CYP2F1 (cytochrome P450 family 2 subfamily F member 1) - Rat Genome Database

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Gene: CYP2F1 (cytochrome P450 family 2 subfamily F member 1) Homo sapiens
Analyze
Symbol: CYP2F1
Name: cytochrome P450 family 2 subfamily F member 1
RGD ID: 1351527
HGNC Page HGNC:2632
Description: Enables oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen. Involved in naphthalene catabolic process. Located in intracellular membrane-bounded organelle.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: C2F1; CYP2F; CYPIIF1; cytochrome P450 2F1; cytochrome P450, family 2, subfamily F, polypeptide 1; cytochrome P450, subfamily IIF, polypeptide 1; flavoprotein-linked monooxygenase; MGC126121; microsomal monooxygenase; xenobiotic monooxygenase
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Pig
Green Monkey
Alliance Orthologs
More Info more info ...
Related Pseudogenes: CYP2F2P   CYP2T1P   CYP2T3P  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381941,114,432 - 41,128,381 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1941,114,432 - 41,128,381 (+)EnsemblGRCh38hg38GRCh38
GRCh371941,620,337 - 41,634,286 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361946,312,193 - 46,326,121 (+)NCBINCBI36Build 36hg18NCBI36
Build 341946,312,192 - 46,326,121NCBI
Celera1938,420,521 - 38,434,443 (+)NCBICelera
Cytogenetic Map19q13.2NCBI
HuRef1938,052,253 - 38,066,192 (+)NCBIHuRef
CHM1_11941,620,070 - 41,634,000 (+)NCBICHM1_1
T2T-CHM13v2.01943,935,308 - 43,949,263 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
(S)-amphetamine  (ISO)
1,1-dichloroethene  (ISO)
1,2-dimethylhydrazine  (ISO)
1-aminobenzotriazole  (EXP)
1-naphthyl isothiocyanate  (ISO)
1-nitronaphthalene  (ISO)
1-Phenyl-1,2-ethanediol  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP,ISO)
1H-pyrazole  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4-dibromophenyl 2,4,5-tribromophenyl ether  (ISO)
2-palmitoylglycerol  (EXP)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
3-methyleneindolenine  (EXP)
4,4'-sulfonyldiphenol  (ISO)
4-(ethoxymethylene)-2-phenyloxazol-5-one  (ISO)
4-hydroxystyrene  (ISO)
5-fluorouracil  (EXP)
5-methoxy-2-\{[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl\}-1H-benzimidazole  (ISO)
6-propyl-2-thiouracil  (ISO)
8-Br-cAMP  (EXP)
acetamide  (ISO)
acrylamide  (ISO)
actinomycin D  (EXP)
aflatoxin B1  (ISO)
all-trans-retinoic acid  (ISO)
alpha-naphthoflavone  (EXP)
amiodarone  (ISO)
ammonium chloride  (ISO)
atrazine  (ISO)
benzbromarone  (ISO)
benzene  (EXP,ISO)
benzo[a]pyrene  (EXP,ISO)
bis(2-ethylhexyl) phthalate  (EXP,ISO)
bisphenol A  (ISO)
bisphenol F  (ISO)
Butylbenzyl phthalate  (ISO)
cadmium dichloride  (ISO)
carbon nanotube  (ISO)
clofibrate  (ISO)
crocidolite asbestos  (ISO)
cycloheximide  (EXP)
cylindrospermopsin  (EXP)
dexamethasone  (ISO)
dibenzofuran  (ISO)
dibutyl phthalate  (ISO)
dicyclanil  (ISO)
diethyl phthalate  (ISO)
diethylstilbestrol  (ISO)
diiodine  (ISO)
diisobutyl phthalate  (ISO)
diisononyl phthalate  (ISO)
diquat  (ISO)
doxorubicin  (ISO)
endosulfan  (ISO)
epoxiconazole  (ISO)
fenofibrate  (ISO)
finasteride  (ISO)
fluensulfone  (ISO)
flurbiprofen  (ISO)
flutamide  (ISO)
gefitinib  (EXP)
indometacin  (ISO)
inulin  (ISO)
kojic acid  (ISO)
L-ethionine  (ISO)
lycopene  (ISO)
methapyrilene  (ISO)
mono(2-ethylhexyl) phthalate  (ISO)
N-nitrosodiethylamine  (ISO)
naphthalene  (EXP,ISO)
naphthalene 1,2-oxide  (ISO)
nickel atom  (ISO)
nickel sulfate  (ISO)
nonanoic acid  (ISO)
ochratoxin A  (ISO)
oleanolic acid  (ISO)
omeprazole  (ISO)
ozone  (ISO)
paracetamol  (ISO)
paraquat  (ISO)
parathion  (EXP)
pentane-2,3-dione  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (ISO)
phenobarbital  (EXP,ISO)
phenol  (ISO)
phorbol 13-acetate 12-myristate  (ISO)
pirinixic acid  (ISO)
