Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4060
Gene name Gene Name - the full gene name approved by the HGNC.
Lumican
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LUM
Synonyms (NCBI Gene) Gene synonyms aliases
LDC, SLRR2D
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q21.33
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the small leucine-rich proteoglycan (SLRP) family that includes decorin, biglycan, fibromodulin, keratocan, epiphycan, and osteoglycin. In these bifunctional molecules, the protein moiety binds collagen fibrils and the highly
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT735118 hsa-miR-450b-5p qRT-PCR 31776299
MIRT1122429 hsa-miR-4282 CLIP-seq
MIRT1122430 hsa-miR-4330 CLIP-seq
MIRT1122431 hsa-miR-4760-3p CLIP-seq
MIRT1122432 hsa-miR-490-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005201 Function Extracellular matrix structural constituent NAS 10892350
GO:0005515 Function Protein binding IPI 25304424, 32814053
GO:0005518 Function Collagen binding IBA 21873635
GO:0005518 Function Collagen binding IDA 10892350
GO:0005576 Component Extracellular region HDA 27068509
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600616 6724 ENSG00000139329
Protein
UniProt ID P51884
Protein name Lumican (Keratan sulfate proteoglycan lumican) (KSPG lumican)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01462 LRRNT 36 66 Leucine rich repeat N-terminal domain Family
PF13855 LRR_8 67 102 Leucine rich repeat Repeat
PF13855 LRR_8 136 171 Leucine rich repeat Repeat
PF13516 LRR_6 182 197 Leucine Rich repeat Repeat
PF13855 LRR_8 205 266 Leucine rich repeat Repeat
Tissue specificity TISSUE SPECIFICITY: Cornea and other tissues.
Sequence
MSLSAFTLFLALIGGTSGQYYDYDFPLSIYGQSSPNCAPECNCPESYPSAMYCDELKLKS
VPMVPP
GIKYLYLRNNQIDHIDEKAFENVTDLQWLILDHNLLENSKIKGRVFSKLKQLKK
LHINHNNLTESVGPLPKSLEDLQLTHNKITKLGSFEGLVNLTFIHLQHNRLKEDAVSAAF
KGLKSLEYLDLSFNQIARLPSGLPVSLLTLYLDNNKISNIPDEYFKRFNALQYLRLSHNE
LADSGIPGNSFNVSSLVELDLSYNKL
KNIPTVNENLENYYLEVNQLEKFDIKSFCKILGP
LSYSKIKHLRLDGNRISETSLPPDMYECLRVANEVTLN
Sequence length 338
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Proteoglycans in cancer   Keratan sulfate biosynthesis
Keratan sulfate degradation
Integrin cell surface interactions
Defective CHST6 causes MCDC1
Defective ST3GAL3 causes MCT12 and EIEE15
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Facioscapulohumeral muscular dystrophy Muscular Dystrophy, Facioscapulohumeral rs387907319, rs397514623, rs1057519614, rs1598416221, rs886041918, rs886042417, rs1057519644, rs1245372794, rs1555642277, rs1555644339, rs1555647265, rs886044369, rs1568350731, rs377471712, rs2075161300
View all (2 more)
12868502
Associations from Text Mining
Disease Name Relationship Type References
Acute Aortic Syndrome Associate 22228989, 27403433
Adenocarcinoma Associate 25961303, 38250763
Adenocarcinoma of Lung Associate 25961303
Aneuploidy Inhibit 31760859
Aneurysm Stimulate 29929532
Aortic Dissection Associate 22228989
Aortic Valve Stenosis Associate 26742884
Ascites Associate 27500424
Atherosclerosis Associate 15970583
Bone Cysts Aneurysmal Associate 32859633