br. J. Haematol. 112 (1), 138-147 (2001) PUBMED 11167794 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DA619102.1, AY154467.1 and BC028069.1. On Mar 9, 2013 this sequence version replaced gi:188497620. Summary: This gene encodes a member of the CATERPILLER family of cytoplasmic proteins. The encoded protein, which contains an N-terminal pyrin domain, a NACHT domain, a NACHT-associated domain, and a C-terminus leucine-rich repeat region, functions as an attenuating factor of inflammation by suppressing inflammatory responses in activated monocytes. Mutations in this gene cause familial cold autoinflammatory syndrome type 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]. Transcript Variant: This variant (2) uses an alternate splice site in the central coding region, compared to variant 3, resulting in an isoform (2) that is 1 aa shorter than isoform 3. 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 :: AY095146.1, BC028069.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025089 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-65 DA619102.1 1-65 66-2697 AY154467.1 13-2644 2698-3580 BC028069.1 2588-3470 3581-3880 AY154467.1 3528-3827 FEATURES Location/Qualifiers source 1..3880 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="19" /map="19q13.42" gene 1..3880 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /note="NLR family, pyrin domain containing 12" /db_xref="GeneID:91662" /db_xref="HGNC:22938" /db_xref="HPRD:14803" /db_xref="MIM:609648" exon 1..518 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /inference="alignment:Splign:1.39.8" misc_feature 179..181 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /note="upstream in-frame stop codon" CDS 230..3415 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /note="isoform 2 is encoded by transcript variant 2; nucleotide-binding oligomerization domain, leucine rich repeat and pyrin domain containing 12; NACHT, LRR and PYD domains-containing protein 12; PYRIN-containing APAF1-like protein 7; monarch 1; regulated by nitric oxide" /codon_start=1 /product="NACHT, LRR and PYD domains-containing protein 12 isoform 2" /protein_id="NP_653288.1" /db_xref="GI:21955154" /db_xref="CCDS:CCDS12864.1" /db_xref="GeneID:91662" /db_xref="HGNC:22938" /db_xref="HPRD:14803" /db_xref="MIM:609648" /translation="
MLRTAGRDGLCRLSTYLEELEAVELKKFKLYLGTATELGEGKIPWGSMEKAGPLEMAQLLITHFGPEEAWRLALSTFERINRKDLWERGQREDLVRDTPPGGPSSLGNQSTCLLEVSLVTPRKDPQETYRDYVRRKFRLMEDRNARLGECVNLSHRYTRLLLVKEHSNPMQVQQQLLDTGRGHARTVGHQASPIKIETLFEPDEERPEPPRTVVMQGAAGIGKSMLAHKVMLDWADGKLFQGRFDYLFYINCREMNQSATECSMQDLIFSCWPEPSAPLQELIRVPERLLFIIDGFDELKPSFHDPQGPWCLCWEEKRPTELLLNSLIRKKLLPELSLLITTRPTALEKLHRLLEHPRHVEILGFSEAERKEYFYKYFHNAEQAGQVFNYVRDNEPLFTMCFVPLVCWVVCTCLQQQLEGGGLLRQTSRTTTAVYMLYLLSLMQPKPGAPRLQPPPNQRGLCSLAADGLWNQKILFEEQDLRKHGLDGEDVSAFLNMNIFQKDINCERYYSFIHLSFQEFFAAMYYILDEGEGGAGPDQDVTRLLTEYAFSERSFLALTSRFLFGLLNEETRSHLEKSLCWKVSPHIKMDLLQWIQSKAQSDGSTLQQGSLEFFSCLYEIQEEEFIQQALSHFQVIVVSNIASKMEHMVSSFCLKRCRSAQVLHLYGATYSADGEDRARCSAGAHTLLVQLPERTVLLDAYSEHLAAALCTNPNLIELSLYRNALGSRGVKLLCQGLRHPNCKLQNLRLKRCRISSSACEDLSAALIANKNLTRMDLSGNGVGFPGMMLLCEGLRHPQCRLQMIQLRKCQLESGACQEMASVLGTNPHLVELDLTGNALEDLGLRLLCQGLRHPVCRLRTLWLKICRLTAAACDELASTLSVNQSLRELDLSLNELGDLGVLLLCEGLRHPTCKLQTLRLGICRLGSAACEGLSVVLQANHNLRELDLSFNDLGDWGLWLLAEGLQHPACRLQKLWLDSCGLTAKACENLYFTLGINQTLTDLYLTNNALGDTGVRLLCKRLSHPGCKLRVLWLFGMDLNKMTHSRLAALRVTKPYLDIGC
