Hs05660311_cn

• Gene Symbol: FAM9B
• Assay Reference Genome Location: Chr.X:9034165 on build GRCh38
• Cytoband: Xp22.31

Target Gene Details

• Entrez Gene ID: 171483
• Gene Name: family with sequence similarity 9 member B
• Gene Aliases: TEX39B
• Location: Chr.X:9024232-9197176 on Build GRCh38
• Assay Gene Location: Overlaps Intron 8 - Exon 9

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM9B	NM_205849.3			NP_995321.1
	XM_011545464.2			XP_011543766.1
	AF494344.1			AAN07163.1
	AK128470.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv526672	Chr.X:8856093 - 9048808 on Build GRCh38	Gain	FAM9B
nsv515590	Chr.X:8952896 - 9048808 on Build GRCh38	Gain	FAM9B
nsv6791	Chr.X:9029888 - 9064100 on Build GRCh38	Insertion	FAM9B

More Information

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

Gene Ontology Categories:

Process(es)

spermatid development

Function(s)

protein binding