Gene
SPATA32
spermatogenesis associated 32
- HGNC 26349↗(opens in a new tab)
- Ensembl gene ENSG00000184361↗(opens in a new tab)
- NCBI Gene 124783↗(opens in a new tab)
Summary
- Cytogenetic location
- 17q21.31
- Coordinates
- Chromosome 17: 45,254,393–45,262,094 (GRCh38)
- Exons
- 5 exons across 7.7 kb
- Protein
- 384 amino acids
- Also known as
- FLJ25414, AEP2, VAD1.2
- Previous symbols
- C17orf46, TEX34
- MANE Select transcript
- ENST00000331780.5NM_152343.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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How SPATA32 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 1.3 kb of the gene's 7.7 kb; 1,155 of those bases code for the protein.
External links
Gene records
Transcript
Protein
Clinical
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
Cite this page
Dante Labs. (n.d.). SPATA32 gene: spermatogenesis associated 32. Retrieved 17 October 2026, from https://dantelabs.com/genes/spata32
Dante Labs. SPATA32 gene: spermatogenesis associated 32 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/spata32
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