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

Chr.2:96680173 on build GRCh38
Cytoband
2q11.2
Assay ID Hs04599066_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 20
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 CNNM4 KANSL3 FER1L5 NEURL3 LMAN2L LOC105373496
nsv469775 Chr.2:96575189 - 96746754 on Build GRCh38 Loss KANSL3 FER1L5 LMAN2L
nsv526313 Chr.2:96667755 - 96994882 on Build GRCh38 Loss CNNM3 CNNM4 FER1L5 LOC101927053 ANKRD39 SEMA4C MIR3127 LMAN2L FAM178B ANKRD23
dgv607e201 Chr.2:95855884 - 97561622 on Build GRCh38 Deletion FER1L5 NEURL3 LOC100506076 LOC653924 ANKRD36 ANKRD23 LOC107984110 CNNM4 DUSP2 ANKRD36B ASTL STARD7 ANKRD36C SNRNP200 KANSL3 LOC101927053 TMEM127 NCAPH LMAN2L LOC105373495 ADRA2B ARID5A ITPRIPL1 CNNM3 STARD7-AS1 CIAO1 ANKRD39 FAHD2CP SEMA4C GPAT2 MIR3127 LOC105373496 LOC100506123 FAM178B FAHD2B
nsv834306 Chr.2:96575378 - 96747201 on Build GRCh38 Loss KANSL3 FER1L5 LMAN2L
nsv834307 Chr.2:96655710 - 96813529 on Build GRCh38 Loss CNNM4 FER1L5 MIR3127 LMAN2L
nsv1135873 Chr.2:95981454 - 97579645 on Build GRCh38 Deletion FER1L5 NEURL3 LOC100506076 LOC653924 ANKRD36 ANKRD23 LOC107984110 CNNM4 DUSP2 ANKRD36B ASTL STARD7 ANKRD36C SNRNP200 KANSL3 LOC101927053 TMEM127 NCAPH LMAN2L LOC105373495 ADRA2B ARID5A ITPRIPL1 CNNM3 STARD7-AS1 CIAO1 ANKRD39 FAHD2CP SEMA4C GPAT2 MIR3127 LOC105373496 LOC100506123 FAM178B FAHD2B
esv3425717 Chr.2:95859900 - 97515905 on Build GRCh38 Duplication FER1L5 NEURL3 LOC100506076 LOC653924 ANKRD36 ANKRD23 LOC107984110 CNNM4 DUSP2 ANKRD36B ASTL STARD7 ANKRD36C SNRNP200 KANSL3 LOC101927053 TMEM127 NCAPH LMAN2L LOC105373495 ADRA2B ARID5A ITPRIPL1 CNNM3 STARD7-AS1 CIAO1 ANKRD39 FAHD2CP SEMA4C GPAT2 MIR3127 LOC105373496 LOC100506123 FAM178B FAHD2B

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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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