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2024-03-28 17:18:54, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_058186               1384 bp    mRNA    linear   PRI 15-JUN-2013
DEFINITION  Homo sapiens family with sequence similarity 3, member B (FAM3B),
            transcript variant 1, mRNA.
ACCESSION   NM_058186
VERSION     NM_058186.3  GI:46255029
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 1384)
  AUTHORS   Li,Z., Mou,H., Wang,T., Xue,J., Deng,B., Qian,L., Zhou,Y., Gong,W.,
            Wang,J.M., Wu,G., Zhou,C.F., Fang,J. and Le,Y.
  TITLE     A non-secretory form of FAM3B promotes invasion and metastasis of
            human colon cancer cells by upregulating Slug expression
  JOURNAL   Cancer Lett. 328 (2), 278-284 (2013)
   PUBMED   23059759
  REMARK    GeneRIF: These results suggest that FAM3B-258 promotes colon cancer
            cell invasion and metastasis through upregulation of Slug.
REFERENCE   2  (bases 1 to 1384)
  AUTHORS   He,M., Wu,C., Xu,J., Guo,H., Yang,H., Zhang,X., Sun,J., Yu,D.,
            Zhou,L., Peng,T., He,Y., Gao,Y., Yuan,J., Deng,Q., Dai,X., Tan,A.,
            Feng,Y., Zhang,H., Min,X., Yang,X., Zhu,J., Zhai,K., Chang,J.,
            Qin,X., Tan,W., Hu,Y., Lang,M., Tao,S., Li,Y., Li,Y., Feng,J.,
            Li,D., Kim,S.T., Zhang,S., Zhang,H., Zheng,S.L., Gui,L., Wang,Y.,
            Wei,S., Wang,F., Fang,W., Liang,Y., Zhai,Y., Chen,W., Miao,X.,
            Zhou,G., Hu,F.B., Lin,D., Mo,Z. and Wu,T.
  TITLE     A genome wide association study of genetic loci that influence
            tumour biomarkers cancer antigen 19-9, carcinoembryonic antigen and
            alpha fetoprotein and their associations with cancer risk
  JOURNAL   Gut (2013) In press
   PUBMED   23300138
  REMARK    Publication Status: Available-Online prior to print
REFERENCE   3  (bases 1 to 1384)
  AUTHORS   Davila,S., Froeling,F.E., Tan,A., Bonnard,C., Boland,G.J.,
            Snippe,H., Hibberd,M.L. and Seielstad,M.
  TITLE     New genetic associations detected in a host response study to
            hepatitis B vaccine
  JOURNAL   Genes Immun. 11 (3), 232-238 (2010)
   PUBMED   20237496
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   4  (bases 1 to 1384)
  AUTHORS   Yang,J., Robert,C.E., Burkhardt,B.R., Young,R.A., Wu,J., Gao,Z. and
            Wolf,B.A.
  TITLE     Mechanisms of glucose-induced secretion of pancreatic-derived
            factor (PANDER or FAM3B) in pancreatic beta-cells
  JOURNAL   Diabetes 54 (11), 3217-3228 (2005)
   PUBMED   16249448
  REMARK    GeneRIF: PANDER is secreted from 2 types of pancreatic cells,
            glucose stimulates its secretion in beta cell and primary islets
            but not in alpha-cells, it is likely cosecreted with insulin, and
            structure and conformation is vital for PANDER secretion.
REFERENCE   5  (bases 1 to 1384)
  AUTHORS   Yang,J., Gao,Z., Robert,C.E., Burkhardt,B.R., Gaweska,H.,
            Wagner,A., Wu,J., Greene,S.R., Young,R.A. and Wolf,B.A.
  TITLE     Structure-function studies of PANDER, an islet specific cytokine
            inducing cell death of insulin-secreting beta cells
  JOURNAL   Biochemistry 44 (34), 11342-11352 (2005)
   PUBMED   16114871
  REMARK    GeneRIF: Helices B and C and the second disulfide bond of PANDER
            are essential for PANDER-induced beta-cell death.
REFERENCE   6  (bases 1 to 1384)
  AUTHORS   Clark,H.F., Gurney,A.L., Abaya,E., Baker,K., Baldwin,D., Brush,J.,
            Chen,J., Chow,B., Chui,C., Crowley,C., Currell,B., Deuel,B.,
            Dowd,P., Eaton,D., Foster,J., Grimaldi,C., Gu,Q., Hass,P.E.,
            Heldens,S., Huang,A., Kim,H.S., Klimowski,L., Jin,Y., Johnson,S.,
            Lee,J., Lewis,L., Liao,D., Mark,M., Robbie,E., Sanchez,C.,
            Schoenfeld,J., Seshagiri,S., Simmons,L., Singh,J., Smith,V.,
            Stinson,J., Vagts,A., Vandlen,R., Watanabe,C., Wieand,D., Woods,K.,
            Xie,M.H., Yansura,D., Yi,S., Yu,G., Yuan,J., Zhang,M., Zhang,Z.,
            Goddard,A., Wood,W.I., Godowski,P. and Gray,A.