pregnenolone 16alpha-carbonitrile  (ISO)
rifampicin  (EXP)
rotenone  (ISO)
serpentine asbestos  (EXP)
sevoflurane  (ISO)
silver atom  (ISO)
silver(0)  (ISO)
skatole  (EXP)
sodium arsenate  (ISO)
sodium arsenite  (ISO)
styrene  (ISO)
styrene oxide  (ISO)
tamoxifen  (ISO)
tauroursodeoxycholic acid  (ISO)
tetrachloromethane  (ISO)
thioacetamide  (ISO)
titanium dioxide  (ISO)
toluene  (EXP)
toluene 2,4-diisocyanate  (ISO)
tremolite asbestos  (ISO)
trichloroethene  (ISO)
triphenyl phosphate  (ISO)
triptonide  (ISO)
vinclozolin  (ISO)
zinc atom  (EXP)
zinc(0)  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:1974816   PMID:2045106   PMID:8432525   PMID:8587134   PMID:8619884   PMID:8889548   PMID:9539103   PMID:10383923   PMID:11827709   PMID:12477932   PMID:12598524   PMID:15128046  
PMID:16883522   PMID:17327131   PMID:17943660   PMID:19343046   PMID:20198857   PMID:21873635   PMID:22232929   PMID:22397853   PMID:29171455  


Genomics

Comparative Map Data
CYP2F1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381941,114,432 - 41,128,381 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1941,114,432 - 41,128,381 (+)EnsemblGRCh38hg38GRCh38
GRCh371941,620,337 - 41,634,286 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361946,312,193 - 46,326,121 (+)NCBINCBI36Build 36hg18NCBI36
Build 341946,312,192 - 46,326,121NCBI
Celera1938,420,521 - 38,434,443 (+)NCBICelera
Cytogenetic Map19q13.2NCBI
HuRef1938,052,253 - 38,066,192 (+)NCBIHuRef
CHM1_11941,620,070 - 41,634,000 (+)NCBICHM1_1
T2T-CHM13v2.01943,935,308 - 43,949,263 (+)NCBIT2T-CHM13v2.0
Cyp2f2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39726,819,380 - 26,833,085 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl726,819,334 - 26,833,085 (+)EnsemblGRCm39 Ensembl
GRCm38727,119,955 - 27,133,660 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl727,119,909 - 27,133,660 (+)EnsemblGRCm38mm10GRCm38
MGSCv37727,904,974 - 27,918,679 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36726,828,735 - 26,842,420 (+)NCBIMGSCv36mm8
Celera721,696,833 - 21,710,532 (+)NCBICelera
Cytogenetic Map7A3NCBI
cM Map715.82NCBI
Cyp2f4
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8191,543,768 - 91,557,553 (+)NCBIGRCr8
mRatBN7.2182,416,107 - 82,429,897 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl182,416,130 - 82,429,896 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx187,819,674 - 87,833,401 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0196,305,887 - 96,319,672 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0189,575,540 - 89,589,267 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0183,933,974 - 83,947,804 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl183,933,942 - 83,947,821 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0185,144,699 - 85,158,525 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4182,191,741 - 82,204,629 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1182,269,851 - 82,282,739 (+)NCBI
Celera176,831,247 - 76,843,408 (+)NCBICelera
RH 3.4 Map1841.6RGD
Cytogenetic Map1q21NCBI
LOC102004212
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955578531,353 - 541,684 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955578530,094 - 541,951 (+)NCBIChiLan1.0ChiLan1.0
CYP2F1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22047,333,165 - 47,355,081 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11949,201,512 - 49,223,265 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01938,124,921 - 38,137,574 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11946,632,134 - 46,644,048 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1946,632,134 - 46,643,748 (+)Ensemblpanpan1.1panPan2
