Not currently registered for phenotyping at IMPC
Phenotyping is currently not planned for a knockout strain of this gene.
Gene Summary
IMPC Data Collections
- No Body Weight Data
- No Embryo Imaging Data
- No Viability Data
Phenotyping is currently not planned for a knockout strain of this gene.
The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.
Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.
The table below shows human diseases predicted to be associated to Bid by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Spongiform Encephalopathy With Neuropsychiatric Features | Gliosis | OMIM:606688 | |
Mitochondrial Complex Iv Deficiency, Nuclear Type 6 | Gliosis | OMIM:615119 | |
Diabetes Insipidus, Neurohypophyseal | Gliosis | OMIM:125700 | |
Spinocerebellar Ataxia, Autosomal Recessive 27 | Gliosis | OMIM:618369 | |
Immunodeficiency 83, Susceptibility To Viral Infections | Gliosis | OMIM:613002 | |
Developmental And Epileptic Encephalopathy 14 | Gliosis | OMIM:614959 | |
Huntington Disease | Gliosis | OMIM:143100 | |
Pontocerebellar Hypoplasia, Type 4 | Gliosis | OMIM:225753 | |
Congenital Neuronal Ceroid Lipofuscinosis | Abnormal astrocyte morphology, Gliosis, Agenesis of corpus callosum | ORPHA:168486 | |
Amyotrophic Lateral Sclerosis 15 With Or Without Frontotemporal Dementia | Gliosis | OMIM:300857 | |
Encephalopathy, Acute, Infection-Induced, Susceptibility To, 3 | Gliosis, Pneumonia | OMIM:608033 | |
Pick Disease Of Brain | Gliosis | OMIM:172700 | |
Spastic Paraplegia 50, Autosomal Recessive | Gliosis | OMIM:612936 | |
Spinocerebellar Ataxia, Autosomal Recessive 2 | Gliosis | OMIM:213200 | |
Primary Non-Essential Cutis Verticis Gyrata | Gliosis | ORPHA:357225 | |
Encephalopathy, Familial, With Neuroserpin Inclusion Bodies | Gliosis | OMIM:604218 | |
Adducted Thumbs Syndrome | Myelin-dependent gliosis | OMIM:201550 | |
Sporadic Creutzfeldt-Jakob Disease | Recurrent aspiration pneumonia, Gliosis, Astrocytosis | ORPHA:204 | |
Hemimegalencephaly | Gliosis | ORPHA:99802 | |
Combined Oxidative Phosphorylation Deficiency 14 | Gliosis | OMIM:614946 | |
Pyruvate Dehydrogenase E1-Alpha Deficiency | Gliosis, Cerebellar gliosis, Basal ganglia gliosis, Partial agenesis of the corpus callosum, Recu... | ORPHA:79243 | |
Neuropathy, Hereditary Motor And Sensory, Okinawa Type | Gliosis | OMIM:604484 | |
Leukoencephalopathy, Hereditary Diffuse, With Spheroids 1 | Gliosis | OMIM:221820 | |
Lissencephaly, X-Linked, 2 | Gliosis, Agenesis of corpus callosum | OMIM:300215 | |
Rigidity And Multifocal Seizure Syndrome, Lethal Neonatal | Gliosis | OMIM:614498 | |
Microcephaly 10, Primary, Autosomal Recessive | Gliosis | OMIM:615095 | |
Leukoencephalopathy With Vanishing White Matter | Gliosis | OMIM:603896 | |
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1 | Gliosis | OMIM:105550 | |
Cerebrooculofacioskeletal Syndrome 1 | Gliosis, Agenesis of corpus callosum, Recurrent pneumonia | OMIM:214150 | |
Spinocerebellar Ataxia 17 | Gliosis | OMIM:607136 | |
X-Linked Intellectual Disability-Short Stature-Overweight Syndrome | Gliosis, Pulmonary fibrosis | ORPHA:457240 | |
Duodenal Atresia | Annular pancreas, Abnormality of the pulmonary artery, Abnormality of the pancreas | ORPHA:1203 | |
Polycystic Lipomembranous Osteodysplasia With Sclerosing Leukoencephalopathy 1 | Gliosis | OMIM:221770 | |
Combined Oxidative Phosphorylation Deficiency 24 | Gliosis, Agenesis of corpus callosum | OMIM:616239 | |
Frontotemporal Dementia With Motor Neuron Disease | Gliosis | ORPHA:275872 | |
L-2-Hydroxyglutaric Aciduria | Gliosis | OMIM:236792 | |
Leigh Syndrome | Gliosis | OMIM:256000 | |
Huntington Disease-Like 1 | Gliosis | ORPHA:157941 | |
Spinocerebellar Ataxia, X-Linked 3 | Gliosis, Recurrent respiratory infections | OMIM:301790 | |
Intellectual Developmental Disorder, X-Linked 12 | Gliosis | OMIM:300957 | |
Mitochondrial Complex Iv Deficiency, Nuclear Type 5 | Gliosis | OMIM:220111 | |
Charcot-Marie-Tooth Disease With Ptosis And Parkinsonism | Gliosis | OMIM:118301 | |
