SPATA7 gene

spermatogenesis associated 7

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

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]

From UniProt:

Involved in photoreceptor cells maintenance (By similarity). It is required for recruitment and proper localization of RPGRIP1 to the photoreceptor connecting cilium (CC), as well as protein trafficking across the CC to the outer segments.

Covered on Genetics Home Reference:

From NCBI Gene:

  • Leber congenital amaurosis 3

From UniProt:

Leber congenital amaurosis 3 (LCA3): A severe dystrophy of the retina, typically becoming evident in the first years of life. Visual function is usually poor and often accompanied by nystagmus, sluggish or near-absent pupillary responses, photophobia, high hyperopia and keratoconus. [MIM:604232]

Retinitis pigmentosa autosomal recessive (ARRP): A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. [MIM:268000]

Cytogenetic Location: 14q31.3, which is the long (q) arm of chromosome 14 at position 31.3

Molecular Location: base pairs 88,385,638 to 88,470,350 on chromosome 14 (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: 14q31.3, which is the long (q) arm of chromosome 14 at position 31.3
  • HEL-S-296
  • HSD-3.1
  • HSD3
  • LCA3