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Phenotypes Associated with This Genotype
Genotype
MGI:7336104
Allelic
Composition
Sdccag8em1Lji/Sdccag8em1Lji
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sdccag8em1Lji mutation (0 available); any Sdccag8 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 45% of mice die within 24 hours of birth
• only 9.1% of mice, lower than the expected 25%, are seen at birth

growth/size/body
• mice have reduced body weight at P30
• small cysts form in the cortical region of the kidney at P30
• kidneys progressively deteriorate from P90 to P180, with renal cysts spreading beyond the cortical region to the corticomedullary junction and becoming enlarged, and renal parenchyma replaced by interstitial infiltrates
• mice have normal body size at birth but are smaller at P30, indicating developmental retardation
• mice show kidney enlargement as early as P30 and kidneys become progressively larger at P90 and deformed at P180

reproductive system
• all males are infertile

vision/eye
• apoptosis is detected in the outer nuclear layer at P21, indicating that outer segment protein mislocalization occurs after photoreceptor cell death
• photoreceptors show progressive mislocalization of phototransduction proteins
• mice exhibit shortened connecting cilium and disorganized outer segment compartments, with significantly deteriorated disk membranes at P60, indicating that structure of photoreceptor cilia is destroyed
• photoreceptor outer segments are about half as short as that of controls at P30
• shortening of the outer segments progresses rapidly from P30 to P180
• mice show reduced cone outer segment at P180
• early-onset and rapidly progressive photoreceptor degeneration; rods degenerate earlier and faster than cones, presenting as rod-cone degeneration
• loss of cones is seen at P180 but not at P90, indicating late-onset cone degeneration
• mice have only 4 rows of photoreceptor nuclei left in the outer nuclear layer at P90 and two rows at P180, indicating severe retinal degeneration
• mice have only around 6 rows of photoreceptor nuclei lining the retinal outer nuclear layer at P30
• shortening of the outer nuclear layer progresses rapidly from P30 to P180
• scotopic ERG shows that a-wave amplitudes are decreased by 53% at P30
• scotopic ERG responses decline by 78% at P90 and by 93% by P180
• photopic ERG shows that b-wave amplitudes are decreased by 38% at P30
• photopic ERG responses decrease by 71% at P90 and 91% by P180

cellular
• primary cilium formation is seen only in 8% of mouse embryonic fibroblasts (MEFs) compared to 80% of wild-type MEFs
• the average lengths of cilia in MEFs are shorter
• renal epithelial cilia are completely absent in the distal convoluted tubules and cortical collecting ducts of the kidneys
• mice exhibit shortened connecting cilium and disorganized outer segment compartments, with significantly deteriorated disk membranes at P60, indicating that structure of photoreceptor cilia is destroyed
• apoptosis is detected in the outer nuclear layer at P21, indicating that outer segment protein mislocalization occurs after photoreceptor cell death

homeostasis/metabolism
• 24 hour urine albumin to creatinine ratios are elevated 3.3 times compared to wild-type, indicating proteinuria and chronic kidney disease progression by P180

limbs/digits/tail
• 100% penetrance of preaxial polydactyly in the hindlimbs
• bilateral polydactyly is predominant, accounting for 80% of mice
• among the mice with unilateral polydactyly 75% present with right-sided polydactyly

nervous system
• photoreceptors show progressive mislocalization of phototransduction proteins
• mice exhibit shortened connecting cilium and disorganized outer segment compartments, with significantly deteriorated disk membranes at P60, indicating that structure of photoreceptor cilia is destroyed
• photoreceptor outer segments are about half as short as that of controls at P30
• shortening of the outer segments progresses rapidly from P30 to P180
• mice show reduced cone outer segment at P180
• early-onset and rapidly progressive photoreceptor degeneration; rods degenerate earlier and faster than cones, presenting as rod-cone degeneration
• loss of cones is seen at P180 but not at P90, indicating late-onset cone degeneration

renal/urinary system
• 24 hour urine albumin to creatinine ratios are elevated 3.3 times compared to wild-type, indicating proteinuria and chronic kidney disease progression by P180
• mice exhibit early-onset nephronophthisis
• mice display nephronophthisis and develop chronic kidney disease with an earlier onset than Sdccag8em2Lji homozygotes
• renal epithelial cilia are completely absent in the distal convoluted tubules and cortical collecting ducts of the kidneys
• small cysts form in the cortical region of the kidney at P30
• kidneys progressively deteriorate from P90 to P180, with renal cysts spreading beyond the cortical region to the corticomedullary junction and becoming enlarged, and renal parenchyma replaced by interstitial infiltrates
• mice show kidney enlargement as early as P30 and kidneys become progressively larger at P90 and deformed at P180
• mice show rapidly progressive renal fibrosis, from mild fibrosis surrounding the dilated tubules at P30 and P90 to extensive collagen deposits distributed across renal tissue at P180

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Bardet-Biedl syndrome 16 DOID:0110138 OMIM:615993
J:328191


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
11/12/2024
MGI 6.24
The Jackson Laboratory