Hs04560486_cn

• Gene Symbol: FER1L5
• Assay Reference Genome Location: Chr.2:96652620 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 7

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	6	1241	BAC86403.1
	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	FER1L5 KANSL3 ARID5A LOC105373496 NEURL3 LMAN2L CNNM4
nsv469775	Chr.2:96575189 - 96746754 on Build GRCh38	Loss	FER1L5 KANSL3 LMAN2L
nsv834306	Chr.2:96575378 - 96747201 on Build GRCh38	Loss	FER1L5 KANSL3 LMAN2L
dgv607e201	Chr.2:95855884 - 97561622 on Build GRCh38	Deletion	ANKRD39 ITPRIPL1 ARID5A NCAPH FAHD2CP ANKRD36B DUSP2 LMAN2L TMEM127 CIAO1 ANKRD36 KANSL3 GPAT2 LOC101927053 STARD7 LOC653924 CNNM3 LOC100506076 ANKRD36C CNNM4 LOC105373496 ADRA2B NEURL3 ANKRD23 ASTL SEMA4C SNRNP200 FAM178B MIR3127 FER1L5 FAHD2B LOC105373495 STARD7-AS1 LOC107984110 LOC100506123
nsv1135873	Chr.2:95981454 - 97579645 on Build GRCh38	Deletion	ANKRD39 ITPRIPL1 ARID5A NCAPH FAHD2CP ANKRD36B DUSP2 LMAN2L TMEM127 CIAO1 ANKRD36 KANSL3 GPAT2 LOC101927053 STARD7 LOC653924 CNNM3 LOC100506076 ANKRD36C CNNM4 LOC105373496 ADRA2B NEURL3 ANKRD23 ASTL SEMA4C SNRNP200 FAM178B MIR3127 FER1L5 FAHD2B LOC105373495 STARD7-AS1 LOC107984110 LOC100506123
esv3425717	Chr.2:95859900 - 97515905 on Build GRCh38	Duplication	ANKRD39 ITPRIPL1 ARID5A NCAPH FAHD2CP ANKRD36B DUSP2 LMAN2L TMEM127 CIAO1 ANKRD36 KANSL3 GPAT2 LOC101927053 STARD7 LOC653924 CNNM3 LOC100506076 ANKRD36C CNNM4 LOC105373496 ADRA2B NEURL3 ANKRD23 ASTL SEMA4C SNRNP200 FAM178B MIR3127 FER1L5 FAHD2B LOC105373495 STARD7-AS1 LOC107984110 LOC100506123

More Information

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation

Panther Classification:

Molecular Function -

membrane trafficking regulatory protein

Gene Ontology Categories:

Process(es)

myoblast fusion