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See other FER1L5 CNV Assays ›
Gene Symbol
FER1L5
Assay Reference Genome
Location

Chr.2:96651929 on build GRCh38
Cytoband
2q11.2
Assay ID Hs05863453_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

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 6 - Exon 7
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
AK126032.1 BAC86403.1
AY461813.1 AAS19933.1
DB083434.1

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

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More Information


Set Membership:

 Intragenic Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s)


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