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Symbol
Name
ID

Ostm1
osteopetrosis associated transmembrane protein 1
MGI:2655574

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Cranial hyperostosis	Micrognathia	Microcephaly	Flared metaphysis	Hip subluxation	Increased bone mineral density	Osteopetrosis	Decreased osteoclast count
Disease(s) Associated with OSTM1
autosomal recessive osteopetrosis 5

Mouse Phenotypes

abnormal mental foramen morphology

abnormal incisor morphology

short lower incisors

absent incisors

short incisors

abnormal molar morphology

abnormal molar crown morphology

abnormal molar root morphology

abnormal dentin mineralization

failure of tooth eruption

abnormal maxilla morphology

abnormal maxillary zygomatic process morphology

abnormal deltoid tuberosity morphology

abnormal femur morphology

short femur

abnormal long bone morphology

abnormal rib morphology

decreased bone mineral density

abnormal compact bone morphology

abnormal trabecular bone morphology

osteopetrosis

abnormal skeleton development

failure of bone ossification

failure of bone resorption

Availability

Mouse Genotype

Ostm1^gl/Ostm1^gl

Ostm1^om/Ostm1^om

Ostm1^gl/Ostm1^om

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 04/09/2024 MGI 6.23