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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Arl6tm2Vcs
targeted mutation 2, Val C Sheffield
MGI:5310744
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Arl6tm2Vcs/Arl6tm2Vcs B6.129-Arl6tm2Vcs MGI:7449243
hm2
Arl6tm2Vcs/Arl6tm2Vcs involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5310750


Genotype
MGI:7449243
hm1
Allelic
Composition
Arl6tm2Vcs/Arl6tm2Vcs
Genetic
Background
B6.129-Arl6tm2Vcs
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Arl6tm2Vcs mutation (4 available); any Arl6 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice are born at normal Mendelian ratios but die within 2-3 h after birth likely due to congenital heart defects

cardiovascular system
• all embryos exhibit complete atrioventricular septum defect at E14.5

homeostasis/metabolism
• mice exhibit cyanosis at postpartum

respiratory system
• at E14.5, the size of the growing nasal septum is reduced toward the ventral side
• mice exhibit panting at postpartum

craniofacial
• frontal part of the cranial base is dysmorphic at E18.5; the spheno-ethmoidal and intrasphenoidal synchondroses are cleaved in the midline of the cranial base
• no cartilaginous tissues are present in unmineralized areas in the midline of the cranial base at E18.5
• at E18.5, the cranial base is longitudinally shortened and bilaterally expanded, with a big gap in the midline cartilaginous structures including the synchondrosis
• at E14.5, the cranial base is already partially fused at intrasphenoidal and spheno-occipital synchondroses and shows an abnormal gap in the midline
• no condensation of ectomesenchymal cells is detectable in the developing cranial base at E12.5
• at E18.5, the basioccipital bone occasionally shows a gap filled with fibroblastic-like cells in the mid-sagittal portion of the calcified tissues surrounded by well-defined periosteum at both ends
• cranial base is longitudinally shorter at E18.5, as determined by the distance from the anterior border of maxilla to the anterior edge of basioccipital bone
• at E18.5, the spheno-ethmoidal and intrasphenoidal synchondroses are cleaved in the midline of the cranial base
• no defined intrasphenoidal synchondrosis connecting the presphenoid and the basisphenoid is detected at E18.5
• a bilateral pair of rod-like trabecular cartilages are not fused in the midline and are instead filled with fibrous connective tissues
• at E18.5, the spheno-occipital synchondrosis is partially cleaved and longitudinally elongated compared to the other synchondroses
• cartilage tissues of spheno-occipital synchondrosis appear to expand laterally and thicken dorso-ventrally but fail to fuse in the midline
• contour of the frontal bone to the nasal bone is steeper
• however, no obvious changes are detected in the morphology or length of the calvarium
• marked defects in sphenoidal bones at E18.5
• at E18.5, the width of the basisphenoid is significantly increased relative to that in wild-type controls
• at E14.5, the primordium of basisphenoid is not properly shaped, presenting a huge hall in the middle
• round foramen in the midline of the basisphenoid at E18.5
• presphenoid is sometimes totally absent at E18.5
• presphenoid is severely hypomorphic at E18.5
• the cartilaginous primordium of presphenoid is absent at E14.5
• a huge solitary upper incisor is found in the premaxilla at E18.5
• no unmineralized mid-sagittal mesenchymal structures are observed
• no tooth buds are seen at E18.5 or a single hall is occasionally observed at the center
• no gross abnormalities are seen on other parts of tooth germs including molars
• at E14.5, the bilateral dental laminae are formed in close proximity and fused to form single and a shallow invagination in the midline with excess condensation of ectomesenchymal cells
• at E18.5, premaxillary bones are fused in the midline completely or incompletely, sometimes with a single hall at the center
• premaxillary shelves are hypomorphic or missing at E18.5
• fused premaxilla are occasionally observed at E14.5
• bilateral vomer wings are already fused and filled with bone at E18.5; no unmineralized mid-sagittal mesenchymal structures are observed
• at E14.5, ectomesenchymal cells condense only at the tip of the nasal septum, possibly corresponding to the midline fusion of the vomer wings seen at E18.5
• mice exhibit a dome-shaped cranium at postpartum, due to the presence of a shorter cranial base against the normal growing calvarium
• approximately one third of mice exhibit cleft lip and/or cleft palate at E18.5
• approximately one third of mice exhibit cleft lip and/or cleft palate at E18.5
• approximately one third of mice exhibit an unfused secondary palate at E18.5
• at E14.5, the size of the growing nasal septum is reduced toward the ventral side

