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MGI:Cyp1b1

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Cyp1b1
Protein Name(s) cytochrome P450, family 1, subfamily b, polypeptide 1,
External Links
MGI MGI:88590

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0001525

angiogenesis

MGI:MGI:3829820
PMID:19005183[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2154690

P

From MGI

GO:0004497

monooxygenase activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0503

F

From MGI

GO:0005506

iron ion binding

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001128
InterPro:IPR002401

F

From MGI

GO:0005783

endoplasmic reticulum

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0256

C

From MGI

GO:0005792

microsome

MGI:MGI:3713192
PMID:17166882[2]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005792

microsome

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:Q64678

C

From MGI

GO:0005792

microsome

MGI:MGI:82204
PMID:1910294[3]

IDA: Inferred from Direct Assay

C

From MGI

GO:0006725

cellular aromatic compound metabolic process

MGI:MGI:1097753
PMID:9377560[4]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0006725

cellular aromatic compound metabolic process

MGI:MGI:1099570
PMID:9367523[5]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0006725

cellular aromatic compound metabolic process

MGI:MGI:1333452
PMID:10051580[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2154690

P

From MGI

GO:0006725

cellular aromatic compound metabolic process

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:Q64678

P

From MGI

GO:0006725

cellular aromatic compound metabolic process

MGI:MGI:82204
PMID:1910294[3]

IDA: Inferred from Direct Assay

P

From MGI

GO:0008210

estrogen metabolic process

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:Q64678

P

From MGI

GO:0009055

electron carrier activity

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001128

F

From MGI

GO:0009404

toxin metabolic process

MGI:MGI:1333452
PMID:10051580[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2154690

P

From MGI

GO:0009404

toxin metabolic process

MGI:MGI:3713192
PMID:17166882[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2154690

P

From MGI

GO:0009636

response to toxin

MGI:MGI:3794487
PMID:16377763[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2154690

P

From MGI

GO:0016020

membrane

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0472

C

From MGI

GO:0016491

oxidoreductase activity

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:Q64678

F

From MGI

GO:0016705

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001128
InterPro:IPR017972
InterPro:IPR002401

F

From MGI

GO:0016712

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

MGI:MGI:1099570
PMID:9367523[5]

IDA: Inferred from Direct Assay

F

From MGI

GO:0016712

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

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

UniProtKB:Q16678

F

From MGI

GO:0020037

heme binding

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001128
InterPro:IPR002401

F

From MGI

GO:0043542

endothelial cell migration

MGI:MGI:3829820
PMID:19005183[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2154690

P

From MGI

GO:0046872

metal ion binding

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0479

F

From MGI

GO:0055114

oxidation-reduction process

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:Q64678

P

From MGI

GO:0061298

retina vasculature development in camera-type eye

MGI:MGI:3829820
PMID:19005183[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2154690

P

From MGI

GO:0070330

aromatase activity

MGI:MGI:2152096

IEA: Inferred from Electronic Annotation

EC:1.14.14.1

F

From MGI

GO:0071603

endothelial cell-cell adhesion

MGI:MGI:3829820
PMID:19005183[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2154690

P

From MGI

NOT

GO:0018894

dibenzo-p-dioxin metabolic process

MGI:MGI:3688815
PMID:16636061[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2154690

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. 1.0 1.1 1.2 1.3 Tang Y et al. (2009) CYP1B1 expression promotes the proangiogenic phenotype of endothelium through decreased intracellular oxidative stress and thrombospondin-2 expression. Blood 113: 744-54 PubMed GONUTS page
  2. 2.0 2.1 Shertzer HG et al. (2007) 7H-dibenzo[c,g]carbazole metabolism by the mouse and human CYP1 family of enzymes. Carcinogenesis 28: 1371-8 PubMed GONUTS page
  3. 3.0 3.1 Pottenger LH et al. (1991) Purification and immunological characterization of a novel cytochrome P450 from C3H/10T1/2 cells. Arch Biochem Biophys 286: 488-97 PubMed GONUTS page
  4. Alexander DL et al. (1997) Ah receptor regulation of CYP1B1 expression in primary mouse embryo-derived cells. Cancer Res 57: 4498-506 PubMed GONUTS page
  5. 5.0 5.1 Savas U et al. (1997) Biological oxidations and P450 reactions. Recombinant mouse CYP1B1 expressed in Escherichia coli exhibits selective binding by polycyclic hydrocarbons and metabolism which parallels C3H10T1/2 cell microsomes, but differs from human recombinant CYP1B1. Arch Biochem Biophys 347: 181-92 PubMed GONUTS page
  6. 6.0 6.1 Buters JT et al. (1999) Cytochrome P450 CYP1B1 determines susceptibility to 7, 12-dimethylbenz[a]anthracene-induced lymphomas. Proc Natl Acad Sci U S A 96: 1977-82 PubMed GONUTS page
  7. Uno S et al. (2006) Oral benzo[a]pyrene in Cyp1 knockout mouse lines: CYP1A1 important in detoxication, CYP1B1 metabolism required for immune damage independent of total-body burden and clearance rate. Mol Pharmacol 69: 1103-14 PubMed GONUTS page
  8. Dragin N et al. (2006) For dioxin-induced birth defects, mouse or human CYP1A2 in maternal liver protects whereas mouse CYP1A1 and CYP1B1 are inconsequential. J Biol Chem 281: 18591-600 PubMed GONUTS page
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