GGRNA Home | Help | Advanced search

2020-10-24 07:06:54, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_018192               3715 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens leprecan-like 1 (LEPREL1), transcript variant 1, mRNA.
ACCESSION   NM_018192
VERSION     NM_018192.3  GI:197313660
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 3715)
  AUTHORS   Mordechai,S., Gradstein,L., Pasanen,A., Ofir,R., El Amour,K.,
            Levy,J., Belfair,N., Lifshitz,T., Joshua,S., Narkis,G.,
            Elbedour,K., Myllyharju,J. and Birk,O.S.
  TITLE     High myopia caused by a mutation in LEPREL1, encoding prolyl
            3-hydroxylase 2
  JOURNAL   Am. J. Hum. Genet. 89 (3), 438-445 (2011)
   PUBMED   21885030
  REMARK    GeneRIF: High myopia is caused by a mutation in LEPREL1, encoding
            prolyl 3-hydroxylase 2.
REFERENCE   2  (bases 1 to 3715)
  AUTHORS   Fernandes,R.J., Farnand,A.W., Traeger,G.R., Weis,M.A. and Eyre,D.R.
  TITLE     A role for prolyl 3-hydroxylase 2 in post-translational
            modification of fibril-forming collagens
  JOURNAL   J. Biol. Chem. 286 (35), 30662-30669 (2011)
   PUBMED   21757687
  REMARK    GeneRIF: P3H2 has preferred substrate sequences among the classes
            of 3Hyp sites in clade A collagen chains
REFERENCE   3  (bases 1 to 3715)
  AUTHORS   Shah,R., Smith,P., Purdie,C., Quinlan,P., Baker,L., Aman,P.,
            Thompson,A.M. and Crook,T.
  TITLE     The prolyl 3-hydroxylases P3H2 and P3H3 are novel targets for
            epigenetic silencing in breast cancer
  JOURNAL   Br. J. Cancer 100 (10), 1687-1696 (2009)
   PUBMED   19436308
  REMARK    GeneRIF: The restriction of silencing in P3H2 to breast carcinomas,
            and its association with oestrogen-receptor-positive cases,
            suggests that P3H2 may be a breast-cancer-specific tumour
            suppressor.
REFERENCE   4  (bases 1 to 3715)
  AUTHORS   Tiainen,P., Pasanen,A., Sormunen,R. and Myllyharju,J.
  TITLE     Characterization of recombinant human prolyl 3-hydroxylase
            isoenzyme 2, an enzyme modifying the basement membrane collagen IV
  JOURNAL   J. Biol. Chem. 283 (28), 19432-19439 (2008)
   PUBMED   18487197
  REMARK    GeneRIF: P3H2 is responsible for the hydroxylation of collagen IV,
            which has the highest 3-hydroxyproline content of all collagens. It
            is thus possible that P3H2 mutations may lead to a disease with
            changes in basement membranes.
REFERENCE   5  (bases 1 to 3715)
  AUTHORS   Vranka,J.A., Sakai,L.Y. and Bachinger,H.P.
  TITLE     Prolyl 3-hydroxylase 1, enzyme characterization and identification
            of a novel family of enzymes
  JOURNAL   J. Biol. Chem. 279 (22), 23615-23621 (2004)
   PUBMED   15044469
REFERENCE   6  (bases 1 to 3715)
  AUTHORS   Jarnum,S., Kjellman,C., Darabi,A., Nilsson,I., Edvardsen,K. and
            Aman,P.
  TITLE     LEPREL1, a novel ER and Golgi resident member of the Leprecan
            family
  JOURNAL   Biochem. Biophys. Res. Commun. 317 (2), 342-351 (2004)
   PUBMED   15063763
REFERENCE   7  (bases 1 to 3715)
  AUTHORS   Thelin-Jarnum,S., Lassen,C., Panagopoulos,I., Mandahl,N. and
            Aman,P.
  TITLE     Identification of genes differentially expressed in TLS-CHOP
            carrying myxoid liposarcomas
  JOURNAL   Int. J. Cancer 83 (1), 30-33 (1999)
   PUBMED   10449603
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from DA879789.1, AJ430351.2,
            AK125134.1, BC005029.1, BU621129.1 and BU737886.1.
            On Aug 28, 2008 this sequence version replaced gi:27764881.
