Hs04691329_cn

• Gene Symbol: FER1L5
• Assay Reference Genome Location: Chr.2:96666297 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 14

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

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

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