CYP2F1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11112,973,776 - 112,986,419 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1112,974,847 - 112,986,123 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1112,376,173 - 112,388,674 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01113,572,083 - 113,584,693 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1113,573,209 - 113,584,285 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11113,131,608 - 113,144,122 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01112,763,587 - 112,776,096 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01113,757,678 - 113,770,190 (+)NCBIUU_Cfam_GSD_1.0
CYP2F1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl649,017,008 - 49,029,388 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1649,014,912 - 49,032,207 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2644,701,834 - 44,707,747 (-)NCBISscrofa10.2Sscrofa10.2susScr3
LOC103235509
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1635,270,229 - 35,286,326 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366607313,409,873 - 13,430,845 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in CYP2F1
51 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19q13.12-13.2(chr19:37319377-42738688)x3 copy number gain See cases [RCV000050636] Chr19:37319377..42738688 [GRCh38]
Chr19:37810279..43242840 [GRCh37]
Chr19:42502119..47934680 [NCBI36]
Chr19:19q13.12-13.2		 pathogenic
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3 copy number gain See cases [RCV000133888] Chr19:11227942..44626354 [GRCh38]
Chr19:11338618..45129651 [GRCh37]
Chr19:11199618..49821491 [NCBI36]
Chr19:19p13.2-q13.31		 pathogenic
GRCh37/hg19 19q13.12-13.2(chr19:37582250-41630908)x3 copy number gain See cases [RCV000239839] Chr19:37582250..41630908 [GRCh37]
Chr19:19q13.12-13.2		 pathogenic
NM_000774.5(CYP2F1):c.15dup (p.Thr6fs) duplication not specified [RCV000454539] Chr19:41116202..41116203 [GRCh38]
Chr19:41622107..41622108 [GRCh37]
Chr19:19q13.2		 benign
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
NM_000774.5(CYP2F1):c.163C>T (p.Leu55Phe) single nucleotide variant not specified [RCV004282357] Chr19:41116351 [GRCh38]
Chr19:41622256 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.784C>T (p.Arg262Trp) single nucleotide variant not specified [RCV004304103] Chr19:41122095 [GRCh38]
Chr19:41628000 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.181G>A (p.Glu61Lys) single nucleotide variant not specified [RCV004298151] Chr19:41116464 [GRCh38]
Chr19:41622369 [GRCh37]
Chr19:19q13.2		 likely benign
NM_000774.5(CYP2F1):c.798G>C (p.Gln266His) single nucleotide variant not provided [RCV000947950] Chr19:41122109 [GRCh38]
Chr19:41628014 [GRCh37]
Chr19:19q13.2		 benign
NM_000774.5(CYP2F1):c.1172T>C (p.Leu391Pro) single nucleotide variant not provided [RCV000947951] Chr19:41125512 [GRCh38]
Chr19:41631417 [GRCh37]
Chr19:19q13.2		 benign
NM_000774.5(CYP2F1):c.335-8C>G single nucleotide variant not provided [RCV000950847] Chr19:41120339 [GRCh38]
Chr19:41626244 [GRCh37]
Chr19:19q13.2		 benign
NM_000774.5(CYP2F1):c.293G>C (p.Arg98Pro) single nucleotide variant not provided [RCV000968967] Chr19:41116576 [GRCh38]
Chr19:41622481 [GRCh37]
Chr19:19q13.2		 benign
NM_000774.5(CYP2F1):c.1110C>T (p.Arg370=) single nucleotide variant not provided [RCV000967518] Chr19:41124864 [GRCh38]
Chr19:41630769 [GRCh37]
Chr19:19q13.2		 benign
GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3 copy number gain not provided [RCV000845733] Chr19:28271106..49213832 [GRCh37]
Chr19:19q11-13.33		 pathogenic
NM_000774.5(CYP2F1):c.1132C>T (p.Arg378Cys) single nucleotide variant not specified [RCV004321777] Chr19:41124886 [GRCh38]
Chr19:41630791 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.640G>A (p.Gly214Ser) single nucleotide variant not specified [RCV004283906] Chr19:41121613 [GRCh38]
Chr19:41627518 [GRCh37]
Chr19:19q13.2		 uncertain significance