  TITLE     The secreted protein discovery initiative (SPDI), a large-scale
            effort to identify novel human secreted and transmembrane proteins:
            a bioinformatics assessment
  JOURNAL   Genome Res. 13 (10), 2265-2270 (2003)
   PUBMED   12975309
  REMARK    Erratum:[Genome Res. 2003 Dec;13(12):2759]
REFERENCE   7  (bases 1 to 1384)
  AUTHORS   Zhu,Y., Xu,G., Patel,A., McLaughlin,M.M., Silverman,C., Knecht,K.,
            Sweitzer,S., Li,X., McDonnell,P., Mirabile,R., Zimmerman,D.,
            Boyce,R., Tierney,L.A., Hu,E., Livi,G.P., Wolf,B.,
            Abdel-Meguid,S.S., Rose,G.D., Aurora,R., Hensley,P., Briggs,M. and
            Young,P.R.
  TITLE     Cloning, expression, and initial characterization of a novel
            cytokine-like gene family
  JOURNAL   Genomics 80 (2), 144-150 (2002)
   PUBMED   12160727
  REMARK    GeneRIF: Localized to the islets of Langerhans.
REFERENCE   8  (bases 1 to 1384)
  AUTHORS   Reymond,A., Friedli,M., Henrichsen,C.N., Chapot,F., Deutsch,S.,
            Ucla,C., Rossier,C., Lyle,R., Guipponi,M. and Antonarakis,S.E.
  TITLE     From PREDs and open reading frames to cDNA isolation: revisiting
            the human chromosome 21 transcription map
  JOURNAL   Genomics 78 (1-2), 46-54 (2001)
   PUBMED   11707072
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AK125528.1, BI712971.1, BC057829.1, AY358459.1 and BF514643.1.
            On Apr 7, 2004 this sequence version replaced gi:21361797.
            
            Transcript Variant: This variant (1) represents the longer
            transcript and encodes the longer isoform (a).
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK125528.1, AL561378.3 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084, ERS025085 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-361               AK125528.1         3-363
            362-565             BI712971.1         324-527
            566-928             BC057829.1         488-850
            929-1088            AY358459.1         797-956
            1089-1384           BF514643.1         145-440
FEATURES             Location/Qualifiers
     source          1..1384
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="21"
                     /map="21q22.3"
     gene            1..1384
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /note="family with sequence similarity 3, member B"
                     /db_xref="GeneID:54097"
                     /db_xref="HGNC:1253"
                     /db_xref="HPRD:10552"
                     /db_xref="MIM:608617"
     exon            1..165
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /inference="alignment:Splign:1.39.8"
     variation       92
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:148108671"
     CDS             147..854
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /note="isoform a precursor is encoded by transcript
                     variant 1; pancreatic derived factor; D21M16SJHU19e;
                     cytokine-like protein 2-21; pancreatic-derived factor;
                     protein FAM3B"
                     /codon_start=1
                     /product="protein FAM3B isoform a precursor"
                     /protein_id="NP_478066.3"
                     /db_xref="GI:46255030"
                     /db_xref="CCDS:CCDS13671.1"
                     /db_xref="GeneID:54097"
                     /db_xref="HGNC:1253"
                     /db_xref="HPRD:10552"
                     /db_xref="MIM:608617"
                     /translation="
MRPLAGGLLKVVFVVFASLCAWYSGYLLAELIPDAPLSSAAYSIRSIGERPVLKAPVPKRQKCDHWTPCPSDTYAYRLLSGGGRSKYAKICFEDNLLMGEQLGNVARGINIAIVNYVTGNVTATRCFDMYEGDNSGPMTKFIQSAAPKSLLFMVTYDDGSTRLNNDAKNAIEALGSKEIRNMKFRSSWVFIAAKGLELPSEIQREKINHSDAKNNRYSGWPAEIQIEGCIPKERS
"
     sig_peptide     147..233
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P58499.2)"
     mat_peptide     234..851
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /product="Protein FAM3B"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P58499.2)"
     exon            166..309
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /inference="alignment:Splign:1.39.8"
     variation       179
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374924359"
     variation       185
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186901119"
     variation       186
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2838012"
     variation       194
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61734881"
     variation       195
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371282791"
     variation       208
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112776726"
     variation       237
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:138471782"
     variation       269
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:149569625"
     variation       278
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149282476"
     variation       280
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369146230"
     variation       287
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148283845"
     exon            310..433
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /inference="alignment:Splign:1.39.8"
     variation       319
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141359085"
     variation       367
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191085667"
     variation       386
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371339927"
     variation       387
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146229700"
     variation       407
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376038821"
     exon            434..492
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /inference="alignment:Splign:1.39.8"
     variation       439
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369029304"
     variation       491
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373278221"
