Symbol Name ID |
Ndn
necdin, MAGE family member MGI:97290 |
Darker colors indicate more annotations |
Human Phenotypes | Decreased fetal movement |
Feeding difficulties in infancy |
Nasogastric tube feeding in infancy |
Poor suck |
Tube feeding |
Atypical behavior |
Autistic behavior |
Autism |
Polyphagia |
Attention deficit hyperactivity disorder |
Self-injurious behavior |
Weak cry |
Hypernasal speech |
Disease(s) Associated with NDN | |||||||||||||
Prader-Willi syndrome |
Mouse Phenotypes | abnormal spatial learning |
excessive scratching |
impaired coordination |
decreased thermal nociceptive threshold |
increased thermal nociceptive threshold |
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Availability | Mouse Genotype | |||||
Ndntm1.1Mus/Ndn+ | ||||||
Ndntm1Ky/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 03/19/2024 MGI 6.23 |
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