Hs03878293_cn

• Gene Symbol: SLC35F4
• Assay Reference Genome Location: Chr.14:57581085 on build GRCh38
• Cytoband: 14q22.3

Target Gene Details

• Entrez Gene ID: 341880
• Gene Name: solute carrier family 35 member F4
• Gene Aliases: C14orf36, c14_5373
• Location: Chr.14:57563922-57982329 on Build GRCh38
• Assay Gene Location: Within Exon 9

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLC35F4	NM_001206920.1			NP_001193849.1
	NM_001306087.1			NP_001293016.1
	XM_011536720.2			XP_011535022.1
	XM_011536721.2			XP_011535023.1
	XM_011536723.2			XP_011535025.1
	XM_011536724.2			XP_011535026.1
	XM_011536725.1			XP_011535027.1
	XM_017021258.1			XP_016876747.1
	XM_017021259.1	6	4764	XP_016876748.1
	XM_017021260.1			XP_016876749.1
	XM_017021261.1	4	1053	XP_016876750.1
	BC101318.1
	BC101320.1
	BC101321.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1046422	Chr.14:57198718 - 58129812 on Build GRCh38	Gain	C14orf105 AP5M1 C14orf37 NAA30 SLC35F4 EXOC5
nsv1289	Chr.14:57579311 - 57590530 on Build GRCh38	Deletion	SLC35F4
nsv1043109	Chr.14:57545677 - 57618153 on Build GRCh38	Loss	SLC35F4

More Information

Additional Information:

For this assay, SNP(s) [rs147425664] 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)

transport