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Glycogen Storage Disease ( GSD ) Type IV
Test number: 8113
Gene: GSDIV Price: £ 48.00 (including VAT)
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Update 25/11/2011 price of Glycogen Storage Disease ( GSD ) Type IV in Norwegian Forest Cats has been reduced to £49.95 (VAT included)
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Breed
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Norwegian Forest Cat
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The Disease |
Glycogen storage disease type IV (GSD IV) of the Norwegian forest cat is an
inherited abnormality of glucose metabolism. Normally, excess glucose is stored in
many tissues as glycogen. If energy is needed, glucose molecules are removed from
glycogen. The ability to add and remove glucose molecules from glycogen efficiently
is dependent on its highly branched structure. The glycogen branching enzyme
(GBE) is an enzyme of glycogen synthesis necessary to produce the branching
structure.
Deficiency of GBE activity leads to abnormal glycogen accumulation in myocytes,
hepatocytes, and neurones, causing variably progressive, benign to lethal organ
dysfunctions.
Most affected kittens die at or soon after bird, presumably due to hypoglycemia.
Survivors of the perinatal period appear clinically normal until onset of progressive
neuromuscular degeneration at 5 month of age.
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Description |
By DNA testing, the responsible mutation can be shown directly. This method
provides a very high accuracy test and can be done at any age. It offers the
possibility to distinguish not only between affected and clear cats, but also to identify
clinically healthy carriers. This is an essential information for controlling the disease
in the breed, as carriers are able to spread the disease in the population, but can not
be identified by means of common laboratory diagnostic.
To ensure maximum test reliability, the test is always performed in two independent
test runs per sample.
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Trait of Inheritance |
The mutation and inheritance
The mutation in the GBE1 gene which has been suggested to cause GSD-IV has
recently been published by the group of John C. Fyfe at the University of Michigan,
USA.
GSD IV is inherited as an autosomal recessive trait. So there are three conditions a
cat can be: it can be clear or homozygous normal (genotype N/N) meaning that it
does not carry the mutation and will not develop GSD IV. Since it also cannot pass
the mutation onto its offspring, it can be mated to any other cat.
A cat which has one copy of the GBE1 gene with the mutation and one copy without
the mutation is called a carrier or heterozygous (genotype N/GSD-IV); while it will not
be affected by GSD IV, it can pass the mutation onto its offspring and should
therefore only be mated to clear cats.
Affected kitten have two GBE1 gene copies with the mutation (genotype GSDIV/
GSD-IV or homozygous affected); they will always pass the mutated gene onto
their offspring.
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Inheritance : AUTOSOMAL
RECESSIVE
trait
Sire
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Dam
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Offspring
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clear
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clear
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100% clear
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clear
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carrier
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50% clear + 50%
carriers
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clear
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affected
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100% carriers
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carrier
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clear
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50% clear + 50%
carriers
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carrier
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carrier
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25% clear + 25% affected
+ 50% carriers
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carrier
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affected
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50% carriers + 50%
affected
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affected
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clear
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100% carriers
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affected
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carrier
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50% carriers + 50%
affected
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affected
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affected
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100% affected
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Clear
Genotype: N / N [ Homozygous normal ]
The cat is noncarrier of the mutant gene.
It is very unlikely that the cat will develop Glycogen Storage Disease ( GSD ) Type IV. The cat will never pass the mutation to its offspring, and therefore it can be bred to any other cat.
Carrier
Genotype: N / GSDIV [ Heterozygous ]
The cat carries one copy of the mutant gene and one
copy of the normal gene.
It is very unlikely that the cat will develop Glycogen Storage Disease ( GSD ) Type IV but since it carries the mutant gene, it can pass it on to its offspring with the probability of 50%. Carriers should only be bred to clear cats. Avoid breeding carrier to carrier because 25% of their offspring is expected to be affected (see table above)
Affected
Genotype: GSDIV / GSDIV [ Homozygous mutant ]
The cat carries two copies of the mutant gene and
therefore it will pass the mutant gene to its entire offspring.
The cat is likely to develop Glycogen Storage Disease ( GSD ) Type IV and will pass the mutant gene to its entire offspring
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Turnaround |
2-3 weeks
We will run this test 2 independant times on your sample to ensure that the result is 100% accurate
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Price
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£ 48.00 (including VAT)
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See also: |
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HCM 1 (Hypertrophic Cardiomyopathy)
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Osteochondrodysplasia (Scottish Fold Osteodystrophy) OCD
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HCM (Hypertrophic Cardiomyopathy HCM3/HCR)
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PKD (Feline Polycystic Kidney Disease)
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PK Deficiency (Pyruvate Kinase Deficiency)
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Progressive Retinal Atrophy ( rdAc - PRA )
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SMA (Spinal Muscular Atrophy )
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Serological Evaluation of blood Groups
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Hypokalemia / Familial Episodic Hypokalaemic Polymyopathy (BHK)
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Head Defect (BHD)
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Alpha-Mannosidosis (AMD)
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Congenital Myasthenic Syndrome (CMS) / Hereditary Myopathy
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Gangliosidosis GM1
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Gangliosidosis GM2
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Gangliosidosis GM2
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Mucopolysaccharidosis Type VI (MPS VI MPS6)
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Mucopolysaccharidosis type VII (MPS VII / MPS7)
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Myotonia Congenita (Fainting Goat)
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Progressive Retinal Atrophy (pd-PRA)
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Progressive Retinal Atrophy (rdy-PRA)
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Hypotrichosis and Short Life Expectancy
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Progressive Retinal Atrophy in Bengal (PRA-b / b-PRA)
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Special Offer: HCM, HCR, GSD4, PKD, PRA, PK-Def., SMA, Blood Groups
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Primary Congenital Glaucoma (PCG)
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Persian DNA bundle (PKD + pd-PRA + AMD + Blood Groups)
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Burmese DNA bundle (Hypokalemia (BHK) + Head Defect + Gangliosidosis (GM2) + Blood Groups
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Birma DNA bundle (PKD + pd-PRA + Hypotrichiose + MPS6 + Blood Groups)
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Maine Coon DNA bundle (HCM1 + SMA + PK-Def + FXI + Blood Groups)
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Ragdoll DNA bundle (HCM1 + HCM3 + PKD + pd-PRA + Blood groups)
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Polydactyly (extra toes) / polydactylism / Polydactyl / hyperdactyly
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Unlisted DNA test
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Blue Eyes
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