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Results for "lamellar cataracts": 2 genes, 124 gene sets

Name

LI5 Gene

Lamellar ichthyosis 5

ICR1 Gene

ichthyosis congenita I, erythromatous lamellar ichthyosis, ichthyosiform erythroderma

lamellar cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the lamellar cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperferritinemia, hereditary, with congenital cataracts Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperferritinemia, hereditary, with congenital cataracts from the curated CTD Gene-Disease Associations dataset.

Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.

HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS from the curated CTD Gene-Disease Associations dataset.

congenital cataracts Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital cataracts in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataracts Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cataracts in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Cataracts in type 2 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Cataracts in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Age-related nuclear cataracts Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related nuclear cataracts phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

presenile cataracts Gene Set

From HPO Gene-Disease Associations

genes associated with the presenile cataracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile zonular cataracts Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile zonular cataracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nuclear cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the nuclear cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

anterior subcapsular cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the anterior subcapsular cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

anterior polar cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the anterior polar cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

polar cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the polar cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sutural cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sutural cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

subcapsular cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the subcapsular cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

posterior subcapsular cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the posterior subcapsular cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

total cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the total cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

anterior cortical cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the anterior cortical cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cortical cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cortical cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated OMIM Gene-Disease Associations dataset.

galactokinase deficiency with cataracts Gene Set

From OMIM Gene-Disease Associations

genes associated with the galactokinase deficiency with cataracts phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital cataracts, hearing loss, and neurodegeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital cataracts, hearing loss, and neurodegeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital cataracts, facial dysmorphism, and neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital cataracts, facial dysmorphism, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

branchiootorenal syndrome 1, with or without cataracts Gene Set

From OMIM Gene-Disease Associations

genes associated with the branchiootorenal syndrome 1, with or without cataracts phenotype from the curated OMIM Gene-Disease Associations dataset.

?partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Bilateral Cataracts (Disorder) Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Bilateral Cataracts (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hyperferritinemia, Hereditary, With Congenital Cataracts Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hyperferritinemia, Hereditary, With Congenital Cataracts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Partial Lipodystrophy, Congenital Cataracts, And Neurodegeneration Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Partial Lipodystrophy, Congenital Cataracts, And Neurodegeneration Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Bilateral Cataracts Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Bilateral Cataracts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hemorrhagic Destruction Of The Brain, Subependymal Calcification, And Cataracts Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hemorrhagic Destruction Of The Brain, Subependymal Calcification, And Cataracts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cryohydrocytosis, Stomatin-Deficient, With Mental Retardation, Seizures, Cataracts, And Massive Hepatosplenomegaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cryohydrocytosis, Stomatin-Deficient, With Mental Retardation, Seizures, Cataracts, And Massive Hepatosplenomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Cataracts, Hearing Loss, And Neurodegeneration Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Cataracts, Hearing Loss, And Neurodegeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease 3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease 3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Congenital muscular dystrophy with cataracts and intellectual disability Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Congenital muscular dystrophy with cataracts and intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Congenital cataracts-facial dysmorphism-neuropathy syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Congenital cataracts-facial dysmorphism-neuropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cataracts Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Cataracts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cataracts (operation) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Cataracts (operation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Age-related cataracts Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Age-related cataracts phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Age-related cataracts (age at onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Age-related cataracts (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Age-related nuclear cataracts Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Age-related nuclear cataracts phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Cataracts in type 2 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Cataracts in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Cataracts Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Cataracts phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Lamellar ichthyosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lamellar ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

lamellar body Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

epidermal lamellar body Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the epidermal lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

alveolar lamellar body membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the alveolar lamellar body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

alveolar lamellar body Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the alveolar lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

lamellar body membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the lamellar body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

lamellar body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the lamellar body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

epidermal lamellar body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the epidermal lamellar body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

lamellar body membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the lamellar body membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Lamellar ichthyosis, type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lamellar ichthyosis, type 2 from the curated CTD Gene-Disease Associations dataset.

Ichthyosis, Lamellar, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis, Lamellar, 5 from the curated CTD Gene-Disease Associations dataset.

