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See other KRT86 CNV Assays ›
Gene Symbol
KRT86
Assay Reference Genome
Location

Chr.12:52307760 on build GRCh38
Cytoband
12q13.13
Assay ID Hs03835722_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 3892

Gene Name:

 keratin 86

Gene Aliases:

 HB6, Hb1, K86, KRTHB1, KRTHB6, MNX

Location:

 Chr.12:52270507-52309163 on Build GRCh38

Assay Gene Location:

 Within Intron 9
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
KRT86 NM_001320198.1 NP_001307127.1
XM_005268866.4 XP_005268923.1
XM_017019296.1 XP_016874785.1
AK292237.1
AK297794.1
BC069585.1 AAH69585.1
X99142.1 CAA67579.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv1503n100 Chr.12:52285116 - 52394255 on Build GRCh38 Gain KRT86 KRT82 KRT85 KRT84 KRT81 KRT83
esv2759899 Chr.12:52169480 - 52391735 on Build GRCh38 Gain C12orf80 KRT86 KRT85 KRT7 KRT80 KRT87P KRT84 LINC00592 KRT81 KRT83
dgv29e180 Chr.12:52291976 - 52389509 on Build GRCh38 Gain KRT86 KRT85 KRT84 KRT83
nsv516938 Chr.12:52283925 - 52394228 on Build GRCh38 Gain+Loss KRT86 KRT82 KRT85 KRT84 KRT81 KRT83
dgv487e212 Chr.12:52294699 - 52388067 on Build GRCh38 Gain KRT86 KRT85 KRT84 KRT83
dgv200n27 Chr.12:52297319 - 52395144 on Build GRCh38 Gain KRT86 KRT82 KRT85 KRT84 KRT83
dgv9e209 Chr.12:52294216 - 52390216 on Build GRCh38 Duplication KRT86 KRT85 KRT84 KRT83
dgv2630n54 Chr.12:52287930 - 52395144 on Build GRCh38 Gain KRT86 KRT82 KRT85 KRT84 KRT81 KRT83
esv27319 Chr.12:52287366 - 52389709 on Build GRCh38 Gain+Loss KRT86 KRT85 KRT84 KRT81 KRT83
dgv70e55 Chr.12:52282619 - 52398149 on Build GRCh38 Gain KRT86 KRT82 KRT85 KRT84 KRT81 KRT83
esv2760832 Chr.12:52294900 - 52389052 on Build GRCh38 Gain KRT86 KRT85 KRT84 KRT83

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More Information


Additional Information:

For this assay, SNP(s) [rs73111108] 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:

Process(es)


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