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Symbol
Name
ID
Nsd2
nuclear receptor binding SET domain protein 2
MGI:1276574
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Micrognathia
Craniofacial asymmetry
Microcephaly
Frontal bossing
Calvarial skull defect
Dolichocephaly
Preaxial hand polydactyly
Short thumb
Arachnodactyly
Short hallux
Preaxial foot polydactyly
Metatarsus adductus
Radioulnar synostosis
Pseudoepiphyses of the metacarpals
Split hand
Hip dislocation
Sacral dimple
Hypoplastic pubic rami
Hip dysplasia
Abnormality of the thorax
Rib fusion
Rib segmentation abnormalities
Abnormal sternal ossification
Abnormality of the vertebral column
Abnormal vertebral morphology
Abnormal form of the vertebral bodies
Vertebral fusion
Kyphosis
Scoliosis
Osteoporosis
Delayed skeletal maturation
Disease(s) Associated with NSD2
Wolf-Hirschhorn syndrome

Mouse Phenotypes
malocclusion
abnormal sternum ossification
failure of sternum ossification
Availability Mouse Genotype
Nsd2tm1Ykan/Nsd2tm1Ykan
Nsd2tm1Ykan/Nsd2+

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
10/15/2019
MGI 6.14
The Jackson Laboratory