Morc2a Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Morc2a
microrchidia 2A
MGI:1921772

170 phenotypes from 5 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Morc2a^{em1(IMPC)Wtsi}/Morc2a⁺ C57BL/6N-Morc2a^{em1(IMPC)Wtsi}/WtsiOulu	decreased circulating HDL cholesterol level	J:211773
Morc2a^{em1(IMPC)Wtsi}/Morc2a^{em1(IMPC)Wtsi} C57BL/6N-Morc2a^{em1(IMPC)Wtsi}/WtsiOulu	aberrant origin of the right subclavian artery	J:239583
	abnormal adrenal gland morphology	J:239583
	abnormal anterior cerebral artery morphology	J:239583
	abnormal atrioventricular cushion morphology	J:239583
	abnormal brain internal capsule morphology	J:239583
	abnormal brain morphology	J:239583
	abnormal carpal bone morphology	J:239583
	abnormal celiac artery morphology	J:239583
	abnormal choroid plexus morphology	J:239583
	abnormal clavicle morphology	J:239583
	abnormal common bile duct morphology	J:239583
	abnormal diaphragm morphology	J:239583
	abnormal dorsal pancreas topology	J:239583
	abnormal ductus venosus topology	J:239583
	abnormal external auditory canal morphology	J:239583
	abnormal eye muscle morphology	J:239583
	abnormal facial nerve topology	J:239583
	abnormal forebrain morphology	J:239583
	abnormal forelimb morphology	J:239583
	abnormal head morphology	J:239583
	abnormal hindbrain morphology	J:239583
	abnormal humerus morphology	J:239583
	abnormal hyoid bone body morphology	J:239583
	abnormal hypoglossal nerve topology	J:239583
	abnormal incisor morphology	J:239583
	abnormal inferior vena cava morphology	J:239583
	abnormal infrahyoid muscle connection	J:239583
	abnormal inner ear morphology	J:239583
	abnormal interatrial septum morphology	J:239583
	abnormal internal carotid artery topology	J:239583
	abnormal intestine placement	J:239583
	abnormal intrathoracic topology of vagus nerve	J:239583
	abnormal jaw morphology	J:239583
	abnormal left lung morphology	J:239583
	abnormal lens morphology	J:239583
	abnormal liver morphology	J:239583
	abnormal liver vasculature morphology	J:239583
	abnormal masticatory muscle morphology	J:239583
	abnormal Meckel's cartilage morphology	J:239583
	abnormal middle ear morphology	J:239583
	abnormal middle ear ossicle morphology	J:239583
	abnormal Mullerian duct morphology	J:239583
	abnormal nasal cavity morphology	J:239583
	abnormal nasal septum morphology	J:239583
	abnormal occipital bone morphology	J:239583
	abnormal olfactory bulb morphology	J:239583
	abnormal olfactory bulb position	J:239583
	abnormal olfactory nerve morphology	J:239583
	abnormal optic cup morphology	J:239583
	abnormal optic stalk morphology	J:239583
	abnormal pectinate muscle morphology	J:239583
	abnormal pineal gland morphology	J:239583
	abnormal pituitary gland morphology	J:239583
	abnormal radius morphology	J:239583
	abnormal rib morphology	J:239583
	abnormal right lung morphology	J:239583
	abnormal salivary gland morphology	J:239583
	abnormal scapula morphology	J:239583
	abnormal sphenoid bone morphology	J:239583
	abnormal stapes morphology	J:239583
	abnormal subclavian artery origin	J:239583
	abnormal testis morphology	J:239583
	abnormal thymus topology	J:239583
	abnormal thyroid gland morphology	J:239583
abnormal ulna morphology	J:239583
abnormal ureter topology	J:239583
abnormal vertebral arch morphology	J:239583
abnormal vertebral artery origin	J:239583
abnormal vertebral body morphology	J:239583
abnormal vitelline vein connection	J:239583
abnormal vomeronasal organ morphology	J:239583
abnormal Wolffian duct morphology	J:239583
abnormal Wolffian duct topology	J:239583
absent connection between subcutaneous lymph vessels and lymph sac	J:239583
absent digastric muscle	J:239583
absent ductus venosus valve	J:239583
absent external auditory canal	J:239583
absent eye muscles	J:239583
absent humerus	J:239583
