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SPATA7, spermatogenesis associated 7

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SPATA7, spermatogenesis associated 7

  • This gene, originally isolated from testis, is also expressed in retina. Mutations in this gene are associated with Leber congenital amaurosis and juvenile retinitis pigmentosa. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]

  • Gene Synonyms (HEL-S-296, HSD-3.1, HSD3, LCA3, spermatogenesis-associated protein 7, epididymis secretory protein Li 296, epididymis secretory sperm binding protein, spermatogenesis-associated protein HSD3,)
  • NCBI Gene ID: 55812
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>V9HVY9
    UNIPROT ID#>>Q9P0W8
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

spermatogenesis associated 7 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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