Name

absent outer ear Gene Set

From MPO Gene-Phenotype Associations

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

abnormal kidney outer medulla outer stripe morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney outer medulla outer stripe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

outer ear morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the outer ear morphogenesis biological process from the curated GO Biological Process Annotations dataset.

neoplasm of the outer ear Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of the outer ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the outer ear Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the outer ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal outer ear morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal outer ear morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

outer ear Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue outer ear in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

absent outer dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent/shortened outer dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent/shortened outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent inner and outer dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent inner and outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent photoreceptor outer segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent photoreceptor outer segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cochlear outer hair cell electromotility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cochlear outer hair cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear outer hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent outer hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent earlobe Gene Set

From HPO Gene-Disease Associations

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

absent middle ear ossicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent middle ear ossicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent inner ear vestibule Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent inner ear vestibule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent inner ear Gene Set

From MPO Gene-Phenotype Associations

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

OB outer plexiform layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in OB outer plexiform layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Main olfactory bulb, outer plexiform layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Main olfactory bulb, outer plexiform layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

AOB, outer plexiform layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in AOB, outer plexiform layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

outer SZ in dorsomedial frontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in dorsomedial frontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in dorsomedial frontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in dorsomedial frontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in orbital frontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in orbital frontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in rostral perirhinal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in rostral perirhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in lateral temporal-occipital cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in midinferior temporal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in midinferior temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in primary visual cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in posteroinferior (ventral) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in posteroinferior (ventral) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in frontal polar cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in frontal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in posterosuperior (dorsal) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in posterosuperior (dorsal) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in medial temporal-occipital cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in primary somatosensory cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in primary auditory cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in ventrolateral prefrontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in ventrolateral prefrontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in ventrolateral prefrontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in ventrolateral prefrontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer plexiform zone in extrastriate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer plexiform zone in extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in rostral cingulate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in rostral cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in inferolateral temporal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in inferolateral temporal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in subgenual (subcallosal) cingulate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in subgenual (subcallosal) cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in posterosuperior (dorsal) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in posterosuperior (dorsal) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in caudal midinferior temporal cortex (area TF) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in dorsomedial extrastriate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in dorsomedial extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in primary somatosensory cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in posteroinferior (ventral) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in posteroinferior (ventral) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in (rostral) midinferior temporal cortex (area 36) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in (rostral) midinferior temporal cortex (area 36) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in midlateral extrastriate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in midlateral extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in lateral temporal-occipital cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in dorsolateral prefrontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in dorsolateral prefrontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in posterior parahippocampal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in dorsolateral prefrontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in dorsolateral prefrontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in caudal midinferior temporal cortex (area TF) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in dorsomedial parietal cortex (area 7m) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in dorsomedial parietal cortex (area 7m) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer portion of medial ganglionic eminence Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer portion of medial ganglionic eminence relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in posterior parahippocampal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in frontal polar cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in frontal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in ventromedial extrastriate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in ventromedial extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in temporal polar cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in temporal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in dysgranular insular cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in dysgranular insular cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in medial temporal-occipital cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in caudal cingulate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in caudal cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in dorsomedial extrastriate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in dorsomedial extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in midcingulate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in midcingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in superolateral temporal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in orbital frontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in orbital frontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in superolateral temporal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in granular insular cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in granular insular cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in primary visual cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in caudal perirhinal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in caudal perirhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in midlateral extrastriate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in midlateral extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in midlateral temporal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in midlateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in posteror frontal cortex (motor cortex) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer portion of lateral ganglionic eminence Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer portion of lateral ganglionic eminence relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in posteror frontal cortex (motor cortex) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in ventromedial extrastriate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in ventromedial extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

outer acrosomal membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

intrinsic component of cell outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of cell outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

condensed nuclear chromosome outer kinetochore Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed nuclear chromosome outer kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intrinsic component of mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

outer dynein arm Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the outer dynein arm cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

extrinsic component of mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the extrinsic component of mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

outer mucus layer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the outer mucus layer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

photoreceptor outer segment Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the photoreceptor outer segment cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

integral component of mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the integral component of mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

nuclear outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

mitochondrial outer membrane translocase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial outer membrane translocase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cell outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

outer dense fiber Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the outer dense fiber cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

integral component of cell outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the integral component of cell outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

nuclear outer membrane-endoplasmic reticulum membrane network Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the nuclear outer membrane-endoplasmic reticulum membrane network cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intrinsic component of nuclear outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of nuclear outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

nuclear pore outer ring Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the nuclear pore outer ring cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

external side of cell outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the external side of cell outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

