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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
//

Annotations:

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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