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.2:96685263 on build GRCh38
Cytoband
2q11.2
Assay ID Hs05869094_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:

 Within Intron 21
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
XM_017005223.1 XP_016860712.1
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 NEURL3 KANSL3 CNNM4 FER1L5 ARID5A LOC105373496 LMAN2L
nsv469775 Chr.2:96575189 - 96746754 on Build GRCh38 Loss KANSL3 FER1L5 LMAN2L
nsv526313 Chr.2:96667755 - 96994882 on Build GRCh38 Loss ANKRD39 CNNM4 FAM178B FER1L5 LOC101927053 MIR3127 CNNM3 ANKRD23 SEMA4C LMAN2L
nsv834306 Chr.2:96575378 - 96747201 on Build GRCh38 Loss KANSL3 FER1L5 LMAN2L
nsv834307 Chr.2:96655710 - 96813529 on Build GRCh38 Loss CNNM4 FER1L5 MIR3127 LMAN2L
dgv607e201 Chr.2:95855884 - 97561622 on Build GRCh38 Deletion LOC100506123 FAHD2CP LOC101927053 SNRNP200 STARD7 ADRA2B LOC105373496 ANKRD39 NEURL3 DUSP2 KANSL3 ARID5A ANKRD36C NCAPH ASTL LOC100506076 LOC107984110 CIAO1 LOC105373495 LMAN2L CNNM4 LOC653924 CNNM3 ANKRD23 ANKRD36B ANKRD36 FAHD2B TMEM127 STARD7-AS1 FAM178B FER1L5 ITPRIPL1 MIR3127 GPAT2 SEMA4C
nsv1135873 Chr.2:95981454 - 97579645 on Build GRCh38 Deletion LOC100506123 FAHD2CP LOC101927053 SNRNP200 STARD7 ADRA2B LOC105373496 ANKRD39 NEURL3 DUSP2 KANSL3 ARID5A ANKRD36C NCAPH ASTL LOC100506076 LOC107984110 CIAO1 LOC105373495 LMAN2L CNNM4 LOC653924 CNNM3 ANKRD23 ANKRD36B ANKRD36 FAHD2B TMEM127 STARD7-AS1 FAM178B FER1L5 ITPRIPL1 MIR3127 GPAT2 SEMA4C
esv3425717 Chr.2:95859900 - 97515905 on Build GRCh38 Duplication LOC100506123 FAHD2CP LOC101927053 SNRNP200 STARD7 ADRA2B LOC105373496 ANKRD39 NEURL3 DUSP2 KANSL3 ARID5A ANKRD36C NCAPH ASTL LOC100506076 LOC107984110 CIAO1 LOC105373495 LMAN2L CNNM4 LOC653924 CNNM3 ANKRD23 ANKRD36B ANKRD36 FAHD2B TMEM127 STARD7-AS1 FAM178B FER1L5 ITPRIPL1 MIR3127 GPAT2 SEMA4C

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