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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
Craniofacial asymmetry
Micrognathia
Microcephaly
Preaxial hand polydactyly
Short thumb
Short hallux
Preaxial foot polydactyly
Pseudoepiphyses of the metacarpals
Split hand
Metatarsus adductus
Radioulnar synostosis
Hip dislocation
Sacral dimple
Hip dysplasia
Rib fusion
Rib segmentation abnormalities
Abnormal sternal ossification
Abnormal form of the vertebral bodies
Vertebral fusion
Kyphosis
Scoliosis
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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
02/05/2019
MGI 6.13
The Jackson Laboratory