LOCUS       NM_001164447            1395 bp    mRNA    linear   PRI 01-FEB-2024
DEFINITION  Homo sapiens family with sequence similarity 90 member A10
            (FAM90A10), mRNA.
ACCESSION   NM_001164447 NR_046351 XM_496957
VERSION     NM_001164447.1
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     PROVISIONAL REFSEQ: This record has not yet been subject to final
            NCBI review. The reference sequence was derived from AC084121.13.
            
            On or before Nov 12, 2021 this sequence version replaced
            NR_046351.1, XM_496957.5.
            
            Summary: FAM90A10 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 SAMEA2148874,
                              SAMEA2151119 [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000533716.2/ ENSP00000497650.1
            RefSeq Select criteria :: based on single protein-coding transcript
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-123               AC084121.13        69047-69169         c
            124-323             AC084121.13        68353-68552         c
            324-432             AC084121.13        67786-67894         c
            433-1395            AC084121.13        66158-67120         c
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="FAM90A10"
                     /gene_synonym="FAM90A10P"
                     /note="family with sequence similarity 90 member A10"
                     /db_xref="GeneID:441328"
                     /db_xref="HGNC:HGNC:32258"
                     /db_xref="MIM:613047"
     CDS             1..1395
                     /gene="FAM90A10"
                     /gene_synonym="FAM90A10P"
                     /note="putative protein FAM90A10P; family with sequence
                     similarity 90 member A10, pseudogene"
                     /codon_start=1
                     /product="putative protein FAM90A10"
                     /protein_id="NP_001157919.1"
                     /db_xref="CCDS:CCDS94255.1"
                     /db_xref="GeneID:441328"
                     /db_xref="HGNC:HGNC:32258"
                     /db_xref="MIM:613047"
                     /translation="MMARRDPKSWAKRLVRAQTLQKQRRAPVGPRAPPPDEEDPRLKC
                     KNCGAFGHTARSTTCPMKCWKAALVPATLGKKEGKENLKPWKPRGEANPGPLNKDKGE
                     KEERPRQQDPQRKALLHMFSGKPPEKPLPNGKGSTESSEHLRVASGPMPVHTTSKRPR
                     VDPVLADRSATEMSGRGSVLASLSPLRKASLSSSSSLGPKERQTGAAADIPQPAFRHQ
                     GPEPLLVVKPTHSSPEGGCREVPQAASKTHGLLQAARPQAQDKRPAVTSQPCPPAATH
                     SLGLGSNLSFGPGAKRPAQAPIQACLNFPKKPRLGPFQIPESAIQGGELGAPENLQPP
                     PAATELGPSTSPQMGRRTPAQVPSVDWQPPHSTPCLPTAQACTMSHHPAAGHDGAQPL
                     RVLFRRLENGRWSSSLLAAPSFHSPEKPGAFLAQSPHVSEKSEAPCVRVPPSVLYEDL
                     QVSSSSEDSDSDLE"
     exon            1..123
                     /gene="FAM90A10"
                     /gene_synonym="FAM90A10P"
                     /inference="alignment:Splign:2.1.0"
     exon            124..323
                     /gene="FAM90A10"
                     /gene_synonym="FAM90A10P"
                     /inference="alignment:Splign:2.1.0"
     exon            324..432
                     /gene="FAM90A10"
                     /gene_synonym="FAM90A10P"
                     /inference="alignment:Splign:2.1.0"
     exon            433..1395
                     /gene="FAM90A10"
                     /gene_synonym="FAM90A10P"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 atgatggcac gtcgggaccc caaatcttgg gccaagagac tggtgagagc ccagaccctc
       61 cagaagcagc ggagggcccc agttgggcca agggctcccc cgcccgatga agaagatccc
      121 aggctcaagt gcaaaaactg cggggccttt ggccacacgg ccagaagtac cacgtgcccc
      181 atgaagtgct ggaaggcagc cctggttcca gcgaccttgg ggaaaaagga agggaaggaa
      241 aacctgaaac catggaagcc ccggggtgaa gccaacccgg ggcccttgaa caaggataag
      301 ggagagaagg aagagagacc aaggcaacaa gacccgcaga ggaaggctct cctccacatg
      361 ttttccggga aacctccaga gaagccgctg ccgaatggaa aaggatccac ggaatcttct
      421 gagcatctga gggttgcaag cgggccaatg ccggtccaca caaccagtaa gaggccgcgc
      481 gtggaccctg tcctcgctga tcgctcagct accgaaatgt ctggcagggg ctccgtcttg
      541 gcttcactgt ctcccctcag aaaagccagc ctgagctcct cctcaagtct tggaccaaag
      601 gaaagacaga caggggctgc ggccgacatc cctcagcctg cattcaggca ccagggcccc
      661 gagcctctcc tcgtggtgaa gccgacacac agcagccctg agggtggctg ccgagaagtt
      721 ccccaggctg cctccaaaac ccacggcctg ctccaggccg ccagacccca ggcacaagac
      781 aaacgtcctg cggtgacctc acagccctgc ccgccagccg ccacacacag cttgggccta
      841 ggctccaatc tcagcttcgg gccgggagcc aagagacctg cccaggctcc gattcaggct
      901 tgcctgaact tccccaagaa accgagactg ggtcccttcc agatccccga aagcgccatc
      961 cagggaggtg agctgggggc cccggagaat ctccaacctc cgccagccgc aaccgaactt
     1021 ggaccaagta cgtcgcccca gatgggcagg aggacaccgg cccaggtgcc cagcgtcgac
     1081 tggcagcctc cgcacagcac accttgcctg cctactgccc aggcctgcac catgtcccat
     1141 cacccagcgg ccggccatga tggggcccag cctctcagag tgctcttccg gagactggaa
     1201 aacggacgct ggagctccag cctcctggcc gccccctcat ttcactctcc tgagaagccg
     1261 ggagccttcc tcgctcagag ccctcatgtg tcagagaagt ctgaggctcc ctgtgttcgt
     1321 gtcccaccga gcgtcctcta tgaggacctt caggtttcct cctcctcaga ggacagcgat
     1381 tctgacctgg agtga
//
