Hs04699769_cn

• Gene Symbol: FER1L5
• Assay Reference Genome Location: Chr.2:96660362 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 9 - Intron 10

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

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