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

Chr.7:1536055 on build GRCh38
Cytoband
7p22.3
Assay ID Hs03623201_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 7975

Gene Name:

 MAF bZIP transcription factor K

Gene Aliases:

 NFE2U, P18

Location:

 Chr.7:1530732-1543043 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
MAFK NM_002360.3 NP_002351.1
AF059194.1 AAC14426.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv823970 Chr.7:1428809 - 1562091 on Build GRCh38 Gain LOC100128653 MAFK MICALL2 INTS1 TMEM184A
nsv950786 Chr.7:1381265 - 1675664 on Build GRCh38 Deletion LOC100128653 MAFK PSMG3 MICALL2 INTS1 ELFN1 TFAMP1 TMEM184A PSMG3-AS1 LOC105375303
esv2759499 Chr.7:1159459 - 1650311 on Build GRCh38 Loss LOC101927021 LOC100128653 MAFK PSMG3 ZFAND2A MICALL2 INTS1 UNCX TFAMP1 TMEM184A PSMG3-AS1 LOC105375303
nsv471182 Chr.7:1152053 - 1554022 on Build GRCh38 Loss LOC101927021 LOC100128653 MAFK ZFAND2A MICALL2 INTS1 UNCX TMEM184A
esv3891010 Chr.7:1534767 - 1554022 on Build GRCh38 Loss LOC100128653 MAFK TMEM184A
nsv830880 Chr.7:1493586 - 1650311 on Build GRCh38 Loss LOC100128653 MAFK PSMG3 INTS1 TFAMP1 TMEM184A PSMG3-AS1 LOC105375303
nsv605819 Chr.7:1512080 - 1550644 on Build GRCh38 Loss LOC100128653 MAFK TMEM184A
dgv11136n54 Chr.7:1523105 - 1543652 on Build GRCh38 Loss LOC100128653 MAFK TMEM184A
dgv11135n54 Chr.7:1388817 - 1554022 on Build GRCh38 Loss LOC100128653 MAFK MICALL2 INTS1 TMEM184A
nsv5615 Chr.7:1528557 - 1573208 on Build GRCh38 Deletion LOC100128653 MAFK PSMG3 TMEM184A PSMG3-AS1
nsv605820 Chr.7:1518331 - 1574625 on Build GRCh38 Loss LOC100128653 MAFK PSMG3 TMEM184A PSMG3-AS1

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More Information


Additional Information:

For this assay, SNP(s) [rs77709192] 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) Process(es)


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