Crim1
BMP
CRIM1
ENU mouse mutagenesis
Protein instability
Whole-exome sequencing
Journal
Mammalian genome : official journal of the International Mammalian Genome Society
ISSN: 1432-1777
Titre abrégé: Mamm Genome
Pays: United States
ID NLM: 9100916
Informations de publication
Date de publication:
12 2019
12 2019
Historique:
received:
21
09
2019
accepted:
20
11
2019
pubmed:
30
11
2019
medline:
18
6
2020
entrez:
29
11
2019
Statut:
ppublish
Résumé
Cysteine-rich transmembrane bone morphogenetic protein regulator 1 (CRIM1) is a type I transmembrane protein involved in the organogenesis of many tissues via its interactions with growth factors including BMP, TGF-β, and VEGF. In this study, we used whole-exome sequencing and linkage analysis to identify a novel Crim1 mutant allele generated by ENU mutagenesis in mice. This allele is a missense mutation that causes a cysteine-to-serine substitution at position 140, and is referred to as Crim1
Identifiants
pubmed: 31776724
doi: 10.1007/s00335-019-09822-3
pii: 10.1007/s00335-019-09822-3
doi:
Substances chimiques
Crim1 protein, mouse
0
Bone Morphogenetic Protein Receptors
EC 2.7.11.30
Cysteine
K848JZ4886
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
329-338Références
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