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

Chr.2:96646844 on build GRCh38
Cytoband
2q11.2
Assay ID Hs05855726_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 2
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_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
AK126032.1 BAC86403.1
AY461813.1 AAS19933.1
DB083434.1

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

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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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