LOCUS       NM_001394151            1321 bp    mRNA    linear   PRI 08-APR-2024
DEFINITION  Homo sapiens small integral membrane protein 11B (LOC102723553),
            transcript variant 2, mRNA.
ACCESSION   NM_001394151
VERSION     NM_001394151.1
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 1321)
  AUTHORS   Suzuki,Y., Yamashita,R., Shirota,M., Sakakibara,Y., Chiba,J.,
            Mizushima-Sugano,J., Nakai,K. and Sugano,S.
  TITLE     Sequence comparison of human and mouse genes reveals a homologous
            block structure in the promoter regions
  JOURNAL   Genome Res 14 (9), 1711-1718 (2004)
   PUBMED   15342556
REFERENCE   2  (bases 1 to 1321)
  AUTHORS   Dias Neto,E., Correa,R.G., Verjovski-Almeida,S., Briones,M.R.,
            Nagai,M.A., da Silva,W. Jr., Zago,M.A., Bordin,S., Costa,F.F.,
            Goldman,G.H., Carvalho,A.F., Matsukuma,A., Baia,G.S., Simpson,D.H.,
            Brunstein,A., de Oliveira,P.S., Bucher,P., Jongeneel,C.V.,
            O'Hare,M.J., Soares,F., Brentani,R.R., Reis,L.F., de Souza,S.J. and
            Simpson,A.J.
  TITLE     Shotgun sequencing of the human transcriptome with ORF expressed
            sequence tags
  JOURNAL   Proc Natl Acad Sci U S A 97 (7), 3491-3496 (2000)
   PUBMED   10737800
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            CU633980.13.
            
            Sequence Note: NM_001394151 is annotated on a scaffold that is
            thought to be a false duplication and thus this accession is
            possibly redundant with other RefSeq accessions.
            
            ##Evidence-Data-START##
            Transcript exon combination :: SRR5189652.65357.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           SAMEA1965299, SAMEA1968832
                                           [ECO:0000348]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-364               CU633980.13        1587-1950
            365-453             CU633980.13        5199-5287
            454-642             CU633980.13        25487-25675
            643-1321            CU633980.13        27867-28545
FEATURES             Location/Qualifiers
     source          1..1321
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="21"
                     /map="21p11.2"
     gene            1..1321
                     /gene="LOC102723553"
                     /gene_synonym="SMIM11B"
                     /note="small integral membrane protein 11B"
                     /db_xref="GeneID:102723553"
     exon            1..364
                     /gene="LOC102723553"
                     /gene_synonym="SMIM11B"
                     /inference="alignment:Splign:2.1.0"
     exon            365..453
                     /gene="LOC102723553"
                     /gene_synonym="SMIM11B"
                     /inference="alignment:Splign:2.1.0"
     CDS             442..648
                     /gene="LOC102723553"
                     /gene_synonym="SMIM11B"
                     /note="isoform a is encoded by transcript variant 2"
                     /codon_start=1
                     /product="uncharacterized protein LOC102723553 isoform a"
                     /protein_id="NP_001381080.1"
                     /db_xref="GeneID:102723553"
                     /translation="MNWKVLTGTTYSPWRVRMEFPLCGCLSLILHHFADKEGRTIGRR
                     ESCLATIWTISRPWQAGSLWITLS"
     exon            454..642
                     /gene="LOC102723553"
                     /gene_synonym="SMIM11B"
                     /inference="alignment:Splign:2.1.0"
     exon            643..1321
                     /gene="LOC102723553"
                     /gene_synonym="SMIM11B"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 cccgggcggg gcccaggatt ggttcaagcc tacggtgttg gtccccggag agtctaggga
       61 gacaagcaat cccctggaat ggtgggggaa gcgatgacag cccctggtcc tcatccgcag
      121 ctctggggga agtcgggggg tggggagggc gggtgttgct ccctgagtgt tgggggaagg
      181 gtatggggag aggaccctga actagccccc aggttaccca ggaggagctg aggcccagag
      241 aggttcagcg actcgcccag ggttgcacag cgagcacagg caccgacgtc gccctccgag
      301 gcctgggctt ccagcaggga gagacccgga cacctgtcat cgcttctcgg tggatccctg
      361 aaatatcaga ccttccagct gcctctcatg tacttgtctg ttgggggctt gtgttgatca
      421 ggagtgaatt cacagtctac catgaattgg aaggtcctaa ctgggaccac ctactcccct
      481 tggagggtcc ggatggagtt tcccctctgc ggctgcctct cactcatcct ccaccacttt
      541 gccgacaagg aaggaaggac aatcgggagg agggagtctt gcttggcgac catctggaca
      601 atatctcgcc catggcaagc tggatccctg tggattactt tgagctaaag acatttcata
      661 aaatgggcat gaaggattcc ttcaaatgaa gacgtggaca aaatgattgg tcaggtcctt
      721 tgctctactg ttgaatggag gaggattttt tttttttttc cctcacacag gggttttctt
      781 ggagctcaag tttggatgac cccagacagt aagataatct catcatggta aagttaatat
      841 gaaatatgtg gtctccaaac agcctctccc agaggccagg atcagcaggt ttgagtggat
      901 aattggcttg tggtcatttt ctcataggat ttttctttta gtagtggaaa ctgtttttca
      961 aatcaaattt ggatgccaac tatgtggaac agaagtgtgg ctgctctggt ggaagtggca
     1021 atggtagtcc tagagtctcc ctgtcagcca caccctttgt ctccccctac ccaagggacc
     1081 ctgtggcctg gaaccgcagt gtgaaatgct atatagtgca atgaagtcaa ttcgaagaca
     1141 agagttcttt gcctttctca tctaattttt agttatggat atgagacgct tgttcagaag
     1201 tatggaaaag tatatataat atgttatctt ttagatgtgg gtgtaaatat gcttatgtat
     1261 gcaatatgct tatattttaa cgcataaaca acatgaataa agcaaacact ctagacttct
     1321 c
//