Ichthyosis, Lamellar Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis, Lamellar from the curated CTD Gene-Disease Associations dataset.

Lamellar ichthyosis, type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lamellar ichthyosis, type 3 from the curated CTD Gene-Disease Associations dataset.

lamellar ichthyosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lamellar ichthyosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lamellar Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term lamellar in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

lamellar body Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the lamellar body cellular component from the curated GO Cellular Component Annotations 2015 dataset.

epidermal lamellar body Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the epidermal lamellar body cellular component from the curated GO Cellular Component Annotations 2015 dataset.

alveolar lamellar body membrane Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the alveolar lamellar body membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.

alveolar lamellar body Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the alveolar lamellar body cellular component from the curated GO Cellular Component Annotations 2015 dataset.

lamellar body membrane Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the lamellar body membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.

foam cells with lamellar inclusion bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the foam cells with lamellar inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lamellar cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the lamellar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

small alveolar lamellar bodies Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small alveolar lamellar bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased alveolar lamellar body number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased alveolar lamellar body number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent alveolar lamellar bodies Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent alveolar lamellar bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal alveolar lamellar body morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal alveolar lamellar body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged alveolar lamellar bodies Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged alveolar lamellar bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased alveolar lamellar body number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased alveolar lamellar body number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal compact bone lamellar structure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal compact bone lamellar structure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal epidermal lamellar body morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal epidermal lamellar body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Lamellar Ichthyosis, Type 2 Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lamellar Ichthyosis, Type 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Lamellar Cataract Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Lamellar Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cortical, Lamellar, Or Zonular Nonsenile Cataract Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cortical, Lamellar, Or Zonular Nonsenile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lamellar Macular Hole Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lamellar Macular Hole in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lamellar Pulverulent Cataract Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lamellar Pulverulent Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Foam Cells With Lamellar Inclusion Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Foam Cells With Lamellar Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

alveolar lamellar body Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the alveolar lamellar body cellular component from the curated GO Cellular Component Annotations 2023 dataset.

lamellar body Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the lamellar body cellular component from the curated GO Cellular Component Annotations 2023 dataset.

epidermal lamellar body Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the epidermal lamellar body cellular component from the curated GO Cellular Component Annotations 2023 dataset.

epidermal lamellar body membrane Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the epidermal lamellar body membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset.

lamellar body membrane Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the lamellar body membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset.

alveolar lamellar body membrane Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the alveolar lamellar body membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset.

decreased alveolar lamellar body number Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased alveolar lamellar body number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

enlarged alveolar lamellar bodies Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the enlarged alveolar lamellar bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased alveolar lamellar body number Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased alveolar lamellar body number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal alveolar lamellar body morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal alveolar lamellar body morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

small alveolar lamellar bodies Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the small alveolar lamellar bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal compact bone lamellar structure Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal compact bone lamellar structure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal epidermal lamellar body morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal epidermal lamellar body morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

absent alveolar lamellar bodies Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the absent alveolar lamellar bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

lamellar cataract Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the lamellar cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

alveolar lamellar body Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the alveolar lamellar body cellular component from the curated GO Cellular Component Annotations 2025 dataset.

lamellar body Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the lamellar body cellular component from the curated GO Cellular Component Annotations 2025 dataset.

epidermal lamellar body Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the epidermal lamellar body cellular component from the curated GO Cellular Component Annotations 2025 dataset.

alveolar lamellar body membrane Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the alveolar lamellar body membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset.

epidermal lamellar body membrane Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the epidermal lamellar body membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset.

lamellar body membrane Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the lamellar body membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset.

Lamellar body Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Epidermal lamellar body Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Epidermal lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Lamellar body membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Lamellar body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Alveolar lamellar body membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Alveolar lamellar body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Alveolar lamellar body Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Alveolar lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Epidermal lamellar body membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Epidermal lamellar body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Dendritic lamellar body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Dendritic lamellar body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Lamellar body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Lamellar body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Lamellar body membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Lamellar body membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Epidermal lamellar body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Epidermal lamellar body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Alveolar lamellar body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Alveolar lamellar body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Alveolar lamellar body membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Alveolar lamellar body membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Lamellar ichthyosis Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lamellar ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.