Hs00821495_cn

• Gene Symbol: KRI1
• Assay Reference Genome Location: Chr.19:10559855 on build GRCh38
• Cytoband: 19p13.2

Target Gene Details

• Entrez Gene ID: 65095
• Gene Name: KRI1 homolog
• Gene Aliases: -
• Location: Chr.19:10553085-10566031 on Build GRCh38
• Assay Gene Location: Within Exon 10

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
KRI1	NM_023008.3	10	909	NP_075384.3
	XM_011528190.2	9	840	XP_011526492.1
	AK023011.1	8	687	BAB14357.1
	AK093879.1	9	1021	BAC04240.1
	AK097181.1	2	144
	AK300780.1	10	893
	AK300850.1	10	914
	AL833189.1	9	1562
	BC002890.2	7	574	AAH02890.3
	BC009876.2	1	81	AAH09876.2
	BC112249.1	7	566	AAI12250.1
	BC112251.1	7	566	AAI12252.1
	BC143770.1	7	566

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv833744	Chr.19:10458964 - 10635033 on Build GRCh38	Loss	SLC44A2 CDKN2D MIR1238 AP1M2 KRI1 ATG4D KEAP1 PDE4A S1PR5
nsv833745	Chr.19:10539132 - 10727920 on Build GRCh38	Loss	MIR638 ILF3 SLC44A2 CDKN2D MIR1238 ILF3-AS1 AP1M2 QTRT1 KRI1 ATG4D DNM2

More Information

Additional Information:

For this assay, SNP(s) [rs112414135] 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, Exonic, DGV Variation

Gene Ontology Categories:

Function(s)

poly(A) RNA binding