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UnknownStructure modeling to function prediction of Uncharacterized Human Protein C15orf41.
Not available
S-EPMC6077826 | biostudies-literature
UnknownCharacterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein.
Not available
S-EPMC6539198 | biostudies-literature
UnknownCharacterization of the interactions between Codanin-1 and C15Orf41, two proteins implicated in congenital dyserythropoietic anemia type I disease.
Not available
S-EPMC7092493 | biostudies-literature
UnknownA complex comprising C15ORF41 and Codanin-1: the products of two genes mutated in congenital dyserythropoietic anaemia type I (CDA-I).
Not available
S-EPMC7261414 | biostudies-literature
UnknownGenetic and functional insights into CDA-I prevalence and pathogenesis.
Not available
S-EPMC7613268 | biostudies-literature
GenomicsModelling erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) for diagnosis and molecular dissection.
Congenital Dyserythropoietic Anaemia type 1 (CDA-I) is an inherited anaemia arising primarily from mutations in C15orf41 and CDAN1, however the molecular mechanisms that cause the disease remain to be fully elucidated. We use an in vitro culture system to study multiple stages of erythropoiesis from...
ORGANISM(S): Homo sapiens 
2020-11-02 | GSE125175 | GEO
UnknownWhole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development.
Not available
S-EPMC8519060 | biostudies-literature
UnknownMolecular complex detection in protein interaction networks through reinforcement learning.
Not available
S-EPMC10394916 | biostudies-literature
GenomicsModelling erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) for diagnosis and molecular dissection.
Modelling erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) for diagnosis and molecular dissection.
PRJNA515475 | ENA
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 
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