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Gene : CDAN1 Homo sapiens

Name  ? codanin 1 Cytological Location  15q15.2
Brief Description  codanin 1
Description  This gene encodes a protein that appears to play a role in nuclear envelope integrity, possibly related to microtubule attachments. Mutations in this gene cause congenital dyserythropoietic anemia type I, a disease resulting in morphological and functional abnormalities of erythropoiesis. [provided by RefSeq, Jul 2009]
  • synonyms:
  • CDAN1A,
  • OTTHUMG00000175801,
  • uc001zql.4,
  • HGNC:1713,
  • congenital dyserythropoietic anemia, type I,
  • CDAN1,
  • NM_138477,
  • AF525398,
  • CDAI,
  • PRO1295,
  • CDA1,
  • CDAI,
  • DLT,
  • CDA-I
  • identifiers:
  • 146059,
  • ENSG00000140326,
  • CDAN1

Genome feature

Region: gene ? Length: 13590  
Location: 15:42723544-42737133 reverse strand Cyto location: 15q15.2

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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]


Homologue Displayer


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

3740 SN Ps

5 Cross References

18 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results