NC_000019.9:g.(?_39904727)_(42931301_?)dup duplication Diamond-Blackfan anemia [RCV003122291]|MEGF8-related Carpenter syndrome [RCV003105286]|Maple syrup urine disease [RCV003105287]|TWIST1-related craniosynostosis [RCV003105285] Chr19:39904727..42931301 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.523G>C (p.Val175Leu) single nucleotide variant not provided [RCV000950848] Chr19:41121496 [GRCh38]
Chr19:41627401 [GRCh37]
Chr19:19q13.2		 benign
NM_000774.5(CYP2F1):c.524T>G (p.Val175Gly) single nucleotide variant not provided [RCV000950849] Chr19:41121497 [GRCh38]
Chr19:41627402 [GRCh37]
Chr19:19q13.2		 benign
GRCh37/hg19 19q13.2(chr19:41304025-41928997)x3 copy number gain not provided [RCV001007048] Chr19:41304025..41928997 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1198A>T (p.Ser400Cys) single nucleotide variant not specified [RCV004608507] Chr19:41125538 [GRCh38]
Chr19:41631443 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.304C>T (p.Pro102Ser) single nucleotide variant not specified [RCV004608508] Chr19:41116587 [GRCh38]
Chr19:41622492 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.22A>G (p.Ile8Val) single nucleotide variant not specified [RCV004608509] Chr19:41116210 [GRCh38]
Chr19:41622115 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1051G>A (p.Ala351Thr) single nucleotide variant not specified [RCV004608504] Chr19:41124805 [GRCh38]
Chr19:41630710 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1405G>A (p.Asp469Asn) single nucleotide variant not specified [RCV004608506] Chr19:41128011 [GRCh38]
Chr19:41633916 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1405G>C (p.Asp469His) single nucleotide variant not specified [RCV004608510] Chr19:41128011 [GRCh38]
Chr19:41633916 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.503C>A (p.Thr168Lys) single nucleotide variant not specified [RCV004302879] Chr19:41121476 [GRCh38]
Chr19:41627381 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.650A>G (p.Tyr217Cys) single nucleotide variant not specified [RCV004121965] Chr19:41121961 [GRCh38]
Chr19:41627866 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1319C>T (p.Ser440Leu) single nucleotide variant not specified [RCV004210026] Chr19:41127925 [GRCh38]
Chr19:41633830 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1382C>T (p.Pro461Leu) single nucleotide variant not specified [RCV004086963] Chr19:41127988 [GRCh38]
Chr19:41633893 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.46G>A (p.Val16Ile) single nucleotide variant not specified [RCV004235778] Chr19:41116234 [GRCh38]
Chr19:41622139 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1243G>A (p.Asp415Asn) single nucleotide variant not specified [RCV004208713] Chr19:41125583 [GRCh38]
Chr19:41631488 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.14G>A (p.Ser5Asn) single nucleotide variant not specified [RCV004098265] Chr19:41116202 [GRCh38]
Chr19:41622107 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1279A>G (p.Met427Val) single nucleotide variant not specified [RCV004172886] Chr19:41125619 [GRCh38]
Chr19:41631524 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.359G>A (p.Arg120Gln) single nucleotide variant not specified [RCV004074346] Chr19:41120371 [GRCh38]
Chr19:41626276 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1211C>T (p.Thr404Met) single nucleotide variant not specified [RCV004242422] Chr19:41125551 [GRCh38]
Chr19:41631456 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1354G>A (p.Ala452Thr) single nucleotide variant not specified [RCV004199673] Chr19:41127960 [GRCh38]
Chr19:41633865 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1472G>A (p.Arg491His) single nucleotide variant not specified [RCV004225844] Chr19:41128078 [GRCh38]