            
            Summary: This gene encodes a member of the prolyl 3-hydroxylase
            subfamily of 2-oxo-glutarate-dependent dioxygenases. These enzymes
            play a critical role in collagen chain assembly, stability and
            cross-linking by catalyzing post-translational 3-hydroxylation of
            proline residues. Mutations in this gene are associated with
            nonsyndromic severe myopia with cataract and vitreoretinal
            degeneration, and downregulation of this gene may play a role in
            breast cancer. Alternatively spliced transcript variants encoding
            multiple isoforms have been observed for this gene. [provided by
            RefSeq, Dec 2011].
            
            Transcript Variant: This variant (1) represents the longer
            transcript and encodes the longer isoform (a).
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK125134.1, AJ430351.2 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025081, ERS025082 [ECO:0000350]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-190               DA879789.1         1-190
            191-895             AJ430351.2         1-705
            896-2726            AK125134.1         701-2531
            2727-2979           BC005029.1         1922-2174
            2980-3596           BU621129.1         17-633              c
            3597-3715           BU737886.1         1-119               c
FEATURES             Location/Qualifiers
     source          1..3715
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="3"
                     /map="3q28"
     gene            1..3715
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /note="leprecan-like 1"
                     /db_xref="GeneID:55214"
                     /db_xref="HGNC:19317"
                     /db_xref="HPRD:17270"
                     /db_xref="MIM:610341"
     exon            1..868
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    359..361
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /note="upstream in-frame stop codon"
     CDS             389..2515
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /EC_number="1.14.11.7"
                     /note="isoform a precursor is encoded by transcript
                     variant 1; prolyl 3-hydroxylase 3; prolyl 3-hydroxylase 2;
                     myxoid liposarcoma-associated protein 4"
                     /codon_start=1
                     /product="prolyl 3-hydroxylase 2 isoform a precursor"
                     /protein_id="NP_060662.2"
                     /db_xref="GI:27764882"
                     /db_xref="CCDS:CCDS3294.1"
                     /db_xref="GeneID:55214"
                     /db_xref="HGNC:19317"
                     /db_xref="HPRD:17270"
                     /db_xref="MIM:610341"
                     /translation="
MRERIWAPPLLLLLPLLLPPPLWGGPPDSPRRELELEPGPLQPFDLLYASGAAAYYSGDYERAVRDLEAALRSHRRLREIRTRCARHCAARHPLPPPPPGEGPGAELPLFRSLLGRARCYRSCETQRLGGPASRHRVSEDVRSDFQRRVPYNYLQRAYIKLNQLEKAVEAAHTFFVANPEHMEMQQNIENYRATAGVEALQLVDREAKPHMESYNAGVKHYEADDFEMAIRHFEQALREYFVEDTECRTLCEGPQRFEEYEYLGYKAGLYEAIADHYMQVLVCQHECVRELATRPGRLSPIENFLPLHYDYLQFAYYRVGEYVKALECAKAYLLCHPDDEDVLDNVDYYESLLDDSIDPASIEAREDLTMFVKRHKLESELIKSAAEGLGFSYTEPNYWIRYGGRQDENRVPSGVNVEGAEVHGFSMGKKLSPKIDRDLREGGPLLYENITFVYNSEQLNGTQRVLLDNVLSEEQCRELHSVASGIMLVGDGYRGKTSPHTPNEKFEGATVLKALKSGYEGRVPLKSARLFYDISEKARRIVESYFMLNSTLYFSYTHMVCRTALSGQQDRRNDLSHPIHADNCLLDPEANECWKEPPAYTFRDYSALLYMNDDFEGGEFIFTEMDAKTVTASIKPKCGRMISFSSGGENPHGVKAVTKGKRCAVALWFTLDPLYRELERIQADEVIAILDQEQQGKHELNINPKDEL
"
     sig_peptide     389..460
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="COORDINATES: ab initio prediction:SignalP:4.0"
     mat_peptide     461..2512
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /product="Prolyl 3-hydroxylase 2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IVL5.1)"
     misc_feature    518..619
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IVL5.1);
                     Region: TPR 1"
     misc_feature    830..931
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IVL5.1);
                     Region: TPR 2"
     misc_feature    1016..1117
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IVL5.1);
                     Region: TPR 3"
     misc_feature    1304..1405
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IVL5.1);
