FBXO38
Protein-coding gene in the species Homo sapiens
FBXO38 Identifiers Aliases FBXO38 , Fbx38, HMN2D, MOKA, SP329, F-box protein 38, FBX38External IDs OMIM : 608533 ; MGI : 2444639 ; GeneCards : FBXO38 Gene location (Mouse ) Chr. Chromosome 18 (mouse) Band 18| 18 E1 Start 62,504,155 bp End 62,548,695 bp
Wikidata
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. Mice deficient in Fbxo38 gene have defective spermatogenesis and are growth retarded.
References
1 2 3 GRCh38: Ensembl release 89: ENSG00000145868 – Ensembl , May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000042211 – Ensembl , May 2017
↑ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
↑ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
↑ Dibus N, Korinek V, Cermak L (23 June 2022). "FBXO38 Ubiquitin Ligase Controls Centromere Integrity via ZXDA/B Stability" . Frontiers in Cell and Developmental Biology . 10 929288. doi :10.3389/fcell.2022.929288 . PMC 9260856 . PMID 35813202 .
↑ Dibus N, Zobalova E, Monleon MA, Korinek V, Filipp D, Petrusova J, et al. (13 June 2022). "FBXO38 Ubiquitin Ligase Controls Sertoli Cell Maturation" . Frontiers in Cell and Developmental Biology . 10 914053. doi :10.3389/fcell.2022.914053 . PMC 9234700 . PMID 35769260 .