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Gene : GLDN Homo sapiens

Name  ? gliomedin Cytological Location  15q21.2
Brief Description  gliomedin
Description  This gene encodes a protein that contains olfactomedin-like and collagen-like domains. The encoded protein, which exists in both transmembrane and secreted forms, promotes formation of the nodes of Ranvier in the peripheral nervous system. Mutations in this gene cause a form of lethal congenital contracture syndrome in human patients. Autoantibodies to the encoded protein have been identified in sera form patients with multifocal motor neuropathy. [provided by RefSeq, May 2017]
  • synonyms:
  • GLDN,
  • HGNC:29514,
  • CRGL2,
  • CLOM,
  • CRG-L2,
  • UNC-112,
  • UNC-112,
  • AY358144,
  • uc002aba.4,
  • COLM,
  • collomin,
  • colmedin,
  • COLM,
  • CLOM,
  • OTTHUMG00000131746,
  • CRG-L2,
  • LCCS11,
  • NM_181789
  • identifiers:
  • 342035,
  • ENSG00000186417,
  • GLDN

Genome feature

Region: gene ? Length: 71711  
Location: 15:51341655-51413365 Cyto location: 15q21.2

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Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer

Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

3756 SN Ps

4 Cross References

17 Data Sets

16 Homologues

0 Located Features

97 Rna Seq Results