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Gene · 34

ACADM: acyl-CoA dehydrogenase medium chain

12 sourcesgene-search-2026-11-11-0.2.0

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ConductScience Library. ACADM: acyl-CoA dehydrogenase medium chain. Genes, record 34. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/34

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Gene

Symbol
ACADM
HGNC
Name
acyl-CoA dehydrogenase medium chain
HGNC
NCBI Gene ID
34
NCBI Gene
HGNC ID
HGNC:89
HGNC
Ensembl
ENSG00000117054
NCBI Gene
Aliases
ACAD1, MCAD, MCADH
NCBI Gene
Type
protein-coding
NCBI Gene

Proteins1

Reviewed human proteins whose Swiss-Prot entry states the gene.

UniProt entryProteinLengthStructuresGene stated in
P11310Medium-chain specific acyl-CoA dehydrogenase, mitochondrial4217Ensembl, GeneID, HGNC

Source UniProt

Patents38

Patents whose sequence listing contains this protein's exact sequence. A patent can list a sequence without claiming it.

PublicationPublishedSEQ ID NOProteinSource
JP 2026067851 A2026-04-21109P11310Espacenet
JP 2026004568 A2026-01-1436260P11310Espacenet
EP 4650780 A22025-11-198853P11310Espacenet
JP 2025517970 A2025-06-128853P11310Espacenet
JP 2025062604 A2025-04-141856P11310Espacenet
US 11813258 B22023-11-143P11310Espacenet
JP 2023521663 A2023-05-25108P11310Espacenet
US 11446398 B22022-09-201856P11310Espacenet
JP 2022524081 A2022-04-27104827P11310Espacenet
JP 2022519460 A2022-03-2427P11310Espacenet

1 to 10 of 38

See all 38 patents

Drugs0

Drugs a ChEMBL mechanism record says act on the gene's protein, through Open Targets.

None in this release.

Trials0

Trials of those drugs. A trial joins the gene only through a drug that acts on it.

None in this release.

NIH grants1,226

NIH grants whose papers are about the gene, through NIH's grant-paper links.

GrantTitleACADM papersNewest fiscal year
P30DK020572Michigan Diabetes Research Center (MDRC)62025
P30DK056341Washington University Nutrition Obesity Research Center62025
P30CA016672Cancer Center Support Grant42025
P30DK026743UCSF Liver Center42025
ZIABC005562Xenobiotic receptors42025
ZIABC005708Xenobiotic metabolism, cancer chemoprevention and cancer biomarkers42025
P01AI063302The intersection of innate and adaptive immunity to intracellular pathogens32025
P30AG028716Duke Claude D. Pepper Older Americans Independence Center32025
P30DK020541NYR-Diabetes Research Center (NYR-DRC)32025
P30DK052574Host-environment interactions in the pathophysiology of digestive disease32025

1 to 10 of 1,226Source NIH's project files

See all 1,226 nih grants

Papers1,869

Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.

TitleJournalYearPMIDFound bySource
Medium-chain acyl-CoA dehydrogenase deficiency: A ten-year single-center case series from India.Clin Chim Acta202642749071PubTator, text miningPubMed
When to think of genetic causes for rhabdomyolysis? A Brazilian single-center exploratory study.Arq Neuropsiquiatr202642595308PubTator, text miningPubMed
Medium Chain Acyl-CoA Dehydrogenase Deficiency; an Unexpected Cause of Neonatal Ketoacidosis.JIMD Rep202642578122PubTator, text miningPubMed
Evaluating the potential causal relationship between carnitine-related metabolites and breast cancer: a Mendelian randomization and transcriptomic analysis.Arch Med Sci202642540481PubTator, text miningPubMed
Dynamic regulation of lysine and arginine metabolism promotes immune evasion by limiting T cell function in cancer.Sci Immunol202642497246PubTator, text miningPubMed
Distinct Molecular Signature of Earlobe Keloids: Integrated Transcriptomic Analysis of Extracellualr Matrix, Metalloproteinase, and Metabolic Pathways.Aesthetic Plast Surg202642414644PubTator, text miningPubMed
Mutant KRAS-driven selective mRNA translation reveals mechanisms and therapeutic vulnerabilities in cancer.Cell Rep202642284146PubTator, text miningPubMed
ACADM-mediated fatty acid β-oxidation pathway in atherosclerosis and abdominal aortic aneurysm.Eur Heart J202642247143PubTator, text miningPubMed
Expanding the Utility of Exome Sequencing in Preventive and Population Genetics.Am J Med Genet A202642212615PubTator, text miningPubMed
Identification of 19 Pathogenic Variants in a Clinically Heterogeneous Cohort With Suspected Inborn Errors of Metabolism.Clin Genet202641968882PubTator, text miningPubMed

1 to 10 of 1,869

See all 1,869 papers

Sources 12

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
  • GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
  • HGNCCC0
  • NCBI GenePublic domain (US government)
  • NIH's project files and grant-paper linksPublic domain
  • Open TargetsCC0 1.0
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • EMBL-EBI's patent proteinsEMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use
  • GenBank's patent filesGenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/
  • HGNCCC0: https://www.genenames.org/about/license/
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH's project files and grant-paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this gene from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/genes/v1/34

GET https://conductscience.org/api/genes/v1/34/patents?page=2