Chr19:41633983 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.238G>A (p.Gly80Arg) single nucleotide variant not specified [RCV004250097] Chr19:41116521 [GRCh38]
Chr19:41622426 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1066G>A (p.Val356Met) single nucleotide variant not specified [RCV004276513] Chr19:41124820 [GRCh38]
Chr19:41630725 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1192G>A (p.Asp398Asn) single nucleotide variant not specified [RCV004252753] Chr19:41125532 [GRCh38]
Chr19:41631437 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1214C>T (p.Pro405Leu) single nucleotide variant not specified [RCV004297584] Chr19:41125554 [GRCh38]
Chr19:41631459 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.409A>T (p.Met137Leu) single nucleotide variant not specified [RCV004354116] Chr19:41120421 [GRCh38]
Chr19:41626326 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1316A>G (p.Glu439Gly) single nucleotide variant not specified [RCV004339651] Chr19:41127922 [GRCh38]
Chr19:41633827 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1052C>T (p.Ala351Val) single nucleotide variant not specified [RCV004367939] Chr19:41124806 [GRCh38]
Chr19:41630711 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1297C>T (p.Arg433Cys) single nucleotide variant not specified [RCV004367941] Chr19:41127903 [GRCh38]
Chr19:41633808 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1327C>T (p.Arg443Cys) single nucleotide variant not specified [RCV004367942] Chr19:41127933 [GRCh38]
Chr19:41633838 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.148G>C (p.Asp50His) single nucleotide variant not specified [RCV004367947] Chr19:41116336 [GRCh38]
Chr19:41622241 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.586C>T (p.Leu196Phe) single nucleotide variant not specified [RCV004367951] Chr19:41121559 [GRCh38]
Chr19:41627464 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.871A>G (p.Thr291Ala) single nucleotide variant not specified [RCV004367953] Chr19:41122870 [GRCh38]
Chr19:41628775 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.974A>T (p.Gln325Leu) single nucleotide variant not specified [RCV004367954] Chr19:41124728 [GRCh38]
Chr19:41630633 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1015G>A (p.Ala339Thr) single nucleotide variant not specified [RCV004367938] Chr19:41124769 [GRCh38]
Chr19:41630674 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1445G>A (p.Arg482Gln) single nucleotide variant not specified [RCV004367946] Chr19:41128051 [GRCh38]
Chr19:41633956 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.790T>C (p.Phe264Leu) single nucleotide variant not specified [RCV004367952] Chr19:41122101 [GRCh38]
Chr19:41628006 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.13A>T (p.Ser5Cys) single nucleotide variant not specified [RCV004367943] Chr19:41116201 [GRCh38]
Chr19:41622106 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.386T>A (p.Ile129Asn) single nucleotide variant not specified [RCV004367949] Chr19:41120398 [GRCh38]
Chr19:41626303 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.382T>G (p.Ser128Ala) single nucleotide variant not specified [RCV004367948] Chr19:41120394 [GRCh38]
Chr19:41626299 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.434G>A (p.Arg145Gln) single nucleotide variant not specified [RCV004367950] Chr19:41120446 [GRCh38]
Chr19:41626351 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1152+4C>A single nucleotide variant EBV-positive nodal T- and NK-cell lymphoma [RCV004560219] Chr19:41124910 [GRCh38]
Chr19:41630815 [GRCh37]
Chr19:19q13.2		 likely benign
NM_000774.5(CYP2F1):c.7A>G (p.Ser3Gly) single nucleotide variant not specified [RCV004913295] Chr19:41116195 [GRCh38]
Chr19:41622100 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.425T>C (p.Ile142Thr) single nucleotide variant not specified [RCV004913301] Chr19:41120437 [GRCh38]
