LOCUS       NM_001423528            1395 bp    mRNA    linear   PRI 27-AUG-2024
DEFINITION  Homo sapiens family with sequence similarity 90 member A3
            (FAM90A3), mRNA.
ACCESSION   NM_001423528
VERSION     NM_001423528.1
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.
REFERENCE   1  (bases 1 to 1395)
  AUTHORS   Bosch,N., Escaramis,G., Mercader,J.M., Armengol,L. and Estivill,X.
  TITLE     Analysis of the multi-copy gene family FAM90A as a copy number
            variant in different ethnic backgrounds
  JOURNAL   Gene 420 (2), 113-117 (2008)
   PUBMED   18602769
REFERENCE   2  (bases 1 to 1395)
  AUTHORS   Bosch,N., Caceres,M., Cardone,M.F., Carreras,A., Ballana,E.,
            Rocchi,M., Armengol,L. and Estivill,X.
  TITLE     Characterization and evolution of the novel gene family FAM90A in
            primates originated by multiple duplication and rearrangement
            events
  JOURNAL   Hum Mol Genet 16 (21), 2572-2582 (2007)
   PUBMED   17684299
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 AF228730.8.
            
            Summary: FAM90A3 belongs to subfamily II of the primate-specific
            FAM90A gene family, which originated from multiple duplications and
            rearrangements (Bosch et al., 2007 [PubMed 17684299]). For
            background information on the FAM90A gene family, as well as
            information on the evolution of FAM90A genes, see FAM90A1 (MIM
            613041).[supplied by OMIM, Oct 2009].
            
            ##Evidence-Data-START##
            RNAseq introns :: single sample supports all introns SAMEA2151119
                              [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000506444.1/ ENSP00000514262.1
            RefSeq Select criteria :: based on single protein-coding transcript
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-123               AF228730.8         224275-224397
            124-323             AF228730.8         224892-225091
            324-432             AF228730.8         225550-225658
            433-1395            AF228730.8         226323-227285
FEATURES             Location/Qualifiers
     source          1..1395
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="8"
                     /map="8p23.1"
     gene            1..1395
                     /gene="FAM90A3"
                     /gene_synonym="FAM90A3P"
                     /note="family with sequence similarity 90 member A3"
                     /db_xref="GeneID:389611"
                     /db_xref="HGNC:HGNC:32251"
                     /db_xref="MIM:613042"
     CDS             1..1395
                     /gene="FAM90A3"
                     /gene_synonym="FAM90A3P"
                     /note="family with sequence similarity 90 member A3,
                     pseudogene"
                     /codon_start=1
                     /product="protein FAM90A3"
                     /protein_id="NP_001410457.1"
                     /db_xref="GeneID:389611"
                     /db_xref="HGNC:HGNC:32251"
                     /db_xref="MIM:613042"
                     /translation="MMARRDPTSWAKRLVRAQTLQKQRRAPVGPRAPPPDEEDPRLKC
                     KNCGAFGHTARSTRCPMKCWKAALVPATLGKKEGKENLKPWKPRVEANPGPLNKDKGE
                     KEERPRQQDPQRKALLHMFSGKPPEKPLPNGKGSTEPSDYLRVASGPMPVHTTSKRPR
                     VDPVLADGSATEMSDRGSVLASLSPLRKASLSSSSSLGPKERQTGAAADIPQPAVRHQ
                     GREPLLVVKPTHSSPEGGCREVPQAASKTHGLLQAARPQAQDKRPAVTSQPCPPAATH
                     SLGLGSNLSFGPGAKRPAQAPIQACLNFPKKPRLGPFQIPESAIQGGELGAPENLQPP
                     PAATELGPSTSPQMGRRTPAQVPSVERQPPHSRPCLPTAQACTMSHHSAASHDGAQPL
                     RVLFRRLENGRWSSSLLAAPSFHSPEKPGAFLAQSPHVSEKSEAPCVRVPPSVLYEDL
                     QVSSSSEDSDSDLE"
     exon            1..123
                     /gene="FAM90A3"
                     /gene_synonym="FAM90A3P"
                     /inference="alignment:Splign:2.1.0"
     exon            124..323
                     /gene="FAM90A3"
                     /gene_synonym="FAM90A3P"
                     /inference="alignment:Splign:2.1.0"
     exon            324..432
                     /gene="FAM90A3"
                     /gene_synonym="FAM90A3P"
                     /inference="alignment:Splign:2.1.0"
     exon            433..1395
                     /gene="FAM90A3"
                     /gene_synonym="FAM90A3P"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 atgatggcac gtcgggaccc cacatcttgg gccaagagac tggtgagagc ccagaccctc
       61 cagaagcagc ggagggcccc agttgggcca agggctcccc cgcccgatga agaagatccc
      121 aggctcaagt gcaaaaactg cggggccttt ggccacacgg ccagaagtac caggtgcccc
      181 atgaagtgct ggaaggcagc cctggttcca gcgaccttgg ggaaaaagga agggaaggaa
      241 aacctgaaac catggaagcc ccgggttgaa gccaacccgg ggcccttgaa caaggataag
      301 ggagagaagg aagagagacc aaggcaacaa gacccgcaga ggaaggctct cctccacatg
      361 ttttccggga aacctccaga gaagccgctg ccgaatggaa aaggatccac ggaaccttct
      421 gattatctga gggttgcaag cgggccaatg ccggtccaca caaccagtaa gaggccgcgc
      481 gtggaccctg tcctcgctga tggctcagct accgaaatgt ctgacagggg ctccgtcttg
      541 gcttcactgt ctcccctcag aaaagccagc ctgagctcct cctcaagtct tggaccaaag
      601 gaaagacaga caggggctgc ggccgacatc cctcagcctg cagtcaggca ccagggccgc
      661 gagcctctcc tcgtggtgaa gccgacacac agcagccctg agggtggctg ccgagaagtt
      721 ccccaggctg cctccaaaac ccacggcctg ctccaggccg ccagacccca ggcacaagac
      781 aaacgtcctg cggtgacctc acagccctgc ccgccagccg ccacacacag cttgggcctc
      841 ggctccaatc tcagcttcgg gccaggagcc aagagacctg cccaggctcc gattcaggct
      901 tgcctgaact tccccaagaa accgagactg ggtcccttcc agatccccga aagcgccatc
      961 cagggaggtg agctgggggc cccggagaat ctccaacctc cgccagccgc aaccgaactt
     1021 ggaccaagta cgtcgcccca gatgggcagg aggacaccgg cccaggtgcc cagcgtcgaa
     1081 cggcagcctc cgcacagcag accttgcctg cctactgccc aggcctgcac catgtcccat
     1141 cactcagcgg ccagccatga tggggcccag cctctcagag tgctcttccg gagactggaa
     1201 aacggacgct ggagctccag cctcctggcg gccccctcat ttcactctcc tgagaagccg
     1261 ggagccttcc tcgctcagag ccctcatgtg tcagagaagt ctgaggctcc ctgtgttcgt
     1321 gtcccaccga gcgtcctcta tgaggacctt caggtttcct cctcctcaga ggacagcgat
     1381 tctgacctgg agtga
//
