|
XB-GENEPAGE-988823
nsd2 nuclear receptor binding SET domain protein 2
Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology
covering anatomical, gene ontology, and neurobehavioral phenotypes.
|
|---|
| decreased cell migration in cranial neural crest (2 sources), increased size of the head (2 sources), abnormal chondrocranium morphology (1 source), abnormal cranial neural crest (1 source), abnormal craniofacial region morphology (1 source), decreased size of the forebrain (1 source) |
| Diseases
Diseases from the human disease ontology (DO) manually associated with phenotypes
from disease models. Sources are grouped by anatomical (AP) and expression (EP) phenotypes.
|
|---|
| Wolf-Hirschhorn syndrome (4AP sources) |
| Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
|
|---|
| Xla Wt + nsd2 MO (5 sources) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
|
|---|
| Mouse (5 sources): abnormal sternum ossification, decreased fetal size, failure of sternum ossification, neonatal lethality, incomplete penetrance, postnatal lethality, complete penetrance |