" misc_feature 260..505 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /note="Pyrin death domain found in NALP proteins; Region: Pyrin_NALPs; cd08320" /db_xref="CDD:176735" misc_feature 863..1372 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /note="NACHT domain; Region: NACHT; pfam05729" /db_xref="CDD:191357" misc_feature 1910..2827 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /note="Leucine-rich repeats (LRRs), ribonuclease inhibitor (RI)-like subfamily. LRRs are 20-29 residue sequence motifs present in many proteins that participate in protein-protein interactions and have different functions and cellular locations. LRRs correspond...; Region: LRR_RI; cl15309" /db_xref="CDD:199167" misc_feature order(1913..1915,1922..1924,1928..1930,1970..1972, 1982..1984,1988..1990,1997..1999,2003..2005,2057..2059, 2066..2068,2072..2074,2081..2083,2087..2089,2144..2146, 2162..2164,2168..2170,2177..2179,2183..2185,2216..2218, 2225..2227,2231..2233,2240..2242,2246..2248,2288..2290, 2297..2299,2303..2305,2312..2314,2318..2320,2372..2374, 2381..2383,2387..2389,2396..2398,2402..2404,2459..2461, 2468..2470,2474..2476,2483..2485,2489..2491,2543..2545, 2552..2554,2558..2560,2567..2569,2573..2575,2630..2632, 2639..2641,2645..2647,2654..2656,2660..2662,2714..2716, 2723..2725,2729..2731,2738..2740,2744..2746,2801..2803, 2810..2812,2816..2818,2825..2827) /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /note="Leucine-rich repeats; other site" /db_xref="CDD:29015" misc_feature order(1991..1996,2174..2176,2309..2311,2393..2395, 2564..2566,2642..2644,2648..2650,2726..2728,2813..2815) /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /note="Substrate binding site [chemical binding]; other site" /db_xref="CDD:29015" misc_feature 2378..3334 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /note="Leucine-rich repeats (LRRs), ribonuclease inhibitor (RI)-like subfamily. LRRs are 20-29 residue sequence motifs present in many proteins that participate in protein-protein interactions and have different functions and cellular locations. LRRs correspond...; Region: LRR_RI; cd00116" /db_xref="CDD:29015" misc_feature order(2381..2383,2387..2389,2396..2398,2402..2404, 2459..2461,2468..2470,2474..2476,2483..2485,2489..2491, 2543..2545,2552..2554,2558..2560,2567..2569,2630..2632, 2639..2641,2645..2647,2654..2656,2660..2662,2714..2716, 2723..2725,2729..2731,2738..2740,2744..2746,2801..2803, 2810..2812,2816..2818,2825..2827,2831..2833,2885..2887, 2894..2896,2900..2902,2909..2911,2915..2917,2972..2974, 2981..2983,2987..2989,2996..2998,3002..3004,3056..3058, 3065..3067,3071..3073,3080..3082,3086..3088,3143..3145, 3152..3154,3158..3160,3167..3169,3173..3175,3227..3229, 3236..3238,3242..3244,3251..3253,3257..3259,3314..3316, 3323..3325,3329..3331) /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /note="Leucine-rich repeats; other site" /db_xref="CDD:29015" misc_feature order(2477..2482,2651..2653,2822..2824,2906..2908, 3077..3079,3155..3157,3161..3163,3239..3241,3326..3328) /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /note="Substrate binding site [chemical binding]; other site" /db_xref="CDD:29015" misc_feature 2711..2773 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (P59046.2); Region: LRR 1" misc_feature 2798..2863 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (P59046.2); Region: LRR 2" misc_feature 2882..2947 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (P59046.2); Region: LRR 3" misc_feature 2969..3034 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (P59046.2); Region: LRR 4" misc_feature 3053..3115 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (P59046.2); Region: LRR 5" misc_feature 3140..3205 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (P59046.2); Region: LRR 6" misc_feature 3224..3289 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (P59046.2); Region: LRR 7" misc_feature 3311..3376 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (P59046.2); Region: LRR 8" exon 519..599 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /inference="alignment:Splign:1.39.8" exon 600..2301 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /inference="alignment:Splign:1.39.8" variation 1581 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /replace="a" /replace="g" /db_xref="dbSNP:76085152" exon 2302..2472 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /inference="alignment:Splign:1.39.8" variation 