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2024-04-26 13:07:34, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001190441             600 bp    mRNA    linear   PRI 18-APR-2013
DEFINITION  Homo sapiens lectin, galactoside-binding, soluble, 16 (LGALS16),
            mRNA.
ACCESSION   NM_001190441 XM_001721300 XM_001721341 XM_001723341 XM_001723342
            XM_086001 XM_942526
VERSION     NM_001190441.1  GI:298919184
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 600)
  AUTHORS   Than,N.G., Romero,R., Goodman,M., Weckle,A., Xing,J., Dong,Z.,
            Xu,Y., Tarquini,F., Szilagyi,A., Gal,P., Hou,Z., Tarca,A.L.,
            Kim,C.J., Kim,J.S., Haidarian,S., Uddin,M., Bohn,H., Benirschke,K.,
            Santolaya-Forgas,J., Grossman,L.I., Erez,O., Hassan,S.S.,
            Zavodszky,P., Papp,Z. and Wildman,D.E.
  TITLE     A primate subfamily of galectins expressed at the maternal-fetal
            interface that promote immune cell death
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 106 (24), 9731-9736 (2009)
   PUBMED   19497882
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AC093051.2 and AC005515.1.
            On or before Jun 23, 2010 this sequence version replaced
            gi:169213286, gi:169213287, gi:169214329, gi:169214330,
            gi:169213905, gi:169213907.
            
            Sequence Note: The RefSeq transcript and protein were derived from
            genomic sequence to make the sequence consistent with the reference
            genome assembly. The genomic coordinates used for the transcript
            record were based on alignments.
            
            ##Evidence-Data-START##
            Transcript exon combination :: CD386476.1, FJ613352.1 [ECO:0000332]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-59                AC093051.2         3945-4003
            60-136              AC005515.1         3925-4001
            137-347             AC005515.1         4502-4712
            348-600             AC005515.1         6437-6689
FEATURES             Location/Qualifiers
     source          1..600
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="19"
                     /map="19q13.2"
     gene            1..600
                     /gene="LGALS16"
                     /note="lectin, galactoside-binding, soluble, 16"
                     /db_xref="GeneID:148003"
                     /db_xref="HGNC:40039"
     exon            1..59
                     /gene="LGALS16"
                     /inference="alignment:Splign:1.39.8"
     CDS             45..473
                     /gene="LGALS16"
                     /note="beta-galactoside-binding lectin"
                     /codon_start=1
                     /product="galectin-16"
                     /protein_id="NP_001177370.1"
                     /db_xref="GI:298919185"
                     /db_xref="CCDS:CCDS54267.1"
                     /db_xref="GeneID:148003"
                     /db_xref="HGNC:40039"
                     /translation="
MSFLTVPYKLPVSLSVGSCVIIKGTLIDSSINEPQLQVDFYTEMNEDSEIAFHLRVHLGRRVVMNSREFGIWMLEENLHYVPFEDGKPFDLRIYVCLNEYEVKVNGEYIYAFVHRIPPSYVKMIQVWRDVSLDSVLVNNGRR
"
     misc_feature    60..449
                     /gene="LGALS16"
                     /note="Galectin/galactose-binding lectin. This domain
                     exclusively binds beta-galactosides, such as lactose, and
                     does not require metal ions for activity. GLECT domains
                     occur as homodimers or tandemly repeated domains. They are
                     developmentally regulated and may...; Region: GLECT;
                     cd00070"
                     /db_xref="CDD:28952"
     misc_feature    order(60..74,435..449)
                     /gene="LGALS16"
                     /note="dimerization interface [polypeptide binding]; other
                     site"
                     /db_xref="CDD:28952"
     misc_feature    60..74
                     /gene="LGALS16"
                     /note="dimerization swap strand; other site"
                     /db_xref="CDD:28952"
     misc_feature    order(87..95,102..104,111..113,324..332,345..347,351..353,
                     360..362)
                     /gene="LGALS16"
                     /note="putative alternate dimerization interface
                     [polypeptide binding]; other site"
                     /db_xref="CDD:28952"
     misc_feature    order(201..203,207..209,213..215,231..233,237..239,
                     258..260,267..269,273..275)
                     /gene="LGALS16"
                     /note="sugar binding pocket [chemical binding]; other
                     site"
                     /db_xref="CDD:28952"
     exon            60..136
                     /gene="LGALS16"
                     /inference="alignment:Splign:1.39.8"
     variation       121
                     /gene="LGALS16"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10403702"
     variation       135
                     /gene="LGALS16"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113930745"
     exon            137..347
                     /gene="LGALS16"
                     /inference="alignment:Splign:1.39.8"
     variation       139
                     /gene="LGALS16"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201930366"
     variation       179
                     /gene="LGALS16"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138874309"
     variation       208
                     /gene="LGALS16"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116331309"
     variation       219
                     /gene="LGALS16"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35476378"
     variation       223
                     /gene="LGALS16"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149409914"
     variation       226
                     /gene="LGALS16"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184657849"
     variation       262
                     /gene="LGALS16"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147471254"
     variation       300
                     /gene="LGALS16"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187604453"
     variation       334
                     /gene="LGALS16"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1860134"
     exon            348..600
                     /gene="LGALS16"
                     /inference="alignment:Splign:1.39.8"
     variation       360
                     /gene="LGALS16"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:190910422"
     variation       411
                     /gene="LGALS16"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:181925874"
     variation       437
                     /gene="LGALS16"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148828240"
     variation       458
                     /gene="LGALS16"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:186797209"
     variation       466
                     /gene="LGALS16"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367627881"
     variation       484
                     /gene="LGALS16"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191782299"
     variation       527
                     /gene="LGALS16"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112620313"
     variation       584
                     /gene="LGALS16"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:183190594"
ORIGIN      
gaagactggacacaattccgaaggtcgcccagaaggagaggacaatgtcatttctaactgtgccatacaaactgcctgtgtctttgtctgttggttcctgcgtgataatcaaagggacactgatcgactcttctatcaacgaaccacagctgcaggtggatttctacactgagatgaatgaggactcagaaattgccttccatttgcgagtgcacttaggccgtcgtgtggtcatgaacagtcgtgagtttgggatatggatgttggaggagaatttacactatgtgccctttgaggatggcaaaccatttgacttgcgcatctacgtgtgtctcaatgagtatgaggtaaaggtaaatggtgaatacatttatgcctttgtccatcgaatcccgccatcatatgtgaagatgattcaagtgtggagagatgtctccctggactcagtgcttgtcaacaatggacggagatgatcacactcctcattgttgaggaaaccctctttctacctgaccatgggattcctagagcctgctaacagaataatccctcctcaaccccttcccctacacttggtcattaaaacagcaccaaaccgta
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:148003 -> Molecular function: GO:0030395 [lactose binding] evidence: IDA
            GeneID:148003 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA
            GeneID:148003 -> Biological process: GO:0070234 [positive regulation of T cell apoptotic process] evidence: IDA
            GeneID:148003 -> Cellular component: GO:0005575 [cellular_component] evidence: ND

by @meso_cacase at DBCLS
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