Biology:FBXO38
From HandWiki
Short description: Protein-coding gene in the species Homo sapiens
 Generic protein structure example |
F-box only protein 38 (FBXO38) is a protein that in humans is encoded by the FBXO38 gene.
Mutations in the FBXO38 gene are associated with distal spinal muscular atrophy with calf predominance. FBXO38 controls the composition of centromeric chromatin via the stability of ZXDA/B nuclear factors.[1] Mice deficient in Fbxo38 gene have defective spermatogenesis and are growth retarded.[2]
References
- ↑ "FBXO38 Ubiquitin Ligase Controls Centromere Integrity via ZXDA/B Stability". Frontiers in Cell and Developmental Biology 10: 929288. 23 June 2022. doi:10.3389/fcell.2022.929288. PMID 35813202.
- ↑ "FBXO38 Ubiquitin Ligase Controls Sertoli Cell Maturation". Frontiers in Cell and Developmental Biology 10: 914053. 13 June 2022. doi:10.3389/fcell.2022.914053. PMID 35769260.
External links
- FBXO38 human gene location in the UCSC Genome Browser.
- FBXO38 human gene details in the UCSC Genome Browser.
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