Hs04669144_cn

• Gene Symbol: FER1L5
• Assay Reference Genome Location: Chr.2:96667723 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	LMAN2L LOC105373496 NEURL3 CNNM4 ARID5A FER1L5 KANSL3
nsv469775	Chr.2:96575189 - 96746754 on Build GRCh38	Loss	LMAN2L FER1L5 KANSL3
nsv526313	Chr.2:96667755 - 96994882 on Build GRCh38	Loss	LMAN2L LOC101927053 CNNM3 CNNM4 MIR3127 FAM178B ANKRD23 ANKRD39 FER1L5 SEMA4C
nsv834307	Chr.2:96655710 - 96813529 on Build GRCh38	Loss	LMAN2L CNNM4 MIR3127 FER1L5
nsv834306	Chr.2:96575378 - 96747201 on Build GRCh38	Loss	LMAN2L FER1L5 KANSL3
dgv607e201	Chr.2:95855884 - 97561622 on Build GRCh38	Deletion	LOC105373495 LOC105373496 LOC101927053 LOC107984110 LOC100506076 ADRA2B LOC653924 KANSL3 ITPRIPL1 FAHD2CP ANKRD36C ANKRD36B CNNM3 NEURL3 LOC100506123 FAM178B ARID5A DUSP2 ANKRD23 FER1L5 CNNM4 CIAO1 MIR3127 FAHD2B SNRNP200 LMAN2L TMEM127 GPAT2 NCAPH STARD7 ANKRD36 ANKRD39 STARD7-AS1 SEMA4C ASTL
nsv1135873	Chr.2:95981454 - 97579645 on Build GRCh38	Deletion	LOC105373495 LOC105373496 LOC101927053 LOC107984110 LOC100506076 ADRA2B LOC653924 KANSL3 ITPRIPL1 FAHD2CP ANKRD36C ANKRD36B CNNM3 NEURL3 LOC100506123 FAM178B ARID5A DUSP2 ANKRD23 FER1L5 CNNM4 CIAO1 MIR3127 FAHD2B SNRNP200 LMAN2L TMEM127 GPAT2 NCAPH STARD7 ANKRD36 ANKRD39 STARD7-AS1 SEMA4C ASTL
esv3425717	Chr.2:95859900 - 97515905 on Build GRCh38	Duplication	LOC105373495 LOC105373496 LOC101927053 LOC107984110 LOC100506076 ADRA2B LOC653924 KANSL3 ITPRIPL1 FAHD2CP ANKRD36C ANKRD36B CNNM3 NEURL3 LOC100506123 FAM178B ARID5A DUSP2 ANKRD23 FER1L5 CNNM4 CIAO1 MIR3127 FAHD2B SNRNP200 LMAN2L TMEM127 GPAT2 NCAPH STARD7 ANKRD36 ANKRD39 STARD7-AS1 SEMA4C ASTL

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