accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

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

Chr.2:96651929 on build GRCh38
Cytoband
2q11.2
Assay ID Hs05863453_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

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:

 Overlaps Intron 6 - Exon 7
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 FER1L5 ARID5A CNNM4 KANSL3 LOC105373496 LMAN2L
nsv469775 Chr.2:96575189 - 96746754 on Build GRCh38 Loss FER1L5 KANSL3 LMAN2L
nsv834306 Chr.2:96575378 - 96747201 on Build GRCh38 Loss FER1L5 KANSL3 LMAN2L
dgv607e201 Chr.2:95855884 - 97561622 on Build GRCh38 Deletion GPAT2 FAHD2CP LOC105373495 FAHD2B TMEM127 STARD7 ITPRIPL1 STARD7-AS1 FER1L5 ANKRD36C LOC107984110 LOC100506076 CNNM4 LOC101927053 ANKRD36 ADRA2B ANKRD39 ANKRD36B ASTL CIAO1 LMAN2L SEMA4C NCAPH DUSP2 NEURL3 FAM178B LOC100506123 LOC653924 SNRNP200 ARID5A ANKRD23 CNNM3 MIR3127 KANSL3 LOC105373496
nsv1135873 Chr.2:95981454 - 97579645 on Build GRCh38 Deletion GPAT2 FAHD2CP LOC105373495 FAHD2B TMEM127 STARD7 ITPRIPL1 STARD7-AS1 FER1L5 ANKRD36C LOC107984110 LOC100506076 CNNM4 LOC101927053 ANKRD36 ADRA2B ANKRD39 ANKRD36B ASTL CIAO1 LMAN2L SEMA4C NCAPH DUSP2 NEURL3 FAM178B LOC100506123 LOC653924 SNRNP200 ARID5A ANKRD23 CNNM3 MIR3127 KANSL3 LOC105373496
esv3425717 Chr.2:95859900 - 97515905 on Build GRCh38 Duplication GPAT2 FAHD2CP LOC105373495 FAHD2B TMEM127 STARD7 ITPRIPL1 STARD7-AS1 FER1L5 ANKRD36C LOC107984110 LOC100506076 CNNM4 LOC101927053 ANKRD36 ADRA2B ANKRD39 ANKRD36B ASTL CIAO1 LMAN2L SEMA4C NCAPH DUSP2 NEURL3 FAM178B LOC100506123 LOC653924 SNRNP200 ARID5A ANKRD23 CNNM3 MIR3127 KANSL3 LOC105373496

Back To Top

More Information


Set Membership:

 Intragenic Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s)


Back To Top

Related Products