Setsi sa Tlhahlobo ea Liphatsa tsa lefutso bakeng sa Lintja, Likatse le Lipere

Batla pokello ea rona ea tlhahlobo ea DNA ea liphoofolo

Lekola pokello ea rona ea tlhahlobo ea DNA ea liphoofolo e koahelang liteko tsa lefutso bakeng sa lintja, likatse le lipere. Leqephe le leng le le leng la liteko le fana ka lintlha tse qaqileng mabapi le lefutso le amanang le tsona, phetoho, mokhoa oa lefa le bohlokoa ba tleliniki ha bo le teng. Sebaka sena sa polokelo ea boitsebiso se etselitsoe ho tšehetsa balisa, lingaka tsa liphoofolo, lilaboratori le beng ba liphoofolo tse ruuoang lapeng ba batlang tlhahisoleseding e tšepahalang ka mafu a futsitsoeng, matšoao a mebala ea jase le litšobotsi tse ling tsa lefutso. Sebelisa lihloela tsa mefuta e ka tlase kapa batla ka kotloloho tlhahlobo e itseng ea DNA.

Batla database ea rona e ntseng e hola ea liteko tsa DNA ea liphoofolo tse koahelang mafu a futsitsoeng, matšoao a mebala ea jase le litšobotsi tse ling tsa lefutso ho lintja, likatse le lipere.

Seo u ka se fumanang polokelong ena:

Liteko tsa DNA tse amanang le mafu a futsitsoeng liphoofolong
Matšoao a liphatsa tsa lefutso a amanang le 'mala oa jase le litšobotsi tsa' mele
Mefuta e fapaneng e amang bophelo bo botle, baeloji kapa kutloisiso ea lithethefatsi

Each entry in the database describes a specific genetic test, variant or marker identified in dogs, cats or horses. The information may include the associated gene, the mutation or variant involved, inheritance pattern and a short explanation of the biological or clinical relevance of the test.

U batla ho etsa tlhahlobo ea DNA? Batla le ho odara liteko tse fumanehang ka kotloloho ho rona lebenkele la inthanete la tlhahlobo ea liphatsa tsa lefutso.

Batla ka mefuta

Fumana likarolo tse kholo tsa mefuta ea liphoofolo ka kotloloho ho hlahloba pokello e inehetseng ea liteko tsa lefutso la liphoofolo.

Liteko tsa lefutso tsa ntja Liteko tsa liphatsa tsa lefutso tsa Cat Liteko tsa liphatsa tsa lefutso tsa pere

Liteko tsohle tsa DNA

Ntja

Achromatopsia Type 2 In German Shepherd (ACHM2-GS)

Achromatopsia Type 2 ke boemo ba liphatsa tsa lefutso ho Balisa ba Jeremane bo amang bokhoni ba bona ba ho bona mebala, e leng se etsang hore e se ke ea hlola e e-ba mebala. Boemo bona bo bakoa ke liphetoho tsa CNGB3…

Ntja

Achromatopsia Type 2 In Labrador Retriever (ACHM2-LR)

Ntja

Achromatopsia Type 3 In German Shorthaired Pointer (PRAcd)

Ntja

Acral Mutilation Syndrome (AMS)

Katse

Acrodermatitis Enteropathica (AE)

Katse

Acute Intermittent Porphyria In Siamese Variant 2 (AIP-S2)

Katse

Acute Intermittent Porphyria Variant 1 (AIP1)

Katse

Acute Intermittent Porphyria Variant 3 (AIP3)

Katse

Acute Intermittent Porphyria Variant 4 (AIP4)

Ntja

Acute Respiratory Distress Syndrome (ARDS)

Ntja

Batho ba baholo ba Paroxysmal Dyskinesia (APD)

Ntja

Afibrinogenemia (AF)

Katse

Agouti (A)

Ntja

Alaskan Malamute Polyneuropathy (AMPN)

