Skip to search formSkip to main contentSkip to account menu

Codanin-1

Known as: CDAN1 
Codanin-1 (1227 aa, ~134 kDa) is encoded by the human CDAN1 gene. This protein may be involved in nuclear membrane integrity.
National Institutes of Health

Related topics

Related topics

4 relations
CDAN1 geneGenes, RegulatorIntegral Membrane ProteinsTransmembrane Domain

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Codanin-1 Mutations Engineered in Human Erythroid Cells Allow Investigation of Mechanisms Underlying Congenital Dyserythropoietic Anemia
The generation of a functional erythrocyte from a committed progenitor requires significant changes in gene expression during a… 
2018
2018
Fetal-onset congenital dyserythropoietic anemia type 1 due to CDAN1 mutations presenting as hydrops fetalis
Sha Liu, BS, Ying-Na Liu, MS, Li Zhen, PhD, and Dong-Zhi Li, PhD Department of Pediatric Hematology-Oncology, Guangzhou Women and… 
Review
2017
Review
2017
The First Registry for Patients with Congenital Dyserythropoietic Anemia in North America: Design and Preliminary Results
Background Congenital dyserythropoietic anemias (CDA) encompass a heterogeneous group of rare genetic disorders characterized by… 
2016
2016
Table 3. [Selected CDAN1 Allelic Variants].
2014
2014
Codanin-1 Binds to Key Erythroid Genes and Its Knockdown Coupled with Ectopic Mutant Expression Recapitulates the Congenital Dyserythropoietic Anemia Type I (CDA I) Phenotype
Congenital dyserythropoietic anemia type I (CDA I) is an autosomal recessive disorder marked by specific morphological… 
Review
2013
Review
2013
Congenital dyserythropoietic anemia in China: a case report from two families and a review
Congenital dyserythropoietic anemias (CDAs) are a group of hereditary disorders characterized by ineffective erythropoiesis and… 
2006
2006
Evidence of genetic heterogeneity in congenital dyserythropoietic anaemia type I – response to Ahmed et al
We read with interest the correspondence article by Dr Ahmed and colleagues. The authors describe a consanguineous Kuwaiti family… 
2006
2006
We Also Investigated 6 Sporadic Cases with Cda I for Cdan1
gene mutations by bidirectional genomic sequencing. Six mutant alleles were found in these cases, 5 previously reported (3242A T… 
2004
2004
Nuclear Localization of Codanin-1, a Product of a Newly Identified Gene Mutated in Congenital Dyserythropoeitic Anemie Type I.
Congenital dyserythropoietic anemia (CDA) type I is a rare autosomal recessive macrocytic moderate to severe anemia rarely… 
Review
2003
Review
2003
Red cell membrane and erythropoiesis genetic defects.
In recent years, the frontline of red cell membrane research has shifted. Seeking new mutations in known genes has been taken… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)