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

Chr.2:96644810 on build GRCh38
Cytoband
2q11.2
Assay ID Hs04561489_cn
Size
Availability Made To Order
Catalog # 4400291
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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 1
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 CNNM4 LOC105373496 ARID5A NEURL3 KANSL3 LMAN2L 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 CIAO1 LOC100506076 NCAPH KANSL3 LOC101927053 LOC100506123 CNNM4 STARD7-AS1 SNRNP200 TMEM127 LOC653924 MIR3127 NEURL3 FAHD2CP LMAN2L ANKRD36B ANKRD36 LOC105373496 ADRA2B ANKRD36C FAHD2B FAM178B GPAT2 DUSP2 SEMA4C LOC105373495 STARD7 CNNM3 ASTL LOC107984110 ANKRD23 ARID5A ITPRIPL1 FER1L5 ANKRD39
nsv1135873 Chr.2:95981454 - 97579645 on Build GRCh38 Deletion CIAO1 LOC100506076 NCAPH KANSL3 LOC101927053 LOC100506123 CNNM4 STARD7-AS1 SNRNP200 TMEM127 LOC653924 MIR3127 NEURL3 FAHD2CP LMAN2L ANKRD36B ANKRD36 LOC105373496 ADRA2B ANKRD36C FAHD2B FAM178B GPAT2 DUSP2 SEMA4C LOC105373495 STARD7 CNNM3 ASTL LOC107984110 ANKRD23 ARID5A ITPRIPL1 FER1L5 ANKRD39
esv3425717 Chr.2:95859900 - 97515905 on Build GRCh38 Duplication CIAO1 LOC100506076 NCAPH KANSL3 LOC101927053 LOC100506123 CNNM4 STARD7-AS1 SNRNP200 TMEM127 LOC653924 MIR3127 NEURL3 FAHD2CP LMAN2L ANKRD36B ANKRD36 LOC105373496 ADRA2B ANKRD36C FAHD2B FAM178B GPAT2 DUSP2 SEMA4C LOC105373495 STARD7 CNNM3 ASTL LOC107984110 ANKRD23 ARID5A ITPRIPL1 FER1L5 ANKRD39

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More Information


Additional Information:

For this assay, SNP(s) [rs149872911] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s)


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