LOCUS       NM_001372060            2118 bp    mRNA    linear   PRI 29-OCT-2022
DEFINITION  Homo sapiens anomalous homeobox (ANHX), transcript variant 1, mRNA.
ACCESSION   NM_001372060 XM_011534821
VERSION     NM_001372060.1
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
            AC226150.5.
            
            On Aug 6, 2019 this sequence version replaced XM_011534821.3.
            
            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 alignments.
            
            ##Evidence-Data-START##
            RNAseq introns :: single sample supports all introns SAMEA1968968,
                              SAMEA2148093 [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            inferred exon combination :: based on alignments, homology
            MANE Ensembl match        :: ENST00000545940.6/ ENSP00000439513.2
            RefSeq Select criteria    :: based on manual assertion,
                                         conservation, expression
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-71                AC226150.5         897-967
            72-342              AC226150.5         2396-2666
            343-470             AC226150.5         5130-5257
            471-594             AC226150.5         8827-8950
            595-811             AC226150.5         9622-9838
            812-932             AC226150.5         10336-10456
            933-1225            AC226150.5         10946-11238
            1226-1373           AC226150.5         15422-15569
            1374-1458           AC226150.5         17407-17491
            1459-2118           AC226150.5         17803-18462
FEATURES             Location/Qualifiers
     source          1..2118
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="12"
                     /map="12q24.33"
     gene            1..2118
                     /gene="ANHX"
                     /note="anomalous homeobox"
                     /db_xref="GeneID:647589"
                     /db_xref="HGNC:HGNC:40024"
     exon            1..71
                     /gene="ANHX"
                     /inference="alignment:Splign:2.1.0"
     exon            72..342
                     /gene="ANHX"
                     /inference="alignment:Splign:2.1.0"
     CDS             94..1545
                     /gene="ANHX"
                     /note="isoform 1 is encoded by transcript variant 1;
                     anomalous homeobox protein"
                     /codon_start=1
                     /product="anomalous homeobox protein isoform 1"
                     /protein_id="NP_001358989.1"
                     /db_xref="CCDS:CCDS91786.1"
                     /db_xref="GeneID:647589"
                     /db_xref="HGNC:HGNC:40024"
                     /translation="MQSFLTLLKEHEDTCAPPAELVTLAGRLCRDFQDDLAQLQPLVT
                     AILDSQLRLHLLDNADVALACARVLDQQEQQQAACRLLEGCQVPGGSQELVQLWNDIH
                     YRLVMRRLGVAALTPVQKFRCRKRNPPPPSLCPEGLKSRNFPREVREKLHNFAVGVNT
                     NPSKAERENLALETSLTPEQVYNWFANYRRRQRALPQHMKPAQQATAEDPGARERGPD
                     LLQPSGNPRVDSGFVDRPQWSEEREEKGPPQSPQTTQGPWEPLALAPDFPADETVSKP
                     LDVRSLPGGEMYQEGPGHDPATLPLFCPGPGLCPLAAGNDMLNPSLAAPESWLMSLAL
                     ASSKEVSFQTGQLVHSHGLDFMMGPADTAVAVSIATLGDPSPTGFSGPPSGHPQSVQL
                     EEGLGTSSGRTELRVGSFLVTQPPLQAPEFILTQSPPELAPAPSAFPGPVSAMELSQA
                     LPSSQVQCSDSQASGDAFWGARMLLEFSGSSLG"
     exon            343..470
                     /gene="ANHX"
                     /inference="alignment:Splign:2.1.0"
     exon            471..594
                     /gene="ANHX"
                     /inference="alignment:Splign:2.1.0"
     exon            595..811
                     /gene="ANHX"
                     /inference="alignment:Splign:2.1.0"
     exon            812..932
                     /gene="ANHX"
                     /inference="alignment:Splign:2.1.0"
     exon            933..1225
                     /gene="ANHX"
                     /inference="alignment:Splign:2.1.0"
     exon            1226..1373
                     /gene="ANHX"
                     /inference="alignment:Splign:2.1.0"
     exon            1374..1458
                     /gene="ANHX"
                     /inference="alignment:Splign:2.1.0"
     exon            1459..2118
                     /gene="ANHX"
                     /inference="alignment:Splign:2.1.0"
     regulatory      2093..2098
                     /regulatory_class="polyA_signal_sequence"
                     /gene="ANHX"
                     /note="hexamer: ATTAAA"
     polyA_site      2118
                     /gene="ANHX"
                     /note="major polyA site"
ORIGIN      
        1 gcccagcgcc tcctcgccag ccccgggtgc gcgccaagca cgtgcgccgg cgctgaagcg
       61 ggtcccggag gagtggccac gacccagcac aggatgcaga gcttcctgac tctgctgaag
      121 gagcatgagg acacctgtgc acccccggcg gagctggtga cccttgcggg cagactgtgc
      181 cgggacttcc aggatgacct tgcccaactg cagcctttgg tcacagccat tctggacagc
      241 cagctccgcc tgcatctcct ggacaacgca gatgtggccc tggcgtgcgc ccgtgtcctg
      301 gaccagcagg agcagcagca ggcggcttgc cgcctcctgg aggggtgcca ggtgccggga
      361 ggcagccagg agttagtgca gctctggaac gacatccact accgtctggt catgaggagg
      421 ctgggcgtgg ctgcgctcac cccggtgcag aagttccgct gcaggaagag gaaccccccg
      481 cccccctccc tctgcccaga ggggctgaag agccggaact tccccagaga ggttcgtgag
      541 aagctgcaca atttcgctgt gggggtgaac accaacccca gcaaggctga gagggagaac
      601 ttggcattgg agacgagctt gacccctgag caggtgtaca actggtttgc caattaccgg
      661 cgccgccaaa gagcccttcc ccagcacatg aagccagccc agcaggccac agctgaagac
      721 cctggtgcga gggagagggg tcctgacctc ctgcagccct caggcaaccc ccgtgttgac
      781 tctgggtttg tggacaggcc tcagtggtca gaggaacgtg aggaaaaggg gcctccacag
      841 tccccacaga ccacccaagg accatgggag ccactggcct tagccccgga ctttcccgca
      901 gatgagacag tctcaaagcc actggatgtc aggtctctgc caggtggcga gatgtaccag
      961 gaggggcctg gccatgatcc tgccaccctc cccctcttct gccctggccc tggcctctgc
     1021 cctctggctg ctggcaatga catgctgaac ccctctctgg ctgcccctga atcttggctg
     1081 atgtctcttg cactggcgtc ctccaaggaa gtttccttcc agactgggca gctggtccac
     1141 agccatgggc tggacttcat gatgggccct gcagacaccg ctgtggctgt gtccattgcc
     1201 acccttggag atcccagccc tacagggttt tctggccccc ccagcggcca tccccagagc
     1261 gtgcaattgg aggagggtct gggcacaagc agtggacgga cagagctacg ggtgggcagc
     1321 ttcctggtga cacagccccc actgcaagct cctgaattca tcctcaccca gagccctcca
     1381 gagctggccc cagccccatc tgccttcccc ggccctgtgt ctgccatgga gctgagccag
     1441 gccctgccct ccagccaggt gcagtgttct gatagccagg cctctggtga tgccttctgg
     1501 ggagccagga tgctccttga gttttcaggg agcagcctgg gctgagctat ccccaggagc
     1561 cagacagcac cccaggagga gcgggtgtgg atggtctgcc tggtcaacac aaggagttac
     1621 agagctttat cctgaataca aaatgaaggt ccccagagtt cccctggggg ctctgctgaa
     1681 aagcagagat tctttcccac tgccatgttt gaatagtttg gttagcaatt ccctgtagta
     1741 gagaaagcat ttgagaaatg ttcgtgagat cagaagtcaa aggtgggtct gtcccactca
     1801 cgcagcactg gatcagtcgg gctccggggc actcgtgcag agaaggccat tctagagagg
     1861 ggagtgttct gctgctggct gccttgccgt ctgcccgtgc acacagccag acttttccac
     1921 caagttaact gagtgaggta tgaggagtgt tctgagattt ctgtgtgtag gggcttctcc
     1981 cttgagtact gggaggcaaa cctgtctgcg aatggcctag gcagggcaga gtagggtgga
     2041 ttttccctcc aggttgtaat tcactgtgtc tatgacacaa atgttgtagt caattaaagt
     2101 ttaatgtttt gaactccc
//
