Homo sapiens (human): 5660 Help Entry 5660              CDS       T01001                                  Symbol PSAP, GLBA, PARK24, PSAPD, SAP1, SAP2 Name (RefSeq) prosaposin   KO K12382   saposin Organism hsa  Homo sapiens (human) Pathway hsa00600   Sphingolipid metabolism hsa04142   Lysosome Network nt06014  Sphingolipid degradation   Element N00642   Saposin stimulation of GBA and GALC N00643   Loss of saposin stimulation Disease H00057   Parkinson disease H00126   Gaucher disease H00127   Metachromatic leukodystrophy H00135   Krabbe disease H00423   Sphingolipidosis H01239   Combined SAP deficiency Brite KEGG Orthology (KO) [BR:hsa00001]  09100 Metabolism   09103 Lipid metabolism    00600 Sphingolipid metabolism     5660 (PSAP)  09140 Cellular Processes   09141 Transport and catabolism    04142 Lysosome     5660 (PSAP)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04147 Exosome [BR:hsa04147]     5660 (PSAP) Exosome [BR:hsa04147]  Exosomal proteins   Exosomal proteins of other body fluids (saliva and urine)    5660 (PSAP) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SapB_1 SapB_2 SapA Saposin Helicase_C_3 ApoLp-III Xpo1 Motif Other DBs NCBI-GeneID:  5660 NCBI-ProteinID:  NP_002769 OMIM:  176801 HGNC:  9498 Ensembl:  ENSG00000197746 UniProt:  P07602 Structure PDBPDBj LinkDB All DBs Position 10:complement(71816298..71851251) Genome browser AA seq 524 aa AA seqDB search MYALFLLASLLGAALAGPVLGLKECTRGSAVWCQNVKTASDCGAVKHCLQTVWNKPTVKS LPCDICKDVVTAAGDMLKDNATEEEILVYLEKTCDWLPKPNMSASCKEIVDSYLPVILDI IKGEMSRPGEVCSALNLCESLQKHLAELNHQKQLESNKIPELDMTEVVAPFMANIPLLLY PQDGPRSKPQPKDNGDVCQDCIQMVTDIQTAVRTNSTFVQALVEHVKEECDRLGPGMADI CKNYISQYSEIAIQMMMHMQPKEICALVGFCDEVKEMPMQTLVPAKVASKNVIPALELVE PIKKHEVPAKSDVYCEVCEFLVKEVTKLIDNNKTEKEILDAFDKMCSKLPKSLSEECQEV VDTYGSSILSILLEEVSPELVCSMLHLCSGTRLPALTVHVTQPKDGGFCEVCKKLVGYLD RNLEKNSTKQEILAALEKGCSFLPDPYQKQCDQFVAEYEPVLIEILVEVMDPSFVCLKIG ACPSAHKPLLGTEKCIWGPSYWCQNTETAAQCNAVEHCKRHVWN NT seq 1575 nt NT seq  +upstreamnt  +downstreamnt atgtacgccctcttcctcctggccagcctcctgggcgcggctctagccggcccggtcctt ggactgaaagaatgcaccaggggctcggcagtgtggtgccagaatgtgaagacggcgtcc gactgcggggcagtgaagcactgcctgcagaccgtttggaacaagccaacagtgaaatcc cttccctgcgacatatgcaaagacgttgtcaccgcagctggtgatatgctgaaggacaat gccactgaggaggagatccttgtttacttggagaagacctgtgactggcttccgaaaccg aacatgtctgcttcatgcaaggagatagtggactcctacctccctgtcatcctggacatc attaaaggagaaatgagccgtcctggggaggtgtgctctgctctcaacctctgcgagtct ctccagaagcacctagcagagctgaatcaccagaagcagctggagtccaataagatccca gagctggacatgactgaggtggtggcccccttcatggccaacatccctctcctcctctac cctcaggacggcccccgcagcaagccccagccaaaggataatggggacgtttgccaggac tgcattcagatggtgactgacatccagactgctgtacggaccaactccacctttgtccag gccttggtggaacatgtcaaggaggagtgtgaccgcctgggccctggcatggccgacata tgcaagaactatatcagccagtattctgaaattgctatccagatgatgatgcacatgcaa cccaaggagatctgtgcgctggttgggttctgtgatgaggtgaaagagatgcccatgcag actctggtccccgccaaagtggcctccaagaatgtcatccctgccctggaactggtggag cccattaagaagcacgaggtcccagcaaagtctgatgtttactgtgaggtgtgtgaattc ctggtgaaggaggtgaccaagctgattgacaacaacaagactgagaaagaaatactcgac gcttttgacaaaatgtgctcgaagctgccgaagtccctgtcggaagagtgccaggaggtg gtggacacgtacggcagctccatcctgtccatcctgctggaggaggtcagccctgagctg gtgtgcagcatgctgcacctctgctctggcacgcggctgcctgcactgaccgttcacgtg actcagccaaaggacggtggcttctgcgaagtgtgcaagaagctggtgggttatttggat cgcaacctggagaaaaacagcaccaagcaggagatcctggctgctcttgagaaaggctgc agcttcctgccagacccttaccagaagcagtgtgatcagtttgtggcagagtacgagccc gtgctgatcgagatcctggtggaggtgatggatccttccttcgtgtgcttgaaaattgga gcctgcccctcggcccataagcccttgttgggaactgagaagtgtatatggggcccaagc tactggtgccagaacacagagacagcagcccagtgcaatgctgtcgagcattgcaaacgc catgtgtggaactag

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