Katse

Albinism C1 (C1)

Katse

Albinism C2 (C2)

Ntja

Lefu la Alexander (AxD)

Katse

Alpha Mannosidosis (AlphaMan)

Ntja

Alpha-Mannosidosis (AMD)

Katse

Amber (Ka)

Ntja

Amelogenesis Imperfecta In Akita (AI-A)

Ntja

Amelogenesis Imperfecta In Greyhound (AI-G)

Ntja

Amelogenesis Imperfecta Ho Russell Terrier (AI-RT)

Pere

Androgen Insensitivity Syndrome In Quarter Horse (AIS-QH)

Pere

Androgen Insensitivity Syndrome In Thoroughbred Variant 2 (AIS-T2)

Pere

Androgen Insensitivity Syndrome ho Warmblood (AIS-W)

Ntja

Anhidrotic Ectodermal Dysplasia (AED)

Pere

Appaloosa Pattern-1 (PATN1)

Pere

Auditory-pigmentary syndrome SW2 (AS2)

Ntja

Labradoodle Dystrophinopathy ea Australia (DMD-AL)

Katse

Autoimmune Lymphoproliferative Syndrome (ALPS)

Ntja

Autosomal Dominant Pre (DPRA)

Ntja

Bardet-Biedl Syndrome 4 (BBS4)

Ntja

Benign Familial Juvenile Epilepsy (BFJE)

Ntja

Bernard-Soulier Syndrome (BSS-C)

Ntja

Bifid nko ho lintja tsa Çatalburun (BN)

Ntja

Mask o Motšo oa Melanistic (Em)

Ntja

Bothata ba ho Tlopa madi (Bdis)

Katse

Blood Group New 2019 Panel Variant 268ta (BG268TA)

Katse

Mofuta oa B1 oa Tabby B1 (Ta b1)

Katse

Mofuta oa B2 oa Tabby o senyehileng (Ta b2)

Katse

Mofuta oa B3 oa Tabby o senyehileng (Ta b3)

Ntja

Bob Tail (BT)

Ntja

Mofuta oa 2 oa Brachycephaly (BC-2)

Ntja

Brown Bas (bas)

Ntja

Bc e sootho (bc)

Ntja

Brown Bd (bd)

Ntja

Brown Bs (bs)

Katse

Burmese Colourpoint (cb)

Ntja

Canine Double vs single coat (DC1)

Ntja

Canine Double vs single coat (DC2)

Ntja

Canine Leukocyte Adhesion Deficiency (CLAD)

Ntja

Canine Leukocyte Adhesion Deficiency Type Iii (CLAD3)

Ntja

Moriri o Motelele oa Canine (LH)

Ntja

Canine Malignant Hyperthermia (MH)

Ntja

Canine Multiple System Degeneration In Chinese Crested (CMSD-CC)

Ntja

Canine Multiple System Degeneration Ho Kerry Blue Terrier (CMSD-KBT)

Ntja

Canine Scott Syndrome (CSS)

Ntja

Laminopathy ea pelo (CLAM)

Ntja

Cardiomyopathy le lefu la Bana (CJM)

Ntja

Centronuclear Myopathy In Border Collie (CNM-BC)

Ntja

Centronuclear Myopathy Ho Labrador Variant 2 (CNM-L2)

Pere

Cerebellar Abiotrophy (CA)

Ntja

Cerebellar Ataxia In Belgian Shepherd Dog (CA-BSD)

Ntja

Cerebellar Ataxia In Finnish Hound (CA-FH)

Ntja

Cerebellar Cortical Degeneration (CCD)

Ntja

Cerebellar Degeneration-Myositis Complex (CDMC)

Ntja

Cerebellar Hypoplasia In Eurasier (CHP-E)

Ntja

Cerebellar Hypoplasia In White Swiss Shepherd Dog (CHP-WSS)

Pere

Chestnut Variant E (katoloso e)

