Hs04631015_cn

• Gene Symbol: FER1L5
• Assay Reference Genome Location: Chr.2:96669845 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 Exon 18

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_011512124.2	1	680	XP_011510426.1
	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	CNNM4 KANSL3 LOC105373496 LMAN2L ARID5A FER1L5 NEURL3
nsv469775	Chr.2:96575189 - 96746754 on Build GRCh38	Loss	KANSL3 LMAN2L FER1L5
nsv526313	Chr.2:96667755 - 96994882 on Build GRCh38	Loss	MIR3127 CNNM3 CNNM4 ANKRD23 SEMA4C FAM178B LMAN2L ANKRD39 LOC101927053 FER1L5
nsv834307	Chr.2:96655710 - 96813529 on Build GRCh38	Loss	MIR3127 CNNM4 LMAN2L FER1L5
nsv834306	Chr.2:96575378 - 96747201 on Build GRCh38	Loss	KANSL3 LMAN2L FER1L5
dgv607e201	Chr.2:95855884 - 97561622 on Build GRCh38	Deletion	LOC100506123 NCAPH LOC105373496 FAHD2B ANKRD36 FER1L5 LOC105373495 LOC653924 CIAO1 ADRA2B MIR3127 ASTL CNNM3 CNNM4 STARD7 LOC100506076 ANKRD36C ANKRD39 LOC107984110 GPAT2 FAHD2CP NEURL3 ANKRD23 SEMA4C KANSL3 ITPRIPL1 DUSP2 LOC101927053 STARD7-AS1 TMEM127 FAM178B LMAN2L ANKRD36B SNRNP200 ARID5A
nsv1135873	Chr.2:95981454 - 97579645 on Build GRCh38	Deletion	LOC100506123 NCAPH LOC105373496 FAHD2B ANKRD36 FER1L5 LOC105373495 LOC653924 CIAO1 ADRA2B MIR3127 ASTL CNNM3 CNNM4 STARD7 LOC100506076 ANKRD36C ANKRD39 LOC107984110 GPAT2 FAHD2CP NEURL3 ANKRD23 SEMA4C KANSL3 ITPRIPL1 DUSP2 LOC101927053 STARD7-AS1 TMEM127 FAM178B LMAN2L ANKRD36B SNRNP200 ARID5A
esv3425717	Chr.2:95859900 - 97515905 on Build GRCh38	Duplication	LOC100506123 NCAPH LOC105373496 FAHD2B ANKRD36 FER1L5 LOC105373495 LOC653924 CIAO1 ADRA2B MIR3127 ASTL CNNM3 CNNM4 STARD7 LOC100506076 ANKRD36C ANKRD39 LOC107984110 GPAT2 FAHD2CP NEURL3 ANKRD23 SEMA4C KANSL3 ITPRIPL1 DUSP2 LOC101927053 STARD7-AS1 TMEM127 FAM178B LMAN2L ANKRD36B SNRNP200 ARID5A

More Information

• Set Membership: Intragenic, Exonic, DGV Variation

Panther Classification:

Molecular Function -

membrane trafficking regulatory protein

Gene Ontology Categories:

Process(es)

myoblast fusion