Hs05757217_cn

• Gene Symbol: FAM89A
• Assay Reference Genome Location: Chr.1:231033441 on build GRCh38
• Cytoband: 1q42.2

Target Gene Details

• Entrez Gene ID: 375061
• Gene Name: family with sequence similarity 89 member A
• Gene Aliases: C1orf153
• Location: Chr.1:231018958-231040249 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM89A	NM_198552.2			NP_940954.1
	BC009447.1			AAH09447.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3589093	Chr.1:230482037 - 231277190 on Build GRCh38	Gain	LOC101927553 CAPN9 AGT ARV1 TTC13 TRIM67 C1orf198 C1orf131 LOC101927604 LOC149373 GNPAT MIR1182 COG2 FAM89A
nsv1011066	Chr.1:230940432 - 231242850 on Build GRCh38	Gain	C1orf131 ARV1 LOC149373 TTC13 GNPAT TRIM67 MIR1182 FAM89A
nsv1000488	Chr.1:230799658 - 231269735 on Build GRCh38	Gain	C1orf198 C1orf131 LOC101927604 CAPN9 ARV1 LOC149373 TTC13 GNPAT TRIM67 MIR1182 FAM89A

More Information

Additional Information:

For this assay, SNP(s) [rs140562906,rs145865137] 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 -

scaffold/adaptor protein