Pere

Chestnut Variant Ea (extension ea)

Katse

Tsokolate (b)

Katse

Tsokolate (b2)

Ntja

Chondrodysplasia In Karelian Bear Dog And Norwegian Elkhound (CDPA-KBD)

Katse

Cinnamon (bl)

Ntja

Cleft Palate Variant 2 (CP2)

Ntja

CNS Atrophy With Cerebellar Ataxia (CACA)

Ntja

cocoa (eng)

Ntja

Collie Eye Anomaly (CEA)

Ntja

Colour Dilution And Neurological Defects (CDN)

Ntja

Tlatselletsa bofokoli ba 3 (C3Def)

Katse

Congenital Adrenal Hyperplasia (CAH)

Katse

Congenital Erythropoietic Porphyria Variant 1 (CEP1)

Katse

Congenital Erythropoietic Porphyria Variant 2 (CEP2)

Ntja

Congenital Hypothyroidism With Goiter In French Bulldog (CHG-FB)

Ntja

Congenital Hypothyroidism With Goiter In Rat And Toy Fox Terrier (CHG-RFT)

Ntja

Congenital Hypothyroidism With Goiter In Spanish Water Dog (CHG-SWD)

Ntja

Congenital Methemoglobinemia Variant 1 (CM1)

Ntja

Congenital Mirror Movement Disorder ho Weimaraners (CMM1)

Ntja

Congenital Muscular Dystrophy Ho American Staffordshire Terrier (CMD-AST)

Katse

Congenital Myasthenic Syndrome (CMS)

Ntja

Congenital Myasthenic Syndrome In Golden Retriever (CMS-GR)

Ntja

Congenital Myasthenic Syndrome In Heideterrier (CMS-H)

Ntja

Congenital Myasthenic Syndrome Ho Jack Russell Terrier (CMS-JRT)

Ntja

Congenital Myasthenic Syndrome Ho Labrador Retriever (CMS-LR)

Ntja

Congenital Myasthenic Syndrome In Old Danish Pointer (CMS-ODP)

Ntja

Congenital Stationary Night Blindness In Beagle (CSNB-Be)

Ntja

Congenital Stationary Night Blindness In Briard (CSNB-Br)

Katse

Kopal (Copal)

Katse

Koporo (Koporo)

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Mabapi le polokelongtshedimosetso ena ya diteko tsa lefutso

Phatlalatso ena e bokella liteko tsa DNA ea liphoofolo tse koahelang mathata a futsitsoeng, mefuta e fapaneng ea mebala ea jase le litšobotsi tse ling tsa lefutso tse khetholloang ho liphoofolo tse tsamaeang le lipere. Mongolo o mong le o mong oa tlhahlobo o hokahana le leqephe le inehetseng moo tlhaiso-leseling e fumanehang e ka kenyelletsang mofuta o amehang, phetoho kapa phetoho e amehang, mokhoa oa lefa le kakaretso ea tšobotsi kapa boemo bo amanang.

Bakeng sa ho sheba haholoanyane, o ka sheba maqephe a rona a mefuta e ikhethileng ka tlase.

Liteko tsa lefutso tsa ntja Liteko tsa liphatsa tsa lefutso tsa Cat Liteko tsa liphatsa tsa lefutso tsa pere

Sebelisa leqephe lena e le qalo ea ho fumana liteko tsa DNA ka bomong, ebe u tsoela pele ho bala ka mefuta ea liphoofolo bakeng sa pono e tsepamisitsoeng haholoanyane.

DNA Portal ea ka

Setsi sa Tlhahlobo ea Liphatsa tsa lefutso bakeng sa Lintja, Likatse le Lipere

Batla pokello ea rona ea tlhahlobo ea DNA ea liphoofolo

Batla ka mefuta

Liteko tsohle tsa DNA

Mabapi le polokelongtshedimosetso ena ya diteko tsa lefutso