integral component of nuclear outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the integral component of nuclear outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

organelle outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

photoreceptor outer segment membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the photoreceptor outer segment membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

condensed chromosome outer kinetochore Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed chromosome outer kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cytoplasmic side of mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cytoplasmic side of mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial outer membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

outer acrosomal membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

condensed nuclear chromosome outer kinetochore Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the condensed nuclear chromosome outer kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

photoreceptor outer segment membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

outer dynein arm Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

viral outer capsid Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

outer mucus layer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

photoreceptor outer segment Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

chloroplast outer membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

nuclear outer membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

mitochondrial outer membrane translocase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

cell outer membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

outer dense fiber Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

nuclear outer membrane-endoplasmic reticulum membrane network Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the nuclear outer membrane-endoplasmic reticulum membrane network cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

nuclear pore outer ring Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the nuclear pore outer ring cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

outer endospore membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

outer membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

plastid outer membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

organelle outer membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

condensed chromosome outer kinetochore Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the condensed chromosome outer kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

outer Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein import into mitochondrial outer membrane Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein import into mitochondrial outer membrane biological process from the curated GO Biological Process Annotations dataset.

regulation of protein import into mitochondrial outer membrane Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein import into mitochondrial outer membrane biological process from the curated GO Biological Process Annotations dataset.

mitochondrial outer membrane permeabilization involved in programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial outer membrane permeabilization involved in programmed cell death biological process from the curated GO Biological Process Annotations dataset.

outer mitochondrial membrane organization Gene Set

From GO Biological Process Annotations

genes participating in the outer mitochondrial membrane organization biological process from the curated GO Biological Process Annotations dataset.

outer medullary collecting duct development Gene Set

From GO Biological Process Annotations

genes participating in the outer medullary collecting duct development biological process from the curated GO Biological Process Annotations dataset.

mitochondrial outer membrane permeabilization Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial outer membrane permeabilization biological process from the curated GO Biological Process Annotations dataset.

photoreceptor cell outer segment organization Gene Set

From GO Biological Process Annotations

genes participating in the photoreceptor cell outer segment organization biological process from the curated GO Biological Process Annotations dataset.

outer dynein arm assembly Gene Set

From GO Biological Process Annotations

genes participating in the outer dynein arm assembly biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

protein localization to photoreceptor outer segment Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to photoreceptor outer segment biological process from the curated GO Biological Process Annotations dataset.

protein import into mitochondrial outer membrane Gene Set

From GO Biological Process Annotations

genes participating in the protein import into mitochondrial outer membrane biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

renal outer medulla development Gene Set

From GO Biological Process Annotations

genes participating in the renal outer medulla development biological process from the curated GO Biological Process Annotations dataset.

mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

outer acrosomal membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the outer acrosomal membrane cellular component from the curated GO Cellular Component Annotations dataset.

intrinsic component of cell outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of cell outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

condensed nuclear chromosome outer kinetochore Gene Set

From GO Cellular Component Annotations

proteins localized to the condensed nuclear chromosome outer kinetochore cellular component from the curated GO Cellular Component Annotations dataset.

photoreceptor outer segment membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the photoreceptor outer segment membrane cellular component from the curated GO Cellular Component Annotations dataset.

intrinsic component of mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

outer dynein arm Gene Set

From GO Cellular Component Annotations

proteins localized to the outer dynein arm cellular component from the curated GO Cellular Component Annotations dataset.

extrinsic component of mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the extrinsic component of mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

outer mucus layer Gene Set

From GO Cellular Component Annotations

proteins localized to the outer mucus layer cellular component from the curated GO Cellular Component Annotations dataset.

photoreceptor outer segment Gene Set

From GO Cellular Component Annotations

proteins localized to the photoreceptor outer segment cellular component from the curated GO Cellular Component Annotations dataset.

integral component of mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the integral component of mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

nuclear outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the nuclear outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial outer membrane translocase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial outer membrane translocase complex cellular component from the curated GO Cellular Component Annotations dataset.

cell outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the cell outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

outer dense fiber Gene Set

From GO Cellular Component Annotations

proteins localized to the outer dense fiber cellular component from the curated GO Cellular Component Annotations dataset.

integral component of cell outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the integral component of cell outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

nuclear outer membrane-endoplasmic reticulum membrane network Gene Set

From GO Cellular Component Annotations

proteins localized to the nuclear outer membrane-endoplasmic reticulum membrane network cellular component from the curated GO Cellular Component Annotations dataset.

