Gene Gene information from NCBI Gene database.
Entrez ID 6407
Gene name Semenogelin 2
Gene symbol SEMG2
Synonyms (NCBI Gene)
SGII
Chromosome 20
Chromosome location 20q13.12
Summary The secreted protein encoded by this gene is involved in the formation of a gel matrix that encases ejaculated spermatozoa. Proteolysis by the prostate-specific antigen (PSA) breaks down the gel matrix and allows the spermatozoa to move more freely. The e
miRNA miRNA information provided by mirtarbase database.
16
miRTarBase ID miRNA Experiments Reference
MIRT023589 hsa-miR-1-3p Microarray 18668037
MIRT032201 hsa-let-7b-5p Proteomics 18668040
MIRT2323974 hsa-miR-3192 CLIP-seq
MIRT2323975 hsa-miR-3619-3p CLIP-seq
MIRT2323976 hsa-miR-3649 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
GO ID Ontology Definition Evidence Reference
GO:0001669 Component Acrosomal vesicle IBA
GO:0002020 Function Protease binding IPI 8665956
GO:0005515 Function Protein binding IPI 8665956
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
182141 10743 ENSG00000124157
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q02383
Protein name Semenogelin-2 (Semenogelin II) (SGII)
Protein function Participates in the formation of a gel matrix (sperm coagulum) entrapping the accessory gland secretions and ejaculated spermatozoa.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05474 Semenogelin 1 582 Semenogelin Family
Tissue specificity TISSUE SPECIFICITY: Seminal vesicles, and to a much lesser extent, epididymis.
Sequence
Sequence length 582
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
ASTHMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinoma Ovarian Epithelial Associate 33246661
★☆☆☆☆
Found in Text Mining only
Lung Neoplasms Associate 33311447
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 33311447
★☆☆☆☆
Found in Text Mining only
Prostatic Neoplasms Associate 33311447
★☆☆☆☆
Found in Text Mining only