                     Region: TPR 4"
     misc_feature    1802..2398
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /note="Prolyl 4-hydroxylase alpha subunit homologues;
                     Region: P4Hc; smart00702"
                     /db_xref="CDD:197834"
     misc_feature    2117..2398
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /note="2OG-Fe(II) oxygenase superfamily; Region:
                     2OG-FeII_Oxy_3; pfam13640"
                     /db_xref="CDD:205817"
     misc_feature    2501..2512
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8IVL5.1);
                     Region: Prevents secretion from ER (Potential)"
     exon            869..1021
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     variation       1000
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:34128856"
     exon            1022..1211
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     variation       1084
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1719600"
     exon            1212..1343
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     exon            1344..1486
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     variation       1360
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:34558237"
     exon            1487..1576
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     variation       1557
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35904452"
     exon            1577..1617
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     variation       1610
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35737596"
     exon            1618..1712
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     exon            1713..1840
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     variation       1765
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35257648"
     variation       1840
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:34111865"
     exon            1841..1936
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     variation       1896
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35072845"
     exon            1937..2087
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     exon            2088..2205
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     variation       2192
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:34620268"
     variation       2195
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:35067805"
     exon            2206..2281
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     exon            2282..2422
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     variation       2395
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1061534"
     exon            2423..3699
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /inference="alignment:Splign:1.39.8"
     STS             3041..3230
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /standard_name="RH93767"
                     /db_xref="UniSTS:87517"
     STS             3206..3347
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
                     /standard_name="STS-N21495"
                     /db_xref="UniSTS:21296"
     polyA_signal    3574..3579
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
     polyA_site      3596
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
     polyA_signal    3678..3683
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
     polyA_site      3699
                     /gene="LEPREL1"
                     /gene_synonym="MCVD; MLAT4; P3H2"
ORIGIN      
atccacttgtacaaccagaagggagctcacgtgtaaagcgcctcgtccccggccggcctcaagcggcgctagctctctggctggcgctggagtgtgccgcccctggcagccccgccgctgcagcggggagcctgggagagcggctctcggagtctcaggcagcaggaggagcgtgtgagctgtgggcgtccctttaagagcggctggccaggcacggcctccgcctctcagtacgcggagcgccggcggtcacctggggctcgcggagcggccagatcgcggcggagtcggcgcgcttccccgagggaaggtgggagaggggacccggacgcgaggtgccccgaagccctctcgagcgtaaccgtcccgcgcctctctgaggcggaggatgcgggagcgcatctgggcgccgccgctgctgctgctgctgccgctgctactgccgccgccactgtggggcggccccccggacagcccacgccgggagctggagctggagcccgggcctctgcagcccttcgacctgctctacgccagcggcgcggccgcctactacagcggagactacgagcgagcggtgcgcgacttggaagcggcgctgcgcagccaccggcgcctgcgggaaatccgcacgcgctgtgcccgccactgcgcggcgcgccacccgctcccgcccccgccccccggcgagggccccggcgctgagctgccccttttccgctccttgttggggcgggcgcgctgttatcgcagctgtgagacccagcgcctcgggggccccgcatcccgccaccgcgtcagcgaggatgtgcgcagcgacttccagcgcagagtgccctacaactacctgcagcgggcctacatcaagcttaaccagctcgaaaaagcagtggaagcagctcacacatttttcgtggctaaccctgagcacatggaaatgcagcagaacattgagaattacagggcgacagctggtgttgaagcattgcagttggtagacagagaagccaagccacacatggagagttacaatgcaggagttaaacattatgaggctgatgactttgagatggctatcaggcacttcgaacaagccttaagagaatatttcgttgaagatacagaatgccggaccctatgtgaggggcctcagagatttgaagaatatgagtatttagggtataaggctggtctgtatgaagctattgcagatcactacatgcaggtgcttgtttgtcagcatgaatgtgtgagggaacttgccacccgccctggccgcctctctcccatcgagaattttcttcctctgcactatgattacctacagtttgcctactatcgagttggtgagtatgtgaaagccctggagtgtgccaaagcctatcttctatgccatccagatgatgaggatgtcctagacaatgtggattactatgagagtctgctggatgatagcattgacccggcatccattgaggccagagaggatttaacaatgtttgtgaaacgtcataagctggagtctgagctgataaaatcagctgcagaaggtctggggttttcatacactgaaccgaattattggatcagatatggaggacgacaggatgagaatcgggtcccttcaggagtgaacgtagagggagcagaagttcatggattctcaatgggaaaaaagctatcacccaagatagatcgagacctaagagaaggtggtcctctactctatgagaacatcacattcgtctacaactcggagcagctgaacgggactcagcgggttctcctggataacgtcctgtcggaagaacagtgccgggagctccacagcgtggccagtggaatcatgcttgttggtgatggatacagaggaaaaacttcaccccatacacccaatgaaaagtttgaaggtgcaactgtcctgaaagcactcaaatctggttatgaaggtcgagtcccactgaagagcgctcgtctgttttatgacatcagcgaaaaggctcgaaggattgtagaatcttattttatgctgaactcaactctgtatttttcctatacacacatggtctgccgaacagccctgtctggtcagcaggatagaagaaatgacctcagtcatcccatccatgctgacaactgtttgttggatccagaggccaacgaatgctggaaggagcctcctgcttacacatttcgagactatagtgctctcctatatatgaatgatgactttgaaggaggagaattcatattcacagagatggatgctaagactgtgactgcctctataaaaccaaaatgtgggcgcatgatcagcttctcatctggaggagagaaccctcatggggtgaaggcagtcaccaagggaaagaggtgtgctgtggctctgtggttcaccttggacccactttatagagaattggagcgaatacaggctgatgaagtgattgcaattctggatcaagaacagcaagggaagcatgaactgaatatcaaccctaaagatgagctataaaaatgagaaagaatgttctatcaaatatttatttaaattgttaatcttatgagaacctttttatttttgtacagagccatggtataaattaacaggttaatgtcagtcatcagatcttccttctcttcctaaggatgcttgtgttgcctcaatctatcaatctatctttcttgttttgggttgttttctctctctctctctctctctctcttcttagagacatggtctaaccatgttgtctaggatatagggcagtggctattcacagatgtgatgatagcacactggagcctcaaactcttaggctcaggcgatccttcaagcctcccggggagctgggaccacaggcacgtgccaccacacccagctctctttcttggtttttcatcatttcatgtatctatcaaagcccagttcacctcctcccccaaacacacacacacacacacacacacacacacacacacacaattaagttgctgcaaattcaaaagcttagagagaataagcttcttggtggtgaaactacaactctcacgtgtgctccagttctaaaattaacctgtgcctggtctctgaagccctttcttgctctgtgcctttcagccacatccttaggtgctaacggccatgagctccgactctccaaagtgagctccactttgggtctgaggagcccctggcagagtccacgctgcctcaggtatcatgggcgtaatgatcacccaggctccgggagatctcatggatgattactgtatgagacagaggggacttcagtctttccagggccttggtggaatttttggctctggtgttttcgccagacaataaacttacactggaagctttgattcaccctccacagtactccagaaaggactgtcctataagttgtacactttaaaaggtcatgtagaggttgtagtagaatggcttttcaccctggtgactttggaagaaactcttgaatactgcctgcatccgggcaccatggccaggttgcctaggagtggggtccactgatgaaaagaggtgttttgtacttacataagaaaaataaatttctgattgattttaaccgtcatctgcttatattttgggggcccctcctcattgctgctatccagcacacagatttgtgcttgtgtctgatttgtttaataaagggaggcttattttaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:55214 -> Molecular function: GO:0005506 [iron ion binding] evidence: IEA
            GeneID:55214 -> Molecular function: GO:0016702 [oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen] evidence: IEA
            GeneID:55214 -> Molecular function: GO:0019797 [procollagen-proline 3-dioxygenase activity] evidence: IDA
            GeneID:55214 -> Molecular function: GO:0031418 [L-ascorbic acid binding] evidence: IEA
            GeneID:55214 -> Biological process: GO:0008285 [negative regulation of cell proliferation] evidence: IDA
            GeneID:55214 -> Biological process: GO:0019511 [peptidyl-proline hydroxylation] evidence: IDA
            GeneID:55214 -> Biological process: GO:0030198 [extracellular matrix organization] evidence: TAS
            GeneID:55214 -> Biological process: GO:0032963 [collagen metabolic process] evidence: IDA
            GeneID:55214 -> Cellular component: GO:0005604 [basement membrane] evidence: ISS
            GeneID:55214 -> Cellular component: GO:0005783 [endoplasmic reticulum] evidence: IDA
            GeneID:55214 -> Cellular component: GO:0005788 [endoplasmic reticulum lumen] evidence: TAS
            GeneID:55214 -> Cellular component: GO:0005794 [Golgi apparatus] evidence: IDA
ANNOTATIONS from NCBI Entrez Gene (20130726):
            NP_060662 -> EC 1.14.11.7

by @meso_cacase at DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.