intrinsic component of nuclear outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of nuclear outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

nuclear pore outer ring Gene Set

From GO Cellular Component Annotations

proteins localized to the nuclear pore outer ring cellular component from the curated GO Cellular Component Annotations dataset.

external side of cell outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the external side of cell outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

integral component of nuclear outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the integral component of nuclear outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

organelle outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the organelle outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

condensed chromosome outer kinetochore Gene Set

From GO Cellular Component Annotations

proteins localized to the condensed chromosome outer kinetochore cellular component from the curated GO Cellular Component Annotations dataset.

cytoplasmic side of mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the cytoplasmic side of mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

shortened outer dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the shortened outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Mitochondrial outer membrane transport complex, Sam37/metaxin Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial outer membrane transport complex, Sam37/metaxin protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Outer dense fibre protein 2-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Outer dense fibre protein 2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial outer membrane translocase complex, subunit Tom20 domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial outer membrane translocase complex, subunit Tom20 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial outer membrane transport complex protein, metaxin Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial outer membrane transport complex protein, metaxin protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Outer dense fibre protein 2-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Outer dense fibre protein 2-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Vitelline membrane outer layer protein I (VOMI) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Vitelline membrane outer layer protein I (VOMI) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Outer membrane protein Iml2/Tetratricopeptide repeat protein 39 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Outer membrane protein Iml2/Tetratricopeptide repeat protein 39 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial outer membrane translocase complex, subunit Tom22 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial outer membrane translocase complex, subunit Tom22 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

organelle outer membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the organelle outer membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

outer membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the outer membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

mitochondrial outer membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the mitochondrial outer membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

abnormal outer hair cell stereociliary bundle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal outer hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short photoreceptor outer segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short photoreceptor outer segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal outer nuclear layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal outer nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized retinal outer nuclear layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized retinal outer nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal rod cell outer segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal rod cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle outer root sheath morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle outer root sheath morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal outer hair cell kinocilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal outer hair cell kinocilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cochlear outer hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal orientation of outer hair cell stereociliary bundles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal orientation of outer hair cell stereociliary bundles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thick hair follicle outer rooth sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thick hair follicle outer rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal photoreceptor outer segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal photoreceptor outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal olfactory bulb outer nerve layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal olfactory bulb outer nerve layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal outer nuclear layer degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal outer nuclear layer degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear outer hair cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear outer hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized photoreceptor outer segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized photoreceptor outer segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

photoreceptor outer segment degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the photoreceptor outer segment degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

fused outer hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fused outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hair follicle outer rooth sheath hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hair follicle outer rooth sheath hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized outer root sheath cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized outer root sheath cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear outer hair cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear outer hair cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cochlear outer hair cell electromotility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retina outer limiting membrane morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retina outer limiting membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased outer hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased outer hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin hair follicle outer rooth sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin hair follicle outer rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal outer plexiform layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal outer plexiform layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney outer medulla morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney outer medulla morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal outer nuclear layer thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal outer nuclear layer thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney outer medulla inner stripe morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney outer medulla inner stripe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear outer hair cell electromotility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short outer hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized retinal outer plexiform layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized retinal outer plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear outer hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin retinal outer nuclear layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal outer nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cochlear outer hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short cochlear outer hair cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short cochlear outer hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin retinal outer plexiform layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal outer plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cochlear outer hair cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cochlear outer hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal cone cell outer segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Heterotrimeric G-protein signaling pathway-rod outer segment phototransduction Gene Set

From PANTHER Pathways

proteins participating in the Heterotrimeric G-protein signaling pathway-rod outer segment phototransduction pathway from the PANTHER Pathways dataset.

Vpr-mediated induction of apoptosis by mitochondrial outer membrane permeabilization Gene Set

From Reactome Pathways

proteins participating in the Vpr-mediated induction of apoptosis by mitochondrial outer membrane permeabilization pathway from the Reactome Pathways dataset.

