Hs00632031_cn

• Gene Symbol: MON1B
• Assay Reference Genome Location: Chr.16:77199372 on build GRCh38
• Cytoband: 16q23.1

Target Gene Details

• Entrez Gene ID: 22879
• Gene Name: MON1 homolog B, secretory trafficking associated
• Gene Aliases: HSRG1, SAND2, SRG1
• Location: Chr.16:77190919-77199646 on Build GRCh38
• Assay Gene Location: Within Exon 6

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
MON1B	NM_001286639.1	5	2731	NP_001273568.1
	NM_001286640.1	4	2573	NP_001273569.1
	NM_014940.3	6	3058	NP_055755.1
	AB020679.1	6	2742
	AK023374.1
	AK128411.1	3	2600	BAC87427.1
	BU682558.1	1	291

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1056676	Chr.16:77105785 - 77820951 on Build GRCh38	Loss	SYCE1L ADAMTS18 NUDT7 VAT1L MON1B
nsv1055234	Chr.16:76969529 - 77433389 on Build GRCh38	Gain	SYCE1L ADAMTS18 MON1B
dgv3027n100	Chr.16:76614676 - 77688151 on Build GRCh38	Gain	SYCE1L ADAMTS18 MIR4719 LOC101928203 MON1B

More Information

Additional Information:

For this assay, SNP(s) [rs113908772] 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, Exonic, DGV Variation

Gene Ontology Categories:

Process(es)

vesicle-mediated transport
early viral transcription
late viral transcription

Function(s)

protein binding