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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Smarcal1
SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
MGI:1859183
15 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Smarcal1tm1.1Cfbo/Smarcal1tm1.1Cfbo
either: B6.129-Smarcal1tm1.1Cfbo or (involves: 129 * C57BL/6) 		abnormal long bone epiphyseal plate morphology J:183899
abnormal long bone epiphyseal plate proliferative zone J:183899
abnormal long bone hypertrophic chondrocyte zone J:183899
albuminuria J:183899
decreased B cell number J:183899
decreased body length J:183899
decreased body weight J:183899
decreased fibroblast proliferation J:183899
increased physiological sensitivity to xenobiotic J:183899
increased susceptibility to induced morbidity/mortality J:183899
postnatal growth retardation J:183899
short vertebral column J:183899
Smarcal1tm1a(EUCOMM)Wtsi/Smarcal1tm1a(EUCOMM)Wtsi
C57BL/6N-Smarcal1tm1a(EUCOMM)Wtsi/Wtsi 		increased circulating alkaline phosphatase level J:175295
increased hemoglobin content J:175295
increased mean corpuscular hemoglobin J:175295
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
09/03/2024
MGI 6.24 		The Jackson Laboratory