Hs00939901_cn

• Gene Symbol: MFSD4B
• Assay Reference Genome Location: Chr.6:111263847 on build GRCh38
• Cytoband: 6q21

Target Gene Details

• Entrez Gene ID: 91749
• Gene Name: major facilitator superfamily domain containing 4B
• Gene Aliases: KIAA1919, NaGLT1
• Location: Chr.6:111259279-111280005 on Build GRCh38
• Assay Gene Location: Overlaps Intron 2 - Exon 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
MFSD4B	NM_153369.2			NP_699200.2
	XM_017011483.1			XP_016866972.1
	AK093136.1
	AK292735.1
	AK315016.1
	BC036115.1			AAH36115.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1020627	Chr.6:110982539 - 111302511 on Build GRCh38	Gain	SLC16A10 RPF2 GSTM2P1 REV3L MFSD4B
esv3610378	Chr.6:111260647 - 111264325 on Build GRCh38	Loss	MFSD4B
nsv1028349	Chr.6:111184772 - 111371598 on Build GRCh38	Gain	SLC16A10 REV3L MFSD4B

More Information

Additional Information:

For this assay, SNP(s) [rs73532762] 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, Non-exonic, DGV Variation

Panther Classification:

Molecular Function -

transporter

Gene Ontology Categories:

Process(es)

sodium ion transport
carbohydrate transport
transmembrane transport

Function(s)

symporter activity