Model Database: Mouse and Rat Disease Model Search Resource

Contain a total of 149819 items

Category	Name	Genes	Background	Diseases	Publications
Knockin	huTFRC/huCD98HC	SLC3A2	C57BL/6NCya	8 Combined T Cell and B Cell Immunodeficiency Combined Immunodeficiency Combined T and B Cell Immunodeficiency Familial Cold Autoinflammatory Syndrome 3 Immunodeficiency 46 Immune Deficiency Disease Protein-Deficiency Anemia Severe Combined Immunodeficiency	--
Knockin	huTFRC	TFRC	C57BL/6NCya	8 Combined T Cell and B Cell Immunodeficiency Combined Immunodeficiency Combined T and B Cell Immunodeficiency Familial Cold Autoinflammatory Syndrome 3 Immunodeficiency 46 Immune Deficiency Disease Protein-Deficiency Anemia Severe Combined Immunodeficiency	--
Knockin	hTFRC	TFRC	C57BL/6NCya	8 Combined T Cell and B Cell Immunodeficiency Combined Immunodeficiency Combined T and B Cell Immunodeficiency Familial Cold Autoinflammatory Syndrome 3 Immunodeficiency 46 Immune Deficiency Disease Protein-Deficiency Anemia Severe Combined Immunodeficiency	--
Knockin	B6-huTFRC/htau	MAPT	C57BL/6Cya	30 Alzheimer's Disease Autism Spectrum Disorder Atypical Progressive Supranuclear Palsy Syndrome Behavioral Variant of Frontotemporal Dementia Classic Progressive Supranuclear Palsy Syndrome Cardiovascular System Disease Cutis Laxa, Autosomal Recessive, Type Iia Dementia Epilepsy, Idiopathic Generalized Epilepsy Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 Frontotemporal Dementia 1 Leukodystrophy Limb-Girdle Muscular Dystrophy Pick Disease of Brain Progressive Supranuclear Palsy Progressive Non-Fluent Aphasia Parkinson Disease, Late-Onset Parkinson-Dementia Syndrome Semantic Dementia Spondyloepimetaphyseal Dysplasia, Strudwick Type Combined T Cell and B Cell Immunodeficiency Combined Immunodeficiency Combined T and B Cell Immunodeficiency Familial Cold Autoinflammatory Syndrome 3 Immunodeficiency 46 Immune Deficiency Disease Protein-Deficiency Anemia Severe Combined Immunodeficiency	--
Knockin	B6-hTFRC/htau	MAPT	C57BL/6Cya	30 Alzheimer's Disease Autism Spectrum Disorder Atypical Progressive Supranuclear Palsy Syndrome Behavioral Variant of Frontotemporal Dementia Classic Progressive Supranuclear Palsy Syndrome Cardiovascular System Disease Cutis Laxa, Autosomal Recessive, Type Iia Dementia Epilepsy, Idiopathic Generalized Epilepsy Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 Frontotemporal Dementia 1 Leukodystrophy Limb-Girdle Muscular Dystrophy Pick Disease of Brain Progressive Supranuclear Palsy Progressive Non-Fluent Aphasia Parkinson Disease, Late-Onset Parkinson-Dementia Syndrome Semantic Dementia Spondyloepimetaphyseal Dysplasia, Strudwick Type Combined T Cell and B Cell Immunodeficiency Combined Immunodeficiency Combined T and B Cell Immunodeficiency Familial Cold Autoinflammatory Syndrome 3 Immunodeficiency 46 Immune Deficiency Disease Protein-Deficiency Anemia Severe Combined Immunodeficiency	--
