Hs04658748_cn

• Gene Symbol: FER1L5
• Assay Reference Genome Location: Chr.2:96668895 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: Overlaps Intron 15 - Exon 16

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

More Information

• Set Membership: Intragenic, Non-exonic, DGV Variation

Panther Classification:

Molecular Function -

membrane trafficking regulatory protein

Gene Ontology Categories:

Process(es)

myoblast fusion