Chr19:41626342 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1252C>G (p.Gln418Glu) single nucleotide variant not specified [RCV004913297] Chr19:41125592 [GRCh38]
Chr19:41631497 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.1321C>A (p.Leu441Met) single nucleotide variant not specified [RCV004913296] Chr19:41127927 [GRCh38]
Chr19:41633832 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.473G>A (p.Arg158Gln) single nucleotide variant not specified [RCV004913294] Chr19:41120485 [GRCh38]
Chr19:41626390 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.787G>A (p.Asp263Asn) single nucleotide variant not specified [RCV004913293] Chr19:41122098 [GRCh38]
Chr19:41628003 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.609T>G (p.Asn203Lys) single nucleotide variant not specified [RCV004913300] Chr19:41121582 [GRCh38]
Chr19:41627487 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.41C>T (p.Ala14Val) single nucleotide variant not specified [RCV004913298] Chr19:41116229 [GRCh38]
Chr19:41622134 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.619C>A (p.Gln207Lys) single nucleotide variant not specified [RCV004913299] Chr19:41121592 [GRCh38]
Chr19:41627497 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_000774.5(CYP2F1):c.377A>G (p.Gln126Arg) single nucleotide variant not specified [RCV004913292] Chr19:41120389 [GRCh38]
Chr19:41626294 [GRCh37]
Chr19:19q13.2		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1754
Count of miRNA genes:702
Interacting mature miRNAs:792
Transcripts:ENST00000331105, ENST00000439903, ENST00000526093, ENST00000531409, ENST00000532164, ENST00000534009
Prediction methods:Microtar, 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
1559110SCL22_HSerum cholesterol level QTL 22 (human)3.590.000241Lipid levelLDL cholesterol193190759457907594Human
1331657COPD9_HChronic obstructive pulmonary disease QTL 9 (human)1.94Chronic airflow obstructionpost-bronchodilator FEV1193102176057021760Human

Markers in Region
SHGC-132734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371941,632,904 - 41,633,216UniSTSGRCh37
GRCh371941,325,395 - 41,325,707UniSTSGRCh37
Build 361946,017,235 - 46,017,547RGDNCBI36
Celera1938,433,066 - 38,433,378UniSTS
Celera1938,125,804 - 38,126,116RGD
Cytogenetic Map19q13.2UniSTS
HuRef1937,758,653 - 37,758,965UniSTS
HuRef1938,064,815 - 38,065,127UniSTS
TNG Radiation Hybrid Map1915458.0UniSTS
D19S986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371941,634,031 - 41,634,243UniSTSGRCh37
GRCh371941,324,367 - 41,324,579UniSTSGRCh37
Build 361946,016,207 - 46,016,419RGDNCBI36
Celera1938,434,193 - 38,434,405UniSTS
Celera1938,124,776 - 38,124,988RGD
Cytogenetic Map19q13.2UniSTS
HuRef1937,757,625 - 37,757,837UniSTS
HuRef1938,065,942 - 38,066,154UniSTS
Stanford-G3 RH Map191813.0UniSTS
NCBI RH Map19421.9UniSTS
GeneMap99-G3 RH Map191824.0UniSTS
CYP2F1_2820  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371941,633,757 - 41,634,274UniSTSGRCh37
GRCh371941,324,336 - 41,324,853UniSTSGRCh37
Build 361946,016,176 - 46,016,693RGDNCBI36
Celera1938,433,919 - 38,434,436UniSTS
Celera1938,124,745 - 38,125,262RGD
HuRef1938,065,668 - 38,066,185UniSTS
HuRef1937,757,594 - 37,758,111UniSTS


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
visual system