hair follicle outer root sheath Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair follicle outer root sheath in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

outer dental epithelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue outer dental epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

renal outer medulla Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue renal outer medulla in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

outer plexiform layer Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue outer plexiform layer in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

outer hair cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue outer hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Early myoclonic encephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early myoclonic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

epileptic encephalopathy, early infanitle, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the epileptic encephalopathy, early infanitle, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, reducing body, X-linked, early-onset, severe Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, reducing body, X-linked, early-onset, severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 20, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 20, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth retardation, developmental delay, coarse facies, and early death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sarcoidosis, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sarcoidosis, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 23 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 6, autosomal recessive early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 6, autosomal recessive early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macular degeneration, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macular degeneration, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Breast cancer, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Breast cancer, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary myopathy with early respiratory failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary myopathy with early respiratory failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Galactosialidosis, early infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Galactosialidosis, early infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, early-onset severe Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, early-onset severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 28 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 24 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 25 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 26 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 27 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 21 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Scalp ear nipple syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Scalp ear nipple syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Question mark ears, isolated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Question mark ears, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

early endosome lumen Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the early endosome lumen cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

early phagosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the early phagosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

early endosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the early endosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

early endosome membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

early phagosome membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

early phagosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

early endosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

early endosome membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

early recombination nodule Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

Respiratory chain complex I (early intermediate NDUFAF1 assembly), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (early intermediate NDUFAF1 assembly), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.

OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 4 from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 1 from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 2 from the curated CTD Gene-Disease Associations dataset.

Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.

Hairy Ears, Y-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hairy Ears, Y-Linked from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 from the curated CTD Gene-Disease Associations dataset.

Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy from the curated CTD Gene-Disease Associations dataset.

Hereditary Myopathy with Early Respiratory Failure Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Myopathy with Early Respiratory Failure from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 6, Autosomal Recessive Early-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 6, Autosomal Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset.

Cataract, Autosomal Recessive, Early-Onset, Pulverulent Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Autosomal Recessive, Early-Onset, Pulverulent from the curated CTD Gene-Disease Associations dataset.

Sarcoidosis, Early-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sarcoidosis, Early-Onset from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 3 from the curated CTD Gene-Disease Associations dataset.

Early-onset ataxia with oculomotor apraxia and hypoalbuminemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Early-onset ataxia with oculomotor apraxia and hypoalbuminemia from the curated CTD Gene-Disease Associations dataset.

Myopathy, Early-Onset, with Fatal Cardiomyopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Early-Onset, with Fatal Cardiomyopathy from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 from the curated CTD Gene-Disease Associations dataset.

Ear Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ear Diseases from the curated CTD Gene-Disease Associations dataset.

Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset.

Parkinsonism, early onset with mental retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinsonism, early onset with mental retardation from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 7, Autosomal Recessive Early-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 7, Autosomal Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset.

Myopathy, Reducing Body, X-Linked, Early-Onset, Severe Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Early-Onset, Severe from the curated CTD Gene-Disease Associations dataset.

Ear, External Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Ear, External in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

inner ear disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease inner ear disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

cholesteatoma of middle ear Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease cholesteatoma of middle ear in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

external ear cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease external ear cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

external ear disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease external ear disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

early yaws Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease early yaws in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

middle ear squamous cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease middle ear squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

inner ear disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease inner ear disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

early myoclonic encephalopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease early myoclonic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

early invasive cervical adenocarcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease early invasive cervical adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

middle ear cholesteatoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease middle ear cholesteatoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

middle ear carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease middle ear carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

middle ear adenoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease middle ear adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

external ear carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease external ear carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

middle ear cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease middle ear cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

middle ear disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease middle ear disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

early onset absence epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease early onset absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

early coronary disease. Gene Set

From GAD Gene-Disease Associations

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

humoral responses to early food allergens in children Gene Set

From GAD Gene-Disease Associations

genes associated with the disease humoral responses to early food allergens in children in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early postmenopausal bone loss at the spine. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early postmenopausal bone loss at the spine. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset alcoholism/substance abuse. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset alcoholism/substance abuse. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrence and early onset of venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease recurrence and early onset of venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammatory bowel disease (early onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammatory bowel disease (early onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early polyarthritis Gene Set

From GAD Gene-Disease Associations

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

early-onset familial alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early-onset familial alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

periodontitis, early-onset Gene Set

From GAD Gene-Disease Associations

genes associated with the disease periodontitis, early-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

temperament in early childhood Gene Set

From GAD Gene-Disease Associations

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

early cognitive decline Gene Set

From GAD Gene-Disease Associations

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

early marginal bone loss around endosseous dental implants. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early marginal bone loss around endosseous dental implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early-onset prostate cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early-onset prostate cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

altered lipid oxidation and early insulin secretion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease altered lipid oxidation and early insulin secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early-onset alcoholism Gene Set

From GAD Gene-Disease Associations

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

early onset of esrf in pkd1 adult polycystic kidney disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset of esrf in pkd1 adult polycystic kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction (early onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction (early onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, early-onset Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, early-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal loss, early Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal loss, early in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial early onset psoriasis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial early onset psoriasis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity (early onset extreme) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity (early onset extreme) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset of sudden infant death. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset of sudden infant death. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

conversion from colorectal adenoma to early carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease conversion from colorectal adenoma to early carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset ischemic heart disease. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset ischemic heart disease. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrent early fetal loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease recurrent early fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early-stage breast cancers Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early-stage breast cancers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced early insulin response to oral glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced early insulin response to oral glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early-onset aggressive diffuse amyloidosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early-onset aggressive diffuse amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early marginal bone loss around endosseous implants. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early marginal bone loss around endosseous implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonia, early onset primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonia, early onset primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset periodontitis Gene Set

From GAD Gene-Disease Associations

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

early onset of multiple sclerosis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset of multiple sclerosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early occlusion of coronary by-pass Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early occlusion of coronary by-pass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature ovarian failure; menopause, early Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature ovarian failure; menopause, early in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial hypertension of early onset. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial hypertension of early onset. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early-onset periodontitis Gene Set

From GAD Gene-Disease Associations

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

early osteoarthritis Gene Set

From GAD Gene-Disease Associations

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

earlyresponse Gene Set

From GeneRIF Biological Term Annotations

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

earlyageofdiagnosis Gene Set

From GeneRIF Biological Term Annotations

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

earlystage Gene Set

From GeneRIF Biological Term Annotations

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

earlysorting Gene Set

From GeneRIF Biological Term Annotations

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

earlypregnancy Gene Set

From GeneRIF Biological Term Annotations

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

earlyonset Gene Set

From GeneRIF Biological Term Annotations

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

ears Gene Set

From GeneRIF Biological Term Annotations

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

early Gene Set

From GeneRIF Biological Term Annotations

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

earliest Gene Set

From GeneRIF Biological Term Annotations

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

earlywarning Gene Set

From GeneRIF Biological Term Annotations

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

ear1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ear1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ear2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ear2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ear3 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ear3 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

eary Gene Set

From GeneRIF Biological Term Annotations

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

earlydisease Gene Set

From GeneRIF Biological Term Annotations

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

earlylife Gene Set

From GeneRIF Biological Term Annotations

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

earlyprimary Gene Set

From GeneRIF Biological Term Annotations

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

earthquake Gene Set

From GeneRIF Biological Term Annotations

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

earlymid Gene Set

From GeneRIF Biological Term Annotations

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

earlylate Gene Set

From GeneRIF Biological Term Annotations

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

earlystageheart Gene Set

From GeneRIF Biological Term Annotations

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

earlier Gene Set

From GeneRIF Biological Term Annotations

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

earlierstage Gene Set

From GeneRIF Biological Term Annotations

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

ear Gene Set

From GeneRIF Biological Term Annotations

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

earlierafter Gene Set

From GeneRIF Biological Term Annotations

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

earlyphase Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of early endosome to late endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations dataset.

inner ear morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the inner ear morphogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein localization to early endosome Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein localization to early endosome biological process from the curated GO Biological Process Annotations dataset.

inner ear receptor cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of inner ear receptor cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations dataset.

early endosome to golgi transport Gene Set

From GO Biological Process Annotations

genes participating in the early endosome to golgi transport biological process from the curated GO Biological Process Annotations dataset.

protein localization to early endosome Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to early endosome biological process from the curated GO Biological Process Annotations dataset.

regulation of early endosome to late endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations dataset.

positive regulation of early endosome to late endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations dataset.

early endosome to recycling endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations dataset.

inner ear receptor cell development Gene Set

From GO Biological Process Annotations

genes participating in the inner ear receptor cell development biological process from the curated GO Biological Process Annotations dataset.

regulation of inner ear receptor cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations dataset.

inner ear development Gene Set

From GO Biological Process Annotations

genes participating in the inner ear development biological process from the curated GO Biological Process Annotations dataset.

ear development Gene Set

From GO Biological Process Annotations

genes participating in the ear development biological process from the curated GO Biological Process Annotations dataset.

regulation of protein localization to early endosome Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein localization to early endosome biological process from the curated GO Biological Process Annotations dataset.

positive regulation of early endosome to recycling endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations dataset.

negative regulation of inner ear receptor cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations dataset.

inner ear receptor stereocilium organization Gene Set

From GO Biological Process Annotations

genes participating in the inner ear receptor stereocilium organization biological process from the curated GO Biological Process Annotations dataset.

ear morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the ear morphogenesis biological process from the curated GO Biological Process Annotations dataset.

early endosome to late endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the early endosome to late endosome transport biological process from the curated GO Biological Process Annotations dataset.