Knockin	B6-huTFRC/htau*P301L	MAPT	C57BL/6Cya	30 Alzheimer's Disease Autism Spectrum Disorder Atypical Progressive Supranuclear Palsy Syndrome Behavioral Variant of Frontotemporal Dementia Classic Progressive Supranuclear Palsy Syndrome Cardiovascular System Disease Cutis Laxa, Autosomal Recessive, Type Iia Dementia Epilepsy, Idiopathic Generalized Epilepsy Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 Frontotemporal Dementia 1 Leukodystrophy Limb-Girdle Muscular Dystrophy Pick Disease of Brain Progressive Supranuclear Palsy Progressive Non-Fluent Aphasia Parkinson Disease, Late-Onset Parkinson-Dementia Syndrome Semantic Dementia Spondyloepimetaphyseal Dysplasia, Strudwick Type Combined T Cell and B Cell Immunodeficiency Combined Immunodeficiency Combined T and B Cell Immunodeficiency Familial Cold Autoinflammatory Syndrome 3 Immunodeficiency 46 Immune Deficiency Disease Protein-Deficiency Anemia Severe Combined Immunodeficiency	--
Knockin	B6-hTFRC/htau*P301L	MAPT	C57BL/6N;6JCya	30 Alzheimer's Disease Autism Spectrum Disorder Atypical Progressive Supranuclear Palsy Syndrome Behavioral Variant of Frontotemporal Dementia Classic Progressive Supranuclear Palsy Syndrome Cardiovascular System Disease Cutis Laxa, Autosomal Recessive, Type Iia Dementia Epilepsy, Idiopathic Generalized Epilepsy Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 Frontotemporal Dementia 1 Leukodystrophy Limb-Girdle Muscular Dystrophy Pick Disease of Brain Progressive Supranuclear Palsy Progressive Non-Fluent Aphasia Parkinson Disease, Late-Onset Parkinson-Dementia Syndrome Semantic Dementia Spondyloepimetaphyseal Dysplasia, Strudwick Type Combined T Cell and B Cell Immunodeficiency Combined Immunodeficiency Combined T and B Cell Immunodeficiency Familial Cold Autoinflammatory Syndrome 3 Immunodeficiency 46 Immune Deficiency Disease Protein-Deficiency Anemia Severe Combined Immunodeficiency	--
Knockin	B6-huTFRC/htau*P301S	MAPT	C57BL/6Cya	30 Alzheimer's Disease Autism Spectrum Disorder Atypical Progressive Supranuclear Palsy Syndrome Behavioral Variant of Frontotemporal Dementia Classic Progressive Supranuclear Palsy Syndrome Cardiovascular System Disease Cutis Laxa, Autosomal Recessive, Type Iia Dementia Epilepsy, Idiopathic Generalized Epilepsy Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 Frontotemporal Dementia 1 Leukodystrophy Limb-Girdle Muscular Dystrophy Pick Disease of Brain Progressive Supranuclear Palsy Progressive Non-Fluent Aphasia Parkinson Disease, Late-Onset Parkinson-Dementia Syndrome Semantic Dementia Spondyloepimetaphyseal Dysplasia, Strudwick Type Combined T Cell and B Cell Immunodeficiency Combined Immunodeficiency Combined T and B Cell Immunodeficiency Familial Cold Autoinflammatory Syndrome 3 Immunodeficiency 46 Immune Deficiency Disease Protein-Deficiency Anemia Severe Combined Immunodeficiency	--
Knockin	B6-hTFRC/htau*P301S	MAPT	C57BL/6N;6JCya	30 Alzheimer's Disease Autism Spectrum Disorder Atypical Progressive Supranuclear Palsy Syndrome Behavioral Variant of Frontotemporal Dementia Classic Progressive Supranuclear Palsy Syndrome Cardiovascular System Disease Cutis Laxa, Autosomal Recessive, Type Iia Dementia Epilepsy, Idiopathic Generalized Epilepsy Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 Frontotemporal Dementia 1 Leukodystrophy Limb-Girdle Muscular Dystrophy