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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Atxn7
ataxin 7
MGI:2179277
28 phenotypes from 2 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Atxn7em1(IMPC)Bay/Atxn7em1(IMPC)Bay
C57BL/6N-Atxn7em1(IMPC)Bay/BayMmucd 		abnormal bone structure J:211773
increased bone mineral content J:211773
Atxn7tm1Hzo/Atxn7+
involves: 129S7/SvEvBrd 		abnormal Bergmann glial cell morphology J:113150
abnormal motor coordination/balance J:179021
ataxia J:179021
blepharoptosis J:179021
kyphosis J:179021
premature death J:179021
tremors J:179021
weight loss J:179021
Atxn7tm1Hzo/Atxn7+
involves: 129S7/SvEvBrd * C57BL/6 		abnormal cerebellum morphology J:82072
ataxia J:82072
blepharoptosis J:82072
decreased brain size J:82072
decreased locomotor activity J:82072
decreased post-tetanic potentiation J:82072
decreased Purkinje cell size J:82072
decreased retina photoreceptor cell number J:82072
female infertility J:82072
impaired coordination J:82072
kyphosis J:82072
male infertility J:82072
myoclonus J:82072
premature death J:82072
short photoreceptor outer segment J:82072
thin retina inner plexiform layer J:82072
Atxn7tm1Hzo/Atxn7+
involves: 129S7/SvEvBrd * C57BL/6J 		abnormal retina rod cell morphology J:107098
premature death J:107098
Atxn7tm1Hzo/Atxn7tm1Hzo
involves: 129S7/SvEvBrd 		abnormal cerebellum vermis morphology J:179021
abnormal gait J:179021
ataxia J:179021
normal behavior/neurological phenotype J:179021
decreased Purkinje cell size J:179021
premature death J:179021
retina outer nuclear layer degeneration J:179021
retina photoreceptor degeneration J:179021
Atxn7tm1Hzo/Atxn7tm1Hzo
involves: 129S7/SvEvBrd * C57BL/6 		premature death J:82072
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