About   Help   FAQ
Symbol
Name
ID
Smarcal1
SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
MGI:1859183
Phenotype annotations related to renal/urinary system
Darker colors indicate more annotations
Human Phenotypes
Microscopic hematuria
Proteinuria
Nephrotic range proteinuria
Focal segmental glomerulosclerosis
Minimal change glomerulonephritis
Nephropathy
Nephrotic syndrome
Renal insufficiency
Stage 5 chronic kidney disease
Disease(s) Associated with SMARCAL1
Schimke immuno-osseous dysplasia

Mouse Phenotypes
albuminuria
Availability Mouse Genotype
Smarcal1tm1.1Cfbo/Smarcal1tm1.1Cfbo

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
05/14/2024
MGI 6.23
The Jackson Laboratory