Strain listing for Mouse/Human Gene Homologs

The links below offer the most recent strain information for Mouse/Human Gene Homologs , including current ordering and pricing information:

Mouse/Human Gene Homologs

• Alport syndrome
• Alzheimer's
• Arthritis
• Atransferrinemia
• Bruton agammaglobulinemia tyrosine kinase
• Charcot-Marie-Tooth disease, Type 1A
• Chediak-Higashi syndrome
• Down syndrome
• Epilepsy
• GM2-gangliosidosis type I, Tay-Sachs disease
• Gaucher disease, type I
• Granulomatous Disease, Chronic, X-Linked; CGD
• Greig cephalopolysyndactyly syndrome
• Griscelli Syndrome
• (with haemophagocytic syndrome)
• Hermansky-Pudlak syndrome
• Hirschsprung disease
• Huntington's disease (chorea)
• IPEX/XLAAD/DMSD/XPID
• Infantile neuronal ceroid lipofuscinosis
• Kok disease-hyperexplexia, startle disease
• Lesch-Nyhan syndrome
• Li-Fraumeni syndrome
• Marfan syndrome
• Menkes syndrome
• Neurofibromatosis Type I
• Niemann-Pick disease, type C
• Pelger-Huet anomaly
• Pelizaeus-Merzbacher disease
• Peters' Anomaly disease
• Retinitis pigmentosa 12; Leber congenital amaurosis (CLA)
• Rett syndrome
• Spinal Muscular Atrophy with Respiratory Distress Type I (SMARD1)
• Spondyloepiphyseal dysplasia, congenital type
• Susceptibility to Iron Deficiency Anemia
• Tangier's disease
• Usher syndrome, type IB
• (deafness, neurosensory, autosomal recessive, 2, and deafness, autosomal dominant nonsyndromic sensorineural, 11)
• Usher syndrome, type IC (USH1C) (deafness, neurosensory, autosomal recessive 18)
• Usher syndrome, type ID
• (USH1D)
• Waardenburg syndrome, type I
• Waardenburg syndrome, type IIA
• Waardenburg-Shah syndrome
• Wilson disease
• Wiskott-Aldrich syndrome
• aceruloplasminemia
• acromesomelic dysplasia, Hunter-Thompson Type
• adenomatosis polyposis coli
• agammaglobulinemia
• albinism, oculocutaneous type II, OCA2
• albinism, tyrosine negative
• (wildtype)
• amyotrophic lateral sclerosis (ALS)
• aniridia type II
• apolipoprotein A1 deficiency, amyloid polyneuropathy-nephropathy
• ataxia telangiectasia
• ataxia, cerebellar, Cayman type
• autoimmune lymphoproliferative syndrome
• autosomal recessive lissencephaly
• branchiootorenal dysplasia, branchiootic syndrome
• bullous pemphigoid
• congenital contractural arachnodactyly
• congenital goiter with hypothyroidism
• craniometaphyseal dysplasia, autosomal dominant
• cystic fibrosis
• deafness
• deafness, autosomal dominant nonsyndromic sensorineural 22 (DFNA22)
• deafness, autosomal recessive 12 (DFNB12)
• deafness, autosomal recessive nonsyndromic sensorineural 37 (DFNB37)
• deafness, neurosensory, autosomal recessive, 3
• diabetes mellitus, insulin-resistant
• erytropoietic protoporphyria
• fragile site mental retardation 1
• globoid cell leukodystrophy (Krabbe disease)
• glycogen storage disease type II (GSDII)
• granulomatous disease, chronic, autosomal cytochrome-b-positive form 1 (CGD)
• growth hormone deficiency
• hemochromatosis
• homocystinuria
• hypercholesterolemia, familial
• hyperlipoproteinemia, type III
• hypobetalipoproteinemia, familial
• hypohidrotic ectodermal dysplasia
• hypophosphatemic D-resistant rickets, X-linked
• hypothyroidism
• immunodeficiency with hyper-IgM, type I (hyper-IgM syndrome)
• leukocyte adhesion deficiency, type I
• mature onset diabetes of the young - MODY
• migraine, familial hemiplegic, with progressive cerebellar ataxia
• mucopolysaccharidosis III B, Sanfilippo syndrome B
• mucopolysaccharidosis type IIIA, Sanfilippo syndrome type A
• mucopolysaccharidosis type VII, GUSB deficiency
• multiple endocrine neoplasia, type I
• muscular dystrophy (Duchenne and Becker)
• muscular dystrophy, congenital merosin-deficient (CMD)
• muscular dystrophy, limb-girdle
• (type 2B)
• (type 2F)
• myotonia congenita, autosomal dominant, Thomsen disease)
• non-syndromic microphthalmia, cataracts and iris abnormalities
• nonspherocytic hemolytic anemia (NSHA)
• obesity, adrenal insufficiency
• obesity, morbid, with hypogonadism (rare)
• obesity, severe, due to leptin deficiency (rare)
• oculocutaneous albinism type III
• ornithine transcarbamylase deficiency
• osteogenesis imperfecta congenita, Ehlers-Danlos syndrome, type VII, autosomal dominant
• parietal foramina-2
• pemphigus vulgaris
• phenylketonuria
• piebaldism
• pituitary hormone deficiency
• (wildtype)
• retinal degeneration, slow
• retinitis pigmentosa, autosomal recessive
• retinitis pigmentosa, wildtype
• retinoblastoma
• severe combined immunodeficiency disease, autosomal recessive, T-negative/ B-positive type
• situs inversus
• spinocerebellar ataxia 2
• synpolydactyly
• systemic lupus erythematosus
• testicular feminization
• thalassemia, alpha
• thalassemia, beta
• thyroid hormone resistance, generalized
• visceroatrial heterotaxia, autosomal recessive

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