regulation of early endosome to recycling endosome transport Gene Set

From GO Biological Process Annotations

genes participating in the regulation of early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations dataset.

middle ear morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the middle ear morphogenesis biological process from the curated GO Biological Process Annotations dataset.

inner ear receptor cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the inner ear receptor cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

early endosome lumen Gene Set

From GO Cellular Component Annotations

proteins localized to the early endosome lumen cellular component from the curated GO Cellular Component Annotations dataset.

cytoplasmic side of early endosome membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the cytoplasmic side of early endosome membrane cellular component from the curated GO Cellular Component Annotations dataset.

early phagosome Gene Set

From GO Cellular Component Annotations

proteins localized to the early phagosome cellular component from the curated GO Cellular Component Annotations dataset.

early endosome Gene Set

From GO Cellular Component Annotations

proteins localized to the early endosome cellular component from the curated GO Cellular Component Annotations dataset.

early endosome membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the early endosome membrane cellular component from the curated GO Cellular Component Annotations dataset.

Prostate cancer (early onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Prostate cancer (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Monocyte early outgrowth colony forming units Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Monocyte early outgrowth colony forming units phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Obesity (early onset extreme) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Obesity (early onset extreme) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Inflammatory bowel disease (early onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Inflammatory bowel disease (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Myocardial infarction (early onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Myocardial infarction (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Breast cancer (early onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Breast cancer (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

middle ear disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease middle ear disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

inner ear disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease inner ear disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

morphological abnormality of the middle ear Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the morphological abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the ear Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the middle ear ossicles Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the middle ear ossicles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the middle ear Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

stahl ear Gene Set

From HPO Gene-Disease Associations

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

round ear Gene Set

From HPO Gene-Disease Associations

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

crumpled ear Gene Set

From HPO Gene-Disease Associations

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

external ear malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the external ear malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

large earlobe Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the middle ear Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the ear Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neoplasm of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

protruding ear Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

morphological abnormality of the vestibule of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the vestibule of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low-set, posteriorly rotated ears Gene Set

From HPO Gene-Disease Associations

genes associated with the low-set, posteriorly rotated ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior creases of earlobe Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior creases of earlobe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

small earlobe Gene Set

From HPO Gene-Disease Associations

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

recurrent infections in infancy and early childhood Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent infections in infancy and early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of earlobe Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of earlobe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the earlobes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the earlobes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cupped ear Gene Set

From HPO Gene-Disease Associations

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

superiorly displaced ears Gene Set

From HPO Gene-Disease Associations

genes associated with the superiorly displaced ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

early balding Gene Set

From HPO Gene-Disease Associations

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

dilated vestibule of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the dilated vestibule of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the middle ear Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

uplifted earlobe Gene Set

From HPO Gene-Disease Associations

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

fusion of middle ear ossicles Gene Set

From HPO Gene-Disease Associations

genes associated with the fusion of middle ear ossicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lop ear Gene Set

From HPO Gene-Disease Associations

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

abnormal middle ear reflexes Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal middle ear reflexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

large fleshy ears Gene Set

From HPO Gene-Disease Associations

genes associated with the large fleshy ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the ear Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

asymmetry of the ears Gene Set

From HPO Gene-Disease Associations

genes associated with the asymmetry of the ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal location of ears Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal location of ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

functional abnormality of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the functional abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

posteriorly rotated ears Gene Set

From HPO Gene-Disease Associations

genes associated with the posteriorly rotated ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

functional abnormality of the middle ear Gene Set

From HPO Gene-Disease Associations

genes associated with the functional abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neoplasm of the middle ear Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low-set ears Gene Set

From HPO Gene-Disease Associations

genes associated with the low-set ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neoplasm of the ear Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the ear cartilage Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the ear cartilage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of ability to walk in early childhood Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of ability to walk in early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

early onset of sexual maturation Gene Set

From HPO Gene-Disease Associations

genes associated with the early onset of sexual maturation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the middle ear ossicles Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the middle ear ossicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short ear Gene Set

From HPO Gene-Disease Associations

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

long ear Gene Set

From HPO Gene-Disease Associations

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

death in early adulthood Gene Set

From HPO Gene-Disease Associations

genes associated with the death in early adulthood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the external ear Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the external ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Ear Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ear Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Adaptin ear-binding coat-associated protein 1 NECAP-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adaptin ear-binding coat-associated protein 1 NECAP-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retrieval of early ER protein Rer1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retrieval of early ER protein Rer1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Radiation-inducible immediate-early gene IEX-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Radiation-inducible immediate-early gene IEX-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Immediate early response Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Immediate early response protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EAR Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EAR protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein LIN-9/Protein ALWAYS EARLY Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein LIN-9/Protein ALWAYS EARLY protein domain from the InterPro Predicted Protein Domain Annotations dataset.

