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Gene : CWF19L1 Homo sapiens

Name  ? CWF19 like cell cycle control factor 1 Cytological Location  10q24.31
Brief Description  CWF19 like cell cycle control factor 1
Description  This gene encodes a member of the CWF19 protein family. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia-17 and mild cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
  • synonyms:
  • hDrn1,
  • HGNC:25613,
  • OTTHUMG00000018901,
  • FLJ10998,
  • C19L1,
  • CWF19L1,
  • hDrn1,
  • CWF19 like 1, cell cycle control (S. pombe),
  • NM_018294,
  • AK001860,
  • SCAR17,
  • uc001kqq.1,
  • human Dbr1 associated ribonuclease 1
  • identifiers:
  • 55280,
  • ENSG00000095485,
  • CWF19L1

Genome feature

Region: gene ? Length: 35341  
Location: 10:100232298-100267638 reverse strand Cyto location: 10q24.31

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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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]


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

3740 SNPs

5 Cross References

19 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results