Hs01057685_cn

• Gene Symbol: FAM26D
• Assay Reference Genome Location: Chr.6:116558673 on build GRCh38
• Cytoband: 6q22.1

Target Gene Details

• Entrez Gene ID: 221301
• Gene Name: family with sequence similarity 26 member D
• Gene Aliases: C6orf78
• Location: Chr.6:116529013-116561123 on Build GRCh38
• Assay Gene Location: Within Exon 8

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM26D	NM_001256887.2	4	1296	NP_001243816.1
	NM_001256888.2	4	1202	NP_001243817.1
	NM_001256889.2	3	1080	NP_001243818.1
	NM_153036.4	3	1135	NP_694581.1
	XM_005266860.3	2	2070	XP_005266917.1
	XM_011535560.2	5	1390	XP_011533862.1
	XM_011535561.2	4	1239	XP_011533863.1
	XM_011535562.2	6	1571	XP_011533864.1
	XM_011535563.2	4	1184	XP_011533865.1
	XM_011535564.1	4	1145	XP_011533866.1
	XM_017010390.1	5	1318	XP_016865879.1
	XM_017010391.1	5	1273	XP_016865880.1
	XM_017010392.1	5	1335	XP_016865881.1
	AK056801.1	3	1068	BAB71288.1
	AY358252.1	3	1117	AAQ88619.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv830783	Chr.6:116445706 - 116645069 on Build GRCh38	Gain	FAM26E RSPH4A ZUFSP RWDD1 FAM26F TRAPPC3L FAM26D
nsv523972	Chr.6:115958024 - 116809541 on Build GRCh38	Gain	COL10A1 NT5DC1 TSPYL4 FAM26E RSPH4A FAM162B TSPYL1 ZUFSP DSE FAM26F TRAPPC3L FAM26D GPRC6A LOC100287467 RWDD1 FRK TPI1P3 KPNA5

More Information

Additional Information:

For this assay, SNP(s) [rs370724503] 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)

ion transmembrane transport
cation transmembrane transport

Function(s)

cation channel activity