648 1289 1243 958 2344 838 1418 4 303 828 152 1194 3179 3008 27 1707 430 1195 1120 161 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_007930 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_000774 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_135528 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526551 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526552 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526553 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526554 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526555 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026387 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438281 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438282 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320017 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320018 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_430190 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_935755 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC008962 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH011393 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296884 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298082 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK316498 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC109056 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC109057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB853363 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471126 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC413790 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF122239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF122240 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF122241 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF122242 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF122243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF122244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF122245 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  J02906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000331105   ⟹   ENSP00000333534
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1941,114,432 - 41,128,381 (+)Ensembl
Ensembl Acc Id: ENST00000439903   ⟹   ENSP00000443424
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1941,124,855 - 41,128,366 (+)Ensembl
Ensembl Acc Id: ENST00000526093
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1941,114,432 - 41,123,350 (+)Ensembl
Ensembl Acc Id: ENST00000531409
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1941,114,432 - 41,125,817 (+)Ensembl
Ensembl Acc Id: ENST00000532164   ⟹   ENSP00000471416
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1941,114,432 - 41,128,254 (+)Ensembl
Ensembl Acc Id: ENST00000534009   ⟹   ENSP00000470136
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1941,124,718 - 41,125,819 (+)Ensembl
RefSeq Acc Id: NM_000774   ⟹   NP_000765
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381941,114,432 - 41,128,381 (+)NCBI
GRCh371941,620,312 - 41,634,286 (+)NCBI
Build 361946,312,193 - 46,326,121 (+)NCBI Archive
HuRef1938,052,253 - 38,066,192 (+)ENTREZGENE
CHM1_11941,620,054 - 41,634,005 (+)NCBI
T2T-CHM13v2.01943,935,308 - 43,949,263 (+)NCBI
Sequence:
RefSeq Acc Id: NR_135528
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381941,114,432 - 41,128,381 (+)NCBI
CHM1_11941,620,054 - 41,634,005 (+)NCBI
T2T-CHM13v2.01943,935,308 - 43,949,263 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047438280   ⟹   XP_047294236
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381941,114,432 - 41,128,381 (+)NCBI
RefSeq Acc Id: XM_047438281   ⟹   XP_047294237
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381941,114,432 - 41,128,381 (+)NCBI
RefSeq Acc Id: XM_047438282   ⟹   XP_047294238
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381941,114,432 - 41,124,906 (+)NCBI
RefSeq Acc Id: XM_054320016   ⟹   XP_054175991
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01943,935,308 - 43,949,263 (+)NCBI
RefSeq Acc Id: XM_054320017   ⟹   XP_054175992
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01943,935,308 - 43,949,263 (+)NCBI
RefSeq Acc Id: XM_054320018   ⟹   XP_054175993
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01943,935,308 - 43,945,788 (+)NCBI
