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Protein Coding Gene : Cdan1 codanin 1
Primary Identifier  MGI:1916218 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  68968
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to be involved in chromatin organization and import into nucleus. Predicted to act upstream of or within protein localization. Located in endomembrane system and nucleus. Is expressed in several structures, including adipose tissue; central nervous system; eye; genitourinary system; and gut. Human ortholog(s) of this gene implicated in congenital dyserythropoietic anemia and congenital dyserythropoietic anemia type Ia. Orthologous to human CDAN1 (codanin 1).
PHENOTYPE: Mice homozygous for a gene trapped allele exhibit complete embryonic lethality between implantation and somite formation. [provided by MGI curators]
  • synonyms:
  • expressed sequence AW492297,
  • MGI:2139352,
  • expressed sequence AI448026,
  • Cdan1,
  • CDA1,
  • codanin-1,
  • 1500015A01Rik,
  • AI448026,
  • codanin 1,
  • CDA-I,
  • MGI:2138950,
  • AW492297,
  • RIKEN cDNA 1500015A01 gene
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Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 Involved In Mutations

Trail: ProteinCodingGene

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

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