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant | Gliosis | OMIM:169500 | |
Neurodegeneration With Brain Iron Accumulation 2A | Gliosis | OMIM:256600 | |
Pontocerebellar Hypoplasia, Type 2A | Gliosis | OMIM:277470 | |
Pancreatitis, Hereditary | Exocrine pancreatic insufficiency, Pancreatitis, Pancreatic pseudocyst, Pleural effusion, Pancrea... | OMIM:167800 | |
Multiple Acyl-Coa Dehydrogenase Deficiency | Gliosis, Pulmonary hypoplasia | OMIM:231680 | |
Machado-Joseph Disease | Gliosis | OMIM:109150 | |
Familial Acute Necrotizing Encephalopathy | Gliosis | ORPHA:88619 | |
Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal | Gliosis | OMIM:602613 | |
Central Nervous System Calcification-Deafness-Tubular Acidosis-Anemia Syndrome | Gliosis | ORPHA:3240 | |
Neurodegeneration, Childhood-Onset, With Progressive Microcephaly | Gliosis | OMIM:619847 | |
Kleefstra Syndrome Due To A Point Mutation | Gliosis | ORPHA:261652 | |
Progressive Supranuclear Palsy | Gliosis | ORPHA:683 | |
Pelizaeus-Merzbacher Disease, Connatal Form | Gliosis | ORPHA:280210 | |
Frontotemporal Lobar Degeneration With Tdp43 Inclusions, Grn-Related | Gliosis | OMIM:607485 | |
Mitochondrial Dna Depletion Syndrome 4A (Alpers Type) | Gliosis, Astrocytosis | OMIM:203700 | |
Multiple Acyl-Coa Dehydrogenase Deficiency | Gliosis | ORPHA:26791 | |
Leigh Syndrome | Gliosis, Agenesis of corpus callosum | ORPHA:506 | |
Encephalopathy, Progressive, Early-Onset, With Brain Atrophy And Thin Corpus Callosum | Gliosis | OMIM:617193 | |
Mannosidosis, Alpha B, Lysosomal | Gliosis | OMIM:248500 | |
Parkinson Disease 1, Autosomal Dominant | Gliosis | OMIM:168601 | |
Encephalopathy, Progressive, Early-Onset, With Brain Edema And/Or Leukoencephalopathy, 2 | Gliosis | OMIM:618321 | |
Molybdenum Cofactor Deficiency, Complementation Group B | Gliosis | OMIM:252160 | |
Tay-Sachs Disease | Aspiration pneumonia, Gliosis | ORPHA:845 | |
Mitochondrial Complex I Deficiency, Nuclear Type 2 | Gliosis | OMIM:618222 | |
Neurodevelopmental Disorder With Epilepsy And Hemochromatosis | Aspiration pneumonia, Gliosis | OMIM:301072 | |
Papillorenal Syndrome | Gliosis | OMIM:120330 | |
Cutis Laxa, Autosomal Recessive, Type Iid | Gliosis | OMIM:617403 | |
Molybdenum Cofactor Deficiency, Complementation Group A | Gliosis | OMIM:252150 | |
Hereditary Late-Onset Parkinson Disease | Gliosis | ORPHA:411602 | |
D-Bifunctional Protein Deficiency | Gliosis | OMIM:261515 | |
Alacrimia-Choreoathetosis-Liver Dysfunction Syndrome | Gliosis, Recurrent respiratory infections | ORPHA:404454 | |
Oxoglutaric Aciduria | Abnormality of Krebs cycle metabolism | ORPHA:31 | |
Congenital Disorder Of Deglycosylation 1 | Gliosis, Recurrent respiratory infections | OMIM:615273 | |
Cerebrotendinous Xanthomatosis | Abnormal lung morphology, Gliosis | ORPHA:909 | |
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 | Gliosis | OMIM:300868 | |
Supranuclear Palsy, Progressive, 1 | Gliosis, Astrocytosis | OMIM:601104 | |
Dyrk1A-Related Intellectual Disability Syndrome Due To 21Q22.13Q22.2 Microdeletion | Gliosis | ORPHA:268261 | |
Cockayne Syndrome | Gliosis | ORPHA:191 | |
Gabriele-De Vries Syndrome | Gliosis, Agenesis of corpus callosum | ORPHA:506358 | |
Supranuclear Palsy, Progressive, 2 | Gliosis | OMIM:609454 | |
Diets-Jongmans Syndrome | Gliosis | OMIM:618846 | |
Mitochondrial Dna-Associated Leigh Syndrome | Abnormality of Krebs cycle metabolism | ORPHA:255210 |
All available products are supplied via our member's centres or partnerships. When ordering a product from the IMPC you will be redirected to one of their websites or prompted to start an email.
This service may be affected by the Covid-19 pandemic. See how
MGI Allele | Allele Type | Produced |
---|---|---|
Bidtm1a(EUCOMM)Wtsi | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors, ES Cells |
Bidtm1e(EUCOMM)Wtsi | Targeted, non-conditional allele | ES Cells |
Get highlights of the most important data releases, news and events, delivered straight to your email inbox
Subscribe to newsletter