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

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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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