ACER2
Alkaline ceramidase 2
Also known as: ACER2_HUMAN, ALKCDase2, ASAH3L, FLJ41587
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5QJU3
- Gene
- ACER2
- Ensembl
- ENSG00000177076
- Chromosome
- 9
- Canonical length
- 275 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted membrane proteins
OverviewNCBI Gene
The sphingolipid metabolite sphingosine-1-phosphate promotes cell proliferation and survival, whereas its precursor, sphingosine, has the opposite effect. The ceramidase ACER2 hydrolyzes very long chain ceramides to generate sphingosine (Xu et al., 2006 [PubMed 16940153]).[supplied by OMIM, Jul 2010]
Canonical amino-acid sequenceUniProt
275 residues, UniProt reviewed canonical sequence.
>Q5QJU3|ACER2
1 MGAPHWWDQL QAGSSEVDWC EDNYTIVPAI AEFYNTISNV LFFILPPICM CLFRQYATCF
61 NSGIYLIWTL LVVVGIGSVY FHATLSFLGQ MLDELAVLWV LMCALAMWFP RRYLPKIFRN
121 DRGRFKVVVS VLSAVTTCLA FVKPAINNIS LMTLGVPCTA LLIAELKRCD NMRVFKLGLF
181 SGLWWTLALF CWISDRAFCE LLSSFNFPYL HCMWHILICL AAYLGCVCFA YFDAASEIPE
241 QGPVIKFWPN EKWAFIGVPY VSLLCANKKS SVKITLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ACER2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 7
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 58 nTPM
Expression across tissuesHPA
Tissue
- stomach: 58 nTPM
- urinary bladder: 37 nTPM
- placenta: 9.1 nTPM
- adipose tissue: 7.2 nTPM
- pancreas: 6.4 nTPM
- breast: 5.5 nTPM
Single-cell type
- urothelial cells: 1,314 nCPM
- papillary tip epithelial cells: 771 nCPM
- foveolar cells: 749 nCPM
- prostatic club cells: 375 nCPM
- prostatic hillock cells: 331 nCPM
- syncytiotrophoblasts: 242 nCPM
Immune cell
- intermediate monocyte: 0.5 nTPM
- naive CD4 T-cell: 0.2 nTPM
- plasmacytoid DC: 0.2 nTPM
- gdT-cell: 0.1 nTPM
- memory B-cell: 0.1 nTPM
- total PBMC: 0.1 nTPM
Brain region
- thalamus: 14 nTPM
- cerebral cortex: 12 nTPM
- amygdala: 11 nTPM
- pons: 11 nTPM
- hippocampal formation: 11 nTPM
- white matter: 9.6 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.7
- gnomAD pLI
- 0.04
- gnomAD missense Z
- -0.37
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to xenobiotic stimulus
- ceramide catabolic process
- DNA damage response
- DNA damage response, signal transduction by p53 class mediator
- negative regulation of cell adhesion mediated by integrin
- negative regulation of cell-matrix adhesion
- positive regulation of cell population proliferation
- regulation of apoptotic process
- regulation of autophagy
- regulation of glycoprotein biosynthetic process
- response to retinoic acid
- sphingolipid catabolic process
- sphingosine biosynthetic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ACER2 as an antibody target. Whether an autoantibody or antibody against ACER2 could matter depends on whether native ACER2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ACER2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label ACER2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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