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Symbol
Name
ID
Morc2a
microrchidia 2A
MGI:1921772
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Congenital finger flexion contractures
Flexion contracture of finger
Split hand
Joint contracture of the hand
Scoliosis
Disease(s) Associated with MORC2
Charcot-Marie-Tooth disease axonal type 2Z

Mouse Phenotypes
basisphenoid bone foramen
abnormal Meckel's cartilage morphology
fragmented Meckel's cartilage
abnormal occipital bone morphology
absent occipital bone
abnormal sphenoid bone morphology
absent neurocranium
abnormal hyoid bone body morphology
abnormal jaw morphology
abnormal incisor morphology
absent upper incisors
domed cranium
abnormal middle ear ossicle morphology
abnormal stapes morphology
abnormal carpal bone morphology
abnormal humerus morphology
absent humerus
abnormal radius morphology
absent radius
abnormal ulna morphology
abnormal clavicle morphology
abnormal scapula morphology
abnormal rib morphology
abnormal vertebral arch morphology
abnormal vertebral body morphology
absent vertebral body
Availability Mouse Genotype
Morc2aem1(IMPC)Wtsi/Morc2aem1(IMPC)Wtsi
Morc2atm1.1Pngr/Morc2atm1.1Pngr
Tg(Nes-cre)1Kln/0  (conditional)

Contributing Projects:
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
04/16/2024
MGI 6.23
The Jackson Laboratory