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Symbol
Name
ID
Smarcal1
SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
MGI:1859183
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Short neck
Hypoplasia of the capital femoral epiphysis
Wide capital femoral epiphyses
Abnormal femoral head morphology
Lateral displacement of the femoral head
Shallow acetabular fossae
Hypoplastic pelvis
Thoracic kyphosis
Lumbar hyperlordosis
Ovoid vertebral bodies
Platyspondyly
Disproportionate short-trunk short stature
Osteopenia
Spondyloepiphyseal dysplasia
Disease(s) Associated with SMARCAL1
Schimke immuno-osseous dysplasia

Mouse Phenotypes
abnormal long bone epiphyseal plate morphology
abnormal long bone epiphyseal plate proliferative zone
abnormal long bone hypertrophic chondrocyte zone
short vertebral column
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)
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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory