LABOGenetics XXL Cat

General description

LABOGenetics XXL Cat can screen your cat for more than 50 genetic variants. You will receive information on hereditary diseases, genetic risk factors, coat colours and coat characteristics. The determination of the genetic blood group is also included. LABOGenetics XXL Cat is available for cats of all breeds and mixes.

Order details

Test number	9330
Sample material	0.5 ml EDTA blood, 1x special swab (eNAT)
Test duration	10-14 working days

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Congenital myasthenic syndrome (CMS)

Test specifications

Symptom complex	muscular
Inheritance	autosomal recessive
Age of onset	3 weeks
Causality	causally
Gene	COLQ
Mutation	C-T
Literature	OMIA:001621-9685

Progressive retinal atrophy (pd-PRA)

Test specifications

Symptom complex	ophthalmic
Inheritance	autosomal recessive
Age of onset	5 weeks
Causality	causally
Gene	AIPL1
Mutation	C-T
Literature	OMIA:001222-9685

Cystinuria

Test specifications

Symptom complex	urological
Inheritance	autosomal recessive
Age of onset	young age
Causality	causally
Gene	SLC7A9
Mutation	T-A
Literature	OMIA:002023-9685

Gangliosidosis (GM2)

Test specifications

Symptom complex	neurological
Inheritance	autosomal recessive
Age of onset	3 months
Causality	causally
Gene	HEXB
Mutation	DEL
Literature	OMIA:001462-9685

Autoimmune lymphoproliferative syndrome (ALPS)

Test specifications

Symptom complex	immunological
Inheritance	autosomal recessive
Age of onset	8 weeks
Causality	causally
Gene	FASLG
Mutation	INS
Literature	OMIA:002064-9685

Hypertrophic cardiomyopathy (HCM4)

Test specifications

Symptom complex	cardiac
Inheritance	autosomal dominant with incomplete penetrance
Age of onset	1-14 years
Causality	causally
Gene	ALMS1
Mutation	G-C
Literature	OMIA:002316-9685

Factor XI deficiency (F11)

Test specifications

Symptom complex	hematologic
Inheritance	autosomal recessive
Causality	associated
Gene	F11
Mutation	G-A
Literature	OMIA:000363-9685

Acrodermatitis enteropathica (AE)

Test specifications

Symptom complex	dermatologic
Inheritance	autosomal recessive
Age of onset	6-8 weeks
Causality	causally
Gene	SLC39A4
Mutation	C-G
Literature	OMIA:000593-9685

Alpha-Mannosidosis (AMD)

Test specifications

Symptom complex	neurological
Inheritance	autosomal recessive
Causality	causally
Gene	MAN2B1
Mutation	DEL
Literature	OMIA:000625-9685

MDR1 gene variant

Test specifications

Symptom complex	metabolic
Inheritance	autosomal recessive
Causality	causally
Gene	ABCB1
Mutation	DEL
Literature	OMIA:001402-9685

Factor XII deficiency (F12)

Test specifications

Symptom complex	hematologic
Inheritance	autosomal recessive
Causality	associated
Gene	F12
Mutation	DEL
Literature	OMIA:000364-9685

Gangliosidosis (GM2)

Test specifications

Symptom complex	neurological
Inheritance	autosomal recessive
Age of onset	2 months
Causality	causally
Gene	HEXB
Mutation	DEL
Literature	OMIA:001462-9685

Hypotrichosis and short life expectancy

Test specifications

Symptom complex	systemic
Inheritance	autosomal recessive
Age of onset	from birth
Causality	causally
Gene	FOXN1
Mutation	DEL
Literature	OMIA:001949-9685

Progressive retinal atrophy (b-PRA)

Test specifications

Symptom complex	ophthalmic
Inheritance	autosomal recessive
Age of onset	7 weeks
Causality	causally
Gene	KIF3B
Mutation	C-T
Literature	OMIA:002267-9685

Osteochondrodysplasia (OCD)

Test specifications

Symptom complex	skeletal
Inheritance	autosomal dominant
Causality	causally
Gene	TRPV4
Mutation	C-A
Literature	OMIA:000319-9685

Primary congenital glaucoma (PCG)

Test specifications

Symptom complex	ophthalmic
Inheritance	autosomal recessive
Age of onset	from birth
Causality	causally
Gene	LTBP2
Mutation	INS
Literature	OMIA:002017-9685

Hypokalaemia

Test specifications

Symptom complex	muscular
Causality	causally
Gene	WNK4
Mutation	C-T
Literature	OMIA:001759-9685

Gangliosidosis (GM1)

Test specifications

Symptom complex	neurological
Inheritance	autosomal recessive
Age of onset	2 months
Causality	causally
Gene	GLB1
Mutation	C-G
Literature	OMIA:000402-9685

Polycystic kidney disease (PKD)

Test specifications

Symptom complex	nephrological
Inheritance	autosomal dominant
Age of onset	8 months
Causality	causally
Gene	PKD1
Mutation	C-A
Literature	OMIA:000807-9685

Pyruvate kinase deficiency (PK)

Test specifications

Symptom complex	hematologic
Inheritance	autosomal recessive
Causality	causally
Gene	PKLR
Mutation	G-A
Literature	OMIA:000844-9685

Myotonia congenita

Test specifications

Symptom complex	muscular
Causality	causally
Gene	CLCN1
Mutation	G-T
Literature	OMIA:000698-9685

Head Defect

Test specifications

Symptom complex	skeletal
Causality	causally
Gene	ALX1
Mutation	DEL
Literature	OMIA:001551-9685

Mucopolysaccharidosis type VI (MPS6)

Test specifications

Symptom complex	systemic
Causality	causally
Gene	ARSB
Mutation	A-G, C-T
Literature	OMIA:000666-9685

Mucopolysaccharidosis type VII (MPS7)

Test specifications

Symptom complex	skeletal
Age of onset	2 months
Causality	causally
Gene	GUSB
Mutation	G-A
Literature	OMIA:000667-9685

Hypertrophic cardiomyopathy (HCM1)

Test specifications

Symptom complex	cardiac
Inheritance	autosomal dominant
Causality	causally
Gene	MYBPC3
Mutation	C-G
Literature	OMIA:000515-9685

Glycogen storage disease type IV (GSD4)

Test specifications

Symptom complex	neuromuscular
Inheritance	autosomal recessive
Age of onset	5 months
Causality	causally
Gene	GBE1
Mutation	COMPLEX
Literature	OMIA:000420-9685

Hypertrophic cardiomyopathy (HCM3)

Test specifications

Symptom complex	cardiac
Inheritance	autosomal dominant
Causality	causally
Gene	MYBPC3
Mutation	G-A
Literature	OMIA:000515-9685

Progressive retinal atrophy (rdAc-PRA)

Test specifications

Symptom complex	ophthalmic
Inheritance	autosomal recessive
Age of onset	1.5-2 years
Causality	causally
Gene	CEP290
Mutation	A-C
Literature	OMIA:001244-9685

Genetic blood group

Test specifications

Symptom complex	hematologic
Inheritance	Allelische Reihe nach Dominanz: N>c>b
Causality	causally
Gene	CMAH
Mutation	COMPLEX
Literature	OMIA:000119-9685

Spinal muscular atrophy (SMA)

Test specifications

Symptom complex	neuromuscular
Inheritance	autosomal recessive
Age of onset	12 weeks
Causality	causally
Gene	LIX1
Mutation	COMPLEX
Literature	OMIA:002389-9685