Mus musculus Gene: Dym
Summary
InnateDB Gene IDBG-158761.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Dym
Gene Name dymeclin
Synonyms 1810041M12Rik; 4933427L07Rik; C030019K18Rik
Species Mus musculus
Ensembl Gene ENSMUSG00000035765
Encoded Proteins
dymeclin
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000141627:
This gene encodes a protein which is necessary for normal skeletal development and brain function. Mutations in this gene are associated with two types of recessive osteochondrodysplasia, Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia, which involve both skeletal defects and mental retardation. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 18:75018772-75286966
Strand Forward strand
Band E2
Transcripts
ENSMUST00000039608 ENSMUSP00000047054
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0019899 enzyme binding
Biological Process
GO:0007030 Golgi organization
GO:0060348 bone development
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005794 Golgi apparatus
GO:0005886 plasma membrane
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.407736
RefSeq NM_027727 XM_006526219
OMIM
CCDS CCDS29346
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas