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Gene : C12orf57 Homo sapiens

Name  ? chromosome 12 open reading frame 57 Cytological Location  12p13.31
Brief Description  chromosome 12 open reading frame 57
Description  This gene is ubiquitously expressed in human tissues. It is required for development of the human corpus callosum. Mutations in this gene are associated with Temtamy syndrome (TEMTYS). Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]
  • synonyms:
  • HGNC:29521,
  • C12orf57,
  • U47924,
  • gene rich cluster C10 gene,
  • GRCC10,
  • GRCC10,
  • uc058knx.1,
  • C10,
  • NM_138425,
  • C10,
  • OTTHUMG00000169017
  • identifiers:
  • 113246,
  • ENSG00000111678,
  • C12orf57

Genome feature

Region: gene ? Length: 2566  
Location: 12:6943438-6946003 Cyto location: 12p13.31


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Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer

Function

Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

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

17 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results