KEGG   Homo sapiens (human): 5660Help
Entry
5660              CDS       T01001                                 

Gene name
PSAP, GLBA, SAP1
Definition
prosaposin
Orthology
K12382  
saposin
Organism
hsa  Homo sapiens (human)
Pathway
Lysosome
Disease
H00126  
Gaucher disease
H00127  
Metachromatic leukodystrophy (MLD)
H00135  
Krabbe disease
H00423  
Defects in the degradation of sulfatide
H00426  
Defects in the degradation of ganglioside
H01239  
Combined SAP deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 Cellular Processes
  Transport and catabolism
   04142 Lysosome
    5660 (PSAP)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of other body fluids (saliva and urine)
   5660 (PSAP)
BRITE hierarchy
SSDB OrthologParalogGFIT
Motif Motif
Other DBs
NCBI-GI: 
NCBI-GeneID: 
OMIM: 
HGNC: 
HPRD: 
Ensembl: 
Vega: 
UniProt: 
Structure
PDB: 

Jmol
Position
10q21-q22
AA seq 527 aa AA seqDB search
MYALFLLASLLGAALAGPVLGLKECTRGSAVWCQNVKTASDCGAVKHCLQTVWNKPTVKS
LPCDICKDVVTAAGDMLKDNATEEEILVYLEKTCDWLPKPNMSASCKEIVDSYLPVILDI
IKGEMSRPGEVCSALNLCESLQKHLAELNHQKQLESNKIPELDMTEVVAPFMANIPLLLY
PQDGPRSKPQPKDNGDVCQDCIQMVTDIQTAVRTNSTFVQALVEHVKEECDRLGPGMADI
CKNYISQYSEIAIQMMMHMQDQQPKEICALVGFCDEVKEMPMQTLVPAKVASKNVIPALE
LVEPIKKHEVPAKSDVYCEVCEFLVKEVTKLIDNNKTEKEILDAFDKMCSKLPKSLSEEC
QEVVDTYGSSILSILLEEVSPELVCSMLHLCSGTRLPALTVHVTQPKDGGFCEVCKKLVG
YLDRNLEKNSTKQEILAALEKGCSFLPDPYQKQCDQFVAEYEPVLIEILVEVMDPSFVCL
KIGACPSAHKPLLGTEKCIWGPSYWCQNTETAAQCNAVEHCKRHVWN
NT seq 1584 nt NT seq  +upstreamnt  +downstreamnt
atgtacgccctcttcctcctggccagcctcctgggcgcggctctagccggcccggtcctt
ggactgaaagaatgcaccaggggctcggcagtgtggtgccagaatgtgaagacggcgtcc
gactgcggggcagtgaagcactgcctgcagaccgtttggaacaagccaacagtgaaatcc
cttccctgcgacatatgcaaagacgttgtcaccgcagctggtgatatgctgaaggacaat
gccactgaggaggagatccttgtttacttggagaagacctgtgactggcttccgaaaccg
aacatgtctgcttcatgcaaggagatagtggactcctacctccctgtcatcctggacatc
attaaaggagaaatgagccgtcctggggaggtgtgctctgctctcaacctctgcgagtct
ctccagaagcacctagcagagctgaatcaccagaagcagctggagtccaataagatccca
gagctggacatgactgaggtggtggcccccttcatggccaacatccctctcctcctctac
cctcaggacggcccccgcagcaagccccagccaaaggataatggggacgtttgccaggac
tgcattcagatggtgactgacatccagactgctgtacggaccaactccacctttgtccag
gccttggtggaacatgtcaaggaggagtgtgaccgcctgggccctggcatggccgacata
tgcaagaactatatcagccagtattctgaaattgctatccagatgatgatgcacatgcag
gatcagcaacccaaggagatctgtgcgctggttgggttctgtgatgaggtgaaagagatg
cccatgcagactctggtccccgccaaagtggcctccaagaatgtcatccctgccctggaa
ctggtggagcccattaagaagcacgaggtcccagcaaagtctgatgtttactgtgaggtg
tgtgaattcctggtgaaggaggtgaccaagctgattgacaacaacaagactgagaaagaa
atactcgacgcttttgacaaaatgtgctcgaagctgccgaagtccctgtcggaagagtgc
caggaggtggtggacacgtacggcagctccatcctgtccatcctgctggaggaggtcagc
cctgagctggtgtgcagcatgctgcacctctgctctggcacgcggctgcctgcactgacc
gttcacgtgactcagccaaaggacggtggcttctgcgaagtgtgcaagaagctggtgggt
tatttggatcgcaacctggagaaaaacagcaccaagcaggagatcctggctgctcttgag
aaaggctgcagcttcctgccagacccttaccagaagcagtgtgatcagtttgtggcagag
tacgagcccgtgctgatcgagatcctggtggaggtgatggatccttccttcgtgtgcttg
aaaattggagcctgcccctcggcccataagcccttgttgggaactgagaagtgtatatgg
ggcccaagctactggtgccagaacacagagacagcagcccagtgcaatgctgtcgagcat
tgcaaacgccatgtgtggaactag

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