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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Chsy1
chondroitin sulfate synthase 1
MGI:2681120
79 phenotypes from 5 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Chsy1em1(IMPC)Mbp/Chsy1em1(IMPC)Mbp
C57BL/6NCrl-Chsy1em1(IMPC)Mbp/MbpMmucd 		abnormal auditory brainstem response J:211773
abnormal bone structure J:211773
abnormal brain morphology J:211773
abnormal cecum morphology J:211773
abnormal eye morphology J:211773
abnormal liver morphology J:211773
abnormal lymph node morphology J:211773
abnormal retina morphology J:211773
abnormal skin morphology J:211773
abnormal spleen morphology J:211773
abnormal vitreous body morphology J:211773
cataract J:211773
cornea opacity J:211773
decreased body length J:211773
decreased bone mineral content J:211773
decreased bone mineral density J:211773
decreased brain size J:211773
decreased grip strength J:211773
enlarged cecum J:211773
enlarged lymph nodes J:211773
enlarged spleen J:211773
hydrocephaly J:211773
increased mean corpuscular volume J:211773
microphthalmia J:211773
small liver J:211773
urinary bladder obstruction J:211773
Chsy1em1Btlr/Chsy1em1Btlr
C57BL/6J-Chsy1em1Btlr/Btlr 		short femur J:309727
short tibia J:309727
Chsy1m1Btlr/Chsy1m1Btlr
C57BL/6J-Chsy1m1Btlr/Btlr 		short femur J:309727
Chsy1skt/Chsy1skt
STOCK a Chsy1skt/J 		kinked tail J:14274
proportional dwarf J:14274
Chsy1skt/Chsy1skt
Pde6b+/Pde6b+
mixed 		abnormal extracellular matrix morphology J:286529
abnormal photoreceptor outer segment morphology J:286529
abnormal retina outer nuclear layer morphology J:286529
abnormal rod electrophysiology J:286529
decreased a-wave amplitude J:286529
decreased b-wave amplitude J:286529
decreased body size J:286529
decreased macrophage cell number J:286529
decreased neutrophil cell number J:286529
disorganized photoreceptor outer segment J:286529
hippocampal neuron degeneration J:286529
hunched posture J:286529
kidney inflammation J:286529
kinked tail J:286529
microgliosis J:286529
neurodegeneration J:286529
photoreceptor outer segment degeneration J:286529
premature death J:286529
premature hair loss J:286529
retina outer nuclear layer degeneration J:286529
retina photoreceptor degeneration J:286529
thin retina outer nuclear layer J:286529
Chsy1skt/Chsy1tm1Lex
mixed 		abnormal retina morphology J:286529
decreased body size J:286529
kinked tail J:286529
microgliosis J:286529
thin retina outer nuclear layer J:286529
Chsy1tm1Lex/Chsy1tm1Lex
involves: 129S5/SvEvBrd * C57BL/6J 		abnormal axial skeleton morphology J:182757
abnormal bone structure J:182757
abnormal carpal bone morphology J:182757
abnormal craniofacial bone morphology J:182757
abnormal limb bone morphology J:182757
abnormal long bone hypertrophic chondrocyte zone J:182757
abnormal metacarpal bone morphology J:182757
abnormal metatarsal bone morphology J:182757
abnormal phalanx morphology J:182757
abnormal retina morphology J:286529
abnormal rib morphology J:182757
autoimmune arthritis J:171883
brachypodia J:182757
chondrodystrophy J:182757
decreased bone mineral content J:171883
decreased bone mineral density of femur J:171883
decreased bone mineral density of vertebrae J:171883
decreased bone trabecula number J:171883
decreased red blood cell distribution width J:171883
decreased trabecular bone connectivity density J:171883
decreased trabecular bone thickness J:171883
decreased trabecular bone volume J:171883
decreased volumetric bone mineral density J:171883
delayed bone mineralization J:182757
delayed chondrocyte differentiation J:182757
increased mean corpuscular hemoglobin J:171883
microgliosis J:286529
retina degeneration J:171883
short limbs J:182757
short ribs J:182757
thin ribs J:182757
weakness J:171883
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