LNX1 (ligand of numb-protein X 1)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 84708 |
| Gene name | Ligand of numb-protein X 1 |
| Gene symbol | LNX1 |
| Synonyms (NCBI Gene) |
LNXMPDZPDZRN2
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| Chromosome | 4 |
| Chromosome location | 4q12 |
| Summary | This gene encodes a membrane-bound protein that is involved in signal transduction and protein interactions. The encoded product is an E3 ubiquitin-protein ligase, which mediates ubiquitination and subsequent proteasomal degradation of proteins containing |
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miRNA
miRNA information provided by mirtarbase database.
8
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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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Q8TBB1 | ||||||||||||||||||||||||||||||
| Protein name | E3 ubiquitin-protein ligase LNX (EC 2.3.2.27) (Ligand of Numb-protein X 1) (Numb-binding protein 1) (PDZ domain-containing RING finger protein 2) (RING-type E3 ubiquitin transferase LNX) | ||||||||||||||||||||||||||||||
| Protein function | E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent proteasomal degradation of NUMB. E3 ubiquitin ligases accept ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubi | ||||||||||||||||||||||||||||||
| PDB | 3B76 , 5H7R , 5H7S | ||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed in heart, placenta, kidney, pancreas and brain. {ECO:0000269|PubMed:11521506}. | ||||||||||||||||||||||||||||||
| Sequence |
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| Sequence length | 728 | ||||||||||||||||||||||||||||||
| 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 categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
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