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.2:96649657 on build GRCh38
Cytoband
2q11.2
Assay ID Hs04668823_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 4 - Intron 5
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 ARID5A NEURL3 LMAN2L FER1L5 KANSL3 LOC105373496 CNNM4
nsv469775 Chr.2:96575189 - 96746754 on Build GRCh38 Loss LMAN2L FER1L5 KANSL3
dgv607e201 Chr.2:95855884 - 97561622 on Build GRCh38 Deletion DUSP2 MIR3127 LMAN2L ANKRD36 ANKRD36C FAHD2B LOC105373496 CNNM4 FAM178B NEURL3 ADRA2B ASTL SEMA4C STARD7-AS1 TMEM127 CIAO1 ANKRD36B ITPRIPL1 GPAT2 LOC653924 LOC105373495 LOC100506123 LOC101927053 SNRNP200 NCAPH ARID5A LOC100506076 LOC107984110 ANKRD23 FAHD2CP CNNM3 ANKRD39 STARD7 FER1L5 KANSL3
nsv834306 Chr.2:96575378 - 96747201 on Build GRCh38 Loss LMAN2L FER1L5 KANSL3
nsv1135873 Chr.2:95981454 - 97579645 on Build GRCh38 Deletion DUSP2 MIR3127 LMAN2L ANKRD36 ANKRD36C FAHD2B LOC105373496 CNNM4 FAM178B NEURL3 ADRA2B ASTL SEMA4C STARD7-AS1 TMEM127 CIAO1 ANKRD36B ITPRIPL1 GPAT2 LOC653924 LOC105373495 LOC100506123 LOC101927053 SNRNP200 NCAPH ARID5A LOC100506076 LOC107984110 ANKRD23 FAHD2CP CNNM3 ANKRD39 STARD7 FER1L5 KANSL3
esv3425717 Chr.2:95859900 - 97515905 on Build GRCh38 Duplication DUSP2 MIR3127 LMAN2L ANKRD36 ANKRD36C FAHD2B LOC105373496 CNNM4 FAM178B NEURL3 ADRA2B ASTL SEMA4C STARD7-AS1 TMEM127 CIAO1 ANKRD36B ITPRIPL1 GPAT2 LOC653924 LOC105373495 LOC100506123 LOC101927053 SNRNP200 NCAPH ARID5A LOC100506076 LOC107984110 ANKRD23 FAHD2CP CNNM3 ANKRD39 STARD7 FER1L5 KANSL3

Back To Top

More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s)


Back To Top

Related Products