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

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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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