2024-04-26 01:26:16, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_005564 840 bp mRNA linear PRI 15-JUL-2013 DEFINITION Homo sapiens lipocalin 2 (LCN2), mRNA. ACCESSION NM_005564 VERSION NM_005564.3 GI:108936956 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 840) AUTHORS Jang,E., Lee,S., Kim,J.H., Kim,J.H., Seo,J.W., Lee,W.H., Mori,K., Nakao,K. and Suk,K. TITLE Secreted protein lipocalin-2 promotes microglial M1 polarization JOURNAL FASEB J. 27 (3), 1176-1190 (2013) PUBMED 23207546 REMARK GeneRIF: LCN2 is an M1-amplifier in brain microglial cells. REFERENCE 2 (bases 1 to 840) AUTHORS Liu,S., Che,M., Xue,S., Xie,B., Zhu,M., Lu,R., Zhang,W., Qian,J. and Yan,Y. TITLE Urinary L-FABP and its combination with urinary NGAL in early diagnosis of acute kidney injury after cardiac surgery in adult patients JOURNAL Biomarkers 18 (1), 95-101 (2013) PUBMED 23167703 REMARK GeneRIF: Urinary L-FABP and NGAL increased at an early stage after cardiac surgery. The combination of the two biomarkers enhanced the accuracy of the early detection of postoperative acute kidney injury after cardiac surgery before a rise in serum creatinine. REFERENCE 3 (bases 1 to 840) AUTHORS Volpe,V., Raia,Z., Sanguigno,L., Somma,D., Mastrovito,P., Moscato,F., Mellone,S., Leonardi,A. and Pacifico,F. TITLE NGAL controls the metastatic potential of anaplastic thyroid carcinoma cells JOURNAL J. Clin. Endocrinol. Metab. 98 (1), 228-235 (2013) PUBMED 23150684 REMARK GeneRIF: NGAL is a novel target of nuclear factor-kappaB prometastatic activity in thyroid cancer through enhancement of MMP-9 enzymatic activity. REFERENCE 4 (bases 1 to 840) AUTHORS Virzi,G.M., Clementi,A., de Cal,M., Cruz,D.N. and Ronco,C. TITLE Genomics and biological activity of neutrophil gelatinase-associated lipocalin in several clinical settings JOURNAL Blood Purif. 35 (1-3), 139-143 (2013) PUBMED 23343559 REMARK GeneRIF: The NGAL gene is a rapid response gene whose expression is driven in a dose-dependent manner by different stimuli which generally induce tissue damage. (Review) Review article REFERENCE 5 (bases 1 to 840) AUTHORS Sirota,J.C., Walcher,A., Faubel,S., Jani,A., McFann,K., Devarajan,P., Davis,C.L. and Edelstein,C.L. TITLE Urine IL-18, NGAL, IL-8 and serum IL-8 are biomarkers of acute kidney injury following liver transplantation JOURNAL BMC Nephrol 14, 17 (2013) PUBMED 23327592 REMARK GeneRIF: Serum IL-8 and urine IL-18, NGAL, IL-6, and IL-8 are elevated in AKI within the first 24 hours following liver transplantation. Publication Status: Online-Only REFERENCE 6 (bases 1 to 840) AUTHORS Blaser,J., Triebel,S. and Tschesche,H. TITLE A sandwich enzyme immunoassay for the determination of neutrophil lipocalin in body fluids JOURNAL Clin. Chim. Acta 235 (2), 137-145 (1995) PUBMED 7554268 REFERENCE 7 (bases 1 to 840) AUTHORS Bartsch,S. and Tschesche,H. TITLE Cloning and expression of human neutrophil lipocalin cDNA derived from bone marrow and ovarian cancer cells JOURNAL FEBS Lett. 357 (3), 255-259 (1995) PUBMED 7835423 REFERENCE 8 (bases 1 to 840) AUTHORS Chan,P., Simon-Chazottes,D., Mattei,M.G., Guenet,J.L. and Salier,J.P. TITLE Comparative mapping of lipocalin genes in human and mouse: the four genes for complement C8 gamma chain, prostaglandin-D-synthase, oncogene-24p3, and progestagen-associated endometrial protein map to HSA9 and MMU2 JOURNAL Genomics 23 (1), 145-150 (1994) PUBMED 7829063 REFERENCE 9 (bases 1 to 840) AUTHORS Kjeldsen,L., Johnsen,A.H., Sengelov,H. and Borregaard,N. TITLE Isolation and primary structure of NGAL, a novel protein associated with human neutrophil gelatinase JOURNAL J. Biol. Chem. 268 (14), 10425-10432 (1993) PUBMED 7683678 REFERENCE 10 (bases 1 to 840) AUTHORS Triebel,S., Blaser,J., Reinke,H. and Tschesche,H. TITLE A 25 kDa alpha 2-microglobulin-related protein is a component of the 125 kDa form of human gelatinase JOURNAL FEBS Lett. 314 (3), 386-388 (1992) PUBMED 1281792 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from BP272828.1, BC033089.1 and BM977724.1. On Jun 14, 2006 this sequence version replaced gi:38455401. 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 :: CA454137.1, BU168788.