LOCUS       S76982                    80 bp    mRNA    linear   HUM 27-JUL-1995
DEFINITION  HEXA {HEXAdeltass mutation, exon 11} [human, Tay-Sachs disease
            patient, mRNA Partial Mutant, 80 nt].
ACCESSION   S76982
VERSION     S76982.1
KEYWORDS    .
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 80)
  AUTHORS   Boles,D.J. and Proia,R.L.
  TITLE     The molecular basis of HEXA mRNA deficiency caused by the most
            common Tay-Sachs disease mutation
  JOURNAL   Am. J. Hum. Genet. 56 (3), 716-724 (1995)
   PUBMED   7887427
  REMARK    GenBank staff at the National Library of Medicine created this
            entry [NCBI gibbsq 164180] from the original journal article.
FEATURES             Location/Qualifiers
     source          1..80
                     /db_xref="H-InvDB:HIT000216703"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
     gene            1..80
                     /gene="HEXA"
     CDS             1..76
                     /gene="HEXA"
                     /note="Unknown"
                     /codon_start=1
                     /protein_id="AAD14242.1"
                     /translation="PWYLNRISYGPDWKDFYVVEPLAFE"
BASE COUNT           18 a           21 c           20 g           21 t
ORIGIN      
        1 ccctggtacc tgaaccgtat atcctatggc cctgactgga aggatttcta cgtagtggaa
       61 cccctggcat ttgaagctga
//