PXD071037 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Combined Histological and Proteomic Analysis Reveals Muscle Denervation in KMT5B-Related Neurodevelopmental Disorder: A Case Report |
| Description | Background: Patients with neurodevelopmental and neuromuscular disorders often show overlapping clinical phenotypes. Pathogenic variants in KMT5B, a histone lysine methyltransferase, have been linked to neurodevelopmental disorders, yet their effects on human skeletal muscle remain unexplored. We report a patient with KMT5B-linked disease who presented to a neuromuscular specialty clinic with significant involvement of skeletal muscle, where a multi-omics approach established the genetic diagnosis and revealed neuromuscular findings relevant for diagnosis, care and rehabilitation. Methods: Whole-exome sequencing was performed from blood and data was analyzed using the RD-Connect Genome Phenome Analysis Platform. Histological analysis and proteomic profiling were performed on muscle tissue. Results: Whole-exome sequencing revealed a pathogenic heterozygous variant (c.554_557del, p.Tyr185Cysfs*27) in KMT5B. Histological examination revealed fiber-type grouping, angular fibers, increased fast-twitch fiber proportion, and lipid droplet accumulation, indicative of muscle denervation. Proteomic profiling identified 77 dysregulated proteins, including upregulation of sarcomeric proteins, mitochondrial and glycolytic enzymes, acute-phase and complement factors, and extracellular matrix components, reflecting structural remodeling, metabolic adaptation, and inflammatory activation. These findings align with phenotypes observed in Kmt5b mouse models, supporting a role of KMT5B in neuromuscular function. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-01-05 |
| AnnouncementXML | Submission_2026-01-04_16:33:28.029.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Andreas Hentschel |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606; scientific name: Mus musculus (Mouse); NCBI TaxID: NEWT:10090; |
| ModificationList | iodoacetamide derivatized residue |
| Instrument | Q Exactive HF |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2025-11-21 05:21:57 | ID requested | |
| ⏵ 1 | 2026-01-04 16:33:29 | announced | |
Publication List
| 10.3390/jcm14248636; |
| Aksel Kilicarslan O, Gangfu, ß A, K, ö, lbel H, Muhmann D, Polavarapu K, Thompson R, Schmitt LI, Lessard L, Chen L, Eisenk, ö, lbl A, Schara-Schmidt U, Hentschel A, Lochm, ü, ller H, Roos A, Combined Histological and Proteomic Analysis Reveals Muscle Denervation in KMT5B-Related Neurodevelopmental Disorder: A Case Report. J Clin Med, 14(24):(2025) [pubmed] |
Keyword List
| submitter keyword: KMT5B |
| muscle denervation in neurodevelopmental disorders |
| muscle proteomics |
| fast-twitch fiber predominance |
| hypotonia |
| case report |
Contact List
| Prof. Dr. Albert Sickmann |
| contact affiliation | Proteomics, Leibniz-Institut für analytische Wissenschaften -ISAS - e.V., Germany |
| contact email | albert.Sickmann@isas.de |
| lab head | |
| Andreas Hentschel |
| contact affiliation | Leibniz Institut für Analytische Wissenschaften |
| contact email | andreas.hentschel@isas.de |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD071037
- Label: PRIDE project
- Name: Combined Histological and Proteomic Analysis Reveals Muscle Denervation in KMT5B-Related Neurodevelopmental Disorder: A Case Report