Hs06806942_cn

• Gene Symbol: AIM1
• Assay Reference Genome Location: Chr.6:106452751 on build GRCh38
• Cytoband: 6q21

Target Gene Details

• Entrez Gene ID: 202
• Gene Name: absent in melanoma 1
• Gene Aliases: CRYBG1, ST4
• Location: Chr.6:106360808-106570449 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
AIM1	XM_005266839.3			XP_005266896.1
	AK125137.1

Target Gene Details

• Entrez Gene ID: 105377924
• Gene Name: uncharacterized LOC105377924
• Gene Aliases: -
• Location: Chr.6:106451496-106457248 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC105377924	NR_134603.1
	BX105858.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1161442	Chr.6:106196410 - 106519212 on Build GRCh38	Duplication	LOC105377924 AIM1 ATG5
esv3610266	Chr.6:106112750 - 106457586 on Build GRCh38	Gain	LOC105377924 AIM1 ATG5
esv3610272	Chr.6:106259255 - 106458865 on Build GRCh38	Gain	LOC105377924 AIM1 ATG5
dgv6134n100	Chr.6:106081902 - 106464172 on Build GRCh38	Gain	LOC105377924 AIM1 PRDM1 ATG5

More Information

Additional Information:

For this assay, SNP(s) [rs114045992] 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

Gene Ontology Categories:

Process(es)

biological_process

Function(s)

molecular_function
carbohydrate binding