SPATA3 (spermatogenesis associated 3)

Gene Gene information from NCBI Gene database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID 130560
Gene name Spermatogenesis associated 3
Gene symbol SPATA3
Synonyms (NCBI Gene)
TSARG1
Chromosome 2
Chromosome location 2q37.1
miRNA miRNA information provided by mirtarbase database.
196
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (196)
miRTarBase ID miRNA Experiments Reference
MIRT019156 hsa-miR-335-5p Microarray 18185580
MIRT609601 hsa-miR-331-3p HITS-CLIP 23824327
MIRT609600 hsa-miR-4308 HITS-CLIP 23824327
MIRT613537 hsa-miR-345-5p HITS-CLIP 23824327
MIRT609598 hsa-miR-5585-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (5)
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0005929 Component Cilium IEA
GO:0031514 Component Motile cilium IEA
GO:0036126 Component Sperm flagellum IDA 31429579
GO:0042995 Component Cell projection IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
619857 17884 ENSG00000173699
Protein Protein information from UniProt database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NHX4
Protein name Spermatogenesis-associated protein 3 (Testis and spermatogenesis cell-related protein 1) (Testis spermatocyte apoptosis-related protein 1)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15662 SPATA3 1 → 191 Spermatogenesis-associated protein 3 family Family
Sequence
Sequence length 192
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Gene miRNA Gene ontology Other IDs Protein Associated diseases
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)
Show/Hide Unknown Diseases (3)
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
DEMENTIA — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MALE INFERTILITY WITH AZOOSPERMIA OR OLIGOZOOSPERMIA DUE TO SINGLE GENE MUTATION — Orphanet
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Show/Hide Text Mining Associations (1)
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Azoospermia Nonobstructive Nonobstructive azoospermia Pubtator 24012201 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only