CYP2D7 (cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene)) - Rat Genome Database

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Gene: CYP2D7 (cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene)) Homo sapiens
Analyze
Symbol: CYP2D7
Name: cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene)
RGD ID: 1346997
HGNC Page HGNC:2624
Description: Enables aromatase activity. Involved in xenobiotic catabolic process. Located in mitochondrion.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: CYP2D; CYP2D6; CYP2D7AP; CYP2D7P; CYP2D7P1; CYP2D@; cytochrome P450, family 2, subfamily D, polypeptide 7 pseudogene 1; cytochrome P450, subfamily II (debrisoquine, sparteine, etc., -metabolising), polypeptide 7 pseudogene 1; cytochrome P450, subfamily IID (debrisoquine, sparteine, etc., -metabolizing) cluster; cytochrome P4502D6; nonfunctional cytochrome P450 family 2 subfamily D polypeptide 6; P450C2D; P450DB1; Putative cytochrome P450 2D7; RNA40057
RGD Orthologs
Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
NCBI Annotation Information: Note: Genetic polymorphisms result in both protein coding and non-coding alleles of this gene.
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382242,139,576 - 42,144,483 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2242,140,203 - 42,149,455 (-)EnsemblGRCh38hg38GRCh38
GRCh372242,535,587 - 42,540,484 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362240,866,158 - 40,870,519 (-)NCBINCBI36Build 36hg18NCBI36
Build 342240,860,713 - 40,865,074NCBI
Celera2226,342,407 - 26,346,769 (-)NCBICelera
Cytogenetic Map22q13.2NCBI
HuRef2225,502,024 - 25,506,388 (-)NCBIHuRef
CHM1_12242,495,953 - 42,500,315 (-)NCBICHM1_1
T2T-CHM13v2.02242,619,075 - 42,623,972 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:1358797   PMID:1978251   PMID:2574001   PMID:3123997   PMID:11207030   PMID:12171760   PMID:12477932   PMID:15051713   PMID:15128046   PMID:16166400   PMID:16169517   PMID:16400609  
PMID:17494644   PMID:18838503   PMID:21873635   PMID:22111604   PMID:26297049   PMID:30020016   PMID:30040020   PMID:39060884  


Genomics

Comparative Map Data
CYP2D7
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382242,139,576 - 42,144,483 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2242,140,203 - 42,149,455 (-)EnsemblGRCh38hg38GRCh38
GRCh372242,535,587 - 42,540,484 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362240,866,158 - 40,870,519 (-)NCBINCBI36Build 36hg18NCBI36
Build 342240,860,713 - 40,865,074NCBI
Celera2226,342,407 - 26,346,769 (-)NCBICelera
Cytogenetic Map22q13.2NCBI
HuRef2225,502,024 - 25,506,388 (-)NCBIHuRef
CHM1_12242,495,953 - 42,500,315 (-)NCBICHM1_1
T2T-CHM13v2.02242,619,075 - 42,623,972 (-)NCBIT2T-CHM13v2.0
Cyp2d1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr87115,789,026 - 115,793,430 (-)NCBIGRCr8
mRatBN7.27113,908,950 - 113,913,420 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl7113,908,947 - 113,922,084 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx7115,664,160 - 115,668,558 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.07117,888,290 - 117,892,688 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.07117,857,740 - 117,862,138 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.07123,625,641 - 123,630,045 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl7123,625,590 - 123,638,765 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.07123,610,230 - 123,614,634 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.47120,769,701 - 120,774,105 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.17120,803,930 - 120,808,335 (-)NCBI
Celera7110,224,046 - 110,228,450 (-)NCBICelera
Cytogenetic Map7q34NCBI

