Genomic Map
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Target Gene Details
Entrez Gene ID: | 388514 |
Gene Name: | cytochrome P450 family 4 subfamily F member 24, pseudogene |
Gene Aliases: |
- |
Location: |
Chr.19:15759334-15779988 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CYP4F24P | NR_033864.1 | |||
| AK297837.1 | ||||
| AK308750.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1060711 | Chr.19:15745103 - 15817596 on Build GRCh38 | Gain |
 OR10H5
CYP4F24P
OR10H1
|
| esv2671181 | Chr.19:15768634 - 15926128 on Build GRCh38 | Deletion |
CYP4F11
OR10H5
CYP4F24P
LOC102724279
OR10H1
UCA1
CYP4F2
|
| nsv2425 | Chr.19:15764425 - 15794652 on Build GRCh38 | Insertion |
OR10H5
CYP4F24P
|
| esv3334671 | Chr.19:15673766 - 15931354 on Build GRCh38 | Duplication |
CYP4F12
CYP4F11
OR10H5
CYP4F24P
OR10H3
LOC102724279
OR10H1
OR10H2
UCA1
CYP4F2
|
| nsv833766 | Chr.19:15759095 - 15956904 on Build GRCh38 | Loss |
CYP4F11
OR10H4
OR10H5
CYP4F24P
LOC102724279
OR10H1
UCA1
CYP4F2
|
| nsv1064684 | Chr.19:15311319 - 16062011 on Build GRCh38 | Gain |
AKAP8L
PGLYRP2
CYP4F12
CYP4F11
OR10H4
CYP4F22
CYP4F8
CYP4F24P
OR10H3
LINC00905
AKAP8
LOC102724279
OR10H2
WIZ
BRD4
CYP4F3
MIR1470
OR10H5
LINC00661
OR10H1
UCA1
RASAL3
CYP4F2
|
| esv2718244 | Chr.19:15743561 - 15951200 on Build GRCh38 | Deletion |
CYP4F11
OR10H4
OR10H5
CYP4F24P
LOC102724279
OR10H1
UCA1
CYP4F2
|
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Additional Information:
For this assay, SNP(s) [rs78464136] 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
|
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