Homo sapiens (human): 171546
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Entry
171546 CDS
T01001
Symbol
SPTSSA, C14orf147, SPG90A, SPG90B, SSSPTA
Name
(RefSeq) serine palmitoyltransferase small subunit A
KO
K26384
serine palmitoyltransferase small subunit
Organism
hsa
Homo sapiens (human)
Pathway
hsa04071
Sphingolipid signaling pathway
Disease
H00266
Hereditary spastic paraplegia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04071 Sphingolipid signaling pathway
171546 (SPTSSA)
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Gene cluster
GFIT
Motif
Pfam:
SPT_ssu-like
Motif
Other DBs
NCBI-GeneID:
171546
NCBI-ProteinID:
NP_612145
OMIM:
613540
HGNC:
20361
Ensembl:
ENSG00000165389
UniProt:
Q969W0
Structure
PDB
PDBj
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All DBs
Position
14:complement(34432788..34462240)
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AA seq
71 aa
AA seq
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MAGMALARAWKQMSWFYYQYLLVTALYMLEPWERTVFNSMLVSIVGMALYTGYVFMPQHI
MAILHYFEIVQ
NT seq
216 nt
NT seq
+upstream
nt +downstream
nt
atggcggggatggcgctggcgcgggcctggaagcagatgtcctggttctactaccagtac
ctgctggtcacggcgctctacatgctggagccctgggagcggacggtgttcaattccatg
ctggtttccattgtggggatggcactatacacaggatacgtcttcatgccccagcacatc
atggcgatattgcactactttgaaatcgtacaatga
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