LRIG2 (leucine rich repeats and immunoglobulin like domains 2)
Gene | |
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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9860 |
Gene name
Gene Name - the full gene name approved by the HGNC.
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Leucine rich repeats and immunoglobulin like domains 2 |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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LRIG2 |
Synonyms (NCBI Gene)
Gene synonyms aliases
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LIG-2, LIG2, UFS2 |
Disease Acronyms (UniProt)
Disease acronyms from UniProt database
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UFS2 |
Chromosome
Chromosome number
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1 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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1p13.2 |
Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a transmembrane protein containing leucine-rich repeats and immunoglobulin-like domains. The encoded protein promotes epidermal growth factor signalling, resulting in increased proliferation. Its expression in the cytoplasm of glioma cel |
SNPs
SNP information provided by dbSNP.
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miRNA
miRNA information provided by mirtarbase database.
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Transcription factors | |||||||||||||
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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 | O94898 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Protein name | Leucine-rich repeats and immunoglobulin-like domains protein 2 (LIG-2) | ||||||||||||||||||||||||||||||||||||||||||||||||||
Family and domains |
Pfam
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Tissue specificity | TISSUE SPECIFICITY: Detected in all tissues analyzed. {ECO:0000269|PubMed:15145052}. | ||||||||||||||||||||||||||||||||||||||||||||||||||
Sequence | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sequence length | 1065 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Interactions | View interactions |
Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease information provided by ClinVar, GenCC, and GWAS databases.
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