RefSeq Acc Id: NP_000765   ⟸   NM_000774
- UniProtKB: Q32MN5 (UniProtKB/Swiss-Prot),   A7KAV0 (UniProtKB/Swiss-Prot),   A7KAU9 (UniProtKB/Swiss-Prot),   A7KAU8 (UniProtKB/Swiss-Prot),   A7KAU7 (UniProtKB/Swiss-Prot),   A7KAU6 (UniProtKB/Swiss-Prot),   Q8WWJ2 (UniProtKB/Swiss-Prot),   P24903 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000333534   ⟸   ENST00000331105
Ensembl Acc Id: ENSP00000443424   ⟸   ENST00000439903
Ensembl Acc Id: ENSP00000471416   ⟸   ENST00000532164
Ensembl Acc Id: ENSP00000470136   ⟸   ENST00000534009
RefSeq Acc Id: XP_047294236   ⟸   XM_047438280
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047294237   ⟸   XM_047438281
- Peptide Label: isoform X2
- UniProtKB: B4DNV7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294238   ⟸   XM_047438282
- Peptide Label: isoform X3
- UniProtKB: B4DNV7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054175991   ⟸   XM_054320016
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054175992   ⟸   XM_054320017
- Peptide Label: isoform X2
- UniProtKB: B4DNV7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054175993   ⟸   XM_054320018
- Peptide Label: isoform X3
- UniProtKB: B4DNV7 (UniProtKB/TrEMBL)

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P24903-F1-model_v2 AlphaFold P24903 1-491 view protein structure

Promoters
RGD ID:7240039
Promoter ID:EPDNEW_H25765
Type:multiple initiation site
Name:CYP2F1_1
Description:cytochrome P450 family 2 subfamily F member 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381941,114,432 - 41,114,492EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:2632 AgrOrtholog
COSMIC CYP2F1 COSMIC
Ensembl Genes ENSG00000197446 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000331105 ENTREZGENE
  ENST00000331105.7 UniProtKB/Swiss-Prot
  ENST00000439903.2 UniProtKB/TrEMBL
  ENST00000532164 ENTREZGENE
  ENST00000532164.2 UniProtKB/Swiss-Prot
  ENST00000534009.1 UniProtKB/TrEMBL
Gene3D-CATH 1.10.630.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000197446 GTEx
HGNC ID HGNC:2632 ENTREZGENE
Human Proteome Map CYP2F1 Human Proteome Map
InterPro Cyt_P450 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cyt_P450_CS UniProtKB/Swiss-Prot
  Cyt_P450_CYP2_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cyt_P450_E_grp-I UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cyt_P450_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cytochrome_P450_fam2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:1572 UniProtKB/Swiss-Prot
NCBI Gene 1572 ENTREZGENE
OMIM 124070 OMIM
PANTHER CYTOCHROME P450 2F1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CYTOCHROME P450 508A4-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam p450 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB CYP2F1 RGD, PharmGKB
PRINTS EP450I UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EP450ICYP2F UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P450 UniProtKB/Swiss-Prot
PROSITE CYTOCHROME_P450 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF48264 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A075B795_HUMAN UniProtKB/TrEMBL
  A7KAU4_HUMAN UniProtKB/TrEMBL
  A7KAU6 ENTREZGENE
  A7KAU7 ENTREZGENE
  A7KAU8 ENTREZGENE
  A7KAU9 ENTREZGENE
  A7KAV0 ENTREZGENE
  B4DNV7 ENTREZGENE, UniProtKB/TrEMBL
  CP2F1_HUMAN UniProtKB/Swiss-Prot
  H0YGI9_HUMAN UniProtKB/TrEMBL
  P24903 ENTREZGENE
  Q32MN5 ENTREZGENE
  Q8WWJ2 ENTREZGENE
UniProt Secondary A7KAU6 UniProtKB/Swiss-Prot
  A7KAU7 UniProtKB/Swiss-Prot
  A7KAU8 UniProtKB/Swiss-Prot
  A7KAU9 UniProtKB/Swiss-Prot
  A7KAV0 UniProtKB/Swiss-Prot
  Q32MN5 UniProtKB/Swiss-Prot
  Q8WWJ2 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-15 CYP2F1  cytochrome P450 family 2 subfamily F member 1  CYP2F1  cytochrome P450, family 2, subfamily F, polypeptide 1  Symbol and/or name change 5135510 APPROVED