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Unreviewed, UniProtKB/TrEMBL Q9JLE1 (Q9JLE1_MOUSE)

Last modified November 3, 2009. Version 34. Feed History...

Clusters with 100%, 90%, 50% identity | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information

Names and origin

Protein namesSubmitted name:
    P53 tumor suppressor EMBL AAF43276.1
Gene names
Name: Trp53 MGI 98834
OrganismMus musculus (Mouse) EMBL AAF43276.1
Taxonomic identifier10090 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresGliresRodentiaSciurognathiMuroideaMuridaeMurinaeMus

Protein attributes

Sequence length43 AA.
Sequence statusFragment.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence at transcript level.

Ontologies

Gene Ontology (GO)
   Biological processB cell lineage commitment

Inferred from mutant phenotype. Source: MGI

DNA damage response, signal transduction by p53 class mediator resulting in induction of apoptosis

Inferred from genetic interaction. Source: MGI

G1 DNA damage checkpoint

Inferred from mutant phenotype. Source: MGI

T cell differentiation in the thymus

Inferred from genetic interaction. Source: MGI

T cell lineage commitment

Inferred from mutant phenotype. Source: MGI

T cell proliferation during immune response

Inferred from genetic interaction. Source: MGI

cell aging

Inferred from genetic interaction. Source: MGI

cellular response to UV

Inferred from genetic interaction. Source: MGI

central nervous system development

Inferred from genetic interaction. Source: MGI

chromosome organization

Inferred from genetic interaction. Source: MGI

double-strand break repair

Inferred from mutant phenotype. Source: MGI

gastrulation

Inferred from genetic interaction. Source: MGI

in utero embryonic development

Inferred from genetic interaction. Source: MGI

negative regulation of DNA replication

Inferred from direct assay. Source: MGI

negative regulation of apoptosis

Inferred from mutant phenotype. Source: MGI

negative regulation of fibroblast proliferation

Inferred from direct assay. Source: MGI

negative regulation of neuroblast proliferation

Inferred from genetic interaction. Source: MGI

negative regulation of transcription from RNA polymerase II promoter

Inferred from direct assay. Source: MGI

positive regulation of neuron apoptosis

Inferred from direct assay. Source: MGI

positive regulation of transcription from RNA polymerase II promoter

Inferred from direct assay. Source: MGI

protein import into nucleus, translocation

Inferred from direct assay. Source: MGI

rRNA transcription

Inferred from genetic interaction. Source: MGI

regulation of mitochondrial membrane permeability

Inferred from genetic interaction. Source: MGI

release of cytochrome c from mitochondria

Inferred from direct assay. Source: MGI

response to X-ray

Inferred from direct assay. Source: MGI

response to drug

Inferred from direct assay. Source: MGI

response to gamma radiation

Inferred from direct assay. Source: MGI

response to salt stress

Inferred from genetic interaction. Source: MGI

   Cellular componentcytosol

Inferred from direct assay. Source: MGI

nucleus

Inferred from direct assay. Source: MGI

replication fork

Inferred from direct assay. Source: MGI

   Molecular functionprotein binding

Inferred from physical interaction. Source: MGI

transcription factor activity

Inferred from direct assay. Source: MGI

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Experimental info

Non-terminal residue11 EMBL AAF43276.1
Non-terminal residue431 EMBL AAF43276.1

Sequences

Sequence LengthMass (Da)Tools
Q9JLE1-1 [UniParc].

Last modified October 1, 2000. Version 1.
Checksum: D70E9E15774609A1

FASTA434,799
        10         20         30         40 
EALELKDAHA TEESGDSRAH SSYLKTKKGQ STSRHKKTMV KKV 

« Hide

References

[1]"Species-specific regulation of alternative splicing in the C-terminal region of the p53 tumor suppressor gene."
Laverdiere M., Beaudoin J., Lavigueur A.
Nucleic Acids Res. 28:1489-1497(2000) [PubMed: 10684946] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE.
+Additional computationally mapped references.

Cross-references

Sequence databases

AF190269 Genomic DNA. Translation: AAF43276.1.
IPIIPI00406306.
UniGeneMm.222

3D structure databases

HSSPHSSP built from PDB template 1DT7 based on UniProtKB Q9NP68.
ModBaseSearch...

Protein-protein interaction databases

STRINGQ9JLE1.

Genome annotation databases

EnsemblENSMUST00000005371; ENSMUSP00000005371; ENSMUSG00000059552; Mus musculus. [Genome view]
ENSMUST00000108657; ENSMUSP00000104297; ENSMUSG00000059552; Mus musculus. [Genome view]
ENSMUST00000108658; ENSMUSP00000104298; ENSMUSG00000059552; Mus musculus. [Genome view]

Organism-specific databases

MGIMGI:98834. Trp53.

Phylogenomic databases

HOVERGENQ9JLE1.

Gene expression databases

ArrayExpressQ9JLE1.
BgeeQ9JLE1.
GenevestigatorQ9JLE1.

Family and domain databases

InterProIPR015551. Trp53.
[Graphical view]
PANTHERPTHR11447. Trp53. 1 hit.
ProtoNetSearch...

Other Resources

SOURCESearch...

Entry information

Entry nameQ9JLE1_MOUSE
AccessionPrimary (citable) accession number: Q9JLE1
Entry history
Integrated into UniProtKB/TrEMBL: October 1, 2000
Last sequence update: October 1, 2000
Last modified: November 3, 2009
This is version 34 of the entry and version 1 of the sequence. [Complete history]
Entry statusUnreviewed (UniProtKB/TrEMBL)
Names and origin · Protein attributes · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information