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025081, ERS025084 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-13 BP272828.1 1-13 14-818 BC033089.1 1-805 819-840 BM977724.1 1-22 c FEATURES Location/Qualifiers source 1..840 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="9" /map="9q34" gene 1..840 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /note="lipocalin 2" /db_xref="GeneID:3934" /db_xref="HGNC:6526" /db_xref="MIM:600181" exon 1..211 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /inference="alignment:Splign:1.39.8" variation 13 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:12683358" CDS 74..670 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /note="oncogene 24p3; neutrophil gelatinase-associated lipocalin; migration-stimulating factor inhibitor; p25; lipocalin-2; 25 kDa alpha-2-microglobulin-related subunit of MMP-9; siderocalin LCN2" /codon_start=1 /product="neutrophil gelatinase-associated lipocalin precursor" /protein_id="NP_005555.2" /db_xref="GI:38455402" /db_xref="CCDS:CCDS6892.1" /db_xref="GeneID:3934" /db_xref="HGNC:6526" /db_xref="MIM:600181" /translation="
MPLGLLWLGLALLGALHAQAQDSTSDLIPAPPLSKVPLQQNFQDNQFQGKWYVVGLAGNAILREDKDPQKMYATIYELKEDKSYNVTSVLFRKKKCDYWIRTFVPGCQPGEFTLGNIKSYPGLTSYLVRVVSTNYNQHAMVFFKKVSQNREYFKITLYGRTKELTSELKENFIRFSKSLGLPENHIVFPVPIDQCIDG
" sig_peptide 74..133 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /inference="COORDINATES: ab initio prediction:SignalP:4.0" mat_peptide 134..667 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /product="Neutrophil gelatinase-associated lipocalin" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (P80188.2)" misc_feature 134..136 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (P80188.2); other site" misc_feature 215..652 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /note="Lipocalin / cytosolic fatty-acid binding protein family; Region: Lipocalin; pfam00061" /db_xref="CDD:200967" misc_feature 326..328 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /experiment="experimental evidence, no additional details recorded" /note="glycosylation site" /citation=[9] variation 90 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:139418967" variation 99 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="g" /replace="t" /db_xref="dbSNP:147787222" variation 106 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:147142361" variation 126 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:140285982" variation 128 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:201536301" variation 166 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:144354643" variation 179 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:147792047" variation 190 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="g" /replace="t" /db_xref="dbSNP:11556770" variation 203 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:141366243" exon 212..348 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /inference="alignment:Splign:1.39.8" variation 228 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:200107414" variation 266 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:370705191" variation 280 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:373535058" variation 286 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:142623708" variation 299 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:201365744" variation 302 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:377651206" variation 338 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:200876706" exon 349..428 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /inference="alignment:Splign:1.39.8" variation 389 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:367591388" variation 403 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:371653139" variation 411 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:150975968" exon 429..548 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /inference="alignment:Splign:1.39.8" STS 434..575 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /standard_name="RH93784" /db_xref="UniSTS:90193" variation 434 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:2232627" variation 444 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:79993583" variation 455 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:141218430" variation 466 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:373227379" variation 476 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:368926734" variation 504 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="c" /db_xref="dbSNP:145071103" variation 520 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:11927" variation 525 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:199523944" variation 530 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:201570875" variation 