Dym - dymeclin Gene

Also Known as 1810041M12Rik; 4933427L07Rik; C030019K18Rik

Species: Mus musculus

Gene Type: protein coding
Gene ID: 69190

Summary

Predicted to enable enzyme binding activity. Predicted to be involved in Golgi organization and bone development. Predicted to be located in cytoplasm. Predicted to be active in Golgi apparatus. Is expressed in cerebellum; retina inner nuclear layer; and retina outer nuclear layer. Used to study Smith-McCort dysplasia. Human ortholog(s) of this gene implicated in Dyggve-Melchior-Clausen disease; Smith-McCort dysplasia; and osteochondrodysplasia. Orthologous to human DYM (dymeclin). [provided by Alliance of Genome Resources, Apr 2022]

Dym Products (4)

mRNA Protein Name
NM_001403761.1 NP_001390690.1 dymeclin isoform 1
NM_001403762.1 NP_001390691.1 dymeclin isoform 3
NM_001403763.1 NP_001390692.1 dymeclin isoform 4
NM_027727.3 NP_082003.1 dymeclin isoform 2
Protein Preferred Names Protein Names

dymeclin

Orthologs Information

Species Symbol Source ID
Homo sapiens Dym NCBI NCBI:54808