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Gene Symbol
SPRY3
Assay Reference Genome
Location

Chr.X:155696691 on build GRCh38
Cytoband
Xq28
Assay ID Hs04101185_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 10251

Gene Name:

 sprouty RTK signaling antagonist 3

Gene Aliases:

 spry-3

Location:

 Chr.X:155612565-155782459 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SPRY3 NM_001304990.1 NP_001291919.1
DA102958.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv33784 Chr.X:153962665 - 155699588 on Build GRCh38 Gain+Loss MIR3202-1 PLXNA3 GAB3 OPN1MW3 IKBKG FAM3A LOC101927830 MIR1184-3 RPL10 DKC1 FAM223A EMD RAB39B MIR1184-2 TMEM187 SMIM9 CTAG1A TMLHE-AS1 MIR3202-2 DNASE1L1 TAZ SLC10A3 OPN1MW F8A3 HCFC1-AS1 FAM223B CTAG2 VBP1 MPP1 SNORA70 OPN1LW H2AFB1 LAGE3 MTCP1 LOC107987332 G6PD LOC105373386 BRCC3 F8 MIR664B MIR718 F8A1 TKTL1 CMC4 MECP2 F8A2 TMLHE CTAG1B UBL4A SPRY3 CH17-340M24.3 TEX28 FAM50A FLNA SNORA36A GDI1 MIR6858 MIR1184-1 ATP6AP1 H2AFB3 SNORA56 OPN1MW2 H2AFB2 FUNDC2 HCFC1 IRAK1 CLIC2
nsv519485 Chr.X:155507715 - 155699751 on Build GRCh38 Loss TMLHE SPRY3
esv3575080 Chr.X:155683281 - 155699244 on Build GRCh38 Loss SPRY3
nsv510870 Chr.X:155686374 - 155710408 on Build GRCh38 Deletion SPRY3
nsv520699 Chr.X:155545002 - 155699751 on Build GRCh38 Gain TMLHE SPRY3
nsv471607 Chr.X:155652457 - 155812331 on Build GRCh38 Gain+Loss SPRY3
esv2657377 Chr.X:155641695 - 155958434 on Build GRCh38 Deletion SPRY3
nsv511663 Chr.X:155687184 - 155709357 on Build GRCh38 Gain SPRY3
esv29972 Chr.X:154781072 - 155699751 on Build GRCh38 Gain TMLHE-AS1 BRCC3 F8 F8A1 LOC101927830 MIR1184-3 CMC4 MIR1184-1 H2AFB3 F8A3 F8A2 TMLHE H2AFB2 VBP1 MPP1 FUNDC2 H2AFB1 RAB39B MIR1184-2 SMIM9 MTCP1 SPRY3 CLIC2

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More Information


Additional Information:

For this assay, SNP(s) [rs116490668] 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.

Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

Panther Classification:

Molecular Function -

scaffold/adaptor protein

Gene Ontology Categories:

Function(s) Process(es)


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