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Gene : C20orf194 Homo sapiens

Name  ? chromosome 20 open reading frame 194 Cytological Location  20p13
Brief Description  chromosome 20 open reading frame 194
Description  This gene encodes an uncharacterized protein with a C-terminal coiled-coil region. The gene is located on chromosome 20p13 in a 1.8 Mb region linked to a spinocerebellar ataxia phenotype, but this gene does not appear to be a disease candidate. [provided by RefSeq, Dec 2011]
  • synonyms:
  • OTTHUMG00000031742,
  • DKFZp434N061,
  • AL110249,
  • uc002wii.4,
  • NM_001009984,
  • HGNC:17721,
  • C20orf194
  • identifiers:
  • 25943,
  • ENSG00000088854,
  • C20orf194

Genome feature

Region: gene ? Length: 158361  
Location: 20:3249302-3407662 reverse strand Cyto location: 20p13


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Function

Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

0 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

0 Pathways

3753 SN Ps

5 Cross References

15 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results