Hs04682653_cn

• Gene Symbol: FER1L5
• Assay Reference Genome Location: Chr.2:96655594 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 9

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

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