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Gene : CDSN Homo sapiens

Name  ? corneodesmosin Cytological Location  6p21.33
Brief Description  corneodesmosin
Description  This gene encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. The encoded protein undergoes a series of cleavages during corneocyte maturation. This gene is highly polymorphic in human populations, and variation has been associated with skin diseases such as psoriasis, hypotrichosis and peeling skin syndrome. The gene is located in the major histocompatibility complex (MHC) class I region on chromosome 6. [provided by RefSeq, Dec 2014]
  • synonyms:
  • AF030130,
  • S,
  • OTTHUMG00000031150,
  • HYPT2,
  • NM_001264,
  • PSS1,
  • PSS,
  • CDSN,
  • D6S586E,
  • uc011fbm.3,
  • HGNC:1802,
  • HTSS1,
  • HTSS
  • identifiers:
  • 1041,
  • ENSG00000204539,
  • CDSN

Genome feature

Region: gene ? Length: 5360  
Location: 6:31115087-31120446 reverse strand Cyto location: 6p21.33


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

2 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

3740 SN Ps

5 Cross References

15 Data Sets

1 Homologues

0 Located Features

97 Rna Seq Results