Pick Disease of Brain Progressive Supranuclear Palsy Progressive Non-Fluent Aphasia Parkinson Disease, Late-Onset Parkinson-Dementia Syndrome Semantic Dementia Spondyloepimetaphyseal Dysplasia, Strudwick Type Combined T Cell and B Cell Immunodeficiency Combined Immunodeficiency Combined T and B Cell Immunodeficiency Familial Cold Autoinflammatory Syndrome 3 Immunodeficiency 46 Immune Deficiency Disease Protein-Deficiency Anemia Severe Combined Immunodeficiency	--
Knockin	B6-huTFRC/huSNCA(3'UTR)	SNCA	C57BL/6NCya	20 Dementia Dementia, Lewy Body Epilepsy, Idiopathic Generalized Early-Onset Parkinson's Disease Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 Limb-Girdle Muscular Dystrophy Parkinson Disease, Late-Onset Parkinson Disease 1, Autosomal Dominant Parkinson Disease 15, Autosomal Recessive Early-Onset Parkinson Disease 4, Autosomal Dominant Spondyloepimetaphyseal Dysplasia, Strudwick Type Combined T Cell and B Cell Immunodeficiency Combined Immunodeficiency Combined T and B Cell Immunodeficiency Familial Cold Autoinflammatory Syndrome 3 Immunodeficiency 46 Immune Deficiency Disease Protein-Deficiency Anemia Severe Combined Immunodeficiency	--
Knockin	hIGF1R/huTFRC	IGF1R	C57BL/6NCya	22 Acid-Labile Subunit Deficiency Autism Spectrum Disorder Cortical Dysplasia, Complex, with Other Brain Malformations 13 Diaphragmatic Hernia, Congenital Epilepsy Glioma Susceptibility 1 Growth Delay Due to Insulin-Like Growth Factor I Resistance Hematologic Cancer Insulin-Like Growth Factor I Myeloma, Multiple Osteochondritis Dissecans Periventricular Heterotopia with Microcephaly, Autosomal Recessive Seckel Syndrome Three M Syndrome 1 Combined T Cell and B Cell Immunodeficiency Combined Immunodeficiency Combined T and B Cell Immunodeficiency Familial Cold Autoinflammatory Syndrome 3 Immunodeficiency 46 Immune Deficiency Disease Protein-Deficiency Anemia Severe Combined Immunodeficiency	--
Knockin	hTFRC/huCD98HC	SLC3A2	C57BL/6NCya	8 Combined T Cell and B Cell Immunodeficiency Combined Immunodeficiency Combined T and B Cell Immunodeficiency Familial Cold Autoinflammatory Syndrome 3 Immunodeficiency 46 Immune Deficiency Disease Protein-Deficiency Anemia Severe Combined Immunodeficiency	--
Knockin	hIGF1R/huTFRC/huCD98HC	IGF1R	C57BL/6NCya	22 Acid-Labile Subunit Deficiency Autism Spectrum Disorder Cortical Dysplasia, Complex, with Other Brain Malformations 13 Diaphragmatic Hernia, Congenital Epilepsy Glioma Susceptibility 1 Growth Delay Due to Insulin-Like Growth Factor I Resistance Hematologic Cancer Insulin-Like Growth Factor I Myeloma, Multiple Osteochondritis Dissecans Periventricular Heterotopia with Microcephaly, Autosomal Recessive Seckel Syndrome Three M Syndrome 1 Combined T Cell and B Cell Immunodeficiency Combined Immunodeficiency Combined T and B Cell Immunodeficiency Familial Cold Autoinflammatory Syndrome 3 Immunodeficiency 46 Immune Deficiency Disease Protein-Deficiency Anemia Severe Combined Immunodeficiency	--
