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Gene : KRT17 Homo sapiens

Name  ? keratin 17 Cytological Location  17q21.2
Brief Description  keratin 17
Description  This gene encodes the type I intermediate filament chain keratin 17, expressed in nail bed, hair follicle, sebaceous glands, and other epidermal appendages. Mutations in this gene lead to Jackson-Lawler type pachyonychia congenita and steatocystoma multiplex. [provided by RefSeq, Aug 2008]
  • synonyms:
  • PC2,
  • HGNC:6427,
  • KRT17,
  • 39.1,
  • uc002hxh.3,
  • K17,
  • OTTHUMG00000133505,
  • NM_000422,
  • CK-17,
  • PCHC1,
  • PC,
  • PCHC1,
  • keratin 17, type I,
  • X62571
  • identifiers:
  • 3872,
  • ENSG00000128422,
  • KRT17

Genome feature

Region: gene ? Length: 5134  
Location: 17:41619442-41624575 reverse strand Cyto location: 17q21.2


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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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Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

295 SN Ps

5 Cross References

18 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results