Joubert syndrome

Summary
Synonym
  • JBTS
Definition
A ciliopathy that is characterized by congenital malformation of the brainstem and agenesis or hypoplasia of the cerebellar vermis leading to an abnormal respiratory pattern, nystagmus, hypotonia, ataxia, and delay in achieving motor milestones.
Super Class
brain disease ciliopathy
External Links
Disease Ontology
DOID:0050777
Mondo Disease Ontology
ORDO
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 21 - 30 of 31 in total
Gene ID Gene Symbol Description Source
29954 POMT2 protein O-mannosyltransferase 2
50814 NSDHL NAD(P) dependent steroid dehydrogenase-like
51227 PIGP phosphatidylinositol glycan anchor biosynthesis class P
55624 POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
56623 INPP5E inositol polyphosphate-5-phosphatase E
79147 FKRP fukutin related protein
84197 POMK protein O-mannose kinase
84892 POMGNT2 protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)
148789 B3GALNT2 beta-1,3-N-acetylgalactosaminyltransferase 2
160418 TMTC3 transmembrane O-mannosyltransferase targeting cadherins 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
39404 INPP5E Inositol polyphosphate 5-phosphatase E

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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: August 19, 2024