TAX1BP3 (Tax1 binding protein 3)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 30851 |
| Gene name | Tax1 binding protein 3 |
| Gene symbol | TAX1BP3 |
| Synonyms (NCBI Gene) |
TIP-1TIP1
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| Chromosome | 17 |
| Chromosome location | 17p13.2 |
| Summary | This gene encodes a small, highly conserved protein with a single PDZ domain. PDZ (PSD-95/Discs large/ZO-1 homologous) domains promote protein-protein interactions that affect cell signaling, adhesion, protein scaffolding, and receptor and ion transporter |
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miRNA
miRNA information provided by mirtarbase database.
270
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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O14907 | ||||||||||
| Protein name | Tax1-binding protein 3 (Glutaminase-interacting protein 3) (Tax interaction protein 1) (TIP-1) (Tax-interacting protein 1) | ||||||||||
| Protein function | May regulate a number of protein-protein interactions by competing for PDZ domain binding sites. Binds CTNNB1 and may thereby act as an inhibitor of the Wnt signaling pathway. Competes with LIN7A for KCNJ4 binding, and thereby promotes KCNJ4 int | ||||||||||
| PDB | 2KG2 , 2L4S , 2L4T , 2VZ5 , 3GJ9 , 3SFJ , 4E3B , 4NNL , 4NNM | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Ubiquitous. Detected in brain, heart, kidney, lung, small intestine and skeletal muscle. Detected in various cell lines including HeLa. Weakly expressed in peripheral blood leukocytes. {ECO:0000269|PubMed:10940294, ECO:0000269|PubMed:1 | ||||||||||
| Sequence |
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| Sequence length | 124 | ||||||||||
| Interactions | View interactions | ||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (Causal/Unknown) and external databases: GenCC, Orphanet, ClinGen, HPO, DisGeNET, CTD, GWAS Catalog.
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