Hs05855038_cn

• Gene Symbol: FER1L5
• Assay Reference Genome Location: Chr.2:96672971 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 19

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_011512124.2			XP_011510426.1
	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
	XM_017005223.1			XP_016860712.1
	AL133022.1
	AY461813.1			AAS19933.1

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	LOC105373496 ARID5A CNNM4 KANSL3 NEURL3 FER1L5 LMAN2L
nsv469775	Chr.2:96575189 - 96746754 on Build GRCh38	Loss	KANSL3 FER1L5 LMAN2L
nsv526313	Chr.2:96667755 - 96994882 on Build GRCh38	Loss	MIR3127 CNNM4 ANKRD23 SEMA4C FAM178B ANKRD39 CNNM3 LOC101927053 FER1L5 LMAN2L
nsv834307	Chr.2:96655710 - 96813529 on Build GRCh38	Loss	MIR3127 CNNM4 FER1L5 LMAN2L
nsv834306	Chr.2:96575378 - 96747201 on Build GRCh38	Loss	KANSL3 FER1L5 LMAN2L
dgv607e201	Chr.2:95855884 - 97561622 on Build GRCh38	Deletion	ARID5A LOC100506076 FAHD2B CIAO1 ANKRD39 NCAPH LOC101927053 SNRNP200 LOC105373496 LOC653924 ITPRIPL1 SEMA4C LOC100506123 ADRA2B TMEM127 LOC107984110 STARD7 STARD7-AS1 CNNM3 DUSP2 FER1L5 MIR3127 LOC105373495 ASTL GPAT2 ANKRD36B CNNM4 ANKRD23 KANSL3 NEURL3 FAM178B FAHD2CP ANKRD36 LMAN2L ANKRD36C
nsv1135873	Chr.2:95981454 - 97579645 on Build GRCh38	Deletion	ARID5A LOC100506076 FAHD2B CIAO1 ANKRD39 NCAPH LOC101927053 SNRNP200 LOC105373496 LOC653924 ITPRIPL1 SEMA4C LOC100506123 ADRA2B TMEM127 LOC107984110 STARD7 STARD7-AS1 CNNM3 DUSP2 FER1L5 MIR3127 LOC105373495 ASTL GPAT2 ANKRD36B CNNM4 ANKRD23 KANSL3 NEURL3 FAM178B FAHD2CP ANKRD36 LMAN2L ANKRD36C
esv3425717	Chr.2:95859900 - 97515905 on Build GRCh38	Duplication	ARID5A LOC100506076 FAHD2B CIAO1 ANKRD39 NCAPH LOC101927053 SNRNP200 LOC105373496 LOC653924 ITPRIPL1 SEMA4C LOC100506123 ADRA2B TMEM127 LOC107984110 STARD7 STARD7-AS1 CNNM3 DUSP2 FER1L5 MIR3127 LOC105373495 ASTL GPAT2 ANKRD36B CNNM4 ANKRD23 KANSL3 NEURL3 FAM178B FAHD2CP ANKRD36 LMAN2L ANKRD36C

More Information

Additional Information:

For this assay, SNP(s) [rs114903651] 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