about
P129
P688
Mutations in the SPTLC2 subunit of serine palmitoyltransferase cause hereditary sensory and autonomic neuropathy type IIdentification of small subunits of mammalian serine palmitoyltransferase that confer distinct acyl-CoA substrate specificitiesAutophagy regulates sphingolipid levels in the liverORMDL/serine palmitoyltransferase stoichiometry determines effects of ORMDL3 expression on sphingolipid biosynthesisThe Variant p.(Arg183Trp) in SPTLC2 Causes Late-Onset Hereditary Sensory Neuropathy.
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteinë
@sq
proteïne in Serine palmitoyltransferase long chain base subunit 2
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Serine palmitoyltransferase long chain base subunit 2
@en
Serine palmitoyltransferase long chain base subunit 2
@nl
type
label
Serine palmitoyltransferase long chain base subunit 2
@en
Serine palmitoyltransferase long chain base subunit 2
@nl
altLabel
LCB 2
@en
LCB2a
@en
Long chain base biosynthesis protein 2
@en
SPT 2
@en
SPTLC2
@en
long chain base biosynthesis protein 2a
@en
serine palmitoyltransferase 2
@en
serine palmitoyltransferase, subunit II
@en
serine-palmitoyl-CoA transferase 2
@en
prefLabel
Serine palmitoyltransferase long chain base subunit 2
@en
Serine palmitoyltransferase long chain base subunit 2
@nl
P361
P680
P681
P682
P705
P352
P129
P31
P352
P361
P637
XP_011535686
P680
P681
P682
P702
P703
P705
ENSP00000216484
ENSP00000451029
ENSP00000452189