LUM - lumican Gene

Also Known as LDC; SLRR2D

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 4060

About LUM

Cytogenetic location: 12q21.33 Genomic coordinates (GRCh38): 12:91,102,629-91,111,494 (from NCBI)

This gene has 3 transcripts (splice variants), 199 orthologues and 10 paralogues. Broad expression in gall bladder (RPKM 981.2), urinary bladder (RPKM 643.2) and 14 other tissues.

Summary

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 charged hydrophilic glycosaminoglycans regulate interfibrillar spacings. Lumican is the major keratan sulfate proteoglycan of the cornea but is also distributed in interstitial collagenous matrices throughout the body. Lumican may regulate Collagen fibril organization and circumferential growth, corneal transparency, and epithelial cell migration and tissue repair. [provided by RefSeq, Jul 2008]

LUM Products (1)

mRNA Protein Name
NM_002345.4 NP_002336.1 lumican precursor
Molecular Function GO Annotation Evidence References Source
enables collagen binding IDA
IDA: Inferred from direct assay
10892350 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
25304424 GOA
Cellular Component GO Annotation Evidence References Source
part of fibrillar collagen trimer IDA
IDA: Inferred from direct assay
10734230 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

LUM Protein Structure

LRRNT

LRRNT: Leucine rich repeat N-terminal domain (37 - 65)

LRR_8

LRR_8: Leucine rich repeat (66 - 128)

LRR_8

LRR_8: Leucine rich repeat (138 - 196)

LRR_8

LRR_8: Leucine rich repeat (207 - 266)

  • 0
  • 100
  • 200
  • 300
  • 338 a.a.
Protein Preferred Names Protein Names

lumican

  • KSPG lumican

LUM Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
LUM P51884 PRKCA Homo sapiens P17252 32814053
Intra
LUM P51884 PRKCA Homo sapiens P17252 32814053
Intra
LUM P51884 PRKCA Homo sapiens P17252 32814053
Intra
LUM P51884 YWHAG Homo sapiens P61981 32814053
Intra
LUM P51884 YWHAG Homo sapiens P61981 32814053
Intra
LUM P51884 YWHAG Homo sapiens P61981 32814053
Intra
LUM P51884 KAT5 Homo sapiens Q92993 32814053
Intra
LUM P51884 KAT5 Homo sapiens Q92993 32814053
Intra
LUM P51884 KAT5 Homo sapiens Q92993 32814053
Intra
LUM P51884 SETDB1 Homo sapiens Q15047-2 32814053
Intra
LUM P51884 SETDB1 Homo sapiens Q15047-2 32814053
Intra
LUM P51884 SETDB1 Homo sapiens Q15047-2 32814053
Intra
LUM P51884 MMP14 Homo sapiens P50281 25304424
Intra
LUM P51884 MMP14 Homo sapiens P50281
SPR
25304424
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant LUM Proteins

Cat. No. Product Name Accession Purity
HY-P70369 Lumican/LUM Protein, Human (HEK293, His) P51884 (Q19-N338) ≥ 95%, as determined by reducing SDS-PAGE.

LUM Antibodies

Cat. No. Product Name Application Reactivity
HY-P86951 Lumican Antibody (YA6644) WB, IHC-P, ICC/IF, FC Human, Mouse, Rat

Related Diseases

Diseases Alias
Cornea Plana
  • Flat Cornea

Macular Dystrophy, Corneal
  • Macular Corneal Dystrophy

  • MCD

  • Corneal Dystrophy, Macular Type

  • Groenouw Type Ii Corneal Dystrophy

  • Fehr Corneal Dystrophy

  • Macular Dystrophy, Corneal Type 1

  • Mcdc1

  • Macular Corneal Dystrophy Type Ii

  • Macular Corneal Dystrophy, Type Ii

  • Macular Corneal Dystrophy, Type I

  • Mcdc1, Formerly

  • Macular Dystrophy, Corneal, 1

  • Macular Corneal Dystrophy Type 1

  • Corneal Dystrophy Groenouw Type Ii

  • Corneal Dystrophy Macular Type

  • Macular Corneal Dystrophy Type I

  • Dystrophy, Macular, Corneal

Corneal Dystrophy, Posterior Amorphous
  • Posterior Amorphous Corneal Dystrophy

  • PACD

  • Chromosome 12q21.33 Deletion Syndrome

  • Posterior Amorphous Stromal Dystrophy

Degenerative Myopia
  • Pathological Myopia

  • Myopia, Degenerative

  • Degenerative Progressive High Myopia

  • Progressive High Myopia

  • Progressive High Myopia

Stromal Dystrophy
Myopia
  • Near-Sightedness

  • Short-Sightedness

  • Nearsightedness

  • Nearsighted

  • Near Vision

  • Close Sighted

  • Myopic

  • Short-Sighted

  • Near Sighted

Corneal Ectasia
Corneal Dystrophy, Congenital Stromal
  • Congenital Stromal Corneal Dystrophy

  • CSCD

  • Congenital Hereditary Stromal Dystrophy

  • Congenital Hereditary Stromal Dystrophy Of The Cornea

  • Congenital Stromal Dystrophy Of The Cornea

  • Dacs

  • Decorin-Associated Congenital Stromal Corneal Dystrophy

  • Dystrophia Corneae Parenchymatosa Congenita

  • Witschel Dystrophy

  • Dystrophy, Corneal, Stromal, Congenital

Refractive Error
  • Refractive Errors

Corneal Disease
  • Corneal Diseases

  • Corneal Disorders

Ehlers-Danlos Syndrome
  • Eds

  • Cutis Hyperelastica

  • Elastic Skin

  • Ehlers-Danlos Syndromes

  • Ed Syndrome

  • Ehlers Danlos Syndrome

  • Ehlers Danlos Disease

  • Eds - [Ehlers-Danlos Syndrome]

Fuchs' Endothelial Dystrophy
  • Fuchs Endothelial Corneal Dystrophy

  • Fuchs Endothelial Dystrophy

  • Fuchs Dystrophy

  • Fced

  • Fuchs' Corneal Dystrophy

  • Fuchs' Endothelial Corneal Dystrophy

  • Fuchs Atrophy

  • Fuchs Corneal Dystrophy

  • Endoepithelial Corneal Dystrophy

  • Fecd

  • Late Hereditary Endothelial Dystrophy

  • Corneal Dystrophy, Fuchs Endothelial

  • Dystrophy, Corneal, Fuchs Endothelial

  • Corneal Dystrophy, Fuchs' Endothelial, 1

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus LUM VGNC VGNC:31081
Rattus norvegicus LUM RGD RGD:620984
Felis catus LUM VGNC VGNC:68109
Mus musculus LUM MGD MGI:109347
Canis familiaris LUM VGNC VGNC:42865
Macaca mulatta LUM VGNC VGNC:100076
Others LUM NCBI