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Symbol
Name
ID
Slc39a14
solute carrier family 39 (zinc transporter), member 14
MGI:2384851
Phenotype annotations related to skeleton
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Secondary microcephaly
Macrocephaly
Achilles tendon contracture
Ankle clonus
Limb joint contracture
Scoliosis
Disease(s) Associated with SLC39A14
hypermanganesemia with dystonia 2

Mouse Phenotypes
skeleton phenotype
abnormal osteoblast physiology
increased osteoclast cell number
increased femur compact bone thickness
decreased diameter of femur
short femur
abnormal tibia morphology
decreased diameter of tibia
short tibia
decreased length of long bones
scoliosis
decreased bone mineral density
decreased trabecular bone volume
increased trabecular bone volume
decreased bone volume
abnormal compact bone morphology
decreased bone trabecula number
increased bone trabecula number
decreased bone trabecular spacing
increased bone trabecular spacing
decreased trabecular bone connectivity density
decreased trabecular bone mass
increased trabecular bone thickness
osteoporosis
abnormal chondrocyte differentiation
decreased bone mineralization
increased bone mineralization
decreased bone ossification
increased bone ossification
decreased femur stiffness
fragile skeleton
Availability Mouse Genotype
Slc39a14tm1Lex/Slc39a14tm1Lex *
Slc39a14tm1Thir/Slc39a14tm1Thir
Gt(ROSA)26Sortm1(CAG-Slc39a14*L438R)Wvh/Gt(ROSA)26Sor+
Tg(Runx2-icre)1Jtuc/0  (conditional)
Gt(ROSA)26Sortm1(CAG-Slc39a14*L438R)Wvh/Gt(ROSA)26Sor+
Tg(Ctsk-cre)1Rda/0  (conditional)

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
05/07/2024
MGI 6.23
The Jackson Laboratory