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Summary Expression Phenotypes Gene Literature (2) GO Terms (40) Nucleotides (141) Proteins (61) Interactants (205) Wiki
XB-GENEPAGE-1221179
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 mks1

???displayGene.name???: 
Meckel syndrome, type 1

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( Nomenclature history )

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Uncharacterized conserved protein

AI Protein Function :
The mks1 gene encodes a component of the b9 complex localizing to the transition zone of the cilium, forming part of the tectonic-like complex required for ciliogenesis and ciliary membrane composition...[+]


InterPro :
B9 dom

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Diseases: 


Disease Ontology:
Joubert syndrome [+]

MIM:
BARDET-BIEDL SYNDROME 1; BBS1 [+]

External Links:
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???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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