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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
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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:

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

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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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