LIMS2 (LIM zinc finger domain containing 2)
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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55679 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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LIM zinc finger domain containing 2 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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LIMS2 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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LGMD2W, MDRCMTT, PINCH-2, PINCH2 |
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Chromosome
Chromosome number
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2 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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2q14.3 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of a small family of focal adhesion proteins which interacts with ILK (integrin-linked kinase), a protein which effects protein-protein interactions with the extraceullar matrix. The encoded protein has five LIM domains, each do |
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SNPs
SNP information provided by dbSNP.
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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 | Q7Z4I7 | ||||||||||||||||||||||||||||||
| Protein name | LIM and senescent cell antigen-like-containing domain protein 2 (LIM-like protein 2) (Particularly interesting new Cys-His protein 2) (PINCH-2) | ||||||||||||||||||||||||||||||
| Protein function | Adapter protein in a cytoplasmic complex linking beta-integrins to the actin cytoskeleton, bridges the complex to cell surface receptor tyrosine kinases and growth factor receptors. Plays a role in modulating cell spreading and migration. {ECO:0 | ||||||||||||||||||||||||||||||
| PDB | 3IXE | ||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Sequence | |||||||||||||||||||||||||||||||
| Sequence length | 341 | ||||||||||||||||||||||||||||||
| 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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