MEI1 Gene Summary [Human]
Predicted to be involved in meiosis I. Predicted to act upstream of or within gamete generation; meiotic spindle organization; and meiotic telomere clustering. Implicated in gestational trophoblastic neoplasm. [provided by Alliance of Genome Resources, Apr 2022]
Details
| Type | Protein Coding |
| Official Symbol | MEI1 |
| Official Name | meiotic double-stranded break formation protein 1 [Source:HGNC Symbol;Acc:HGNC:28613] |
| Ensembl ID | ENSG00000167077 |
| Bio databases IDs | |
| Aliases | meiotic double-stranded break formation protein 1, spermatogenesis associated 38 |
| Synonyms | 4932408F18Rik, HYDM3, LOC200321, meiotic double-stranded break formation protein 1, SPATA38 |
| Species | Human, Homo sapiens |
| Orthologies |
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
- recurrent hydatidiform mole type 3
- refractive error
- atrial fibrillation
- major depression
- anaplastic thyroid carcinoma
- anaplastic thyroid cancer
- epithelial thyroid cancer
- sarcoidosis
role in cell
- development
- organization
- generation
- meiosis I
Subcellular Expression
Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
- Unknown
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the human MEI1 gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
- meiosis I