dymeclin

Summary
Gene Symbol
  • DYM
Organism
Homo sapiens (human)
NCBI Gene
54808
PubChem
54808
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Cytoplasm
  • Disease variant
  • Dwarfism
  • Golgi apparatus
  • Membrane
  • Myristate
  • Reference proteome
Proteins
Displaying 1 entry
UniProt Protein Name
Q7RTS9
  • Dyggve-Melchior-Clausen syndrome protein
OrthoDB (Group)
Group level
Eukaryota
Group Name
uncharacterized protein
Functional Category
  • E: Amino acid transport and metabolism
  • G: Carbohydrate transport and metabolism
  • O: Posttranslational modification, protein turnover, chaperones
Displaying 1 entry
Gene Ontology
Golgi organization
Displaying 1 entry
InterPro
Dymeclin
Disease
Disease Ontology
Displaying all 4 entries
DO ID Disease Name Source
DOID:0060247 Smith-McCort dysplasia
DOID:0081270 Smith-McCort dysplasia 1
DOID:0111167 Dyggve-Melchior-Clausen disease
DOID:2256 osteochondrodysplasia
Ortholog
Displaying entries 91 - 95 of 95 in total
Species Gene ID OrthoDB Alliance of Genome Resources Orthologous MAtrix
116825467 CHEAB24948
117011796 RHIFE19588
118879841 BALMU02737
122203840 PANLE00636
129018806 9600_0:004664

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024