Gene Gene information from NCBI Gene database.
Entrez ID 4201
Gene name Male-enhanced antigen 1
Gene symbol MEA1
Synonyms (NCBI Gene)
HYSMEA
Chromosome 6
Chromosome location 6p21.1
miRNA miRNA information provided by mirtarbase database.
265
miRTarBase ID miRNA Experiments Reference
MIRT046830 hsa-miR-222-3p CLASH 23622248
MIRT043158 hsa-miR-324-5p CLASH 23622248
MIRT440263 hsa-miR-218-5p HITS-CLIP 23212916
MIRT440263 hsa-miR-218-5p HITS-CLIP 23212916
MIRT1139707 hsa-miR-106a CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16189514, 32296183, 33961781
GO:0005737 Component Cytoplasm IEA
GO:0007283 Process Spermatogenesis IEA
GO:0007283 Process Spermatogenesis TAS 2813404
GO:0008584 Process Male gonad development TAS 2813404
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
143170 6986 ENSG00000124733
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q16626
Protein name Male-enhanced antigen 1 (MEA-1)
Protein function May play an important role in spermatogenesis and/or testis development.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06910 MEA1 66 181 Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in testis.
Sequence
Sequence length 185
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
GLOBAL DEVELOPMENTAL DELAY Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 35 Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INTELLECTUAL DISABILITY Disgenet
★★☆☆☆
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
Maple Syrup Urine Disease Maple Syrup Urine Disease BEFREE 15725595
★☆☆☆☆
Found in Text Mining only
Medullary carcinoma of thyroid Megalencephaly, Polymicrogyria, Polydactyly, Hydrocephalus Syndrome BEFREE 7199015
★☆☆☆☆
Found in Text Mining only
Multiple Endocrine Neoplasia Multiple Endocrine Neoplasia BEFREE 7199015
★☆☆☆☆
Found in Text Mining only