547 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:138858669" variation 548 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:377601677" exon 549..650 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /inference="alignment:Splign:1.39.8" STS 562..646 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /standard_name="PMC152639P4" /db_xref="UniSTS:271237" variation 570 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:368254779" variation 579 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:200989488" variation 608 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:17435161" variation 632 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:149368200" variation 649 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="g" /db_xref="dbSNP:143776517" exon 651..677 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /inference="alignment:Splign:1.39.8" exon 678..822 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /inference="alignment:Splign:1.39.8" variation 693 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:373690406" variation 694 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:112730796" variation 703 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="a" /replace="g" /db_xref="dbSNP:12260" variation 773 /gene="LCN2" /gene_synonym="24p3; MSFI; NGAL" /replace="c" /replace="t" /db_xref="dbSNP:368437949" ORIGIN
actcgccacctcctcttccacccctgccaggcccagcagccaccacagcgcctgcttcctcggccctgaaatcatgcccctaggtctcctgtggctgggcctagccctgttgggggctctgcatgcccaggcccaggactccacctcagacctgatcccagccccacctctgagcaaggtccctctgcagcagaacttccaggacaaccaattccaggggaagtggtatgtggtaggcctggcagggaatgcaattctcagagaagacaaagacccgcaaaagatgtatgccaccatctatgagctgaaagaagacaagagctacaatgtcacctccgtcctgtttaggaaaaagaagtgtgactactggatcaggacttttgttccaggttgccagcccggcgagttcacgctgggcaacattaagagttaccctggattaacgagttacctcgtccgagtggtgagcaccaactacaaccagcatgctatggtgttcttcaagaaagtttctcaaaacagggagtacttcaagatcaccctctacgggagaaccaaggagctgacttcggaactaaaggagaacttcatccgcttctccaaatctctgggcctccctgaaaaccacatcgtcttccctgtcccaatcgaccagtgtatcgacggctgagtgcacaggtgccgccagctgccgcaccagcccgaacaccattgagggagctgggagaccctccccacagtgccacccatgcagctgctccccaggccaccccgctgatggagccccaccttgtctgctaaataaacatgtgccctcaggccaaaaaaaaaaaaaaaaaa
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:3934 -> Molecular function: GO:0002020 [protease binding] evidence: IEA GeneID:3934 -> Molecular function: GO:0005215 [transporter activity] evidence: IEA GeneID:3934 -> Molecular function: GO:0005506 [iron ion binding] evidence: ISS GeneID:3934 -> Molecular function: GO:0036094 [small molecule binding] evidence: IEA GeneID:3934 -> Molecular function: GO:0042803 [protein homodimerization activity] evidence: IEA GeneID:3934 -> Biological process: GO:0006811 [ion transport] evidence: IEA GeneID:3934 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA GeneID:3934 -> Biological process: GO:0009615 [response to virus] evidence: IEA GeneID:3934 -> Biological process: GO:0009635 [response to herbicide] evidence: IEA GeneID:3934 -> Biological process: GO:0010628 [positive regulation of gene expression] evidence: IEA GeneID:3934 -> Biological process: GO:0015891 [siderophore transport] evidence: ISS GeneID:3934 -> Biological process: GO:0031346 [positive regulation of cell projection organization] evidence: IEA GeneID:3934 -> Biological process: GO:0031669 [cellular response to nutrient levels] evidence: IEA GeneID:3934 -> Biological process: GO:0042493 [response to drug] evidence: IEA GeneID:3934 -> Biological process: GO:0042981 [regulation of apoptotic process] evidence: IEA GeneID:3934 -> Biological process: GO:0045087 [innate immune response] evidence: ISS GeneID:3934 -> Biological process: GO:0070207 [protein homotrimerization] evidence: IEA GeneID:3934 -> Biological process: GO:0070301 [cellular response to hydrogen peroxide] evidence: IEA GeneID:3934 -> Biological process: GO:0071222 [cellular response to lipopolysaccharide] evidence: IEA GeneID:3934 -> Biological process: GO:0071347 [cellular response to interleukin-1] evidence: IEA GeneID:3934 -> Biological process: GO:0071356 [cellular response to tumor necrosis factor] evidence: IEA GeneID:3934 -> Cellular component: GO:0005576 [extracellular region] evidence: ISS GeneID:3934 -> Cellular component: GO:0005615 [extracellular space] evidence: IEA GeneID:3934 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA GeneID:3934 -> Cellular component: GO:0005829 [cytosol] evidence: IEA
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