early endosome Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the early endosome cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

EAR2 Gene Set

From MotifMap Predicted Transcription Factor Targets

target genes of the EAR2 transcription factor predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset.

abnormal ear development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ear distance/ position Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ear distance/ position phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased ear pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

inner ear cysts Gene Set

From MPO Gene-Phenotype Associations

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

lowered ear position Gene Set

From MPO Gene-Phenotype Associations

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

early vaginal opening Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ear physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ear pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

early reproductive senescence Gene Set

From MPO Gene-Phenotype Associations

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

abnormal middle ear morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal middle ear morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed inner ear development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed inner ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small ears Gene Set

From MPO Gene-Phenotype Associations

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

early parturition Gene Set

From MPO Gene-Phenotype Associations

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

abnormal middle ear ossicle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal middle ear ossicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

early sexual maturation Gene Set

From MPO Gene-Phenotype Associations

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

prominent ears Gene Set

From MPO Gene-Phenotype Associations

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

ear lobe hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

abnormal blood-inner ear barrier function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood-inner ear barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hearing/vestibular/ear phenotype Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hearing/vestibular/ear phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ear shape Gene Set

From MPO Gene-Phenotype Associations

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

abnormal inner ear canal morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner ear canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

early eyelid opening Gene Set

From MPO Gene-Phenotype Associations

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

abnormal inner ear canal fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner ear canal fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ear morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal inner ear development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed ear emergence Gene Set

From MPO Gene-Phenotype Associations

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

abnormal inner ear morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner ear morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

early cellular replicative senescence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the early cellular replicative senescence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thick ears Gene Set

From MPO Gene-Phenotype Associations

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

decreased ear pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

fusion of middle ear ossicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fusion of middle ear ossicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

big ears Gene Set

From MPO Gene-Phenotype Associations

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

abnormal inner ear vestibule morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner ear vestibule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ear lobe morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ear lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

inner ear hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

ear telangiectases Gene Set

From MPO Gene-Phenotype Associations

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

cup-shaped ears Gene Set

From MPO Gene-Phenotype Associations

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

scaly ears Gene Set

From MPO Gene-Phenotype Associations

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

ear inflammation Gene Set

From MPO Gene-Phenotype Associations

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

macular degeneration, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular degeneration, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal dystrophy, early-onset severe Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal dystrophy, early-onset severe phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, early-onset, with fatal cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, early-onset, with fatal cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

{osteoporosis, early-onset, susceptibility to, autosomal dominant} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {osteoporosis, early-onset, susceptibility to, autosomal dominant} phenotype from the curated OMIM Gene-Disease Associations dataset.

inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 24 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 24 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 26 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 26 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 27 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 27 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

scalp-ear-nipple syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the scalp-ear-nipple syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, mild, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, mild, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

breast cancer, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the breast cancer, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

hepatic failure, early onset, and neurologic disorder Gene Set

From OMIM Gene-Disease Associations

genes associated with the hepatic failure, early onset, and neurologic disorder phenotype from the curated OMIM Gene-Disease Associations dataset.

?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

inflammatory bowel disease 25, early onset, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the inflammatory bowel disease 25, early onset, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, early-onset, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, early-onset, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, congenital with inner ear agenesis, microtia, and microdontia Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, congenital with inner ear agenesis, microtia, and microdontia phenotype from the curated OMIM Gene-Disease Associations dataset.

?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, proximal, with early respiratory muscle involvement Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, proximal, with early respiratory muscle involvement phenotype from the curated OMIM Gene-Disease Associations dataset.

polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

chondrocalcinosis with early-onset osteoarthritis Gene Set

From OMIM Gene-Disease Associations

genes associated with the chondrocalcinosis with early-onset osteoarthritis phenotype from the curated OMIM Gene-Disease Associations dataset.

inflammatory bowel disease 28, early onset, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the inflammatory bowel disease 28, early onset, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

sarcoidosis, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the sarcoidosis, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

question mark ears, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the question mark ears, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

?epileptic encephalopathy, early infantile, 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?epileptic encephalopathy, early infantile, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

[earwax, wet/dry] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [earwax, wet/dry] phenotype from the curated OMIM Gene-Disease Associations dataset.

