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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Arl6
ADP-ribosylation factor-like 6
MGI:1927136
56 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Arl6tm1Vcs/Arl6tm1Vcs
129S.129-Arl6tm1Vcs 		disorganized photoreceptor inner segment J:159222
normal growth/size/body region phenotype J:159222
Arl6tm2Vcs/Arl6tm2Vcs
B6.129-Arl6tm2Vcs 		abnormal basicranium morphology J:257068
abnormal basioccipital bone morphology J:257068
abnormal basisphenoid bone morphology J:257068
abnormal cranial synchondrosis J:257068
abnormal dental lamina morphology J:257068
abnormal ectomesenchyme morphology J:257068
abnormal frontal bone morphology J:257068
abnormal premaxilla morphology J:257068
abnormal presphenoid synchondrosis J:257068
abnormal sphenoid bone morphology J:257068
abnormal sphenooccipital synchondrosis J:257068
abnormal tooth development J:257068
abnormal upper incisor morphology J:257068
abnormal vomer bone morphology J:257068
absent presphenoid bone J:257068
basisphenoid bone foramen J:257068
cleft palate J:257068
cleft secondary palate J:257068
cleft upper lip J:257068
complete atrioventricular septal defect J:257068
cyanosis J:257068
domed cranium J:257068
normal growth/size/body region phenotype J:257068
midface hypoplasia J:257068
neonatal lethality, complete penetrance J:257068
presphenoid bone hypoplasia J:257068
respiratory distress J:257068
short basicranium J:257068
normal skeleton phenotype J:257068
small nasal septum J:257068
sternebra fusion J:257068
Arl6tm2Vcs/Arl6tm2Vcs
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal brain ependyma motile cilium morphology J:180524
abnormal brain ependyma motile cilium physiology J:180524
abnormal brain ventricular system morphology J:180524
abnormal retina neuronal layer morphology J:180524
abnormal retina outer nuclear layer morphology J:180524
abnormal retina photoreceptor morphology J:180524
abnormal sympathetic nervous system physiology J:180524
abnormal telencephalon morphology J:180524
absent photoreceptor inner segment J:180524
absent photoreceptor outer segment J:180524
absent sperm flagellum J:180524
normal behavior/neurological phenotype J:180524
normal cellular phenotype J:180524
decreased brain ependyma motile cilium number J:180524
decreased striatum size J:180524
domed cranium J:180524
hydrocephaly J:180524
increased heart rate J:180524
increased percent body fat/body weight J:180524
increased systemic arterial blood pressure J:180524
male infertility J:180524
small hippocampus J:180524
thin cerebral cortex J:180524
normal vision/eye phenotype J:180524
wide cranial sutures J:180524
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
12/10/2024
MGI 6.24 		The Jackson Laboratory