Gene Gene information from NCBI Gene database.
Entrez ID 101928601
Gene name Meiotic double-stranded break formation protein 4
Gene symbol MEI4
Synonyms (NCBI Gene)
-
Chromosome 6
Chromosome location 6q14.1
miRNA miRNA information provided by mirtarbase database.
10
miRTarBase ID miRNA Experiments Reference
MIRT740506 hsa-miR-7109-3p HITS-CLIP 19536157
MIRT740507 hsa-miR-3614-3p HITS-CLIP 19536157
MIRT740508 hsa-miR-617 HITS-CLIP 19536157
MIRT740509 hsa-miR-6505-3p HITS-CLIP 19536157
MIRT740510 hsa-miR-3164 HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
20
GO ID Ontology Definition Evidence Reference
GO:0000800 Component Lateral element IBA
GO:0000800 Component Lateral element IEA
GO:0000800 Component Lateral element ISS
GO:0005515 Function Protein binding IPI 31704776, 32296183, 38148155
GO:0005694 Component Chromosome IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
618417 43638 ENSG00000269964
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
A8MW99
Protein name Meiosis-specific protein MEI4
Protein function Required for DNA double-strand breaks (DSBs) formation in unsynapsed regions during meiotic recombination. Probably acts by forming a complex with IHO1 and REC114, which activates DSBs formation in unsynapsed regions, an essential step to ensure
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13971 Mei4 1 378 Meiosis-specific protein Mei4 Family
Sequence
Sequence length 385
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
20
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATOPIC ECZEMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATRIAL FIBRILLATION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BENIGN PROSTATIC HYPERPLASIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Malignant neoplasm of lung Lung Cancer GWASDB_DG 21725308
★☆☆☆☆
Found in Text Mining only