LOCUS       NM_001351111             463 bp    mRNA    linear   PRI 17-APR-2022
DEFINITION  Homo sapiens family with sequence similarity 236 member C
            (FAM236C), transcript variant 1, mRNA.
ACCESSION   NM_001351111
VERSION     NM_001351111.1
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     INFERRED REFSEQ: This record is predicted by genome sequence
            analysis and is not yet supported by experimental evidence. The
            reference sequence was derived from AC234776.4.
            
            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 paralogous alignments.
            
            ##Evidence-Data-START##
            RNAseq introns :: single sample supports all introns SAMEA2148874
                              [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000636267.1/ ENSP00000490543.1
            RefSeq Select criteria :: based on expression, longest protein
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-136               AC234776.4         129366-129501       c
            137-312             AC234776.4         129021-129196       c
            313-463             AC234776.4         128715-128865       c
FEATURES             Location/Qualifiers
     source          1..463
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="X"
                     /map="Xq13.1"
     gene            1..463
                     /gene="FAM236C"
                     /gene_synonym="FAM236D"
                     /note="family with sequence similarity 236 member C"
                     /db_xref="GeneID:109729126"
                     /db_xref="HGNC:HGNC:52641"
     exon            1..136
                     /gene="FAM236C"
                     /gene_synonym="FAM236D"
                     /inference="alignment:Splign:2.1.0"
     CDS             101..340
                     /gene="FAM236C"
                     /gene_synonym="FAM236D"
                     /note="isoform 1 is encoded by transcript variant 1;
                     protein FAM236C"
                     /codon_start=1
                     /product="protein FAM236C isoform 1"
                     /protein_id="NP_001338040.1"
                     /db_xref="CCDS:CCDS87763.1"
                     /db_xref="GeneID:109729126"
                     /db_xref="HGNC:HGNC:52641"
                     /translation="MIFTPFLPPADLSVFQNVKGPQKDPEELVAVSDTAEDPSSGTGL
                     PREPALLRGSWRSRFQRALACFIKCFRGGYRALGI"
     exon            137..312
                     /gene="FAM236C"
                     /gene_synonym="FAM236D"
                     /inference="alignment:Splign:2.1.0"
     exon            313..463
                     /gene="FAM236C"
                     /gene_synonym="FAM236D"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 ggccctcggc ctctttgcac cgggcagagt gacgagcttc gccggtgtct tcattgaagt
       61 cctgttggtc cctaccggca catcacacac tcctggaagc atgatcttca ctcccttcct
      121 tccacctgct gacctgtctg tctttcagaa tgtgaaaggg ccgcaaaaag accctgagga
      181 attggttgct gtatctgaca ccgcggagga cccatccagt ggcacaggct tgcccaggga
      241 acctgctctt ctgcgagggt cttggaggag ccggttccag agggccctgg catgtttcat
      301 caagtgcttc aggggaggat accgggcact cggaatctga gaccaccgga gccacagaca
      361 caggcgtgaa cggtgaccga gccccctctg atgctccatg cccctgctcg ccccagtgtc
      421 ccggtcaccg ggcctgaaat aaatgctggc acgcttgact gtt
//
