Hs02251230_cn

• Gene Symbol: MON1B
• Assay Reference Genome Location: Chr.16:77199516 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	2875	NP_001273568.1
	NM_001286640.1	4	2717	NP_001273569.1
	NM_014940.3	6	3202	NP_055755.1
	AB020679.1	6	2886
	AK023374.1
	AK128411.1	3	2744	BAC87427.1
	BU682558.1	1	147

Target Gene Details

• Entrez Gene ID: 100130958
• Gene Name: synaptonemal complex central element protein 1 like
• Gene Aliases: MRP2
• Location: Chr.16:77199452-77213079 on Build GRCh38
• Assay Gene Location: Overlaps Exon 1 - Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SYCE1L	NM_001129979.1			NP_001123451.1

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	NUDT7 MON1B ADAMTS18 VAT1L SYCE1L
nsv1055234	Chr.16:76969529 - 77433389 on Build GRCh38	Gain	MON1B ADAMTS18 SYCE1L
dgv3027n100	Chr.16:76614676 - 77688151 on Build GRCh38	Gain	MON1B LOC101928203 ADAMTS18 MIR4719 SYCE1L

More Information

Additional Information:

For this assay, SNP(s) [rs112674196] 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, Non-exonic, DGV Variation

Gene Ontology Categories:

Process(es)

vesicle-mediated transport
early viral transcription
late viral transcription
synaptonemal complex assembly

Function(s)

protein binding