Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 1543 |
Gene Name: | cytochrome P450 family 1 subfamily A member 1 |
Gene Aliases: |
AHH, AHRR, CP11, CYP1, CYPIA1, P1-450, P450-C, P450DX |
Location: |
Chr.15:74719542-74725610 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 3 - Exon 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CYP1A1 | NM_000499.4 | NP_000490.1 | ||
| NM_001319216.1 | NP_001306145.1 | |||
| NM_001319217.1 | NP_001306146.1 | |||
| XM_017021953.1 | XP_016877442.1 | |||
| AK223108.1 | BAD96828.1 | |||
| AK223113.1 | BAD96833.1 | |||
| AK310810.1 | ||||
| AK313880.1 | ||||
| AM233517.1 | ||||
| AM233518.1 | ||||
| AM233519.1 | ||||
| AM233520.1 | ||||
| AM236046.1 | ||||
| AM236047.1 | ||||
| AY310359.1 | AAQ76692.1 | |||
| AY871801.1 | ||||
| BC023019.1 | AAH23019.1 | |||
| K03191.1 | AAA52139.1 | |||
| M12079.1 | AAA52152.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833055 | Chr.15:74696003 - 74873947 on Build GRCh38 | Loss |
 CYP1A2
EDC3
LMAN1L
SCAMP2
CYP1A1
MIR6882
ULK3
CSK
MIR4513
CPLX3
|
| esv3636907 | Chr.15:74721538 - 74745196 on Build GRCh38 | Loss |
CYP1A1
|
| nsv817698 | Chr.15:74596822 - 74727108 on Build GRCh38 | Gain |
EDC3
CLK3
ARID3B
CYP1A1
LOC102723750
|
| nsv1121512 | Chr.15:72670085 - 75273877 on Build GRCh38 | Deletion |
TBC1D21
HIGD2B
LOC101929333
LMAN1L
UBL7
FAM219B
CYP11A1
LOC107984728
PPCDC
SCAMP5
SCAMP2
REC114
RPP25
ISLR
EDC3
ARID3B
CCDC33
NPTN-IT1
LOXL1-AS1
CSK
COX5A
C15orf39
HCN4
MIR6881
LOC729739
GOLGA6A
MIR4513
LOC105376731
BBS4
LOC732265
CD276
MIR6882
LOC102723750
UBL7-AS1
MPI
LOC283731
PML
ADPGK
CYP1A1
NPTN
STOML1
SEMA7A
CYP1A2
C15orf59-AS1
CLK3
C15orf59
ADPGK-AS1
NEO1
CPLX3
STRA6
GOLGA6C
LOXL1
ULK3
ISLR2
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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