Assay Details

Target Gene Details

Entrez Gene ID:	7484
Gene Name:	Wnt family member 9B
Gene Aliases:	WNT14B, WNT15
Location:	Chr.17:46833201-46886730 on Build GRCh38
Assay Gene Location:	Within Intron 2

Gene Symbol	Transcript Accession	Protein ID
WNT9B	NM_001320458.1	NP_001307387.1
	NM_003396.2	NP_003387.1
	XM_011525178.2	XP_011523480.1
	AB063483.1	BAB70499.1
	AK127268.1	BAC86908.1
	AK127615.1	BAC87058.1
	AY358217.1	AAQ88584.1
	BC064534.1	AAH64534.1

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
esv2656635	Chr.17:46204086 - 47091135 on Build GRCh38	Deletion	WNT3 ARL17B ARL17A WNT9B KANSL1 LOC107987254 LRRC37A NSFP1 NSF MIR5089 LOC107987253 GOSR2 RPRML LRRC37A2
esv2758692	Chr.17:46006548 - 47199967 on Build GRCh38	Gain+Loss	CDC27 WNT3 ARL17B ARL17A MAPT WNT9B RPS2P47 KANSL1 LOC107987254 LRRC37A NSFP1 KANSL1-AS1 NSF MIR5089 LOC107987253 GOSR2 RPRML LRRC37A2

More Information

Additional Information:

For this assay, SNP(s) [rs111474394] 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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System Message

Genomic Map

Assay Details

Target Gene Details

Entrez Gene ID:

Gene Name:

Gene Aliases:

Location:

Assay Gene Location: