LRRC4 (leucine rich repeat containing 4)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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64101 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Leucine rich repeat containing 4 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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LRRC4 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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NAG14, NGL-2 |
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Chromosome
Chromosome number
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7 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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7q32.1 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene is significantly downregulated in primary brain tumors. The exact function of the protein encoded by this gene is unknown. [provided by RefSeq, Jul 2008] |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | ||||||||||||||||||||||||||
| UniProt ID | Q9HBW1 | |||||||||||||||||||||||||
| Protein name | Leucine-rich repeat-containing protein 4 (Brain tumor-associated protein BAG) (Nasopharyngeal carcinoma-associated gene 14 protein) (Netrin-G2 ligand) (NGL-2) | |||||||||||||||||||||||||
| Protein function | Synaptic adhesion protein. Regulates the formation of exitatory synapses through the recruitment of pre-and-postsynaptic proteins. Organize the lamina/pathway-specific differentiation of dendrites. Plays an important role for auditory synaptic r | |||||||||||||||||||||||||
| PDB | 2DL9 , 3ZYI | |||||||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Specifically expressed in brain. {ECO:0000269|PubMed:15967442}. | |||||||||||||||||||||||||
| Sequence |
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| Sequence length | 653 | |||||||||||||||||||||||||
| 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 categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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