Homo sapiens Gene: LGALS7B | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Gene | IDBG-49508.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | LGALS7B | ||||||||||||||||||
Gene Name | lectin, galactoside-binding, soluble, 7B | ||||||||||||||||||
Synonyms | GAL7; LGALS7A | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Gene | ENSG00000178934 | ||||||||||||||||||
Encoded Proteins |
lectin, galactoside-binding, soluble, 7B
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Protein Structure |
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Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||
Entrez Gene | |||||||||||||||||||
Summary |
The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. Differential and in situ hybridization studies indicate that this lectin is specifically expressed in keratinocytes and found mainly in stratified squamous epithelium. A duplicate copy of this gene (GeneID:3963) is found adjacent to, but on the opposite strand on chromosome 19. [provided by RefSeq, Jul 2008] The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. Differential and in situ hybridization studies indicate that this lectin is specifically expressed in keratinocytes and found mainly in stratified squamous epithelium. A duplicate copy of this gene (GeneID:653499) is found adjacent to, but on the opposite strand on chromosome 19. [provided by RefSeq, Jul 2008] The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. Differential and in situ hybridization studies indicate that this lectin is specifically expressed in keratinocytes and found mainly in stratified squamous epithelium. A duplicate copy of this gene (GeneID:653499) is found adjacent to, but on the opposite strand on chromosome 19. [provided by RefSeq, Jul 2008] |
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Gene Information | |||||||||||||||||||
Type | Protein coding | ||||||||||||||||||
Genomic Location | Chromosome 19:38789211-38791749 | ||||||||||||||||||
Strand | Forward strand | ||||||||||||||||||
Band | q13.2 | ||||||||||||||||||
Transcripts |
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Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||
No orthologs found for this gene | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | P47929 | ||||||||||||||||||
TrEMBL | |||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 653499 | ||||||||||||||||||
UniGene | |||||||||||||||||||
RefSeq | NM_001042507 | ||||||||||||||||||
HUGO | HGNC:34447 | ||||||||||||||||||
OMIM | 600615 | ||||||||||||||||||
CCDS | CCDS42565 | ||||||||||||||||||
HPRD | |||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | BC042911 BC061588 BC073743 CH471126 CR456917 L07769 U06643 | ||||||||||||||||||
GenPept | AAA67899 AAA86820 AAH42911 AAH61588 AAH73743 CAG33198 EAW56817 EAW56818 | ||||||||||||||||||
RNA Seq Atlas | 3963 653499 | ||||||||||||||||||