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Spermatogenesis Associated 7 Proteins (SPATA7)

SPATA7, originally isolated from testis, is also expressed in retina. Additionally we are shipping SPATA7 Antibodies (31) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
SPATA7 55812 Q9P0W8
SPATA7 104871 Q80VP2
SPATA7 192225  
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Top SPATA7 Proteins at antibodies-online.com

Showing 5 out of 5 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Wheat germ Human GST tag 2 μg Log in to see 9 Days
$333.33
Details
Yeast Rat His tag   1 mg Log in to see 56 to 66 Days
$3,498.00
Details
HOST_Human Human Un-conjugated   20 μg Log in to see 9 to 11 Days
$785.40
Details

SPATA7 Proteins by Origin and Source

Origin Expressed in Conjugate
Human , ,
,
Mouse (Murine)

Rat (Rattus)

More Proteins for Spermatogenesis Associated 7 (SPATA7) Interaction Partners

Human Spermatogenesis Associated 7 (SPATA7) interaction partners

  1. SPATA7 plays a role in RPGRIP1 (show RPGRIP1 Proteins)-mediated protein trafficking across the connecting cilium of photoreceptor cells. Apoptotic degeneration of these cells triggered by protein mislocalization is a mechanism of disease progression in LCA3/juvenile RP patients

  2. A novel homozygous large deletion in SPATA7 associated with juvenile retinitis pigmentosa has been found in a consanguineous Israeli Muslim Arab family.

  3. Digenic and triallelic mutations of CRB1 (show CRB1 Proteins) and SPATA7 were detected in a Chinese family with Leber congenital amaurosis. The results imply that CRB1 (show CRB1 Proteins) and SPATA7 may not interact with each other directly.

  4. In conclusion, our data established the first linkage association of a loss-of-function mutation in the SPATA7 gene with a typical retinitis pigmentosa (RP) phenotype and not with leber congenital amaurosis or early onset RP.

  5. Mutations in SPATA7 are a rare cause of childhood retinal dystrophy (show MERTK Proteins) accounting for 1.7% of disease in this cohort.

  6. analysis of the SPATA7 mutations in Leber congenital amaurosis and the associated phenotype

  7. isolation and characterization of HSD-3.1 expressed in the testis

  8. Spata7 is expressed in the mature mouse retina.

Mouse (Murine) Spermatogenesis Associated 7 (SPATA7) interaction partners

  1. Spata7 is expressed in the mature mouse retina.

SPATA7 Protein Profile

Protein Summary

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.

Gene names and symbols associated with SPATA7

  • spermatogenesis associated 7 (SPATA7)
  • spermatogenesis associated 7 (Spata7)
  • AI661438 protein
  • B230306G18Rik protein
  • HSD-3.1 protein
  • HSD3 protein
  • LCA3 protein
  • RSD-3 protein
  • Wmp1 protein

Protein level used designations for SPATA7

spermatogenesis-associated protein 7 , spermatogenesis-associated protein HSD3 , spermatogenesis-associated protein 7 homolog , fertility related protein WMP1 , fertility-related protein WMP1 , sperm DNA no.3

GENE ID SPECIES
55812 Homo sapiens
480411 Canis lupus familiaris
100153278 Sus scrofa
510352 Bos taurus
104871 Mus musculus
192225 Rattus norvegicus
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