Hs01488743_cn

• Gene Symbol: CLUL1
• Assay Reference Genome Location: Chr.18:597044 on build GRCh38
• Cytoband: 18p11.32

Target Gene Details

• Entrez Gene ID: 27098
• Gene Name: clusterin like 1
• Gene Aliases: RA337M
• Location: Chr.18:596998-650298 on Build GRCh38
• Assay Gene Location: Overlaps - Exon 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CLUL1	NM_001289036.1			NP_001275965.1
	NM_014410.4			NP_055225.1
	XM_006722322.2			XP_006722385.1
	XM_011525648.2			XP_011523950.1
	XM_011525649.1			XP_011523951.1
	XM_011525652.1			XP_011523954.1
	AK299319.1
	AL713125.1
	BC025381.2			AAH25381.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2716646	Chr.18:596771 - 597053 on Build GRCh38	Deletion	CLUL1
nsv576236	Chr.18:319176 - 794272 on Build GRCh38	Gain	TYMS CETN1 LOC105376854 TYMSOS COLEC12 ENOSF1 CLUL1 YES1
nsv576239	Chr.18:394946 - 712037 on Build GRCh38	Gain	TYMS CETN1 LOC105376854 TYMSOS COLEC12 ENOSF1 CLUL1
esv3641497	Chr.18:551569 - 745897 on Build GRCh38	Gain	TYMS CETN1 TYMSOS ENOSF1 CLUL1 YES1
nsv1060188	Chr.18:575087 - 863351 on Build GRCh38	Gain	TYMS CETN1 TYMSOS ENOSF1 CLUL1 YES1
esv3893055	Chr.18:415105 - 743226 on Build GRCh38	Gain	TYMS CETN1 LOC105376854 TYMSOS COLEC12 ENOSF1 CLUL1 YES1
nsv482935	Chr.18:10001 - 2900002 on Build GRCh38	Loss	TYMS CETN1 NDC80 LOC105376854 TYMSOS COLEC12 ADCYAP1 THOC1 CBX3P2 CLUL1 LOC101926997 YES1 EMILIN2 MIR8078 LOC388456 USP14 LINC00470 ENOSF1 SMCHD1 ROCK1P1 METTL4
nsv576243	Chr.18:594262 - 631435 on Build GRCh38	Gain	CLUL1
dgv5810n54	Chr.18:351004 - 2238246 on Build GRCh38	Gain	TYMS CETN1 LOC388456 LOC105376854 LINC00470 TYMSOS COLEC12 ENOSF1 ADCYAP1 CLUL1 YES1
nsv576242	Chr.18:567127 - 841320 on Build GRCh38	Gain	TYMS CETN1 TYMSOS ENOSF1 CLUL1 YES1
nsv528169	Chr.18:551688 - 2240220 on Build GRCh38	Loss	TYMS CETN1 LOC388456 LINC00470 TYMSOS ENOSF1 ADCYAP1 CLUL1 YES1
dgv3307n100	Chr.18:469797 - 683607 on Build GRCh38	Gain	TYMS CETN1 LOC105376854 TYMSOS COLEC12 ENOSF1 CLUL1
esv2716645	Chr.18:596452 - 597439 on Build GRCh38	Deletion	CLUL1
nsv833577	Chr.18:521331 - 725019 on Build GRCh38	Gain+Loss	TYMS CETN1 TYMSOS ENOSF1 CLUL1 YES1
nsv576228	Chr.18:69836 - 1506323 on Build GRCh38	Loss	TYMS CETN1 LOC105376854 TYMSOS COLEC12 ADCYAP1 THOC1 CLUL1 YES1 MIR8078 LOC388456 USP14 LINC00470 ENOSF1 ROCK1P1

More Information

Additional Information:

For this assay, SNP(s) [rs73942572] 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, Non-exonic, DGV Variation

Gene Ontology Categories:

Process(es)

cell death