LOCUS       HUMSAPABCD              2171 bp    mRNA    linear   HUM 09-JAN-1995
DEFINITION  Human saposin proteins A-D mRNA, complete cds.
ACCESSION   M32221
VERSION     M32221.1
KEYWORDS    saposin.
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 2171)
  AUTHORS   Kretz,K.A., Carson,G.S., Morimoto,S., Kishimoto,Y., Fluharty,A.L.
            and O'Brien,J.S.
  TITLE     Characterization of a mutation in a family with saposin B
            deficiency: a glycosylation site defect
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 87 (7), 2541-2544 (1990)
   PUBMED   2320574
COMMENT     Original source text: Human lymphoblast, cDNA to mRNA.
            Draft entry and computer-readable sequence for [1] kindly submitted
            by J.S.O'Brien, 22-MAR-1990.
FEATURES             Location/Qualifiers
     source          1..2171
                     /db_xref="H-InvDB:HIT000195459"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /map="10q21-q22"
     gene            1..2171
                     /gene="PSAP"
     CDS             7..1581
                     /gene="PSAP"
                     /note="prosaposin"
                     /codon_start=1
                     /protein_id="AAA60303.1"
                     /db_xref="GDB:G00-120-366"
                     /translation="MYALFLLASLLGAALAGPVLGLKECTRGSAVWCQNVKTASDCGA
                     VKHCLQTVWNKPTVKSLPCDICKDVVTAAGDMLKDNATEEEILVYLEKTCDWLPKPNM
                     SASCKEIVDSYLPVILDIIKGEMSRPGEVCSALNLCESLQKHLAELNHQKQLESNKIP
                     ELDMTEVVAPFMANIPLLLYPQDGPRSKPQPKDNGDVCQDCIQMVTDIQTAVRTNSTF
                     VQALVEHVKEECDRLGPGMADICKNYISQYSEIAIQMMMHMQPKEICALVGFCDEVKE
                     MPMQTLVPAKVASKNVIPALELVEPIKKHEVPAKSDVYCEVCEFLVKEVTKLIDNNKT
                     EKEILDAFDKMCSKLPKSLSEECQEVVDTYGSSILSILLEEVSPELVCSMLHLCSGTR
                     LPALTVHVTQPKDGGFCEVCKKLVGYLDRNLEKNSTKQEILAALEKGCSFLPDPYQKQ
                     CDQFVAEYEPVLIEILVEVMDPSFVCLKIGACPSAHKPLLGTEKCIWGPSYWCQNTET
                     AAQCNAVEHCKRHVWN"
     mat_peptide     184..435
                     /gene="PSAP"
                     /product="saposin A"
     mat_peptide     589..831
                     /gene="PSAP"
                     /product="saposin B"
     mat_peptide     937..1176
                     /gene="PSAP"
                     /product="saposin C"
     mat_peptide     1219..1467
                     /gene="PSAP"
                     /product="saposin D"
     variation       656
                     /gene="PSAP"
                     /note="c in wt; t in saposin B deficiency (Thr->Ile)"
BASE COUNT          496 a          565 c          610 g          500 t
ORIGIN      Chromosome 10, q21-q22.
        1 cgcgctatgt acgccctctt cctcctggcc agcctcctgg gcgcggctct agccggcccg
       61 gtccttggac tgaaagaatg caccaggggc tcggcagtgt ggtgccagaa tgtgaagacg
      121 gcgtccgact gcggggcagt gaagcactgc ctgcagaccg tttggaacaa gccaacagtg
      181 aaatcccttc cctgcgacat atgcaaagac gttgtcaccg cagctggtga tatgctgaag
      241 gacaatgcca ctgaggagga gatccttgtt tacttggaga agacctgtga ctggcttccg
      301 aaaccgaaca tgtctgcttc atgcaaggag atagtggact cctacctccc tgtcatcctg
      361 gacatcatta aaggagaaat gagccgtcct ggggaggtgt gctctgctct caacctctgc
      421 gagtctctcc agaagcacct agcagagctg aatcaccaga agcagctgga gtccaataag
      481 atcccagagc tggacatgac tgaggtggtg gcccccttca tggccaacat ccctctcctc
      541 ctctaccctc aggacggccc ccgcagcaag ccccagccaa aggataatgg ggacgtttgc
      601 caggactgca ttcagatggt gactgacatc cagactgctg tacggaccaa ctccaccttt
      661 gtccaggcct tggtggaaca tgtcaaggag gagtgtgacc gcctgggccc tggcatggcc
      721 gacatatgca agaactatat cagccagtat tctgaaattg ctatccagat gatgatgcac
      781 atgcaaccca aggagatctg tgcgctggtt gggttctgtg atgaggtgaa agagatgccc
      841 atgcagactc tggtccccgc caaagtggcc tccaagaatg tcatccctgc cctggaactg
      901 gtggagccca ttaagaagca cgaggtccca gcaaagtctg atgtttactg tgaggtgtgt
      961 gaattcctgg tgaaggaggt gaccaagctg attgacaaca acaagactga gaaagaaata
     1021 ctcgacgctt ttgacaaaat gtgctcgaag ctgccgaagt ccctgtcgga agagtgccag
     1081 gaggtggtgg acacgtacgg cagctccatc ctgtccatcc tgctggagga ggtcagccct
     1141 gagctggtgt gcagcatgct gcacctctgc tctggcacgc ggctgcctgc actgaccgtt
     1201 cacgtgactc agccaaagga cggtggcttc tgcgaagtgt gcaagaagct ggtgggttat
     1261 ttggatcgca acctggagaa aaacagcacc aagcaggaga tcctggctgc tcttgagaaa
     1321 ggctgcagct tcctgccaga cccttaccag aagcagtgtg atcagtttgt ggcagagtac
     1381 gagcccgtgc tgatcgagat cctggtggag gtgatggatc cttccttcgt gtgcttgaaa
     1441 attggagcct gcccctcggc ccataagccc ttgttgggaa ctgagaagtg tatatggggc
     1501 ccaagctact ggtgccagaa cacagagaca gcagcccagt gcaatgctgt cgagcattgc
     1561 aaacgccatg tgtggaacta ggaggaggaa tattccatct tggcagaaac cacagcattg
     1621 gtttttttct acttgtgtgt ctgggggaat gaacgcacag atctgtttga ctttgttata
     1681 aaaatagggc tcccccacct cccccatttc tgtgtccttt attgtagcat tgctgtctgc
     1741 aagggagccc ctagcccctg gcagacatag ctgcttcagt gccccttttc tctctgctag
     1801 atggatgttg atgcactgga ggtcttttag cctgcccttg catggcgcct gctggaggag
     1861 gagagagctc tgctggcatg agccacagtt tcttgactgg aggccatcaa ccctcttggt
     1921 tgaggccttg ttctgagccc tgacatgtgc ttgggcactg gtgggcctgg gcttctgagg
     1981 tggcctcctg ccctgatcag ggaccctccc cgctttcctg ggcctctcag ttgaaccaaa
     2041 gcagcaaaac aaaggcagtt ttatatgaaa gattagaagc ctggaataat caggcttttt
     2101 aaatgatgta attcccactg taatagcata gggattttgg aagcagctgc tggtggcttg
     2161 ggacatcagt g
//