Variants

.
Variants in CYP2D7
2 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 22q13.2-13.33(chr22:42138114-50739836)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051370]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051370]|See cases [RCV000051370] Chr22:42138114..50739836 [GRCh38]
Chr22:42513525..51178264 [GRCh37]
Chr22:40843471..49525130 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh38/hg38 22q12.3-13.33(chr22:33768441-50739977)x3 copy number gain See cases [RCV000051682] Chr22:33768441..50739977 [GRCh38]
Chr22:34164428..51178405 [GRCh37]
Chr22:32494428..49525271 [NCBI36]
Chr22:22q12.3-13.33		 pathogenic
GRCh38/hg38 22q12.3-13.33(chr22:37061769-50738932)x3 copy number gain See cases [RCV000051684] Chr22:37061769..50738932 [GRCh38]
Chr22:37457809..51177360 [GRCh37]
Chr22:35787755..49524226 [NCBI36]
Chr22:22q12.3-13.33		 pathogenic
GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3 copy number gain See cases [RCV000133646] Chr22:16916608..50739836 [GRCh38]
Chr22:17397498..51178264 [GRCh37]
Chr22:15777498..49525130 [NCBI36]
Chr22:22q11.1-13.33		 pathogenic
GRCh38/hg38 22q13.1-13.33(chr22:40202014-50735806)x3 copy number gain See cases [RCV000134513] Chr22:40202014..50735806 [GRCh38]
Chr22:40598018..51174234 [GRCh37]
Chr22:38927964..49521100 [NCBI36]
Chr22:22q13.1-13.33		 pathogenic
GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3 copy number gain See cases [RCV000134730] Chr22:16916743..50739785 [GRCh38]
Chr22:17397633..51178213 [GRCh37]
Chr22:15777633..49525079 [NCBI36]
Chr22:22q11.1-13.33		 pathogenic
GRCh38/hg38 22q13.2(chr22:41645339-42565798)x1 copy number loss See cases [RCV000136528] Chr22:41645339..42565798 [GRCh38]
Chr22:42041343..42961804 [GRCh37]
Chr22:40371289..41291748 [NCBI36]
Chr22:22q13.2		 uncertain significance
GRCh38/hg38 22q13.2(chr22:41277822-42414957)x3 copy number gain See cases [RCV000136785] Chr22:41277822..42414957 [GRCh38]
Chr22:41673826..42810963 [GRCh37]
Chr22:40003772..41140907 [NCBI36]
Chr22:22q13.2		 pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:41871143-50739836)x1 copy number loss See cases [RCV000136921] Chr22:41871143..50739836 [GRCh38]
Chr22:42267147..51178264 [GRCh37]
Chr22:40597093..49525130 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
GRCh38/hg38 22q13.2-13.33(chr22:42080077-50739836)x3 copy number gain See cases [RCV000142755] Chr22:42080077..50739836 [GRCh38]
Chr22:42476081..51178264 [GRCh37]
Chr22:40806027..49525130 [NCBI36]
Chr22:22q13.2-13.33		 pathogenic
NM_001348386.3(CYP2D7):c.801A>C (p.Pro267=) single nucleotide variant not provided [RCV003437624] Chr22:42141910 [GRCh38]
Chr22:42537920 [GRCh37]
Chr22:22q13.2		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1644
Count of miRNA genes:732
Interacting mature miRNAs:868
Transcripts:ENST00000358097, ENST00000424775, ENST00000433992, ENST00000435101, ENST00000435688
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407252997GWAS901973_Hlow density lipoprotein cholesterol measurement QTL GWAS901973 (human)9e-16low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)224214251342142515Human
406989668GWAS638644_Hresponse to tamoxifen QTL GWAS638644 (human)3e-65response to tamoxifen224214250842142509Human
406989738GWAS638714_Hresponse to tamoxifen QTL GWAS638714 (human)4e-21response to tamoxifen224214250842142509Human
406890121GWAS539097_Htotal cholesterol measurement QTL GWAS539097 (human)2e-12total cholesterol measurementblood total cholesterol level (CMO:0000051)224214266942142670Human
406890955GWAS539931_Hnon-high density lipoprotein cholesterol measurement QTL GWAS539931 (human)1e-09non-high density lipoprotein cholesterol measurementblood non-high density lipoprotein cholesterol level (CMO:0003967)224214266942142670Human
407178312GWAS827288_Hschizophrenia, intelligence, self reported educational attainment QTL GWAS827288 (human)2e-15schizophrenia, intelligence, self reported educational attainment224214158742141588Human
407250856GWAS899832_Hnon-high density lipoprotein cholesterol measurement QTL GWAS899832 (human)2e-10non-high density lipoprotein cholesterol measurementblood non-high density lipoprotein cholesterol level (CMO:0003967)224214251342142515Human
407028338GWAS677314_Htestosterone measurement QTL GWAS677314 (human)2e-09testosterone measurementserum testosterone level (CMO:0000568)224214250842142509Human
406887249GWAS536225_Hautism spectrum disorder, schizophrenia QTL GWAS536225 (human)4e-09autism spectrum disorder, schizophrenia224214111742141118Human
406989744GWAS638720_Hresponse to tamoxifen QTL GWAS638720 (human)7e-11response to tamoxifen224214261742142618Human
406887126GWAS536102_Hintelligence QTL GWAS536102 (human)3e-10intelligence224214238942142390Human
406989589GWAS638565_Hresponse to tamoxifen QTL GWAS638565 (human)5e-35response to tamoxifen224214250842142509Human
406990490GWAS639466_Hintelligence QTL GWAS639466 (human)4e-10intelligence224214238942142390Human
407092792GWAS741768_Hexecutive function measurement QTL GWAS741768 (human)9e-09executive function measurement224214209342142094Human
406989593GWAS638569_Hresponse to tamoxifen QTL GWAS638569 (human)4e-09response to tamoxifen224214250742142508Human
406891003GWAS539979_Hlow density lipoprotein cholesterol measurement QTL GWAS539979 (human)1e-13low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)224214266942142670Human

