Hs04645246_cn

• Gene Symbol: FER1L5
• Assay Reference Genome Location: Chr.2:96661704 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: Overlaps Intron 11 - Exon 12

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
	AY461813.1			AAS19933.1
	DW009988.1

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

More Information

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

Panther Classification:

Molecular Function -

membrane trafficking regulatory protein

Gene Ontology Categories:

Process(es)

myoblast fusion