LOCUS       NM_001348072             465 bp    mRNA    linear   PRI 13-FEB-2021
DEFINITION  Homo sapiens family with sequence similarity 236 member B
            (FAM236B), transcript variant 1, mRNA.
ACCESSION   NM_001348072
VERSION     NM_001348072.1
KEYWORDS    RefSeq; MANE Select.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AC240504.3 and AA436071.1.
            
            ##Evidence-Data-START##
            Transcript exon combination :: HY003745.1, AA436071.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           SAMEA1968968, SAMEA2148093
                                           [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000596535.3/ ENSP00000489894.1
            RefSeq Select criteria :: based on expression, longest protein
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-66                AC240504.3         88947-89012
            67-233              AA436071.1         4-170
            234-234             AC240504.3         89357-89357
            235-447             AA436071.1         172-384
            448-465             AC240504.3         89725-89742
FEATURES             Location/Qualifiers
     source          1..465
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="X"
                     /map="Xq13.1"
     gene            1..465
                     /gene="FAM236B"
                     /note="family with sequence similarity 236 member B"
                     /db_xref="GeneID:100132304"
                     /db_xref="HGNC:HGNC:52640"
     exon            1..136
                     /gene="FAM236B"
                     /inference="alignment:Splign:2.1.0"
     CDS             101..340
                     /gene="FAM236B"
                     /note="isoform 1 is encoded by transcript variant 1;
                     family with sequence similarity 235 member B; protein
                     FAM236B"
                     /codon_start=1
                     /product="protein FAM236B isoform 1"
                     /protein_id="NP_001335001.1"
                     /db_xref="CCDS:CCDS87760.1"
                     /db_xref="GeneID:100132304"
                     /db_xref="HGNC:HGNC:52640"
                     /translation="MIFTPFLPPADLSVFQNVKGLQNDPEEWVAVSDATEDPSGGTGL
                     PREPALLRGSWRSRFQRALACFTKCFRGGYRALGI"
     exon            137..312
                     /gene="FAM236B"
                     /inference="alignment:Splign:2.1.0"
     exon            313..465
                     /gene="FAM236B"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 ggccctcggc ctctttgcac ccggcagagt gacgagcttc gccggtgtct tcaacgaagt
       61 cctgtcggtc cctaccggca catcacacac tcctggaagc atgatcttca ctcccttcct
      121 tccacctgct gacctgtctg tctttcagaa tgtgaaaggg ctgcaaaacg accctgagga
      181 atgggtggct gtgtctgacg ccacggagga cccatccggt ggcacaggct tgcccaggga
      241 acctgctctt ctgcgagggt cttggaggag ccggttccag agagccctgg catgtttcac
      301 caagtgtttc aggggaggat accgggcact cggaatctga gaccaccgga gccacagaca
      361 cagagccatg aacggtgacc aagccccttc tgctgctcca tgcccctgct cgccgcagtg
      421 tcccagtcac caggcctgaa ataaatgctg gcacgcttga ctgtt
//
