LABOKLIN (UK)|Genetic Diseases | Dogs| Factor VII Deficiency
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Factor VII Deficiency
Breeds
Airedale , Alaskan Klee Kai , Beagle , Giant Schnauzer , Scottish Deerhound .
The Disease
Factor VII deficiency is a mild bleeding disorder caused by lack of factor VII (proconvertin) which plays a role in the blood clotting system. Affected dogs bruise easily and nosebleeds maybe seen. There is often prolonged bleeding after surgery or trauma and, in the cases of major surgical procedures or trauma, bleeding maybe severe.

The condition may go unnoticed for long time and discovered only when a surgery is performed or if the dog had an accident, in both cases increased bleeding will be noticed which can be difficult to control. Your vet will suspect a bleeding disorder.

Trait of Inheritance
Factor V Deficiency follows an autosomal recessive mode of inheritance.

Inheritance : AUTOSOMAL RECESSIVE trait


 

Sire

  Dam   Offspring
         
Clear
x
Clear
>
100% Clear
         
clear
x
carrier
>
50%  Clear + 50% carriers
         
clear
x
affected
>
100% carriers
         
carrier
x
Clear
>
50%  Clear + 50% carriers
         
carrier
x
carrier
>
25% clear + 25% affected + 50% carriers
         
carrier
x
affected
>
50% carriers + 50% affected
         
affected
x
Clear
>
100%  carriers
         
affected
x
carrier
>
50% carriers + 50% affected
         
affected
x
affected
>
100% affected

 


Clear

Genotype: N / N [ Homozygous normal ]

The dog is noncarrier of the mutant gene.

The dog will never develop Factor VII Deficiency and therefore it can be bred to any other dog.

 

Carrier

Genotype: N / FVII [ Heterozygous ]

The dog carries one copy of the mutant gene and one copy of the normal gene.

The dog will never develop Factor VII Deficiency 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 dogs.

Avoid breeding carrier to carrier because 25% of their offspring is expected to be affected (see table above)

 

Affected

Genotype: FVII / FVII [ Homozygous mutant ]

 

The dog carries two copies of the mutant gene and therefore it will pass the mutant gene to its entire offspring.

The dog will develop Factor VII Deficiency and will pass the mutant gene to its entire offspring
Description

Recently, the mutation responsible for this condition has been identified by Dr Urs Giger and researchers at the University of Pennsylvania. The test is now available at LABOKLIN. Factor VII deficiency follows a recessive trait of inheritance, the test identify a dog as affected (2 copies of the abnormal gene), clear (0 copies of the abnormal gene) or carrier (1 copy of the abnormal gene). Only affected dogs with two copies of the affected gene will develop the disease. Since this is am autosomal recessive condition, carrier dogs will not develop the disease but will pass the mutation to their offspring.

Sample Requirements
Whole blood in EDTA tube (0.5 - 1 ml) or Buccal Swabs.
Turnaround
withing 7 working days
Price
£ 49.99 (including VAT)

To order:

  • Download Order Form from this link pdf

  • Complete the order form and send it together with your samples to the following address:

    Laboklin (UK),   61 Mouldsworth Ave, Manchester M20 1GG

See Also:
Copper Toxicosis  
Degenerative Myelopathy  
Globoid Cell Leukodystrophy (Krabbe Disease)  
CSNB (Congenital Stationary Night Blindness)  
CLAD (Canine Leukocyte Adhesion Deficiency)  
Cystinuria  
von-Willebrand disease type II (vWD II)  
PK Deficiency (Pyruvate Kinase Deficiency)  
Fucosidosis  
PFK Deficiency (Phosphofructokinase deficiency)  
Myotonia Congenita  
MH (Malignant Hyperthermia)  
X-SCID (X-Linked Severe Combined Immunodeficiency)  
GM1-Gangliosidosis  
Narcolepsy  
GRMD (Golden Retriever Muscular Dystrophy)  
MPS ( Mucopolysaccharidosis type VII)  
Hereditary Myopathy / Centronuclear Myopathy (HMLR, CNM)  
Canine Cyclic Neutropenia (Gray Collie Syndrome)  
cord1- PRA ( Cone-rod dystrophy 1 )  
prcd - PRA ( Progressive Retinal Atrophy )  
L-2-HGA ( L- 2 - hydroxyglutaric aciduria )  
von Willebrand disease Type I (vWD I)  
von Willebrand disease Type III (vWD III)  
Neuronal Ceroid Lepofuscinosis ( NCL )  
Trapped Neutrophil Syndrome ( TNS ) *  
crd PRA (Cone-rod dystrophy form of PRA)  
PDP 1 Deficiency (Pyruvate Dehydrogenase Phosphatase 1 Deficiency)  
rcd1 PRA (Progressive Retinal Atrophy)  
rcd3 PRA (Progressive Retinal Atrophy)  
rcd1a PRA (Progressive Retinal Atrophy)  
MDR1 Gene Defect / Ivermectin Sensitivity  
Exercise Induced Collapse ( EIC )  
Dwarfism (Pituitary Dwarfism / Hypopituitarism)  
PRA (Progressive Retinal Atrophy)  

 
 
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