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

Chr.2:96687049 on build GRCh38
Cytoband
2q11.2
Assay ID Hs05825721_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:

 Within Intron 24
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 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
XM_017005223.1 XP_016860712.1
AL133022.1
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 ARID5A KANSL3 NEURL3 LMAN2L FER1L5 LOC105373496 CNNM4
nsv469775 Chr.2:96575189 - 96746754 on Build GRCh38 Loss KANSL3 LMAN2L FER1L5
nsv526313 Chr.2:96667755 - 96994882 on Build GRCh38 Loss SEMA4C ANKRD39 CNNM3 FAM178B ANKRD23 LOC101927053 MIR3127 LMAN2L FER1L5 CNNM4
dgv607e201 Chr.2:95855884 - 97561622 on Build GRCh38 Deletion DUSP2 SEMA4C ANKRD39 TMEM127 STARD7-AS1 SNRNP200 LMAN2L LOC100506123 CNNM4 ASTL STARD7 LOC653924 FAM178B ANKRD23 LOC107984110 GPAT2 FAHD2CP ITPRIPL1 NCAPH FAHD2B LOC105373495 CIAO1 NEURL3 LOC101927053 ANKRD36C FER1L5 ANKRD36 ARID5A KANSL3 LOC100506076 ADRA2B CNNM3 ANKRD36B MIR3127 LOC105373496
nsv834306 Chr.2:96575378 - 96747201 on Build GRCh38 Loss KANSL3 LMAN2L FER1L5
nsv834307 Chr.2:96655710 - 96813529 on Build GRCh38 Loss MIR3127 LMAN2L FER1L5 CNNM4
nsv1135873 Chr.2:95981454 - 97579645 on Build GRCh38 Deletion DUSP2 SEMA4C ANKRD39 TMEM127 STARD7-AS1 SNRNP200 LMAN2L LOC100506123 CNNM4 ASTL STARD7 LOC653924 FAM178B ANKRD23 LOC107984110 GPAT2 FAHD2CP ITPRIPL1 NCAPH FAHD2B LOC105373495 CIAO1 NEURL3 LOC101927053 ANKRD36C FER1L5 ANKRD36 ARID5A KANSL3 LOC100506076 ADRA2B CNNM3 ANKRD36B MIR3127 LOC105373496
esv3425717 Chr.2:95859900 - 97515905 on Build GRCh38 Duplication DUSP2 SEMA4C ANKRD39 TMEM127 STARD7-AS1 SNRNP200 LMAN2L LOC100506123 CNNM4 ASTL STARD7 LOC653924 FAM178B ANKRD23 LOC107984110 GPAT2 FAHD2CP ITPRIPL1 NCAPH FAHD2B LOC105373495 CIAO1 NEURL3 LOC101927053 ANKRD36C FER1L5 ANKRD36 ARID5A KANSL3 LOC100506076 ADRA2B CNNM3 ANKRD36B MIR3127 LOC105373496

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More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s)


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