Skip Header

Contribute Send feedback
Read comments (0) or add your own

Unreviewed, UniProtKB/TrEMBL Q9QXH2 (Q9QXH2_MOUSE)

Last modified January 19, 2010. Version 35. 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:
    Cyclin D1 EMBL AAF23491.1
Gene names
Name: Ccnd1 MGI 88313
OrganismMus musculus (Mouse) EMBL AAF23491.1
Taxonomic identifier10090 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresGliresRodentiaSciurognathiMuroideaMuridaeMurinaeMus

Protein attributes

Sequence length23 AA.
Sequence statusFragment.
Protein existenceEvidence at transcript level.

Ontologies

Keywords
   Molecular functionCyclin EMBL AAF23491.1
Gene Ontology (GO)
   Biological processG1/S DNA damage checkpoint

Inferred from electronic annotation. Source: Compara

G1/S transition of mitotic cell cycle

Inferred from electronic annotation. Source: Compara

Leydig cell differentiation

Inferred from electronic annotation. Source: Compara

Wnt receptor signaling pathway through beta-catenin

Inferred from mutant phenotype. Source: MGI

endoplasmic reticulum unfolded protein response

Inferred from direct assay. Source: MGI

fat cell differentiation

Inferred from direct assay. Source: MGI

lactation

Inferred from genetic interaction. Source: MGI

liver development

Inferred from electronic annotation. Source: Compara

mammary gland alveolus development

Inferred from genetic interaction. Source: MGI

mammary gland epithelial cell proliferation

Inferred from genetic interaction. Source: MGI

negative regulation of Wnt receptor signaling pathway

Inferred from mutant phenotype. Source: MGI

negative regulation of epithelial cell differentiation

Inferred from genetic interaction. Source: MGI

organ regeneration

Inferred from electronic annotation. Source: Compara

positive regulation of cell proliferation

Inferred from electronic annotation. Source: Compara

positive regulation of cyclin-dependent protein kinase activity

Inferred from electronic annotation. Source: Compara

positive regulation of protein amino acid phosphorylation

Inferred from electronic annotation. Source: Compara

protein amino acid phosphorylation

Inferred from direct assay. Source: MGI

re-entry into mitotic cell cycle

Inferred from direct assay. Source: MGI

response to UV-A

Inferred from electronic annotation. Source: Compara

response to X-ray

Inferred from electronic annotation. Source: Compara

response to calcium ion

Inferred from electronic annotation. Source: Compara

response to corticosterone stimulus

Inferred from electronic annotation. Source: Compara

response to drug

Inferred from electronic annotation. Source: Compara

response to estrogen stimulus

Inferred from electronic annotation. Source: Compara

response to ethanol

Inferred from electronic annotation. Source: Compara

response to iron ion

Inferred from electronic annotation. Source: Compara

response to magnesium ion

Inferred from electronic annotation. Source: Compara

response to organic cyclic substance

Inferred from electronic annotation. Source: Compara

response to organic nitrogen

Inferred from electronic annotation. Source: Compara

response to vitamin E

Inferred from electronic annotation. Source: Compara

   Cellular componentcyclin-dependent protein kinase holoenzyme complex

Inferred from physical interaction. Source: MGI

cytoplasm

Inferred from electronic annotation. Source: Compara

nucleus

Inferred from direct assay. Source: MGI

   Molecular functioncyclin-dependent protein kinase regulator activity

Inferred from direct assay. Source: MGI

protein complex binding

Inferred from electronic annotation. Source: Compara

protein kinase activity

Inferred from direct assay. Source: MGI

protein kinase binding

Inferred from electronic annotation. Source: Compara

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Experimental info

Non-terminal residue231 EMBL AAF23491.1

Sequences

Sequence LengthMass (Da)Tools
Q9QXH2-1 [UniParc].

Last modified May 1, 2000. Version 1.
Checksum: 5DA4617C73E3341F

FASTA232,748
        10         20 
MEHQLLCCEV ETIRRAYPDT NLL 

« Hide

References

[1]Eto I.
Submitted (DEC-1999) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF212040 Genomic DNA. Translation: AAF23491.1.
IPIIPI00109561.
UniGeneMm.273049

3D structure databases

ModBaseSearch...

Protein-protein interaction databases

STRINGQ9QXH2.

Genome annotation databases

EnsemblENSMUST00000093962; ENSMUSP00000091495; ENSMUSG00000070348; Mus musculus. [Genome view]

Organism-specific databases

MGIMGI:88313. Ccnd1.

Phylogenomic databases

HOVERGENQ9QXH2.
InParanoidQ9QXH2.

Gene expression databases

ArrayExpressQ9QXH2.
BgeeQ9QXH2.
GenevestigatorQ9QXH2.

Family and domain databases

ProtoNetSearch...

Other Resources

SOURCESearch...

Entry information

Entry nameQ9QXH2_MOUSE
AccessionPrimary (citable) accession number: Q9QXH2
Entry history
Integrated into UniProtKB/TrEMBL: May 1, 2000
Last sequence update: May 1, 2000
Last modified: January 19, 2010
This is version 35 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