Hs03740945_cn

• Gene Symbol: MSMB
• Assay Reference Genome Location: Chr.10:46045097 on build GRCh38
• Cytoband: 10q11.22

Target Gene Details

• Entrez Gene ID: 4477
• Gene Name: microseminoprotein beta
• Gene Aliases: HPC13, IGBF, MSP, MSPB, PN44, PRPS, PSP, PSP-94, PSP57, PSP94
• Location: Chr.10:46033305-46046269 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
MSMB	NM_002443.3			NP_002434.1
	NM_138634.2			NP_619540.1
	AK312108.1
	BC005257.1			AAH05257.1
	BF680662.1
	BM856408.1
	S67815.1			AAB29732.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1041519	Chr.10:45991149 - 46080365 on Build GRCh38	Gain	TIMM23 MSMB NCOA4
esv3577172	Chr.10:45959639 - 46146408 on Build GRCh38	Gain	TIMM23 PARGP1 MSMB AGAP7P NCOA4
nsv1042912	Chr.10:46009162 - 46116183 on Build GRCh38	Loss	MSMB AGAP7P NCOA4
nsv508583	Chr.10:45881821 - 46146976 on Build GRCh38	Deletion	TIMM23 PARGP1 MSMB AGAP7P NCOA4
esv3623185	Chr.10:45995694 - 46106028 on Build GRCh38	Gain	TIMM23 MSMB NCOA4
nsv6643	Chr.10:46040213 - 46075212 on Build GRCh38	Insertion	MSMB
nsv550853	Chr.10:46001360 - 46085061 on Build GRCh38	Gain	TIMM23 MSMB NCOA4

More Information

Additional Information:

For this assay, SNP(s) [rs73318181] 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

Panther Classification:

Molecular Function -

intercellular signal molecule

Gene Ontology Categories:

Process(es)

biological_process

Function(s)

molecular_function
protein binding