PSAP
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Homo sapiens |
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PSAP is differentially expressed in 311 experiments: 106 organism parts: bone marrow, cerebellum, ... (104 more);, 209 disease states: normal, acute myeloid leukemia, ... (207 more);, 119 cell types 398 cell lines 47 compound treatments and 78 other conditions. |
| Synonyms |
SAP1, GLBA |
| Orthologs |
psap
(Danio rerio)
PSAP
(Bos taurus)
PSAP
(Gallus gallus)
ENSCING00000006331
(Ciona intestinalis)
Sap-r
(Drosophila melanogaster)
psap
(Xenopus laevis)
PSAP
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology ID |
GO:0008289, GO:0016021, GO:0008047, GO:0007596, GO:0005615, GO:0005576, GO:0005739, GO:0006869, GO:0005794, GO:0005764, GO:0006629, GO:0006665, GO:0043085, GO:0043231, GO:0043408, GO:0002576, GO:0006687, GO:0043202, GO:0030168, GO:0060736, GO:0060742 |
| Gene Ontology Term |
lipid transport, positive regulation of catalytic activity, extracellular space, lysosome, Golgi apparatus, lipid binding, extracellular region, blood coagulation, intracellular membrane-bounded organelle, regulation of MAPKKK cascade, lipid metabolic process, sphingolipid metabolic process, enzyme activator activity, integral to membrane, mitochondrion, platelet degranulation, prostate gland growth, glycosphingolipid metabolic process, epithelial cell differentiation involved in prostate gland development, lysosomal lumen, platelet activation |
| InterPro Term |
SapA, SaposinB, Saposin, SapB_1, SapB_2, Saposin_chordata |
| InterPro ID |
IPR007856, IPR008139, IPR008138, IPR008373, IPR003119, IPR021165 |
| Ensembl Family Description |
PROACTIVATOR POLYPEPTIDE PRECURSOR[CONTAINS SAPOSIN A SAPOSIN B SAPOSIN B SAPOSIN C SAPOSIN D |
| Ensembl Family |
ENSFM00250000002893 |
| UniProt Accession |
P07602, Q53Y86, Q5BJH1, C9JIZ6, B1AVU8, F5H0X6, F8W6Z6 |
| EMBL-Bank ID |
M60258, M60255, M60257, BC001503, J03015, J03077, M12710, D00422, BC091483, CR456746, AL731541, BC004275, BC007612, CH471083, M86181, BT006849, M32221, AC073370, X57107, X57108 |
| Description |
prosaposin [Source:HGNC Symbol;Acc:9498] |
| Ensembl Protein ID |
ENSP00000378387, ENSP00000378392, ENSP00000378394, ENSP00000378398, ENSP00000362212, ENSP00000384385, ENSP00000350063 |
| Gene-Disease Assocation |
GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY, METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY, COMBINED SAPOSIN DEFICIENCY, KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY |
| UniGene ID |
Hs.523004 |
| RefSeq ID |
NM_001042465, NM_001042466, NP_002769, NP_001035931, NP_001035930, NM_002778 |
| HGNC Symbol |
PSAP |
| Ensembl Gene ID |
ENSG00000197746 |
| Entrez Gene ID |
5660 |
| Ensembl Transcript ID |
ENST00000373120, ENST00000493143, ENST00000495196, ENST00000404083, ENST00000357471, ENST00000394940, ENST00000394936, ENST00000394934, ENST00000394929 |
| Design Element |
ENST00000404083, ENST00000394936, ENST00000495196, ENST00000394934, g11386146_3p_s_at, 200871_s_at, J03077_s_at, ENST00000394929, g337761_3p_a_at, 200866_s_at, ENST00000357471, ENST00000373120, 36795_at, ENST00000493143, ENST00000394940 |
| Search EB-eye |
ENSG00000197746
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