Symbol Name ID |
Nhlh2
nescient helix loop helix 2 MGI:97324 |
Darker colors indicate more annotations |
Human Phenotypes | Camptodactyly |
Generalized joint hypermobility |
Delayed skeletal maturation |
Osteopenia |
Osteoporosis |
Disease(s) Associated with NHLH2 | |||||
hypogonadotropic hypogonadism |
Mouse Phenotypes | abnormal bone structure |
decreased bone mineral content |
decreased bone mineral density |
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Availability | Mouse Genotype | |||
Nhlh2em1(IMPC)Mbp/Nhlh2em1(IMPC)Mbp | ||||
Nhlh2tm1b(KOMP)Mbp/Nhlh2tm1b(KOMP)Mbp |
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 06/12/2024 MGI 6.13 |
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