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See other NKAIN4 CNV Assays ›
Gene Symbol
NKAIN4
Assay Reference Genome
Location

Chr.20:63249214 on build GRCh38
Cytoband
20q13.33
Assay ID Hs04040542_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 128414

Gene Name:

 Na+/K+ transporting ATPase interacting 4

Gene Aliases:

 C20orf58, FAM77A, bA261N11.2

Location:

 Chr.20:63240784-63254904 on Build GRCh38

Assay Gene Location:

 Within Intron 4
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NKAIN4 NM_152864.3 NP_690603.3
XM_005260192.1 XP_005260249.1
XM_005260194.3 XP_005260251.1
XM_011528527.1 XP_011526829.1
XM_011528528.2 XP_011526830.1
XM_011528529.2 XP_011526831.1
XM_017027636.1 XP_016883125.1
XM_017027637.1 XP_016883126.1
XM_017027638.1 XP_016883127.1
XM_017027639.1 XP_016883128.1
AK126246.1
AK225765.1
AK308958.1
BC041812.1 AAH41812.1
BG708360.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv522880 Chr.20:63239113 - 63264557 on Build GRCh38 Loss NKAIN4 BIRC7 LOC107985425 FLJ16779
nsv953306 Chr.20:63151949 - 63571247 on Build GRCh38 Deletion LOC100130152 PPDPF SRMS MIR3196 LOC102723788 CHRNA4 FLJ16779 NKAIN4 ARFGAP1 YTHDF1 KCNQ2 BIRC7 EEF1A2 FNDC11 COL20A1 PTK6 LOC107985425 LOC100130587 MIR124-3 MIR4326 HELZ2
nsv525279 Chr.20:63221277 - 63323323 on Build GRCh38 Loss NKAIN4 ARFGAP1 BIRC7 MIR3196 COL20A1 LOC107985425 FLJ16779 MIR4326
nsv9825 Chr.20:62775470 - 63601330 on Build GRCh38 Gain LOC107985428 LINC00029 LOC100130152 PPDPF CHRNA4 BHLHE23 ARFGAP1 KCNQ2 LINC01056 EEF1A2 FNDC11 COL9A3 SLC17A9 GMEB2 LOC107985425 DPH3P1 HAR1B HAR1A MRGBP SRMS MIR3196 LOC102723788 FLJ16779 LINC00659 GID8 OGFR-AS1 NKAIN4 YTHDF1 DIDO1 TCFL5 BIRC7 LOC63930 COL20A1 PTK6 LOC100130587 MIR124-3 MIR4326 HELZ2 OGFR
nsv3446 Chr.20:63237764 - 63282515 on Build GRCh38 Deletion NKAIN4 ARFGAP1 BIRC7 MIR3196 LOC107985425 FLJ16779
nsv586562 Chr.20:63217271 - 63268953 on Build GRCh38 Gain NKAIN4 BIRC7 MIR3196 LOC107985425 FLJ16779
nsv834032 Chr.20:63213997 - 63308161 on Build GRCh38 Loss NKAIN4 ARFGAP1 YTHDF1 BIRC7 MIR3196 COL20A1 LOC107985425 FLJ16779 MIR4326

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More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s)


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