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Symbol
Name
ID
Slc10a7
solute carrier family 10 (sodium/bile acid cotransporter family), member 7
MGI:1924025
Phenotype annotations related to skeleton
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations

Mouse Phenotypes
skeleton phenotype
abnormal neurocranium morphology
short frontal bone
small occipital bone
small parietal bone
abnormal enamel morphology
abnormal enamel rod pattern
abnormal mandibular angle morphology
abnormal nasal bone morphology
short nasal bone
abnormal phalanx morphology
abnormal tarsal bone morphology
short humerus
short radius
abnormal femur morphology
short femur
short tibia
abnormal metatarsal bone morphology
abnormal long bone epiphyseal plate morphology
abnormal long bone epiphyseal plate proliferative zone
decreased width of hypertrophic chondrocyte zone
decreased long bone epiphyseal plate size
disorganized long bone epiphyseal plate
abnormal long bone epiphysis morphology
decreased length of long bones
increased diameter of long bones
decreased bone mineral density
decreased compact bone volume
decreased trabecular bone volume
decreased bone volume
decreased trabecular bone thickness
abnormal cartilage morphology
increased bone ossification
Availability Mouse Genotype
Slc10a7tm1a(EUCOMM)Hmgu/Slc10a7tm1a(EUCOMM)Hmgu *

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
04/16/2024
MGI 6.23
The Jackson Laboratory