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See other CYP4F12 CNV Assays ›
Gene Symbol
CYP4F12
Assay Reference Genome
Location

Chr.19:15682805 on build GRCh38
Cytoband
19p13.12
Assay ID Hs04488631_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 66002

Gene Name:

 cytochrome P450 family 4 subfamily F member 12

Gene Aliases:

 CYPIVF12, F22329_1

Location:

 Chr.19:15673018-15698819 on Build GRCh38

Assay Gene Location:

 Within Intron 5
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
CYP4F12 NM_023944.3 NP_076433.3
NR_117085.1
XM_006722850.3 XP_006722913.1
XM_011528202.2 XP_011526504.1
XM_011528203.2 XP_011526505.1
XM_011528204.2 XP_011526506.1
XM_011528205.2 XP_011526507.1
XM_011528207.2 XP_011526509.1
XM_011528208.2 XP_011526510.1
XM_017027172.1 XP_016882661.1
AB035130.1 BAB18269.1
AB035131.1 BAB18270.1
AK074412.1
AK075435.1
AL832171.1 CAI46131.1
AY008841.1 AAG33247.1
AY358977.1 AAQ89336.1
BC035350.1 AAH35350.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv470128 Chr.19:15653261 - 15728555 on Build GRCh38 Gain CYP4F3 CYP4F12 OR10H2
esv2421519 Chr.19:15668643 - 15719658 on Build GRCh38 Duplication CYP4F12
esv2758747 Chr.19:15669231 - 15740451 on Build GRCh38 Gain+Loss CYP4F12 OR10H2
esv3334671 Chr.19:15673766 - 15931354 on Build GRCh38 Duplication CYP4F24P OR10H1 OR10H3 UCA1 CYP4F11 LOC102724279 CYP4F2 OR10H5 CYP4F12 OR10H2
nsv978781 Chr.19:15682273 - 15685174 on Build GRCh38 Duplication CYP4F12
dgv28n64 Chr.19:15669207 - 15719658 on Build GRCh38 Gain CYP4F12
dgv3452n100 Chr.19:15679275 - 15714929 on Build GRCh38 Gain CYP4F12
dgv3446n100 Chr.19:15661423 - 15714929 on Build GRCh38 Gain CYP4F12
nsv9671 Chr.19:15666486 - 15723022 on Build GRCh38 Gain CYP4F12
esv2760506 Chr.19:15666091 - 15726410 on Build GRCh38 Gain+Loss CYP4F12
esv3643776 Chr.19:15672308 - 15725395 on Build GRCh38 Gain CYP4F12
nsv436858 Chr.19:15670801 - 15720751 on Build GRCh38 Insertion CYP4F12
esv22534 Chr.19:15667246 - 15726197 on Build GRCh38 Gain+Loss CYP4F12
dgv6289n54 Chr.19:15663105 - 15724712 on Build GRCh38 Gain CYP4F12
nsv526168 Chr.19:15669937 - 15748902 on Build GRCh38 Gain OR10H3 CYP4F12 OR10H2
nsv1064684 Chr.19:15311319 - 16062011 on Build GRCh38 Gain RASAL3 AKAP8L CYP4F24P OR10H1 CYP4F8 CYP4F22 CYP4F11 BRD4 LOC102724279 WIZ LINC00905 CYP4F2 CYP4F12 OR10H3 UCA1 OR10H4 LINC00661 AKAP8 CYP4F3 OR10H5 MIR1470 PGLYRP2 OR10H2
dgv137e55 Chr.19:15666599 - 15728649 on Build GRCh38 Gain CYP4F12 OR10H2

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More Information


Additional Information:

For this assay, SNP(s) [rs115854510] 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:

Molecular Function -

oxygenase

Gene Ontology Categories:

Function(s) Process(es)


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