absent intracranial segment of vertebral artery	J:239583
absent intrahepatic inferior vena cava segment	J:239583
absent mandibular nerve	J:239583
absent Mullerian ducts	J:239583
absent neurocranium	J:239583
absent occipital bone	J:239583
absent optic chiasm	J:239583
absent pituitary gland	J:239583
absent posterior communicating artery	J:239583
absent radius	J:239583
absent salivary gland	J:239583
absent segment of anterior cerebral artery	J:239583
absent stapedial artery	J:239583
absent superior cervical ganglion	J:239583
absent upper incisors	J:239583
absent ventral pancreas	J:239583
absent vertebral body	J:239583
absent Wolffian ducts	J:239583
aphakia	J:239583
athymia	J:239583
basisphenoid bone foramen	J:239583
blood in lymph vessels	J:239583
diaphragmatic hernia	J:239583
double inlet heart right ventricle	J:239583
double outlet right ventricle	J:239583
embryonic growth retardation	J:239583
enlarged brain ventricles	J:239583
facial cleft	J:239583
fragmented Meckel's cartilage	J:239583
heterochrony	J:239583
holoprosencephaly	J:239583
increased trigeminal neuroma incidence	J:239583
intracerebral hemorrhage	J:239583
left sided brachiocephalic trunk	J:239583
liver cyst	J:239583
muscular ventricular septal defect	J:239583
oligodactyly	J:239583
perimembraneous ventricular septal defect	J:239583
persistent dorsal ophthalmic artery	J:239583
persistent truncus arteriosus	J:239583
preweaning lethality, complete penetrance	J:211773
reduced sympathetic cervical ganglion size	J:239583
retroesophageal left subclavian artery	J:239583
right aortic arch	J:239583
short tongue	J:239583
small adrenal glands	J:239583
small dorsal pancreas	J:239583
small kidney	J:239583
small ovary	J:239583
small pancreas	J:239583
small thymus	J:239583
small thyroid gland	J:239583
small trigeminal ganglion	J:239583
small ventral pancreas	J:239583
subcutaneous edema	J:239583
thoracoschisis	J:239583
tongue hypoplasia	J:239583
Morc2a^em1Snupy/Morc2a⁺ involves: C57BL/6	abnormal action potential	J:341847
	abnormal cognition	J:341847
	abnormal myelination	J:341847
	ataxia	J:341847
	cerebellum atrophy	J:341847
	decreased locomotor activity	J:341847
	decreased nerve conduction velocity	J:341847
	decreased Purkinje cell number	J:341847
	decreased spinal cord ventral horn cell number	J:341847
	impaired coordination	J:341847
	increased neuron apoptosis	J:341847
	limb grasping	J:341847
	normal muscle phenotype	J:341847
	paraparesis	J:341847
	prenatal lethality, incomplete penetrance	J:341847
	skeletal muscle atrophy	J:341847
	skeletal muscle fiber atrophy	J:341847
Morc2a^em1Snupy/Morc2a^em1Snupy involves: C57BL/6	prenatal lethality, complete penetrance	J:341847
Morc2a^tm1.1Pngr/Morc2a^tm1.1Pngr Tg(Nes-cre)1Kln/0 involves: 129P2/OlaHsd * C57BL/6 * SJL	abnormal corpora quadrigemina morphology	J:332344
	abnormal neuron physiology	J:332344
	normal behavior/neurological phenotype	J:332344
	decreased body size	J:332344
	decreased body weight	J:332344
	decreased grip strength	J:332344
	decreased locomotor activity	J:332344
	domed cranium	J:332344
	enhanced contextual conditioning behavior	J:332344
	impaired coordination	J:332344
	increased brain size	J:332344
	increased midbrain size	J:332344
	premature death	J:332344
Morc2a^tm1.2Pngr/Morc2a^tm1.2Pngr involves: 129P2/OlaHsd * C57BL/6N * FVB/N	decreased embryo size	J:332344
	embryonic lethality during organogenesis, complete penetrance	J:332344
Morc2a^{tm1b(KOMP)Wtsi}/Morc2a⁺ C57BL/6N-Morc2a^{tm1b(KOMP)Wtsi}/Bay	abnormal gait	J:211773
Morc2a^{tm1b(KOMP)Wtsi}/Morc2a^{tm1b(KOMP)Wtsi} C57BL/6N-Morc2a^{tm1b(KOMP)Wtsi}/Bay	prenatal lethality prior to heart atrial septation	J:211773
	preweaning lethality, complete penetrance	J:211773

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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