Product Details

Assay Reference Genome
Location

Chr.14:88424282 on build GRCh38
Cytoband
14q31.3
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

For this assay, SNP(s) [rs73327418] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Target Gene Details

Entrez Gene ID
55812
Gene Symbol
SPATA7
Gene Name
spermatogenesis associated 7
Gene Aliases
HEL-S-296, HSD-3.1, HSD3, LCA3
Location
Chr.14:88385638-88470350 on build GRCh38
Assay Gene Location
Within Intron 6
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
SPATA7 NM_001040428.3 NP_001035518.1
NM_018418.4 NP_060888.2
XM_005267851.1 XP_005267908.1
XM_005267852.1 XP_005267909.1
XM_005267854.1 XP_005267911.1
XM_005267855.1 XP_005267912.1
XM_006720204.1 XP_006720267.1
XM_006720205.1 XP_006720268.1
XM_011536951.1 XP_011535253.1
XM_011536952.1 XP_011535254.1
XM_011536953.1 XP_011535255.1
XM_017021452.1 XP_016876941.1
XM_017021453.1 XP_016876942.1
XM_017021454.1 XP_016876943.1
XM_017021455.1 XP_016876944.1
XM_017021456.1 XP_016876945.1
XM_017021457.1 XP_016876946.1
AF144487.3 AAF66077.2
AF144488.2 AAF66078.1
AK055864.1
AK225746.1
AK290631.1
AK293007.1
AL136604.1 CAB66539.1
BC090875.1 AAH90875.1
CR533563.1 CAG38594.1
CR936777.1
DA568174.1
EU668353.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
esv2748992 Chr14:88423494 - 88424309 on Build GRCh38 Deletion SPATA7
esv2568808 Chr14:88422888 - 88424373 on Build GRCh38 Deletion SPATA7

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