skeleton
N
• primary rib chondrocytes isolated from E18.5 embryos show normal induction of Gli1 expression in response to smoothened agonist (SAG), suggesting that the transcriptional response to hedgehog signaling is normal
• frontal part of the cranial base is dysmorphic at E18.5; the spheno-ethmoidal and intrasphenoidal synchondroses are cleaved in the midline of the cranial base
• no cartilaginous tissues are present in unmineralized areas in the midline of the cranial base at E18.5
• at E18.5, the cranial base is longitudinally shortened and bilaterally expanded, with a big gap in the midline cartilaginous structures including the synchondrosis
• at E14.5, the cranial base is already partially fused at intrasphenoidal and spheno-occipital synchondroses and shows an abnormal gap in the midline
• no condensation of ectomesenchymal cells is detectable in the developing cranial base at E12.5
• at E18.5, the basioccipital bone occasionally shows a gap filled with fibroblastic-like cells in the mid-sagittal portion of the calcified tissues surrounded by well-defined periosteum at both ends
• cranial base is longitudinally shorter at E18.5, as determined by the distance from the anterior border of maxilla to the anterior edge of basioccipital bone
• at E18.5, the spheno-ethmoidal and intrasphenoidal synchondroses are cleaved in the midline of the cranial base
• no defined intrasphenoidal synchondrosis connecting the presphenoid and the basisphenoid is detected at E18.5
• a bilateral pair of rod-like trabecular cartilages are not fused in the midline and are instead filled with fibrous connective tissues
• at E18.5, the spheno-occipital synchondrosis is partially cleaved and longitudinally elongated compared to the other synchondroses
• cartilage tissues of spheno-occipital synchondrosis appear to expand laterally and thicken dorso-ventrally but fail to fuse in the midline
• contour of the frontal bone to the nasal bone is steeper
• however, no obvious changes are detected in the morphology or length of the calvarium
• marked defects in sphenoidal bones at E18.5
• at E18.5, the width of the basisphenoid is significantly increased relative to that in wild-type controls
• at E14.5, the primordium of basisphenoid is not properly shaped, presenting a huge hall in the middle
• round foramen in the midline of the basisphenoid at E18.5
• presphenoid is sometimes totally absent at E18.5
• presphenoid is severely hypomorphic at E18.5
• the cartilaginous primordium of presphenoid is absent at E14.5
• a huge solitary upper incisor is found in the premaxilla at E18.5
• no unmineralized mid-sagittal mesenchymal structures are observed
• no tooth buds are seen at E18.5 or a single hall is occasionally observed at the center
• no gross abnormalities are seen on other parts of tooth germs including molars
• at E14.5, the bilateral dental laminae are formed in close proximity and fused to form single and a shallow invagination in the midline with excess condensation of ectomesenchymal cells
• at E18.5, premaxillary bones are fused in the midline completely or incompletely, sometimes with a single hall at the center
• premaxillary shelves are hypomorphic or missing at E18.5
• fused premaxilla are occasionally observed at E14.5
• bilateral vomer wings are already fused and filled with bone at E18.5; no unmineralized mid-sagittal mesenchymal structures are observed
• at E14.5, ectomesenchymal cells condense only at the tip of the nasal septum, possibly corresponding to the midline fusion of the vomer wings seen at E18.5
• mice exhibit a dome-shaped cranium at postpartum, due to the presence of a shorter cranial base against the normal growing calvarium
• 63% of mice exhibit asymmetric fusion of sternum at E18.5
• however, appendicular long bones appear morphologically normal

growth/size/body
N
• mice show normal body weight at E18.5
• a huge solitary upper incisor is found in the premaxilla at E18.5
• no unmineralized mid-sagittal mesenchymal structures are observed
• no tooth buds are seen at E18.5 or a single hall is occasionally observed at the center
• no gross abnormalities are seen on other parts of tooth germs including molars
• at E14.5, the bilateral dental laminae are formed in close proximity and fused to form single and a shallow invagination in the midline with excess condensation of ectomesenchymal cells
• approximately one third of mice exhibit cleft lip and/or cleft palate at E18.5
• approximately one third of mice exhibit cleft lip and/or cleft palate at E18.5
• approximately one third of mice exhibit an unfused secondary palate at E18.5
• at E14.5, the size of the growing nasal septum is reduced toward the ventral side
• no condensation of ectomesenchymal cells is detectable in the developing cranial base at E12.5

embryo
• no condensation of ectomesenchymal cells is detectable in the developing cranial base at E12.5

digestive/alimentary system
• approximately one third of mice exhibit cleft lip and/or cleft palate at E18.5
• approximately one third of mice exhibit an unfused secondary palate at E18.5

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Bardet-Biedl syndrome 3 DOID:0110125 OMIM:600151
J:257068




Genotype
MGI:5310750
hm2
Allelic
Composition
Arl6tm2Vcs/Arl6tm2Vcs
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Arl6tm2Vcs mutation (4 available); any Arl6 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
N
• inner nuclear and ganglion cell layers of retina are normal

nervous system
• ependymal cilia display a chaotic beating pattern
• reduced number and misshapen ependymal cell cilia
• paddle shaped cilia with terminal dilatations seen in culture
• reduced number of ependymal cell cilia
• severe hydrocephalus
• corpus striatum reduced in size
• increased renal sympathetic nerve activity

reproductive system
• sperm in seminiferous tubules of 4 month old homozygotes lack flagella
• males fail to produce offspring

craniofacial
• splaying of cranial sutures

cellular
N
• primary cilia are normal
• reduced number and misshapen ependymal cell cilia
• paddle shaped cilia with terminal dilatations seen in culture
• reduced number of ependymal cell cilia
• sperm in seminiferous tubules of 4 month old homozygotes lack flagella
• ependymal cilia display a chaotic beating pattern

adipose tissue
• increased fat mass but body weight is normal

cardiovascular system
• increased 24 hour arterial blood pressure

behavior/neurological
N
• mice are not hyperphagic

skeleton
• splaying of cranial sutures





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory