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Field	Query

Alzheimer disease
Amyotrophic lateral sclerosis
Autism
Bipolar disorder
COXPD
Cancer
Cardiovascular diseases
Diabetes mellitus, type II
Epilepsy
Farber lipogranulomatosis
Inflammatory bowel disease
Lung disease
Major depressive disorder
Multiple sclerosis
Muscular atrophy
Neutropenia, severe congenital
Other
Parkinson disease
Post-traumatic stress disorder
Postpartum depression
Rare disease
Schizophrenia

	Field	Term

General Information:

Id:	7,069 (click here to show other Interactions for entry)
Diseases:	Bardet-Biedl syndrome Joubert syndrome Meckel syndrome
Organism:	Mus musculus
Publication type:	article
Reference:	[PMID: 22179047]

Interaction Information:

Comment	B9D1 was identified as a gene that was localized at the base of the cilia and its knockdown produced significant inhibition of Shh signalling without obvious effects on cilia integrity.
Formal Description Interaction-ID: 69519	gene/protein B9D1 affects_activity of process smoothened signaling pathway

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