Gene Gene information from NCBI Gene database.
Entrez ID 122258
Gene name Sperm acrosome associated 7
Gene symbol SPACA7
Synonyms (NCBI Gene)
C13orf28
Chromosome 13
Chromosome location 13q34
miRNA miRNA information provided by mirtarbase database.
10
miRTarBase ID miRNA Experiments Reference
MIRT2114198 hsa-miR-1539 CLIP-seq
MIRT2114199 hsa-miR-1976 CLIP-seq
MIRT2114200 hsa-miR-3155 CLIP-seq
MIRT2114201 hsa-miR-3155b CLIP-seq
MIRT2114202 hsa-miR-3183 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:0001669 Component Acrosomal vesicle IDA 22495889
GO:0001669 Component Acrosomal vesicle IEA
GO:0005576 Component Extracellular region IEA
GO:0007338 Process Single fertilization IEA
GO:0031410 Component Cytoplasmic vesicle IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96KW9
Protein name Sperm acrosome-associated protein 7
Protein function Involved in fertilization. Seems not to play a direct role in sperm-egg binding or gamete fusion.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15307 SPACA7 19 126 Sperm acrosome-associated protein 7 Family
Tissue specificity TISSUE SPECIFICITY: Expressed in spermatozoa (at protein level) (PubMed:22495889). {ECO:0000269|PubMed:22495889}.
Sequence
MAVSQGDGTLCFVLLLCCWQETELRPRTVIPGSPTEIPFSSKQEDMSELLDEILVQEILD
LNKTTPSEMPSTASTLSTPLHAGIDENYQAGGSENYHELLENLQFSPGIEVKISNDEANA
NANLHG
DPSENYRGPQVSPGSEKSVSSKEKNSKNTQYENLSILDQILQNIGRSSGNIFHK
EQQRTSAQRRSQGSQ
Sequence length 195
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
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
CARDIOVASCULAR DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CENTRAL NERVOUS SYSTEM CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GLIOBLASTOMA MULTIFORME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations