Homo sapiens Protein: MKS1
Summary
InnateDB Protein IDBP-587767.2
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MKS1
Protein Name Meckel syndrome, type 1
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000442096
InnateDB Gene IDBG-60797 (MKS1)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
They are also associated with 33 interaction(s) predicted by orthology.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 33 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0042384 cilium assembly
GO:0060271 cilium morphogenesis
Cellular Component
GO:0005737 cytoplasm
GO:0005813 centrosome
GO:0036038 TCTN-B9D complex
GO:0036064 ciliary basal body
Protein Structure and Domains
PDB ID
InterPro IPR010796 B9 domain
PFAM PF07162
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9NXB0
PhosphoSite PhosphoSite-Q9NXB0
TrEMBL F5H5Y8
UniProt Splice Variant
Entrez Gene 54903
UniGene Hs.408843
RefSeq NP_001159399
HUGO HGNC:7121
OMIM 609883
CCDS CCDS54148
HPRD 07900
IMGT
EMBL AC005962 AK000352 AK310815 BC010061 CR457229 DQ185029
GenPept AAH10061 AAZ94714 BAA91105 CAG33510