Hs04561489_cn

• Gene Symbol: FER1L5
• Assay Reference Genome Location: Chr.2:96644810 on build GRCh38
• Cytoband: 2q11.2

Target Gene Details

• Entrez Gene ID: 90342
• Gene Name: fer-1 like family member 5
• Gene Aliases: -
• Location: Chr.2:96642719-96704887 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FER1L5	NM_001293083.1			NP_001280012.1
	XM_011512110.2			XP_011510412.1
	XM_011512111.2			XP_011510413.1
	XM_011512113.2			XP_011510415.1
	XM_011512114.2			XP_011510416.1
	XM_011512115.2			XP_011510417.1
	XM_011512116.2			XP_011510418.1
	XM_011512117.2			XP_011510419.1
	XM_011512118.2			XP_011510420.1
	XM_011512119.2			XP_011510421.1
	XM_011512120.2			XP_011510422.1
	XM_011512122.2			XP_011510424.1
	XM_011512125.2			XP_011510427.1
	XM_011512126.2			XP_011510428.1
	XM_011512127.2			XP_011510429.1
	XM_011512128.2			XP_011510430.1
	XM_017005222.1			XP_016860711.1
	AK126032.1			BAC86403.1
	AY461813.1			AAS19933.1
	DB083434.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2720413	Chr.2:96472591 - 96793459 on Build GRCh38	Deletion	FER1L5 KANSL3 ARID5A CNNM4 LMAN2L LOC105373496 NEURL3
nsv469775	Chr.2:96575189 - 96746754 on Build GRCh38	Loss	FER1L5 KANSL3 LMAN2L
dgv607e201	Chr.2:95855884 - 97561622 on Build GRCh38	Deletion	KANSL3 ADRA2B LOC105373495 FAHD2CP ITPRIPL1 GPAT2 CIAO1 FAM178B FAHD2B CNNM4 LMAN2L MIR3127 LOC101927053 NCAPH ANKRD23 STARD7-AS1 ANKRD36 FER1L5 ARID5A ANKRD39 TMEM127 LOC107984110 SEMA4C LOC100506076 ANKRD36B NEURL3 CNNM3 LOC100506123 SNRNP200 STARD7 LOC653924 ASTL ANKRD36C LOC105373496 DUSP2
nsv834306	Chr.2:96575378 - 96747201 on Build GRCh38	Loss	FER1L5 KANSL3 LMAN2L
nsv1135873	Chr.2:95981454 - 97579645 on Build GRCh38	Deletion	KANSL3 ADRA2B LOC105373495 FAHD2CP ITPRIPL1 GPAT2 CIAO1 FAM178B FAHD2B CNNM4 LMAN2L MIR3127 LOC101927053 NCAPH ANKRD23 STARD7-AS1 ANKRD36 FER1L5 ARID5A ANKRD39 TMEM127 LOC107984110 SEMA4C LOC100506076 ANKRD36B NEURL3 CNNM3 LOC100506123 SNRNP200 STARD7 LOC653924 ASTL ANKRD36C LOC105373496 DUSP2
esv3425717	Chr.2:95859900 - 97515905 on Build GRCh38	Duplication	KANSL3 ADRA2B LOC105373495 FAHD2CP ITPRIPL1 GPAT2 CIAO1 FAM178B FAHD2B CNNM4 LMAN2L MIR3127 LOC101927053 NCAPH ANKRD23 STARD7-AS1 ANKRD36 FER1L5 ARID5A ANKRD39 TMEM127 LOC107984110 SEMA4C LOC100506076 ANKRD36B NEURL3 CNNM3 LOC100506123 SNRNP200 STARD7 LOC653924 ASTL ANKRD36C LOC105373496 DUSP2

More Information

Additional Information:

For this assay, SNP(s) [rs149872911] 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 -

membrane trafficking regulatory protein

Gene Ontology Categories:

Process(es)

myoblast fusion