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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Chrd
chordin
MGI:1313268
100 phenotypes from 2 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Chrdtm1Emdr/Chrdtm1Emdr
129S6.129-Chrdtm1Emdr 		abnormal ear position J:146769
abnormal outer ear development J:146769
abnormal pharyngeal arch artery morphology J:146769
absent mandible J:146769
athymia J:146769
cleft palate J:146769
persistent truncus arteriosus J:146769
short mandible J:146769
Chrdtm1Emdr/Chrdtm1Emdr
either: B6SJL.129-Chrdtm1Emdr or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J) 		abnormal aortic arch morphology J:83662
abnormal artery morphology J:83662
abnormal brachiocephalic trunk morphology J:83662
abnormal common carotid artery morphology J:83662
abnormal cranial ganglia morphology J:83662
abnormal ear position J:83662
abnormal embryonic tissue morphology J:83662
abnormal extraembryonic tissue morphology J:83662
abnormal laryngeal cartilage morphology J:83662
abnormal mandible morphology J:83662
abnormal mesoderm development J:83662
abnormal middle ear morphology J:83662
abnormal neural crest cell migration J:83662
abnormal neural plate morphology J:83662
abnormal oropharynx morphology J:83662
abnormal pharyngeal pouch morphology J:83662
abnormal secondary palate development J:83662
abnormal thoracic vertebrae morphology J:83662
abnormal thyroid gland morphology J:83662
abnormal trigeminal ganglion morphology J:83662
abnormal tympanic ring morphology J:83662
abnormal vertebral arch development J:83662
abnormal vestibulocochlear ganglion morphology J:83662
absent arcus anterior J:83662
absent auditory tube J:83662
absent esophagus J:83662
absent inner ear J:83662
absent mandibular angle J:83662
absent mandibular condyloid process J:83662
absent mandibular coronoid process J:83662
absent mesoderm J:83662
absent nodose ganglion J:83662
absent notochord J:83662
absent parathyroid glands J:83662
absent petrosal ganglion J:83662
absent pharyngeal arches J:83662
absent pulmonary trunk J:83662
absent somites J:83662
absent temporal bone squamous part J:83662
athymia J:83662
cleft secondary palate J:83662
cricoid cartilage hypoplasia J:83662
cyanosis J:83662
decreased body size J:83662
decreased embryo size J:83662
decreased tympanic ring size J:83662
embryonic lethality between somite formation and embryo turning, complete penetrance J:83662
enlarged allantois J:83662
fusion of basioccipital and basisphenoid bone J:83662
heart right ventricle hypertrophy J:83662
hemorrhage J:83662
hydrops fetalis J:83662
hyoid bone hypoplasia J:83662
increased vasodilation J:83662
lethality throughout fetal growth and development, incomplete penetrance J:83662
microcephaly J:83662
palatal shelves fail to meet at midline J:83662
perinatal lethality, complete penetrance J:83662
persistent truncus arteriosus J:83662
presphenoid bone hypoplasia J:83662
retroesophageal right subclavian artery J:83662
right aortic arch J:83662
short zygomatic arch J:83662
small ears J:83662
small geniculate ganglion J:83662
small mandible J:83662
small nodose ganglion J:83662
small otic capsule J:83662
small otic vesicle J:83662
small petrosal ganglion J:83662
small pharynx J:83662
small temporal bone J:83662
small trachea J:83662
small vertebral body J:83662
thyroid cartilage hypoplasia J:83662
thyroid gland hypoplasia J:83662
Chrdtm1Emdr/Chrdtm1Emdr
involves: 129S1/Sv * 129X1/SvJ 		abnormal brain development J:123318
abnormal miniature excitatory postsynaptic currents J:123318
abnormal response to novel object J:123318
abnormal spatial learning J:123318
decreased exploration in new environment J:123318
enhanced long-term potentiation J:123318
enhanced paired-pulse facilitation J:123318
hyperactivity J:123318
increased neurotransmitter release J:123318
normal nervous system phenotype J:123318
perinatal lethality, incomplete penetrance J:123318
Chrdtm1Emdr/Chrdtm1Emdr
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J 		abnormal cardiovascular development J:60303
abnormal ear development J:60303
abnormal inner ear development J:60303
abnormal outer ear development J:60303
abnormal pharyngeal arch morphology J:60303
perinatal lethality, complete penetrance J:60303
Chrdtm1Emdr/Chrdtm1Emdr
involves: 129S1/Sv * 129X1/SvJ * ICR 		normal mortality/aging J:137629
normal renal/urinary system phenotype J:130204
normal reproductive system phenotype J:130204
Chrdtm2.1Vlcg/Chrdtm2.1Vlcg
involves: 129S6/SvEvTac * C57BL/6NTac 		no abnormal phenotype detected J:200671
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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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory