|
Symbol Name ID |
Ndn
necdin, MAGE family member MGI:97290 |
| Darker colors indicate more annotations |
| Human Phenotypes | Stroke |
Decreased response to growth hormone stimulation test |
Small pituitary gland |
Ventriculomegaly |
Perisylvian polymicrogyria |
Abnormal cerebral white matter morphology |
Poor fine motor coordination |
Poor gross motor coordination |
Delayed speech and language development |
Psychosis |
Atypical behavior |
Autistic behavior |
Autism |
Polyphagia |
Attention deficit hyperactivity disorder |
Self-injurious behavior |
Intellectual disability |
Intellectual disability, borderline |
Intellectual disability, mild |
Intellectual disability, moderate |
Excessive daytime somnolence |
Sleep abnormality |
Abnormal rapid eye movement sleep |
Sleep apnea |
Central sleep apnea |
Obstructive sleep apnea |
Hyporeflexia |
Brain imaging abnormality |
Global developmental delay |
Motor delay |
Specific learning disability |
Seizure |
Impaired pain sensation |
Impaired temperature sensation |
| Disease(s) Associated with NDN | ||||||||||||||||||||||||||||||||||
| Prader-Willi syndrome |
| Mouse Phenotypes | abnormal hypothalamus morphology |
abnormal sensory neuron innervation pattern |
abnormal proprioceptive neuron morphology |
abnormal dorsal root ganglion morphology |
abnormal lumbar dorsal root ganglion morphology |
abnormal pre-Botzinger complex physiology |
abnormal central pattern generator function |
abnormal nervous system electrophysiology |
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| Availability | Mouse Genotype | ||||||||
| Ndntm1.1Mus/Ndn+ | |||||||||
| Ndntm1Ky/Ndn+ | |||||||||
| Ndntm2Stw/Ndn+ | |||||||||
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 04/30/2024 MGI 6.23 |
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