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SPATA32 (spermatogenesis associated 32)
Gene
Gene Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
124783
Gene nameGene Name - the full gene name approved by the HGNC.
Spermatogenesis associated 32
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
SPATA32
SynonymsGene synonyms aliases
AEP2, C17orf46, TEX34, VAD1.2
ChromosomeChromosome number
17
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q21.31
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
Gene Gene ontology Other IDs Protein Associated diseases
GO ID Ontology Definition Evidence Reference
GO:0003779 Function Actin binding IBA 21873635
GO:0005515 Function Protein binding IPI 32296183
GO:0007283 Process Spermatogenesis IBA 21873635
GO:0048471 Component Perinuclear region of cytoplasm IBA 21873635
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene Gene ontology Other IDs Protein Associated diseases
MIM
HGNC
e!Ensembl
Protein
Gene Gene ontology Other IDs Protein Associated diseases
UniProt ID Q96LK8
Protein name Spermatogenesis-associated protein 32 (Testis-expressed protein 34)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15310 VAD1-2
138 → 383
Vitamin A-deficiency (VAD) rat model signalling
 Family
Sequence
Sequence length 384
Interactions View interactions
Associated diseases
Gene Gene ontology Other IDs Protein Associated diseases
Causal
Disease name Disease term dbSNP ID References
Asthma Asthma rs324981, rs121912630, rs150116809, rs4950928, rs708494, rs1581842283 31619474
Unknown
Disease name Disease term dbSNP ID References
Respiratory tract diseases Respiratory Tract Diseases 30595370

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