2024-04-26 17:43:01, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001258005 1510 bp mRNA linear PRI 01-JUL-2013 DEFINITION Homo sapiens chitinase, acidic (CHIA), transcript variant 9, mRNA. ACCESSION NM_001258005 VERSION NM_001258005.1 GI:384367987 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 1510) AUTHORS Di Rosa,M., De Gregorio,C., Malaguarnera,G., Tuttobene,M., Biazzo,F. and Malaguarnera,L. TITLE Evaluation of AMCase and CHIT-1 expression in monocyte macrophages lineage JOURNAL Mol. Cell. Biochem. 374 (1-2), 73-80 (2013) PUBMED 23129258 REMARK GeneRIF: results showed that the expression of AMCase and CHIT-1 were differently modulated in monocyte macrophages at different stage of maturation. The behavior of these two active chitinase suggests that in the immune response their role is complementary. REFERENCE 2 (bases 1 to 1510) AUTHORS Aminuddin,F., Akhabir,L., Stefanowicz,D., Pare,P.D., Connett,J.E., Anthonisen,N.R., Fahy,J.V., Seibold,M.A., Burchard,E.G., Eng,C., Gulsvik,A., Bakke,P., Cho,M.H., Litonjua,A., Lomas,D.A., Anderson,W.H., Beaty,T.H., Crapo,J.D., Silverman,E.K. and Sandford,A.J. TITLE Genetic association between human chitinases and lung function in COPD JOURNAL Hum. Genet. 131 (7), 1105-1114 (2012) PUBMED 22200767 REMARK GeneRIF: study demonstrated genetic associations between chitinase gene variants and lung function level and rate of decline in chronic obstructive pulmonary disease patients from the Lung Health Study; also functional effect of the rs3818822 polymorphism on AMCase levels and activity was demonstrated REFERENCE 3 (bases 1 to 1510) AUTHORS Birben,E., Sackesen,C., Kazani,S., Tincer,G., Karaaslan,C., Durgunsu,B., Gursel,I., Wechsler,M.E., Israel,E. and Kalayci,O. TITLE The effects of an insertion in the 5'UTR of the AMCase on gene expression and pulmonary functions JOURNAL Respir Med 105 (8), 1160-1169 (2011) PUBMED 21511453 REMARK GeneRIF: A ten base pair insertion in the second exon in the 5'UTR region of the AMCase gene may modify the gene expression and thus may affect the severity of asthma. REFERENCE 4 (bases 1 to 1510) AUTHORS Gu,Z., Cao,Z. and Jin,M. TITLE Expression and role of acidic mammalian chitinase and eotaxin-3 in chronic rhinosinusitis with nasal polyps JOURNAL J Otolaryngol Head Neck Surg 40 (1), 64-69 (2011) PUBMED 21303604 REMARK GeneRIF: AMCase and eotaxin-3 may be important mediators in the pathogenesis of nasal polyps. The increased AMCase and eotaxin-3 might lead to nasal polyp formation and growth. REFERENCE 5 (bases 1 to 1510) AUTHORS Park,S.K., Heo,K.W., Hur,D.Y. and Yang,Y.I. TITLE Chitinolytic activity in nasal polyps JOURNAL Am J Rhinol Allergy 25 (1), 12-14 (2011) PUBMED 21711963 REMARK GeneRIF: increased chitinolytic activity in nasal polyps REFERENCE 6 (bases 1 to 1510) AUTHORS Chou,Y.T., Yao,S., Czerwinski,R., Fleming,M., Krykbaev,R., Xuan,D., Zhou,H., Brooks,J., Fitz,L., Strand,J., Presman,E., Lin,L., Aulabaugh,A. and Huang,X. TITLE Kinetic characterization of recombinant human acidic mammalian chitinase JOURNAL Biochemistry 45 (14), 4444-4454 (2006) PUBMED 16584180 REMARK GeneRIF: human AMCase has only one pH optimum for k(cat)/K(m) between pH 4 and 5. Steady state kinetics shows that human AMCase has 'low' intrinsic transglycosidase activity, which leads to the observation of apparent substrate inhibition. REFERENCE 7 (bases 1 to 1510) AUTHORS Zhu,Z., Zheng,T., Homer,R.J., Kim,Y.K., Chen,N.Y., Cohn,L., Hamid,Q. and Elias,J.A. TITLE Acidic mammalian chitinase in asthmatic Th2 inflammation and IL-13 pathway activation JOURNAL Science 304 (5677), 1678-1682 (2004) PUBMED 15192232 REMARK GeneRIF: expressed in exaggerated quantities in human asthma REFERENCE 8 (bases 1 to 1510) AUTHORS Goto,M., Fujimoto,W., Nio,J., Iwanaga,T. and Kawasaki,T. TITLE Immunohistochemical demonstration of acidic mammalian chitinase in the mouse salivary gland and gastric mucosa JOURNAL Arch. Oral Biol. 48 (10), 701-707 (2003) PUBMED 12971947 REFERENCE 9 (bases 1 to 1510) AUTHORS Boot,R.G., Blommaart,E.F., Swart,E., Ghauharali-van der Vlugt,K., Bijl,N., Moe,C., Place,A. and Aerts,J.M. TITLE Identification of a novel acidic mammalian chitinase distinct from chitotriosidase JOURNAL J. Biol. Chem. 276 (9), 6770-6778 (2001) PUBMED 11085997 REFERENCE 10 (bases 1 to 1510) AUTHORS Saito,A., Ozaki,K., Fujiwara,T., Nakamura,Y. and Tanigami,A. TITLE Isolation and mapping of a human lung-specific gene, TSA1902, encoding a novel chitinase family member JOURNAL Gene 239 (2), 325-331 (1999) PUBMED 10548734 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK290702.1, AB025008.1, AF290004.1, AY911311.1, AL356387.16 and BC036339.1. Summary: The protein encoded by this gene degrades chitin, which is found in the cell wall of most fungi as well as in arthropods and some nematodes. The encoded protein can also stimulate interleukin 13 expression, and variations in this gene can lead to asthma susceptibility. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]. Transcript Variant: This variant (9) lacks exons and contains another exon in the 5' coding region, initiating translation at a downstream AUG compared to variant 4. The encoded isoform (b, also known as TSA1902-S) has a shorter N-terminus and lacks a signal peptide compared to isoform c. Variants 3, 6, 8, and 9 all encode the same isoform (b). 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## CDS exon combination :: AY911311.1, AY911310.1 [ECO:0000331] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-10 AK290702.1 1-10 11-64 AB025008.1 1-54 65-164 AF290004.1 1-100 165-367 AY911311.1 1-203 368-368 AL356387.16 4433-4433 369-952 AY911311.1 205-788 953-1510 BC036339.1 795-1352 FEATURES Location/Qualifiers source 1..1510 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="1" /map="1p13.2" gene 1..1510 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /note="chitinase, acidic" /db_xref="GeneID:27159" /db_xref="HGNC:17432" /db_xref="MIM:606080" exon 1..99 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /inference="alignment:Splign:1.39.8" variation 16..18 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="" /replace="ct" /db_xref="dbSNP:34698010" variation 16..17 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="" /replace="ct" /db_xref="dbSNP:374234404" variation 22 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:116488064" variation 44 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:12026825" variation 72 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:149411814" variation 75 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="g" /db_xref="dbSNP:146385552" variation 88 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:139768111" variation 97 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:142723581" exon 100..192 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /inference="alignment:Splign:1.39.8" variation 103 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="g" /db_xref="dbSNP:193167990" variation 123 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="g" /replace="t" /db_xref="dbSNP:376415475" variation 126 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:367796033" variation 131 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="g" /replace="t" /db_xref="dbSNP:371120238" variation 134 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:200693541" variation 136..137 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="" /replace="aagcc" /db_xref="dbSNP:201649523" variation 137..138 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="" /replace="agccaatct" /db_xref="dbSNP:200345479" variation 138..139 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="" /replace="gccaatctag" /db_xref="dbSNP:143789088" variation 140..141 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="" /replace="caatctaggc" /db_xref="dbSNP:375930070" variation 146 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:374220212" variation 151 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="g" /replace="t" /db_xref="dbSNP:201988572" variation 155 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="g" /replace="t" /db_xref="dbSNP:17027394" variation 163 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:376159900" variation 165 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:200929969" variation 166 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:373861430" variation 170 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="g" /db_xref="dbSNP:368020028" variation 178 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="g" /replace="t" /db_xref="dbSNP:371398270" variation 182 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:200053948" variation 185 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:375003916" exon 193..222 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /inference="alignment:Splign:1.39.8" exon 223..279 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /inference="alignment:Splign:1.39.8" variation 226 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:368828123" variation 233 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="c" /db_xref="dbSNP:143910053" variation 262 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:147282128" variation 269 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:3818822" variation 279 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:201556508" exon 280..418 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /inference="alignment:Splign:1.39.8" variation 368 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:2786156" variation 407 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:72693264" misc_feature 416..418 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /note="upstream in-frame stop codon" exon 419..543 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /inference="alignment:Splign:1.39.8" CDS 422..1369 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /EC_number="3.2.1.14" /note="isoform b is encoded by transcript variant 9; acidic mammalian chitinase; lung-specific protein TSA1902" /codon_start=1 /product="acidic mammalian chitinase isoform b" /protein_id="NP_001244934.1" /db_xref="GI:384367988" /db_xref="CCDS:CCDS58017.1" /db_xref="GeneID:27159" /db_xref="HGNC:17432" /db_xref="MIM:606080" /translation="
