ACSF2
Medium-chain acyl-CoA ligase ACSF2, mitochondrial
Also known as: ACSF2_HUMAN, ACSMW, FLJ20920
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96CM8
- Gene
- ACSF2
- Ensembl
- ENSG00000167107
- Chromosome
- 17
- Canonical length
- 615 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Microtubules,Cytosol
OverviewNCBI Gene
Enables medium-chain fatty acid-CoA ligase activity. Predicted to be involved in fatty acid metabolic process. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
615 residues, UniProt reviewed canonical sequence.
>Q96CM8|ACSF2
1 MAVYVGMLRL GRLCAGSSGV LGARAALSRS WQEARLQGVR FLSSREVDRM VSTPIGGLSY
61 VQGCTKKHLN SKTVGQCLET TAQRVPEREA LVVLHEDVRL TFAQLKEEVD KAASGLLSIG
121 LCKGDRLGMW GPNSYAWVLM QLATAQAGII LVSVNPAYQA MELEYVLKKV GCKALVFPKQ
181 FKTQQYYNVL KQICPEVENA QPGALKSQRL PDLTTVISVD APLPGTLLLD EVVAAGSTRQ
241 HLDQLQYNQQ FLSCHDPINI QFTSGTTGSP KGATLSHYNI VNNSNILGER LKLHEKTPEQ
301 LRMILPNPLY HCLGSVAGTM MCLMYGATLI LASPIFNGKK ALEAISRERG TFLYGTPTMF
361 VDILNQPDFS SYDISTMCGG VIAGSPAPPE LIRAIINKIN MKDLVVAYGT TENSPVTFAH
421 FPEDTVEQKA ESVGRIMPHT EARIMNMEAG TLAKLNTPGE LCIRGYCVML GYWGEPQKTE
481 EAVDQDKWYW TGDVATMNEQ GFCKIVGRSK DMIIRGGENI YPAELEDFFH THPKVQEVQV
541 VGVKDDRMGE EICACIRLKD GEETTVEEIK AFCKGKISHF KIPKYIVFVT NYPLTISGKI
601 QKFKLREQME RHLNLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ACSF2 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.25
- Highest tissue expression
- 133 nTPM
Expression across tissuesHPA
Tissue
- kidney: 133 nTPM
- adrenal gland: 69 nTPM
- thyroid gland: 40 nTPM
- skeletal muscle: 40 nTPM
- liver: 34 nTPM
- colon: 26 nTPM
Single-cell type
- proximal tubule cells: 467 nCPM
- cytotrophoblasts: 136 nCPM
- myonuclei: 116 nCPM
- adipocytes: 113 nCPM
- enterocytes: 111 nCPM
- adrenal cortex cells: 105 nCPM
Immune cell
- myeloid DC: 16 nTPM
- eosinophil: 15 nTPM
- memory B-cell: 8.7 nTPM
- intermediate monocyte: 7.7 nTPM
- non-classical monocyte: 7 nTPM
- plasmacytoid DC: 6.3 nTPM
Brain region
- choroid plexus: 9.4 nTPM
- medulla oblongata: 9.3 nTPM
- basal ganglia: 9 nTPM
- spinal cord: 8.7 nTPM
- thalamus: 7.9 nTPM
- cerebellum: 7.5 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)
- 0.65
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.98
- DepMap mean gene effect
- -0.15
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ACSF2 as an antibody target. Whether an autoantibody or antibody against ACSF2 could matter depends on whether native ACSF2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ACSF2 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 ACSF2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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