Hs05036126_cn

• Gene Symbol: FAM49B
• Assay Reference Genome Location: Chr.8:129853008 on build GRCh38
• Cytoband: 8q24.21

Target Gene Details

• Entrez Gene ID: 51571
• Gene Name: family with sequence similarity 49 member B
• Gene Aliases: BM-009, L1
• Location: Chr.8:129839593-130016697 on Build GRCh38
• Assay Gene Location: Within Intron 14

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM49B	NM_001256763.1			NP_001243692.1
	NM_016623.4			NP_057707.3
	NR_046359.1
	NR_046360.1
	NR_046361.1
	XM_005250966.3			XP_005251023.1
	XM_011517108.2			XP_011515410.1
	XM_011517109.2			XP_011515411.1
	XM_011517110.2			XP_011515412.1
	XM_011517111.2			XP_011515413.1
	XM_011517112.2			XP_011515414.1
	XM_011517113.2			XP_011515415.1
	XM_011517114.2			XP_011515416.1
	XM_011517115.2			XP_011515417.1
	XM_011517116.2			XP_011515418.1
	XM_011517117.2			XP_011515419.1
	XM_011517118.2			XP_011515420.1
	XM_011517120.2			XP_011515422.1
	XM_011517121.2			XP_011515423.1
	XM_011517122.2			XP_011515424.1
	XM_011517123.2			XP_011515425.1
	XM_011517124.2			XP_011515426.1
	XM_011517125.2			XP_011515427.1
	XM_017013539.1			XP_016869028.1
	XM_017013540.1			XP_016869029.1
	XM_017013541.1			XP_016869030.1
	XM_017013542.1			XP_016869031.1
	XM_017013543.1			XP_016869032.1
	XM_017013544.1			XP_016869033.1
	XM_017013545.1			XP_016869034.1
	XM_017013546.1			XP_016869035.1
	XM_017013547.1			XP_016869036.1
	XM_017013548.1			XP_016869037.1
	XM_017013549.1			XP_016869038.1
	XM_017013550.1			XP_016869039.1
	XM_017013551.1			XP_016869040.1
	XM_017013552.1			XP_016869041.1
	XM_017013553.1			XP_016869042.1
	XM_017013554.1			XP_016869043.1
	XM_017013555.1			XP_016869044.1
	XM_017013556.1			XP_016869045.1
	XM_017013557.1			XP_016869046.1
	XM_017013558.1			XP_016869047.1
	XM_017013559.1			XP_016869048.1
	XM_017013560.1			XP_016869049.1
	XM_017013561.1			XP_016869050.1
	XM_017013562.1			XP_016869051.1
	AF208851.1			AAF64265.1
	AK001226.1			BAA91566.1
	AK002059.1			BAA92062.1
	AK130372.1
	AY364259.1			AAQ76818.1
	AY598320.1			AAT06731.1
	BC003599.1			AAH03599.1
	BC016345.1			AAH16345.1
	BC017297.2			AAH17297.1
	CR749628.1			CAH18422.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1018045	Chr.8:129851398 - 130110398 on Build GRCh38	Gain	FAM49B ASAP1-IT2 ASAP1 MIR5194

More Information

Additional Information:

For this assay, SNP(s) [rs77924175] 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:

Function(s)

protein binding