| Name | uncharacterized LOC101929726 |
| Description | Involved in myoblast fusion involved in skeletal muscle regeneration. Predicted to be active in Golgi membrane; endoplasmic reticulum membrane; and plasma membrane. Implicated in Carey-Fineman-Ziter syndrome. [provided by Alliance of Genome Resources, Mar 2025] |
| Synonyms | hMINION, MYMX, MINION |
| NCBI Gene ID | 101929726 |
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| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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LOC101929726 has 76 functional associations with biological entities spanning 3 categories (disease, phenotype or trait, functional term, phrase or reference, gene, protein or microRNA) extracted from 6 datasets.
Click the + buttons to view associations for LOC101929726 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| ChEA Transcription Factor Targets 2022 | transcription factors binding the promoter of LOC101929726 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. | |
| DisGeNET Gene-Disease Associations | diseases associated with LOC101929726 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. | |
| GO Biological Process Annotations 2023 | biological processes involving LOC101929726 gene from the curated GO Biological Process Annotations 2023 dataset. | |
| GO Cellular Component Annotations 2023 | cellular components containing LOC101929726 protein from the curated GO Cellular Component Annotations 2023 dataset. | |
| MGI Mouse Phenotype Associations 2023 | phenotypes of transgenic mice caused by LOC101929726 gene mutations from the MGI Mouse Phenotype Associations 2023 dataset. | |
| PerturbAtlas Signatures of Differentially Expressed Genes for Mouse Gene Perturbations | gene perturbations changing expression of LOC101929726 gene from the PerturbAtlas Signatures of Differentially Expressed Genes for Gene Perturbations dataset. | |