Point Mutation	B6-hINHBE/ob	Lep	C57BL/6NCya;C57BL/6JCya	9 46,xy Sex Reversal 3 Autism Spectrum Disorder Body Mass Index Quantitative Trait Locus 11 Cortical Dysplasia, Complex, with Other Brain Malformations 13 Hypogonadotropic Hypogonadism 1 with or Without Anosmia Hypogonadotropic Hypogonadism Immune Deficiency Disease Leptin Deficiency or Dysfunction Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract	--
Other	B6-hPCSK9/TG-hAPOC3	PCSK9	C57BL/6NCya	14 3-Methylcrotonyl-Coa Carboxylase Deficiency Abdominal Obesity-Metabolic Syndrome 1 Coronary Artery Disease, Autosomal Dominant, 1 Carnitine Palmitoyltransferase Ii Deficiency, Infantile Dilated Cardiomyopathy Homozygous Familial Hypercholesterolemia Hypercholesterolemia, Familial, 3 Limb-Girdle Muscular Dystrophy Lipodystrophy, Congenital Generalized, Type 1 3-Methylcrotonyl-Coa Carboxylase Deficiency Carnitine Palmitoyltransferase Ii Deficiency, Infantile Dilated Cardiomyopathy Hyperalphalipoproteinemia 1 Lipodystrophy, Congenital Generalized, Type 1	--
Knockin	B6-hSMN2 (SMA)	SMN2	C57BL/6NCya	7 Neuromuscular Disease Neuronopathy, Distal Hereditary Motor, Autosomal Dominant 13 Spinal Muscular Atrophy Spinal Muscular Atrophy, Type I Spinal Muscular Atrophy, Type Iii Spinal Muscular Atrophy, Type Ii Spinal Muscular Atrophy, Type Iv	--
Knockin	B6-3*hSMN2	SMN2	C57BL/6NCya	7 Neuromuscular Disease Neuronopathy, Distal Hereditary Motor, Autosomal Dominant 13 Spinal Muscular Atrophy Spinal Muscular Atrophy, Type I Spinal Muscular Atrophy, Type Iii Spinal Muscular Atrophy, Type Ii Spinal Muscular Atrophy, Type Iv	--
Knockin	B6-4*hSMN2	SMN2	C57BL/6NCya	7 Neuromuscular Disease Neuronopathy, Distal Hereditary Motor, Autosomal Dominant 13 Spinal Muscular Atrophy Spinal Muscular Atrophy, Type I Spinal Muscular Atrophy, Type Iii Spinal Muscular Atrophy, Type Ii Spinal Muscular Atrophy, Type Iv	--
Knockin	huTau(MAPT)	MAPT	C57BL/6JCya	22 Alzheimer's Disease Autism Spectrum Disorder Atypical Progressive Supranuclear Palsy Syndrome Behavioral Variant of Frontotemporal Dementia Classic Progressive Supranuclear Palsy Syndrome Cardiovascular System Disease Cutis Laxa, Autosomal Recessive, Type Iia Dementia Epilepsy, Idiopathic Generalized Epilepsy Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 Frontotemporal Dementia 1 Leukodystrophy Limb-Girdle Muscular Dystrophy Pick Disease of Brain Progressive Supranuclear Palsy Progressive Non-Fluent Aphasia Parkinson Disease, Late-Onset Parkinson-Dementia Syndrome Semantic Dementia Spondyloepimetaphyseal Dysplasia, Strudwick Type	--
Knockin	B6-htau*P301L	MAPT	C57BL/6JCya	22 Alzheimer's Disease Autism Spectrum Disorder Atypical Progressive Supranuclear Palsy Syndrome Behavioral Variant of Frontotemporal Dementia Classic Progressive Supranuclear Palsy Syndrome Cardiovascular System Disease Cutis Laxa, Autosomal Recessive, Type Iia Dementia Epilepsy, Idiopathic Generalized Epilepsy Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 Frontotemporal Dementia 1 Leukodystrophy Limb-Girdle Muscular Dystrophy Pick Disease of Brain Progressive Supranuclear Palsy Progressive Non-Fluent Aphasia Parkinson Disease, Late-Onset Parkinson-Dementia Syndrome Semantic Dementia Spondyloepimetaphyseal Dysplasia, Strudwick Type	--

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