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

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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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