MREAFEQEAKQINKPRLMVTAAVAAGISNIQSGYEIPQLSQYLDYIHVMTYDLHGSWEGYTGENSPLYKYPTDTGSNAYLNVDYVMNYWKDNGAPAEKLIVGFPTYGHNFILSNPSNTGIGAPTSGAGPAGPYAKESGIWAYYEICTFLKNGATQGWDAPQEVPYAYQGNVWVGYDNIKSFDIKAQWLKHNKFGGAMVWAIDLDDFTGTFCNQGKFPLISTLKKALGLQSASCTAPAQPIEPITAAPSGSGNGSGSSSSGGSSGGSGFCAVRANGLYPVANNRNAFWHCVNGVTYQQNCQAGLVFDTSCDCCNWA
" misc_feature <422..1099 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /note="The GH18 (glycosyl hydrolase, family 18) type II chitinases hydrolyze chitin, an abundant polymer of beta-1,4-linked N-acetylglucosamine (GlcNAc) which is a major component of the cell wall of fungi and the exoskeleton of arthropods. Chitinases have...; Region: GH18_chitinase-like; cl10447" /db_xref="CDD:209141" misc_feature <422..1033 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /note="Glyco_18 domain; Region: Glyco_18; smart00636" /db_xref="CDD:197811" misc_feature 1223..1366 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /note="Chitin-binding domain type 2; Region: ChtBD2; smart00494" /db_xref="CDD:197759" variation 425 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:139158262" variation 440 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:199860140" variation 443 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="g" /replace="t" /db_xref="dbSNP:143586120" variation 453 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:144679403" variation 455 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="t" /db_xref="dbSNP:116430435" variation 460 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="c" /db_xref="dbSNP:200617710" variation 480 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:377181497" variation 503 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:369860168" variation 518 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:199874052" variation 533 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="" /replace="c" /db_xref="dbSNP:150563512" exon 544..667 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /inference="alignment:Splign:1.39.8" variation 550 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="g" /replace="t" /db_xref="dbSNP:140904700" variation 562 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:368843945" variation 574 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:148384495" variation 575 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:200134913" variation 631 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:369614927" variation 633 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:376497990" variation 638 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:147103194" variation 643 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:143960572" variation 652 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:139759326" variation 653 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:142137716" variation 659 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="g" /db_xref="dbSNP:151297358" exon 668..853 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /inference="alignment:Splign:1.39.8" variation 691 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:114510939" variation 695 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="t" /db_xref="dbSNP:181434663" variation 722 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:367730751" variation 749 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="g" /replace="t" /db_xref="dbSNP:78293817" variation 754 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="c" /db_xref="dbSNP:139093708" variation 763 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:143107428" variation 765 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:371506503" variation 770 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:143732960" variation 786 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:150309903" variation 801 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:61748620" variation 811 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="g" /replace="t" /db_xref="dbSNP:61748619" variation 821 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:79500525" variation 827 