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ACER3

ACER3, or alkaline ceramidase 3, is a human gene that encodes an enzyme of the alkaline ceramidase family. This family catalyzes the hydrolysis of ceramides to sphingosine and free fatty acids, a key step in sphingolipid metabolism. ACER3 is expressed in multiple tissues and is evolutionarily conserved across vertebrates.

The ACER3 enzyme participates in regulating cellular levels of ceramides and sphingosine, which are bioactive lipids

Subcellular localization is associated with intracellular membranes such as the endoplasmic reticulum and Golgi apparatus, with

Genetic and biochemical studies investigate ACER3 for potential roles in human disease, including disorders linked to

involved
in
signaling
pathways
controlling
cell
growth,
differentiation,
and
apoptosis.
Like
other
alkaline
ceramidases,
ACER3
is
presumed
to
be
a
membrane-bound
protein
with
activity
at
alkaline
pH,
acting
on
various
ceramide
substrates.
some
evidence
for
lysosomal
involvement
in
specific
cell
types.
The
activity
and
expression
of
ACER3
can
be
modulated
by
cellular
conditions,
contributing
to
dynamic
remodeling
of
sphingolipid
metabolism
in
response
to
stress
or
signaling
cues.
impaired
sphingolipid
homeostasis,
neurodegeneration,
and
cancer,
though
direct
causal
relationships
remain
under
study.
The
gene
has
orthologs
in
model
organisms,
which
are
used
to
study
its
physiological
functions
and
regulation.
ACER3
is
studied
alongside
ACER1
and
ACER2
as
part
of
the
family
of
alkaline
ceramidases.