     exon            493..543
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /inference="alignment:Splign:1.39.8"
     variation       497
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:370579027"
     variation       519
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139331735"
     variation       523
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142423610"
     variation       542
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:417708"
     variation       543
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199919585"
     exon            544..631
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /inference="alignment:Splign:1.39.8"
     variation       548..549
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace=""
                     /replace="ct"
                     /db_xref="dbSNP:369832982"
     variation       556
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139452370"
     variation       557
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149676623"
     variation       604
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145464636"
     variation       615
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148783965"
     variation       617
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144944684"
     exon            632..764
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /inference="alignment:Splign:1.39.8"
     variation       633
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187262938"
     variation       641
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370045496"
     variation       685
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200388472"
     variation       692
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111988437"
     variation       725
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377117970"
     variation       730
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147056375"
     variation       746
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201305246"
     variation       757
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371623376"
     exon            765..1384
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /inference="alignment:Splign:1.39.8"
     variation       765
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:183635372"
     variation       802
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141735671"
     variation       847
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:59821562"
     variation       855
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376707862"
     variation       877
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:140493581"
     variation       976
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:188174846"
     polyA_site      1002
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /experiment="experimental evidence, no additional details
                     recorded"
     variation       1041
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191346748"
     polyA_site      1088
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /experiment="experimental evidence, no additional details
                     recorded"
     variation       1134
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377647313"
     variation       1157
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:73905337"
     variation       1166
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142776996"
     variation       1207
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2838024"
     variation       1225
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369859121"
     variation       1321
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:757368"
     variation       1343
                     /gene="FAM3B"
                     /gene_synonym="2-21; C21orf11; C21orf76; ORF9; PANDER;
                     PRED44"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116810029"
ORIGIN      
tttgcccgactggccgcgcacccagctggcccgcccctgcccgacacgaccgctgcccgccccttgccttcctgacccaggggctccgctggctgcggtcgcctgggagctgccgccagggccaggaggggagcggcacctggaagatgcgcccattggctggtggcctgctcaaggtggtgttcgtggtcttcgcctccttgtgtgcctggtattcggggtacctgctcgcagagctcattccagatgcacccctgtccagtgctgcctatagcatccgcagcatcggggagaggcctgtcctcaaagctccagtccccaaaaggcaaaaatgtgaccactggactccctgcccatctgacacctatgcctacaggttactcagcggaggtggcagaagcaagtacgccaaaatctgctttgaggataacctacttatgggagaacagctgggaaatgttgccagaggaataaacattgccattgtcaactatgtaactgggaatgtgacagcaacacgatgttttgatatgtatgaaggtgataactctggaccgatgacaaagtttattcagagtgctgctccaaaatccctgctcttcatggtgacctatgacgacggaagcacaagactgaataacgatgccaagaatgccatagaagcacttggaagtaaagaaatcaggaacatgaaattcaggtctagctgggtatttattgcagcaaaaggcttggaactcccttccgaaattcagagagaaaagatcaaccactctgatgctaagaacaacagatattctggctggcctgcagagatccagatagaaggctgcatacccaaagaacgaagctgacactgcagggtcctgagtaaatgtgttctgtataaacaaatgcagctggaatcgctcaagaatcttatttttctaaatccaacagcccatatttgatgagtattttgggtttgttgtaaaccaatgaacatttgctagttgtatcaaatcttggtacgcagtatttttataccagtattttatgtagtgaagatgtcaattagcaggaaactaaaatgaatggaaattcttaaagggaatgatgtgattcaagctggaaagagggttgggagaaacagcttgtccaggtggagctatgttatgatcagatcgaagtgtgacccctgtgtggtccagacagccctgcagagagaaaacctttattccattatcaccaagcacctcctagtttccgacagtcatctccttctgctgggagaattagcagcagttcagggggcttatgttatgtccttgttcaactcaacttgagctcttgaactcctcctgtgggcctgtgaatgtattcattcattccacaactctgggtg
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:54097 -> Molecular function: GO:0005125 [cytokine activity] evidence: NAS
            GeneID:54097 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA
            GeneID:54097 -> Biological process: GO:0030073 [insulin secretion] evidence: IDA
            GeneID:54097 -> Cellular component: GO:0005576 [extracellular region] evidence: NAS
            GeneID:54097 -> Cellular component: GO:0005615 [extracellular space] evidence: IEA

by @meso_cacase at DBCLS
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