Assay Details

Target Gene Details

Entrez Gene ID:	65125
Gene Name:	WNK lysine deficient protein kinase 1
Gene Aliases:	HSAN2, HSN2, KDP, PPP1R167, PRKWNK1, PSK, p65
Location:	Chr.12:752552-911452 on Build GRCh38
Assay Gene Location:	Within Intron 1

Gene Symbol	Transcript Accession	Protein ID
WNK1	NM_001184985.1	NP_001171914.1
	NM_014823.2	NP_055638.2
	NM_018979.3	NP_061852.3
	NM_213655.4	NP_998820.3
	XM_006719003.2	XP_006719066.1
	XM_011520997.2	XP_011519299.1
	XM_011520998.2	XP_011519300.1
	XM_011520999.2	XP_011519301.1
	XM_011521000.2	XP_011519302.1
	XM_011521001.2	XP_011519303.1
	XM_011521002.2	XP_011519304.1
	XM_011521003.2	XP_011519305.1
	XM_011521004.2	XP_011519306.1
	XM_011521006.2	XP_011519308.1
	XM_011521007.2	XP_011519309.1
	XM_011521008.2	XP_011519310.1
	XM_011521009.2	XP_011519311.1
	XM_017019834.1	XP_016875323.1
	XM_017019835.1	XP_016875324.1
	XM_017019836.1	XP_016875325.1
	XM_017019837.1	XP_016875326.1
	XM_017019838.1	XP_016875327.1
	XM_017019839.1	XP_016875328.1
	AB002342.2	BAA20802.2
	AF061944.1	AAF31483.1
	AJ296290.1	CAC15059.1
	BC141881.1
	JQ358908.1

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
esv2760688	Chr.12:746699 - 767080 on Build GRCh38	Loss	WNK1
esv3548603	Chr.12:756648 - 766334 on Build GRCh38	Deletion	WNK1
nsv826175	Chr.12:757211 - 765961 on Build GRCh38	Loss	WNK1
nsv1119925	Chr.12:739873 - 764441 on Build GRCh38	Deletion	WNK1
nsv1159950	Chr.12:754908 - 760032 on Build GRCh38	Duplication	WNK1
dgv2259n54	Chr.12:757691 - 765362 on Build GRCh38	Loss	WNK1
dgv2253n54	Chr.12:741122 - 859323 on Build GRCh38	Loss	WNK1
nsv556899	Chr.12:741447 - 813242 on Build GRCh38	Loss	WNK1
dgv1335n100	Chr.12:739562 - 764851 on Build GRCh38	Loss	WNK1
esv2759875	Chr.12:225844 - 881378 on Build GRCh38	Gain+Loss	CCDC77 WNK1 LOC100049716 LOC102723544 LOC105369595 B4GALNT3 SLC6A13 KDM5A NINJ2
dgv2260n54	Chr.12:759691 - 764839 on Build GRCh38	Loss	WNK1
nsv556893	Chr.12:628064 - 873155 on Build GRCh38	Gain	WNK1 LOC100049716 NINJ2
dgv2256n54	Chr.12:756804 - 769498 on Build GRCh38	Loss	WNK1
nsv1038532	Chr.12:754667 - 767068 on Build GRCh38	Gain	WNK1
nsv556901	Chr.12:753823 - 760447 on Build GRCh38	Gain	WNK1
esv3628254	Chr.12:759212 - 765324 on Build GRCh38	Loss	WNK1
nsv556935	Chr.12:758819 - 767122 on Build GRCh38	Loss	WNK1
nsv8888	Chr.12:757189 - 765967 on Build GRCh38	Gain	WNK1
dgv41n73	Chr.12:757620 - 767334 on Build GRCh38	Deletion	WNK1
dgv254e199	Chr.12:757309 - 767244 on Build GRCh38	Deletion	WNK1
dgv2251n54	Chr.12:553282 - 1101718 on Build GRCh38	Gain	WNK1 LOC100049716 ERC1 RAD52 LOC105369595 B4GALNT3 NINJ2
dgv431e212	Chr.12:756526 - 766139 on Build GRCh38	Loss	WNK1
esv24614	Chr.12:757566 - 765832 on Build GRCh38	Gain	WNK1
nsv819875	Chr.12:757124 - 765317 on Build GRCh38	Gain	WNK1
esv2745368	Chr.12:757613 - 765631 on Build GRCh38	Deletion	WNK1
nsv518946	Chr.12:745165 - 852170 on Build GRCh38	Loss	WNK1
dgv27e180	Chr.12:757004 - 766773 on Build GRCh38	Deletion	WNK1
esv2870457	Chr.12:756834 - 766834 on Build GRCh38	Deletion	WNK1

More Information

Additional Information:

For this assay, SNP(s) [rs76153366] 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 -

non-receptor serine/threonine protein kinase

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: