Symbol Name ID |
Bmp4
bone morphogenetic protein 4 MGI:88180 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Stroke |
Anterior hypopituitarism |
Photophobia |
Delayed CNS myelination |
Morphological central nervous system abnormality |
Ventriculomegaly |
Cerebral cortical atrophy |
Aplasia/Hypoplasia of the corpus callosum |
Agenesis of corpus callosum |
Inferior cerebellar vermis hypoplasia |
Cerebellar hypoplasia |
Myelopathy |
Spinal cord compression |
Aplasia of the optic tract |
Absent speech |
Hyperreflexia |
Global developmental delay |
Seizure |
Disease(s) Associated with BMP4 | |||||||||||||||||||
atrial heart septal defect | |||||||||||||||||||
ossification of the posterior longitudinal ligament of spine | |||||||||||||||||||
syndromic microphthalmia 6 | |||||||||||||||||||
tooth agenesis |
Mouse Phenotypes | nervous system phenotype |
abnormal radial glial cell morphology |
abnormal neural tube closure |
absent Rathke's pouch |
decreased vestibular hair cell stereocilia number |
abnormal forebrain development |
abnormal hindbrain development |
abnormal midbrain development |
increased astrocyte number |
decreased oligodendrocyte number |
abnormal sensory neuron innervation pattern |
abnormal optic nerve morphology |
abnormal optic disk morphology |
absent optic nerve |
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Availability | Mouse Genotype | ||||||||||||||
Bmp4tm1b(EUCOMM)Hmgu/Bmp4tm1b(EUCOMM)Hmgu | |||||||||||||||
Bmp4tm1Blh/Bmp4tm1Blh | |||||||||||||||
Bmp4tm1b(EUCOMM)Hmgu/Bmp4+ | |||||||||||||||
Bmp4tm1Blh/Bmp4+ | |||||||||||||||
Tg(Eno2-Bmp4)3Jake/0 | |||||||||||||||
Bmp4tm3Blh/Bmp4tm3Blh Foxg1tm1(cre)Skm/Foxg1+ (conditional) |
* |
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 05/14/2024 MGI 6.23 |
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