Homo sapiens Protein: DYX1C1
Summary
InnateDB Protein IDBP-373291.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DYX1C1
Protein Name DYX1C1-CCPG1 readthrough (non-protein coding)
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000402640
InnateDB Gene IDBG-544502 (DYX1C1)
Protein Structure
UniProt Annotation
Function Involved in neuronal migration during development of the cerebral neocortex. May regulate the stability and proteasomal degradation of the estrogen receptors that play an important role in neuronal differentiation, survival and plasticity. Axonemal dynein assembly factor required for ciliary motility. {ECO:0000269PubMed:19423554, ECO:0000269PubMed:23872636}.
Subcellular Localization Nucleus. Cytoplasm.
Disease Associations Dyslexia 1 (DYX1) [MIM:127700]: A relatively common, complex cognitive disorder characterized by an impairment of reading performance despite adequate motivational, educational and intellectual opportunities. It is a multifactorial trait, with evidence for familial clustering and heritability. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry. A chromosomal aberration involving DYX1C1 has been found in a family affected by dyslexia. Translocation t(2;15)(q11;q21).Ciliary dyskinesia, primary, 25 (CILD25) [MIM:615482]: A disorder characterized by abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia. Patients may exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome. {ECO:0000269PubMed:23872636}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Expressed in several tissues, including brain, lung, kidney and testis. In brain localizes to a fraction of cortical neurons and white matter glial cells. {ECO:0000269PubMed:12954984}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 6 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 6 [view]
Protein-Protein 6 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0030331 estrogen receptor binding
Biological Process
GO:0001764 neuron migration
GO:0003341 cilium movement
GO:0007368 determination of left/right symmetry
GO:0033146 regulation of intracellular estrogen receptor signaling pathway
GO:0036158 outer dynein arm assembly
GO:0036159 inner dynein arm assembly
GO:0061136 regulation of proteasomal protein catabolic process
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005886 plasma membrane
Protein Structure and Domains
PDB ID
InterPro IPR007052 CS domain
IPR008978 HSP20-like chaperone
IPR013026 Tetratricopeptide repeat-containing domain
IPR019734 Tetratricopeptide repeat
PFAM PF04969
PF13174
PF13176
PF13181
PRINTS
PIRSF
SMART SM00028
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8WXU2
PhosphoSite PhosphoSite-Q8WXU2
TrEMBL
UniProt Splice Variant
Entrez Gene 161582
UniGene Hs.126403
RefSeq NP_001028731
HUGO HGNC:21493
OMIM 608706
CCDS CCDS32244
HPRD 10568
IMGT
EMBL AC013355 AC022083 AF337549 AK095201 BC062564
GenPept AAH62564 AAL73230 BAC04498