Markers in Region
RH27796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372242,538,391 - 42,538,826UniSTSGRCh37
GRCh372242,524,688 - 42,525,132UniSTSGRCh37
Build 362240,854,632 - 40,855,076RGDNCBI36
Celera2226,330,881 - 26,331,325RGD
Celera2226,344,585 - 26,345,020UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map22q13UniSTS
HuRef2225,504,195 - 25,504,639UniSTS
HuRef2225,490,706 - 25,491,150UniSTS
STS-M33189  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372242,535,869 - 42,536,046UniSTSGRCh37
GRCh372242,522,154 - 42,522,331UniSTSGRCh37
Build 362240,852,098 - 40,852,275RGDNCBI36
Celera2226,342,062 - 26,342,239UniSTS
Celera2226,328,347 - 26,328,524RGD
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map22q13UniSTS
HuRef2225,488,172 - 25,488,349UniSTS
HuRef2225,501,679 - 25,501,856UniSTS
GeneMap99-GB4 RH Map22137.62UniSTS
NCBI RH Map22209.1UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
1204 2432 2788 2243 4939 1723 2340 4 622 1926 464 2265 7255 6429 52 3708 846 1730 1607 170

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001348386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_002570 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_145674 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC213220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC235563 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC254560 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC254562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC254847 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC254995 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC255093 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC256292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308043 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL021878 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY220845 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC108679 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX247885 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068256 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ211354 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ211355 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ915485 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ915486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ915487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ915489 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU093102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU098009 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GQ162806 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GQ162808 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM641840 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HQ670229 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JF307779 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JN618990 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX678711 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M33387 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X07619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X07620 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X16866 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X58467 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X58468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000358097   ⟹   ENSP00000445124
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2242,140,203 - 42,144,549 (-)Ensembl
Ensembl Acc Id: ENST00000424775
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2242,142,737 - 42,143,999 (-)Ensembl
Ensembl Acc Id: ENST00000433992   ⟹   ENSP00000439604
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2242,140,203 - 42,144,577 (-)Ensembl
Ensembl Acc Id: ENST00000435101   ⟹   ENSP00000437680
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2242,140,203 - 42,141,924 (-)Ensembl
Ensembl Acc Id: ENST00000435688
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2242,143,284 - 42,144,549 (-)Ensembl
Ensembl Acc Id: ENST00000610593
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2242,141,242 - 42,144,549 (-)Ensembl
Ensembl Acc Id: ENST00000612115   ⟹   ENSP00000484065
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2242,140,205 - 42,144,577 (-)Ensembl
Ensembl Acc Id: ENST00000614967   ⟹   ENSP00000481168
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2242,140,205 - 42,144,554 (-)Ensembl
Ensembl Acc Id: ENST00000651010
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2242,140,217 - 42,149,455 (-)Ensembl
Ensembl Acc Id: ENST00000711577
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2242,145,452 - 42,149,500 (-)Ensembl
RefSeq Acc Id: NR_002570
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382242,139,576 - 42,144,483 (-)NCBI
GRCh372242,536,214 - 42,540,575 (-)RGD
Build 362240,866,158 - 40,870,519 (-)NCBI Archive
Celera2226,342,407 - 26,346,769 (-)RGD
HuRef2225,502,024 - 25,506,388 (-)RGD
CHM1_12242,495,953 - 42,500,316 (-)NCBI
T2T-CHM13v2.02242,619,075 - 42,623,972 (-)NCBI
Sequence:
RefSeq Acc Id: NR_145674
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382242,139,576 - 42,144,483 (-)NCBI
T2T-CHM13v2.02242,619,075 - 42,623,972 (-)NCBI
Sequence:
Ensembl Acc Id: ENSP00000484065   ⟸   ENST00000612115
Ensembl Acc Id: ENSP00000481168   ⟸   ENST00000614967
Ensembl Acc Id: ENSP00000439604   ⟸   ENST00000433992
Ensembl Acc Id: ENSP00000437680   ⟸   ENST00000435101
Ensembl Acc Id: ENSP00000445124   ⟸   ENST00000358097

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-A0A087X1C5-F1-model_v2 AlphaFold A0A087X1C5 1-515 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:2624 AgrOrtholog
COSMIC CYP2D7 COSMIC
Ensembl Genes ENSG00000205702 Ensembl
  ENSG00000278088 UniProtKB/TrEMBL
Ensembl Transcript ENST00000618719.2 UniProtKB/TrEMBL
Gene3D-CATH 1.10.630.10 UniProtKB/Swiss-Prot
GTEx ENSG00000205702 GTEx
  ENSG00000278088 GTEx
HGNC ID HGNC:2624 ENTREZGENE
Human Proteome Map CYP2D7 Human Proteome Map
InterPro Cyt_P450 UniProtKB/Swiss-Prot
  Cyt_P450_CS UniProtKB/Swiss-Prot
  Cyt_P450_E_grp-I UniProtKB/Swiss-Prot
  Cyt_P450_E_grp-I_CYP2D-like UniProtKB/Swiss-Prot
  Cyt_P450_sf UniProtKB/Swiss-Prot
  Cytochrome_P450_fam2 UniProtKB/Swiss-Prot
KEGG Report hsa:1564 UniProtKB/Swiss-Prot
NCBI Gene 1564 ENTREZGENE
PANTHER CYTOCHROME P450 2D6-RELATED UniProtKB/Swiss-Prot
  CYTOCHROME P450 508A4-RELATED UniProtKB/Swiss-Prot
Pfam p450 UniProtKB/Swiss-Prot
PharmGKB PA134926902 PharmGKB
PRINTS EP450I UniProtKB/Swiss-Prot
  EP450ICYP2D UniProtKB/Swiss-Prot
  P450 UniProtKB/Swiss-Prot
PROSITE CYTOCHROME_P450 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF48264 UniProtKB/Swiss-Prot
UniProt A0A087X1C5 ENTREZGENE, UniProtKB/Swiss-Prot
  F5H6E7_HUMAN UniProtKB/TrEMBL
  Q6XP50 ENTREZGENE
UniProt Secondary Q6XP50 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-15 CYP2D7  cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene)  CYP2D7  cytochrome P450, family 2, subfamily D, polypeptide 7 (gene/pseudogene)  Symbol and/or name change 5135510 APPROVED
2014-12-30 CYP2D7  cytochrome P450, family 2, subfamily D, polypeptide 7 (gene/pseudogene)  CYP2D7  cytochrome P450, family 2, subfamily D, polypeptide 7  Symbol and/or name change 5135510 APPROVED
2014-10-22 CYP2D7  cytochrome P450, family 2, subfamily D, polypeptide 7  CYP2D7P  cytochrome P450, family 2, subfamily D, polypeptide 7, pseudogene  Symbol and/or name change 5135510 APPROVED
2013-11-19 CYP2D7P  cytochrome P450, family 2, subfamily D, polypeptide 7, pseudogene  CYP2D7P1  cytochrome P450, family 2, subfamily D, polypeptide 7 pseudogene 1  Symbol and/or name change 5135510 APPROVED