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ProteomicsInherited anemia-associated mutations disrupt Codanin1 and CDIN1 mutual direct binding
Congenital dyserythropoietic anemia type I (CDA-I) is a rare hereditary disease that causes ineffective erythropoiesis and morphological abnormalities in bone marrow erythroblasts. The congenital abnormalities are manifested by internuclear bridges and Swiss-cheese-like heterochromatin. CDA-I is as...
ORGANISM(S): Homo sapiens (Human) 
2026-09-07 | PXD037661 | Pride
Rare diseases Cdin1 Lc-msms C15orf41 Codanin1 Congenital dyserythropoietic anemia Hdx-ms 
ProteomicsCharacterisation of CDIN1 and Codanin-1 interaction by affinity purification mass spectrometry analysis
Congenital Dyserythropoietic Anaemia type I (CDA-I) is a rare inherited disorder of erythropoiesis, in which erythroid cells display a unique nuclear phenotype referred to as ‘spongy’ heterochromatin. The molecular basis of CDA-I remains unknown, with most cases of CDA-I caused by mutations in CDAN1...
ORGANISM(S): Homo sapiens (Human) 
2026-09-14 | PXD078989 | Pride
Congenital dyserythropoietic anaemia type i (cda-i) Erythropoiesis 
UnknownMechanism of ASF1 engagement by CDAN1.
Not available
S-EPMC11911400 | biostudies-literature
UnknownMechanism of ASF1 Inhibition by CDAN1.
Not available
S-EPMC11326237 | biostudies-literature
UnknownMEIS2 (15q14) gene deletions in siblings with mild developmental phenotypes and bifid uvula: documentation of mosaicism in an unaffected parent.
Not available
S-EPMC8690878 | biostudies-literature
UnknownGenomic insights into local adaptation and phenotypic diversity of Wenchang chickens.
Not available
S-EPMC10823079 | biostudies-literature
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