Hs04570122_cn

• Gene Symbol: FER1L5
• Assay Reference Genome Location: Chr.2:96662670 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 13

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

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