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

Chr.20:63248283 on build GRCh38
Cytoband
20q13.33
Assay ID Hs04044149_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 5
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
dgv519n27 Chr.20:63154307 - 63248817 on Build GRCh38 Loss MIR124-3 BIRC7 NKAIN4 YTHDF1 LOC107985425 MIR3196
nsv522880 Chr.20:63239113 - 63264557 on Build GRCh38 Loss BIRC7 FLJ16779 NKAIN4 LOC107985425
nsv953306 Chr.20:63151949 - 63571247 on Build GRCh38 Deletion PTK6 MIR4326 COL20A1 ARFGAP1 EEF1A2 LOC100130587 LOC100130152 MIR124-3 BIRC7 PPDPF FNDC11 SRMS KCNQ2 FLJ16779 NKAIN4 CHRNA4 HELZ2 YTHDF1 LOC107985425 LOC102723788 MIR3196
nsv586559 Chr.20:63195172 - 63248817 on Build GRCh38 Gain BIRC7 NKAIN4 YTHDF1 LOC107985425 MIR3196
nsv525279 Chr.20:63221277 - 63323323 on Build GRCh38 Loss BIRC7 MIR4326 FLJ16779 NKAIN4 COL20A1 ARFGAP1 LOC107985425 MIR3196
nsv9825 Chr.20:62775470 - 63601330 on Build GRCh38 Gain HAR1A LINC00659 LINC01056 TCFL5 COL20A1 LOC107985428 ARFGAP1 EEF1A2 LOC100130587 OGFR-AS1 LOC100130152 HAR1B MIR124-3 BIRC7 PPDPF OGFR SRMS LOC63930 LOC102723788 MIR3196 DPH3P1 GMEB2 SLC17A9 PTK6 LINC00029 MRGBP MIR4326 BHLHE23 DIDO1 GID8 FNDC11 KCNQ2 COL9A3 FLJ16779 NKAIN4 CHRNA4 HELZ2 YTHDF1 LOC107985425
nsv3446 Chr.20:63237764 - 63282515 on Build GRCh38 Deletion BIRC7 FLJ16779 NKAIN4 ARFGAP1 LOC107985425 MIR3196
dgv520n27 Chr.20:63217271 - 63264568 on Build GRCh38 Loss BIRC7 FLJ16779 NKAIN4 LOC107985425 MIR3196
nsv834032 Chr.20:63213997 - 63308161 on Build GRCh38 Loss BIRC7 MIR4326 FLJ16779 NKAIN4 COL20A1 ARFGAP1 YTHDF1 LOC107985425 MIR3196

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More Information


Additional Information:

For this assay, SNP(s) [rs80345453] 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

Gene Ontology Categories:

Function(s)


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