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Gene Gene information from NCBI Gene database.
Entrez ID 414332
Gene name Lipocalin 10
Gene symbol LCN10
Synonyms (NCBI Gene)
-
Chromosome 9
Chromosome location 9q34.3
Summary Members of the lipocalin family, such as LCN10, have a common structure consisting of an 8-stranded antiparallel beta-barrel that forms a cup-shaped ligand-binding pocket or calyx. Lipocalins generally bind small hydrophobic ligands and transport them to
miRNA miRNA information provided by mirtarbase database.
46 Show/Hide all (46)
miRTarBase ID miRNA Experiments Reference
MIRT712810 hsa-miR-5007-5p HITS-CLIP 19536157
MIRT712809 hsa-miR-192-5p HITS-CLIP 19536157
MIRT712808 hsa-miR-215-5p HITS-CLIP 19536157
MIRT712810 hsa-miR-5007-5p HITS-CLIP 19536157
MIRT712809 hsa-miR-192-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9 Show/Hide all (9)
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region IEA
GO:0006950 Process Response to stress IEA
GO:0006954 Process Inflammatory response IEA
GO:0007507 Process Heart development IEA
GO:0010165 Process Response to X-ray IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612904 20892 ENSG00000187922
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6JVE6
Protein name Epididymal-specific lipocalin-10
Protein function May play a role in male fertility. May act as a retinoid carrier protein within the epididymis.
Family and domains
Sequence
MRQGLLVLALVLVLVLVLAAGSQVQEWYPRESHALNWNKFSGFWYILATATDAQGFLPAR
DKRKLGASVVKVNKVGQLRVLLAFRRGQGCGRAQPRHPGTSGHLWASLSVKGVKAFHVLS
TDYSYGLVYLRLGRATQNYKNLLLFHRQNVSSFQSLKEFMDACDILGLSKAAVILPKDAS
RTHTILP
Sequence length 187
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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 Reference Evidence Score
Malignant lymphoma, large B-cell, diffuse Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Malignant tumor of esophagus Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Thyroid cancer, nonmedullary, 1 Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Heart Failure Heart failure Pubtator 25725476 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only