Gene Gene information from NCBI Gene database.
Entrez ID 29094
Gene name Galectin like
Gene symbol LGALSL
Synonyms (NCBI Gene)
GRPHSPC159
Chromosome 2
Chromosome location 2p14
miRNA miRNA information provided by mirtarbase database.
24
miRTarBase ID miRNA Experiments Reference
MIRT025108 hsa-miR-181a-5p Sequencing 20371350
MIRT029067 hsa-miR-26b-5p Microarray 19088304
MIRT667650 hsa-miR-5088-5p HITS-CLIP 23824327
MIRT667649 hsa-miR-1470 HITS-CLIP 23824327
MIRT667648 hsa-miR-4667-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21044950, 25416956, 32296183
GO:0030246 Function Carbohydrate binding IBA
GO:0030246 Function Carbohydrate binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617902 25012 ENSG00000119862
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q3ZCW2
Protein name Galectin-related protein (Galectin-like protein) (Lectin galactoside-binding-like protein)
Protein function Does not bind lactose, and may not bind carbohydrates.
PDB 2JJ6 , 3B9C
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00337 Gal-bind_lectin 39 172 Galactoside-binding lectin Domain
Sequence
Sequence length 172
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
AMYOTROPHIC LATERAL SCLEROSIS ClinGen, Disgenet
ClinGen, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LIVER CIRRHOSIS, EXPERIMENTAL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Multiple Myeloma Associate 33675538
★☆☆☆☆
Found in Text Mining only
Osteoporosis Associate 29568943
★☆☆☆☆
Found in Text Mining only
Periodontitis Associate 39610070
★☆☆☆☆
Found in Text Mining only
Postural Orthostatic Tachycardia Syndrome Associate 40022872
★☆☆☆☆
Found in Text Mining only
Uterine Cervical Neoplasms Associate 23052694
★☆☆☆☆
Found in Text Mining only