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:139420194" variation 829 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:201390788" variation 840 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:150840174" variation 851 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:201266629" exon 854..973 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /inference="alignment:Splign:1.39.8" variation 861 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:142736771" variation 888 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:139812869" variation 894..895 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="" /replace="tgcccctcaggaag" /db_xref="dbSNP:151326722" variation 896 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:200566957" variation 898..899 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="" /replace="cctcaggaagtgcc" /db_xref="dbSNP:375881947" variation 912 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="" /replace="cctcaggaagtgcc" /db_xref="dbSNP:74706064" variation 931 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:144546962" variation 932 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:375947945" variation 934 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:17027410" variation 935 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:190772785" variation 937 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="g" /replace="t" /db_xref="dbSNP:144182515" variation 946 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:370020615" variation 952 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:182916944" variation 953 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:2275253" variation 960 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="g" /db_xref="dbSNP:189146821" variation 964 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:200092579" variation 968 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:374270214" exon 974..1115 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /inference="alignment:Splign:1.39.8" variation 999 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:2275254" variation 1006 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:151038298" variation 1007 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:201691527" variation 1008 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:374315938" variation 1010 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:142800191" variation 1020 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:373985805" variation 1035 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:141843885" variation 1051 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:76395847" variation 1067 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:36011905" variation 1081 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:368203516" variation 1089 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:143969273" variation 1094 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="g" /db_xref="dbSNP:147768976" variation 1099 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:2820092" variation 1100 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:371701062" variation 1103 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:12094378" exon 1116..1469 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /inference="alignment:Splign:1.39.8" variation 1123 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:372590829" variation 1130 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:140459744" variation 1144 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:199879175" variation 1153 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:377085074" variation 1156 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:150421495" variation 1158 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:145023911" variation 1159 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="t" /db_xref="dbSNP:187769579" variation 1170 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:144623576" variation 1178 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:199811046" variation 1179 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="g" /db_xref="dbSNP:141747675" variation 1184 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:138227985" variation 1204 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="c" /db_xref="dbSNP:376164222" variation 1210 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:35242709" variation 1214 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:149869566" variation 1233 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="g" /replace="t" /db_xref="dbSNP:2256721" variation 1246 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="c" /db_xref="dbSNP:369442393" variation 1253 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="c" /db_xref="dbSNP:368010768" variation 