2394 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /replace="a" /replace="g" /db_xref="dbSNP:199475868" variation 2467 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /replace="a" /replace="c" /db_xref="dbSNP:199475869" exon 2473..2643 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /inference="alignment:Splign:1.39.8" variation 2623 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /replace="a" /replace="g" /db_xref="dbSNP:4806773" exon 2644..2814 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /inference="alignment:Splign:1.39.8" variation 2668 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /replace="c" /replace="t" /db_xref="dbSNP:199475870" exon 2815..2985 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /inference="alignment:Splign:1.39.8" exon 2986..3156 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /inference="alignment:Splign:1.39.8" exon 3157..3327 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /inference="alignment:Splign:1.39.8" exon 3328..3880 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /inference="alignment:Splign:1.39.8" variation 3380 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /replace="c" /replace="t" /db_xref="dbSNP:199475871" variation 3541 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /replace="c" /replace="g" /db_xref="dbSNP:199475872" polyA_signal 3701..3706 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" polyA_site 3721 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /note="This is an internal polyA site. The 3'-most polyA site has not yet been determined." STS 3736..3838 /gene="NLRP12" /gene_synonym="CLR19.3; FCAS2; NALP12; PAN6; PYPAF7; RNO; RNO2" /standard_name="D11S2921" /db_xref="UniSTS:152074" ORIGIN
agaacagccattggtgagtggggcagggcaggagggaactgaagagtgagaaagcattatttcagcaaaaggtctttcctcccttgctctctcctccaaccactggctcagcctctccgcccgctgcctgtgaatgatgcaatggaaggtgtgctggggtcgccctgtgtcccgtgcataggagcatctcagcctccaggtcctctcctttggggctcacggcacccccatgctacgaaccgcaggcagggacggcctctgtcgcctgtccacctacttggaagaactcgaggctgtggaactgaagaagttcaagttatacctggggaccgcgacagagctgggagaaggcaagatcccctggggaagcatggagaaggccggtcccctggaaatggcccagctgctcatcacccacttcgggccagaggaggcctggaggttggctctcagcacctttgagcggataaacaggaaggacctgtgggagagaggacagagagaggacctggtgagggataccccacctggtggcccgtcctcacttgggaaccagtcaacatgccttctggaagtctctcttgtcactccaagaaaagatccccaggaaacctacagggactatgtccgcaggaaattccggctcatggaagaccgcaatgcgcgcctaggggaatgtgtcaacctcagccaccggtacacccggctcctgctggtgaaggagcactcaaaccccatgcaggtccagcagcagcttctggacacaggccggggacacgcgaggaccgtgggacaccaggctagccccatcaagatagagaccctctttgagccagacgaggagcgccccgagccaccgcgcaccgtggtcatgcaaggcgcggcagggataggcaagtccatgctggcacacaaggtgatgctggactgggcggacgggaagctcttccaaggcagatttgattatctcttctacatcaactgcagggagatgaaccagagtgccacggaatgcagcatgcaagacctcatcttcagctgctggcctgagcccagcgcgcctctccaggagctcatccgagttcccgagcgcctccttttcatcatcgacggcttcgatgagctcaagccttctttccacgatcctcagggaccctggtgcctctgctgggaggagaaacggcccacggagctgcttcttaacagcttaattcggaagaagctgctccctgagctatctttgctcatcaccacacggcccacggctttggagaagctccaccgtctgctggagcaccccaggcatgtggagatcctgggcttctctgaggcagaaaggaaggaatacttctacaagtatttccacaatgcagagcaggcgggccaagtcttcaattacgtgagggacaacgagcctctcttcaccatgtgcttcgtccccctggtgtgctgggtggtgtgtacctgcctccagcagcagctggagggtggggggctgttgagacagacgtccaggaccaccactgcagtgtacatgctctacctgctgagtctgatgcaacccaagccgggggccccgcgcctccagcccccacccaaccagagagggttgtgctccttggcggcagatgggctctggaatcagaaaatcctatttgaggagcaggacctccggaagcacggcctagacggggaagacgtctctgccttcctcaacatgaacatcttccagaaggacatcaactgtgagaggtactacagcttcatccacttgagtttccaggaattctttgcagctatgtactatatcctggacgagggggagggcggggcaggcccagaccaggacgtgaccaggctgttgaccgagtacgcgttttctgaaaggagcttcctggcactcaccagccgcttcctgtttggactcctgaacgaggagaccaggagccacctggagaagagtctctgctggaaggtctcgccgcacatcaagatggacctgttgcagtggatccaaagcaaagctcagagcgacggctccaccctgcagcagggctccttggagttcttcagctgcttgtacgagatccaggaggaggagtttatccagcaggccctgagccacttccaggtgatcgtggtcagcaacattgcctccaagatggagcacatggtctcctcgttctgtctgaagcgctgcaggagcgcccaggtgctgcacttgtatggcgccacctacagcgcggacggggaagaccgcgcgaggtgctccgcaggagcgcacacgctgttggtgcagctaccagagaggaccgttctgctggacgcctacagtgaacatctggcagcggccctgtgcaccaatccaaacctgatagagctgtctctgtaccgaaatgccctgggcagccggggggtgaagctgctctgtcaaggactcagacaccccaactgcaaacttcagaacctgaggctgaagaggtgccgcatctccagctcagcctgcgaggacctctctgcagctctcatagccaataagaatttgacaaggatggatctcagtggcaacggcgttggattcccaggcatgatgctgctttgcgagggcctgcggcatccccaatgcaggctgcagatgattcagttgaggaagtgtcagctggagtccggggcttgtcaggagatggcttctgtgctcggcaccaacccacatctggttgagttggacctgacaggaaatgcactggaggatttgggcctgaggttactatgccagggactgaggcacccagtctgcagactacggactttgtggctgaagatctgccgcctcactgctgctgcctgtgacgagctggcctcaactctcagtgtgaaccagagcctgagagagctggacctgagcctgaatgagctgggggacctcggggtgctgctgctgtgtgagggcctcaggcatcccacgtgcaagctccagaccctgcggttgggcatctgccggctgggctctgccgcctgtgagggtctttctgtggtgctccaggccaaccacaacctccgggagctggacttgagtttcaacgacctgggagactggggcctgtggttgctggctgaggggctgcaacatcccgcctgcagactccagaaactgtggctggatagctgtggcctcacagccaaggcttgtgagaatctttacttcaccctggggatcaaccagaccttgaccgacctttacctgaccaacaacgccctaggggacacaggtgtccgactgctttgcaagcggctgagccatcctggctgcaaactccgagtcctctggttatttgggatggacctgaataaaatgacccacagtaggttggcagcgcttcgagtaacaaaaccttatttggacattggctgctgaatggtcctatctgctggctctcccctgagatctggacagaggaagatgggagggtgctcatcacccccccagcataatgatcagcctccttcctagagacagactcatgcagattgagatcaaaagtccctctgcttgggatcaaattaatgtttgacagagctggccaggcgtggtggctcatgtatgtaatcctagcacttcgagaggccgaggcaggtggatcacgaggtcaggagtttgagattagcctggccaagatggtgaaaccctgtctctactaaaaataaaaaaaaattagccaggcatggtggcgggcacctgtagtcccagctactcaggaggctgaggcaggagaatcgcttgaacccgggaggtggaggttgcagtgagccgagatcgcgccactgcactccagcctgggcgacagagtgggactccatctcaaaaaaaaaaaaaaaaaaa
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:91662 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:91662 -> Molecular function: GO:0005524 [ATP binding] evidence: IEA GeneID:91662 -> Molecular function: GO:0008656 [cysteine-type endopeptidase activator activity involved in apoptotic process] evidence: NAS GeneID:91662 -> Biological process: GO:0006919 [activation of cysteine-type endopeptidase activity involved in apoptotic process] evidence: NAS GeneID:91662 -> Biological process: GO:0007165 [signal transduction] evidence: NAS GeneID:91662 -> Biological process: GO:0008588 [release of cytoplasmic sequestered NF-kappaB] evidence: IDA GeneID:91662 -> Biological process: GO:0009968 [negative regulation of signal transduction] evidence: IDA GeneID:91662 -> Biological process: GO:0031953 [negative regulation of protein autophosphorylation] evidence: IDA GeneID:91662 -> Biological process: GO:0032088 [negative regulation of NF-kappaB transcription factor activity] evidence: IDA GeneID:91662 -> Biological process: GO:0043124 [negative regulation of I-kappaB kinase/NF-kappaB cascade] evidence: IDA GeneID:91662 -> Biological process: GO:0045381 [regulation of interleukin-18 biosynthetic process] evidence: NAS GeneID:91662 -> Biological process: GO:0045409 [negative regulation of interleukin-6 biosynthetic process] evidence: IDA GeneID:91662 -> Biological process: GO:0045751 [negative regulation of Toll signaling pathway] evidence: IDA GeneID:91662 -> Biological process: GO:0050710 [negative regulation of cytokine secretion] evidence: IDA GeneID:91662 -> Biological process: GO:0050711 [negative regulation of interleukin-1 secretion] evidence: IDA GeneID:91662 -> Biological process: GO:0050718 [positive regulation of interleukin-1 beta secretion] evidence: NAS GeneID:91662 -> Biological process: GO:0050728 [negative regulation of inflammatory response] evidence: IMP GeneID:91662 -> Biological process: GO:0050729 [positive regulation of inflammatory response] evidence: NAS GeneID:91662 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
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