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Gene Symbol
WNT3A
Assay Reference Genome
Location

Chr.1:228022034 on build GRCh38
Cytoband
1q42.13
Assay ID Hs03362239_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 89780

Gene Name:

 Wnt family member 3A

Gene Aliases:

 -

Location:

 Chr.1:228007022-228067113 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
WNT3A NM_033131.3 NP_149122.1
XM_011544319.2 XP_011542621.1
AB060284.1 BAB61052.1
AK056278.1 BAB71136.1
BC103921.1 AAI03922.1
BC103922.2 AAI03923.1
BC103923.1 AAI03924.1
DA742143.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv826908 Chr.1:227707685 - 228503399 on Build GRCh38 Gain C1orf145 TRIM17 MRPL55 MIR5008 SNAP47 WNT3A TRIM11 MIR3620 LOC107985355 LOC101060022 MIR6742 LOC105373289 OBSCN LOC100506571 IBA57 LOC101927401 HIST3H2A IBA57-AS1 HIST3H3 JMJD4 WNT9A HIST3H2BB ARF1 MIR4666A RNF187 GJC2 PRSS38 GUK1 C1orf35
nsv832803 Chr.1:227967417 - 228125980 on Build GRCh38 Loss MRPL55 C1orf35 ARF1 WNT3A LOC100506571 MIR3620 LOC107985355 LOC101060022
esv32853 Chr.1:227692415 - 228670462 on Build GRCh38 Gain C1orf145 RNA5S16 RNA5S14 MIR5008 SNAP47 TRIM11 MIR3620 RNA5S5 LOC107985355 LOC101060022 RNA5S2 RNA5S4 OBSCN RNA5S12 IBA57 LOC101927401 RNA5S1 RNA5S13 WNT9A DUSP5P1 HIST3H2BB ARF1 GJC2 RHOU TRIM17 BTNL10 MRPL55 RNA5S8 WNT3A RNA5S9 LOC105373132 MIR6742 LOC105373289 RNA5S17 LOC100506571 HIST3H2A RNA5S10 RNA5S7 IBA57-AS1 HIST3H3 JMJD4 MIR4666A RNA5S6 RNA5S15 RNF187 PRSS38 RNA5S3 GUK1 C1orf35 RNA5S11
nsv523935 Chr.1:227850423 - 228494048 on Build GRCh38 Loss C1orf145 TRIM17 MRPL55 MIR5008 WNT3A TRIM11 MIR3620 LOC107985355 LOC101060022 MIR6742 OBSCN LOC100506571 IBA57 LOC101927401 HIST3H2A IBA57-AS1 HIST3H3 WNT9A HIST3H2BB ARF1 MIR4666A RNF187 GJC2 GUK1 C1orf35
nsv516409 Chr.1:227847430 - 228109044 on Build GRCh38 Loss MRPL55 WNT9A MIR5008 C1orf35 ARF1 WNT3A LOC100506571 MIR3620 LOC107985355 LOC101060022
dgv79e214 Chr.1:228018807 - 228026998 on Build GRCh38 Loss WNT3A

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More Information


Additional Information:

For this assay, SNP(s) [rs74696567] 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 -

intercellular signal molecule

Gene Ontology Categories:

Function(s) Process(es)


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