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

Chr.2:96671640 on build GRCh38
Cytoband
2q11.2
Assay ID Hs04645733_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 18
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
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 KANSL3 FER1L5 NEURL3 CNNM4 ARID5A LOC105373496 LMAN2L
nsv469775 Chr.2:96575189 - 96746754 on Build GRCh38 Loss KANSL3 FER1L5 LMAN2L
nsv526313 Chr.2:96667755 - 96994882 on Build GRCh38 Loss ANKRD39 ANKRD23 FER1L5 SEMA4C CNNM4 CNNM3 MIR3127 FAM178B LMAN2L LOC101927053
dgv607e201 Chr.2:95855884 - 97561622 on Build GRCh38 Deletion ANKRD23 ITPRIPL1 SEMA4C ARID5A LOC100506123 LOC100506076 LOC105373496 LOC101927053 ANKRD36 STARD7 ANKRD39 ASTL NEURL3 CNNM4 LMAN2L GPAT2 KANSL3 SNRNP200 FER1L5 NCAPH LOC653924 FAM178B LOC107984110 FAHD2CP CIAO1 LOC105373495 TMEM127 FAHD2B ADRA2B CNNM3 ANKRD36C MIR3127 STARD7-AS1 DUSP2 ANKRD36B
nsv834306 Chr.2:96575378 - 96747201 on Build GRCh38 Loss KANSL3 FER1L5 LMAN2L
nsv834307 Chr.2:96655710 - 96813529 on Build GRCh38 Loss FER1L5 CNNM4 MIR3127 LMAN2L
nsv1135873 Chr.2:95981454 - 97579645 on Build GRCh38 Deletion ANKRD23 ITPRIPL1 SEMA4C ARID5A LOC100506123 LOC100506076 LOC105373496 LOC101927053 ANKRD36 STARD7 ANKRD39 ASTL NEURL3 CNNM4 LMAN2L GPAT2 KANSL3 SNRNP200 FER1L5 NCAPH LOC653924 FAM178B LOC107984110 FAHD2CP CIAO1 LOC105373495 TMEM127 FAHD2B ADRA2B CNNM3 ANKRD36C MIR3127 STARD7-AS1 DUSP2 ANKRD36B
esv3425717 Chr.2:95859900 - 97515905 on Build GRCh38 Duplication ANKRD23 ITPRIPL1 SEMA4C ARID5A LOC100506123 LOC100506076 LOC105373496 LOC101927053 ANKRD36 STARD7 ANKRD39 ASTL NEURL3 CNNM4 LMAN2L GPAT2 KANSL3 SNRNP200 FER1L5 NCAPH LOC653924 FAM178B LOC107984110 FAHD2CP CIAO1 LOC105373495 TMEM127 FAHD2B ADRA2B CNNM3 ANKRD36C MIR3127 STARD7-AS1 DUSP2 ANKRD36B

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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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