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- Table of Contents
Facts about Spermatogenesis-associated protein 7.
.
Human | |
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Gene Name: | SPATA7 |
Uniprot: | Q9P0W8 |
Entrez: | 55812 |
Belongs to: |
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No superfamily |
HSD-3.1; HSD3DKFZp686D07199; LCA3; Leber congenital amaurosis 3; MGC102934; spermatogenesis associated 7; spermatogenesis-associated protein 7; Spermatogenesis-associated protein HSD3
Mass (kDA):
67.719 kDA
Human | |
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Location: | 14q31.3 |
Sequence: | 14; NC_000014.9 (88385638..88470350) |
Cytoplasm, cytoskeleton, cilium axoneme. Cytoplasm, cytoskeleton, cilium basal body. Cytoplasm, cytoskeleton. Cell projection, cilium, photoreceptor outer segment. Localizes to the microtubule network.
PMID: 12736779 by Zhang X., et al. A novel gene, RSD-3/HSD-3.1, encodes a meiotic-related protein expressed in rat and human testis.
PMID: 19268277 by Wang H., et al. Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa.