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Gene : CDIN1 Homo sapiens

Name  ? CDAN1 interacting nuclease 1 Cytological Location  15q14
Brief Description  chromosome 15 open reading frame 41
Description  This gene encodes a protein with two predicted helix-turn-helix domains. Mutations in this gene were found in families with congenital dyserythropoietic anemia type Ib. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]
  • synonyms:
  • uc059hjw.1,
  • OTTHUMG00000172659,
  • C15orf41,
  • C15orf41,
  • chromosome 15 open reading frame 41,
  • HH114,
  • MGC11326,
  • NM_032499,
  • BC006254,
  • HH114,
  • HGNC:26929,
  • FLJ22851,
  • C15orf41
  • identifiers:
  • 84529,
  • ENSG00000186073,
  • CDIN1

Genome feature

Region: gene ? Length: 230638  
Location: 15:36579611-36810248 Cyto location: 15q14


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Function

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0 Pathways

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

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

661 SN Ps

5 Cross References

17 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results