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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Clstn1
calsyntenin 1
MGI:1929895
16 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Clstn1tm1.1Uge/Clstn1tm1.1Uge
involves: C57BL/6 * C57BL/6NTac 		abnormal CNS synaptic transmission J:212386
abnormal dendrite morphology J:212386
abnormal dendritic spine morphology J:212386
abnormal excitatory postsynaptic potential J:212386
abnormal glutamate-mediated receptor currents J:212386
abnormal NMDA-mediated synaptic currents J:212386
normal behavior/neurological phenotype J:212386
decreased excitatory postsynaptic current frequency J:212386
enhanced long-term potentiation J:212386
normal nervous system phenotype J:212386
prolonged excitatory postsynaptic current decay time J:212386
Clstn1tm1b(EUCOMM)Hmgu/Clstn1tm1b(EUCOMM)Hmgu
C57BL/6N-Clstn1tm1b(EUCOMM)Hmgu/H 		decreased bone mineral content J:211773
increased basophil cell number J:211773
increased hematocrit J:211773
increased mean corpuscular volume J:211773
persistence of hyaloid vascular system J:211773
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory