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

More Information

• Set Membership: Intragenic, Exonic, DGV Variation

Panther Classification:

Molecular Function -

membrane trafficking regulatory protein

Gene Ontology Categories:

Process(es)

myoblast fusion