1254 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="g" /db_xref="dbSNP:143551303" variation 1256 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:138073907" variation 1275 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:201456008" variation 1279 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:368211379" variation 1315 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="g" /db_xref="dbSNP:145057685" variation 1324 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:140461957" variation 1325 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:142653250" variation 1364 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:146040153" variation 1386 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="a" /replace="g" /db_xref="dbSNP:373720681" variation 1391 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:139802202" variation 1403 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="c" /replace="t" /db_xref="dbSNP:372826781" variation 1408 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" /replace="g" /replace="t" /db_xref="dbSNP:141163072" polyA_signal 1445..1450 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" polyA_site 1469 /gene="CHIA" /gene_synonym="AMCASE; CHIT2; TSA1902" ORIGIN
aaagcttcatgaaacctcctcgtctgtgcacgaacaggtggccgactctggagcccaggctgttgctttccagtctggtggtgaatcctccatagtctgaagcctttgtgataaccacagaatcagaacatataaaaagctctgcgggactggtgctgactgcaaccatgacaaagcttattctcctcacaggtcttgtccttatactgaatttgcagctcggaacagccagctgaaaactctcctggccattggaggctggaacttcgggactgccccatgaggaaactaaagtacagagaggatttaagcaacttgcccaagatcacacaactagtaggaatcataacttcctctgcagtttggccacagagtccattgcttctaagcattacactaggctgcccgttattactgagaaatgcgtgaagcttttgagcaggaggccaagcagatcaacaagcccaggctgatggtcactgctgcagtagctgctggcatctccaatatccagtctggctatgagatcccccaactgtcacagtacctggactacatccatgtcatgacctacgacctccatggctcctgggagggctacactggagagaacagccccctctacaaatacccgactgacaccggcagcaacgcctacctcaatgtggattatgtcatgaactactggaaggacaatggagcaccagctgagaagctcatcgttggattccctacctatggacacaacttcatcctgagcaacccctccaacactggaattggtgcccccacctctggtgctggtcctgctgggccctatgccaaggagtctgggatctgggcttactacgagatctgtaccttcctgaaaaatggagccactcagggatgggatgcccctcaggaagtgccttatgcctatcagggcaatgtgtgggttggctatgacaacatcaagagcttcgatattaaggctcaatggcttaagcacaacaaatttggaggcgccatggtctgggccattgatctggatgacttcactggcactttctgcaaccagggcaagtttcccctaatctccaccctgaagaaggccctcggcctgcagagtgcaagttgcacggctccagctcagcccattgagccaataactgctgctcccagtggcagcgggaacgggagcgggagtagcagctctggaggcagctcgggaggcagtggattctgtgctgtcagagccaacggcctctaccccgtggcaaataacagaaatgccttctggcactgcgtgaatggagtcacgtaccagcagaactgccaggccgggcttgtcttcgacaccagctgtgattgctgcaactgggcataaacctgacctggtctatattccctagagttccagtctcttttgcttaggacatgttgcccctacctaaagtcctgcaataaaatcagcagtcaaaacatgaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:27159 -> Molecular function: GO:0003796 [lysozyme activity] evidence: NAS GeneID:27159 -> Molecular function: GO:0004568 [chitinase activity] evidence: IDA GeneID:27159 -> Molecular function: GO:0004568 [chitinase activity] evidence: NAS GeneID:27159 -> Molecular function: GO:0008061 [chitin binding] evidence: TAS GeneID:27159 -> Molecular function: GO:0019900 [kinase binding] evidence: IPI GeneID:27159 -> Molecular function: GO:0030246 [carbohydrate binding] evidence: NAS GeneID:27159 -> Biological process: GO:0000272 [polysaccharide catabolic process] evidence: IEA GeneID:27159 -> Biological process: GO:0001101 [response to acid] evidence: TAS GeneID:27159 -> Biological process: GO:0002532 [production of molecular mediator involved in inflammatory response] evidence: IDA GeneID:27159 -> Biological process: GO:0006030 [chitin metabolic process] evidence: NAS GeneID:27159 -> Biological process: GO:0006032 [chitin catabolic process] evidence: IDA GeneID:27159 -> Biological process: GO:0006032 [chitin catabolic process] evidence: NAS GeneID:27159 -> Biological process: GO:0006037 [cell wall chitin metabolic process] evidence: TAS GeneID:27159 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA GeneID:27159 -> Biological process: GO:0006955 [immune response] evidence: NAS GeneID:27159 -> Biological process: GO:0007586 [digestion] evidence: NAS GeneID:27159 -> Biological process: GO:0009620 [response to fungus] evidence: TAS GeneID:27159 -> Biological process: GO:0090197 [positive regulation of chemokine secretion] evidence: IDA GeneID:27159 -> Cellular component: GO:0005615 [extracellular space] evidence: IC GeneID:27159 -> Cellular component: GO:0005615 [extracellular space] evidence: IDA GeneID:27159 -> Cellular component: GO:0005737 [cytoplasm] evidence: ISS GeneID:27159 -> Cellular component: GO:0005737 [cytoplasm] evidence: NAS ANNOTATIONS from NCBI Entrez Gene (20130726): NP_001244934 -> EC 3.2.1.14
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