LOCUS       NM_001348070             422 bp    mRNA    linear   PRI 11-DEC-2022
DEFINITION  Homo sapiens family with sequence similarity 236 member A
            (FAM236A), transcript variant 1, mRNA.
ACCESSION   NM_001348070
VERSION     NM_001348070.2
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
            AC234776.4.
            
            On Dec 4, 2019 this sequence version replaced NM_001348070.1.
            
            Transcript Variant: This variant (1) represents the longer
            transcript and encodes the longer isoform (1).
            
            ##Evidence-Data-START##
            Transcript exon combination :: HY187292.1, AA393776.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           SAMEA1966682, SAMEA1968968
                                           [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000611003.2/ ENSP00000490343.2
            RefSeq Select criteria :: based on expression, longest protein
            ##RefSeq-Attributes-END##
            COMPLETENESS: full length.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-93                AC234776.4         103818-103910       c
            94-269              AC234776.4         103465-103640       c
            270-422             AC234776.4         103158-103310       c
FEATURES             Location/Qualifiers
     source          1..422
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="X"
                     /map="Xq13.1"
     gene            1..422
                     /gene="FAM236A"
                     /gene_synonym="DMRTC1-AS1; LINC00684"
                     /note="family with sequence similarity 236 member A"
                     /db_xref="GeneID:100129407"
                     /db_xref="HGNC:HGNC:44268"
     exon            1..93
                     /gene="FAM236A"
                     /gene_synonym="DMRTC1-AS1; LINC00684"
                     /inference="alignment:Splign:2.1.0"
     CDS             58..297
                     /gene="FAM236A"
                     /gene_synonym="DMRTC1-AS1; LINC00684"
                     /note="isoform 1 is encoded by transcript variant 1;
                     DMRTC1 antisense RNA 1 (non-protein coding); long
                     intergenic non-protein coding RNA 684; protein FAM236A;
                     family with sequence similarity 235 member A"
                     /codon_start=1
                     /product="protein FAM236A isoform 1"
                     /protein_id="NP_001334999.1"
                     /db_xref="CCDS:CCDS87765.1"
                     /db_xref="GeneID:100129407"
                     /db_xref="HGNC:HGNC:44268"
                     /translation="MIFTPFLPPADLSVFQNVKGLQNDPEEWVAVSDATEDPSGGTGL
                     PREPALLRGSWRSRFQRALACFTKCFRGGYRALGI"
     exon            94..269
                     /gene="FAM236A"
                     /gene_synonym="DMRTC1-AS1; LINC00684"
                     /inference="alignment:Splign:2.1.0"
     exon            270..422
                     /gene="FAM236A"
                     /gene_synonym="DMRTC1-AS1; LINC00684"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 ggtgtcttca acgaagtcct gtcggtccct accggcacat cacacactcc tggaagcatg
       61 atcttcactc ccttccttcc acctgctgac ctgtctgtct ttcagaatgt gaaagggctg
      121 caaaacgacc ctgaggaatg ggtggctgtg tctgacgcca cggaggaccc atccggtggc
      181 acaggcttgc ccagggaacc tgctcttctg cgagggtctt ggaggagccg gttccagaga
      241 gccctggcat gtttcaccaa gtgtttcagg ggaggatacc gggcactcgg aatctgagac
      301 caccggagcc acagacacag agccatgaac ggtgaccaag ccccttctgc tgctccatgc
      361 ccctgctcgc cgcagtgtcc cagtcaccag gcctgaaata aatgctggca cgcttgactg
      421 tt
//
