Hs02327416_cn

• Gene Symbol: FAM89A
• Assay Reference Genome Location: Chr.1:231039941 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: Overlaps Intron 1 - Exon 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
nsv1068593	Chr.1:231039753 - 231041054 on Build GRCh38	Deletion	FAM89A
esv3589093	Chr.1:230482037 - 231277190 on Build GRCh38	Gain	TRIM67 CAPN9 LOC101927553 ARV1 FAM89A TTC13 MIR1182 C1orf198 LOC149373 C1orf131 AGT GNPAT LOC101927604 COG2
nsv1121792	Chr.1:231039754 - 231040354 on Build GRCh38	Deletion	FAM89A
nsv1011066	Chr.1:230940432 - 231242850 on Build GRCh38	Gain	TRIM67 LOC149373 C1orf131 ARV1 GNPAT FAM89A TTC13 MIR1182
nsv1000488	Chr.1:230799658 - 231269735 on Build GRCh38	Gain	TRIM67 CAPN9 LOC149373 C1orf131 ARV1 GNPAT FAM89A TTC13 LOC101927604 MIR1182 C1orf198

More Information

• Set Membership: Intragenic, Non-exonic, DGV Variation

Panther Classification:

Molecular Function -

scaffold/adaptor protein