NucleaRDB: Extraction of mutation data from the literature

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This data was extracted from Medline abstracts and full texts (when available) in an automated manner.

The table below describes the selected point mutation and provides links to other documents. The sentence(s) where the point mutation F171L was found are listed after the table.

The mutated residues are also indicated in the family sequence alignments and hyperlinked to the corresponding mutation pages.


Point mutation F171L in NR1I3_MOUSE

Point mutation:F171L
Domain:LBD HELIX 3
General numbering (NucleaRDB): 335
Protein:NR1I3_MOUSE (Nr1i3,Ca)Swiss-Prot
Cross-reference table
Family page
Protein isoforms2
Other point mutations / same protein / same positionPoint mutations at position 171 in NR1I3_MOUSE
Other point mutations / same proteinList of mutations in NR1I3_MOUSE
Family alignments 1I3 Constitutive Androstane alpha (CAR1)
1I Vitamin D3-like (VDR,PXR,CAR)
1 Thyroid hormone like (TR,RAR,ROR,PPAR,VDR
Other point mutations / same position Position 171 in 1I3 Constitutive Androstane alpha (CAR1) family
Position 225 in 1I Vitamin D3-like (VDR,PXR,CAR) family
Position 218 in 1 Thyroid hormone like (TR,RAR,ROR,PPAR,VDR family
Reference:The xenobiotic compound 1,4-bis[2-(3,5-dichloropyridyloxy)]benzene is an agonist ligand for the nuclear receptor CAR.
Tzameli I, Pissios P, Schuetz EG, Moore DD
Mol Cell Biol 2000 May;20(9):2951-8.
Medline
Other point mutations / same articleList
Text sourceHTML and PDF full texts
Validation statusTrue positive

Relevant sentences:

F171L


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F.Horn (nucleardbcmbi.kun.nl), 21-Apr-2005