Genomic Map
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Target Gene Details
Entrez Gene ID: | 57834 |
Gene Name: | cytochrome P450 family 4 subfamily F member 11 |
Gene Aliases: |
CYPIVF11 |
Location: |
Chr.19:15912370-15934866 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 5 - Exon 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CYP4F11 | NM_001128932.1 | NP_001122404.1 | ||
| NM_021187.3 | NP_067010.3 | |||
| AF236085.1 | AAG15889.1 | |||
| AK125714.1 | ||||
| AK289424.1 | ||||
| AL833940.1 | CAD38795.2 | |||
| BC016853.1 | AAH16853.1 | |||
| BM727421.1 | ||||
| BU180723.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2671181 | Chr.19:15768634 - 15926128 on Build GRCh38 | Deletion |
 LOC102724279
CYP4F24P
OR10H1
OR10H5
CYP4F2
UCA1
CYP4F11
|
| esv3334671 | Chr.19:15673766 - 15931354 on Build GRCh38 | Duplication |
LOC102724279
CYP4F24P
OR10H1
OR10H5
OR10H2
CYP4F2
OR10H3
UCA1
CYP4F12
CYP4F11
|
| nsv960801 | Chr.19:15922084 - 15924858 on Build GRCh38 | Duplication |
CYP4F11
|
| nsv833766 | Chr.19:15759095 - 15956904 on Build GRCh38 | Loss |
LOC102724279
CYP4F24P
OR10H1
OR10H4
OR10H5
CYP4F2
UCA1
CYP4F11
|
| nsv1064684 | Chr.19:15311319 - 16062011 on Build GRCh38 | Gain |
OR10H4
OR10H2
MIR1470
CYP4F2
OR10H3
CYP4F8
RASAL3
LINC00661
CYP4F22
PGLYRP2
CYP4F11
LOC102724279
CYP4F24P
OR10H1
OR10H5
AKAP8L
CYP4F3
AKAP8
UCA1
CYP4F12
WIZ
LINC00905
BRD4
|
| esv2718244 | Chr.19:15743561 - 15951200 on Build GRCh38 | Deletion |
LOC102724279
CYP4F24P
OR10H1
OR10H4
OR10H5
CYP4F2
UCA1
CYP4F11
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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