{major affective disorder 3, early onset} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {major affective disorder 3, early onset} phenotype from the curated OMIM Gene-Disease Associations dataset.

growth retardation, developmental delay, coarse facies, and early death Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth retardation, developmental delay, coarse facies, and early death phenotype from the curated OMIM Gene-Disease Associations dataset.

osteochondritis dissecans, short stature, and early-onset osteoarthritis Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteochondritis dissecans, short stature, and early-onset osteoarthritis phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 6, early onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 6, early onset phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal dystrophy, early-onset, and pituitary dysfunction Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 7, autosomal recessive early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 7, autosomal recessive early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 20, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 20, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

pulmonary disease, chronic obstructive, severe early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the pulmonary disease, chronic obstructive, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, reducing body, x-linked, severe early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, reducing body, x-linked, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, early-onset atypical, with myoclonic features Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, early-onset atypical, with myoclonic features phenotype from the curated OMIM Gene-Disease Associations dataset.

?hairy ears, y-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?hairy ears, y-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

EARS2 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for EARS2 from the Pathway Commons Protein-Protein Interactions dataset.

immediate-early-proteins Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term immediate-early-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

Formation of the Early Elongation Complex Gene Set

From Reactome Pathways

proteins participating in the Formation of the Early Elongation Complex pathway from the Reactome Pathways dataset.

Phagosomal maturation (early endosomal stage) Gene Set

From Reactome Pathways

proteins participating in the Phagosomal maturation (early endosomal stage) pathway from the Reactome Pathways dataset.

Synthesis of PIPs at the early endosome membrane Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PIPs at the early endosome membrane pathway from the Reactome Pathways dataset.

Regulation of APC/C activators between G1/S and early anaphase Gene Set

From Reactome Pathways

proteins participating in the Regulation of APC/C activators between G1/S and early anaphase pathway from the Reactome Pathways dataset.

APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 Gene Set

From Reactome Pathways

proteins participating in the APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 pathway from the Reactome Pathways dataset.

Regulation of gene expression in early pancreatic precursor cells Gene Set

From Reactome Pathways

proteins participating in the Regulation of gene expression in early pancreatic precursor cells pathway from the Reactome Pathways dataset.

Early Phase of HIV Life Cycle Gene Set

From Reactome Pathways

proteins participating in the Early Phase of HIV Life Cycle pathway from the Reactome Pathways dataset.

G0 and Early G1 Gene Set

From Reactome Pathways

proteins participating in the G0 and Early G1 pathway from the Reactome Pathways dataset.

Formation of the HIV-1 Early Elongation Complex Gene Set

From Reactome Pathways

proteins participating in the Formation of the HIV-1 Early Elongation Complex pathway from the Reactome Pathways dataset.

inner ear Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue inner ear from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

ear Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue ear from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

ear Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue ear in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

inner ear Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue inner ear in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

corn ear Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue corn ear in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

inner ear vestibulum Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue inner ear vestibulum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

middle ear Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue middle ear in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

ear Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue ear in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Absent corpus callosum cataract immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Absent corpus callosum cataract immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Absent corpus callosum cataract immunodeficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Absent corpus callosum cataract immunodeficiency from the curated CTD Gene-Disease Associations dataset.

Absent patella Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Absent patella from the curated CTD Gene-Disease Associations dataset.

Absent radii and thrombocytopenia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Absent radii and thrombocytopenia from the curated CTD Gene-Disease Associations dataset.

thrombocytopenia-absent radius syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease thrombocytopenia-absent radius syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

thrombocytopenia-absent radius syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease thrombocytopenia-absent radius syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

absent Gene Set

From GeneRIF Biological Term Annotations

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

absent sternal ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the absent sternal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent tibia Gene Set

From HPO Gene-Disease Associations

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

absent fifth fingernail Gene Set

From HPO Gene-Disease Associations

genes associated with the absent fifth fingernail phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent middle phalanx of 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the absent middle phalanx of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent or minimally ossified vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the absent or minimally ossified vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent fingernail Gene Set

From HPO Gene-Disease Associations

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

absent nasal septal cartilage Gene Set

From HPO Gene-Disease Associations

genes associated with the absent nasal septal cartilage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent phalangeal crease Gene Set

From HPO Gene-Disease Associations

genes associated with the absent phalangeal crease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent pigmentation of chest Gene Set

From HPO Gene-Disease Associations

genes associated with the absent pigmentation of chest phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent external genitalia Gene Set

From HPO Gene-Disease Associations

genes associated with the absent external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent nasal bridge Gene Set

From HPO Gene-Disease Associations

genes associated with the absent nasal bridge phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent thumb Gene Set

From HPO Gene-Disease Associations

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

absent ulna Gene Set

From HPO Gene-Disease Associations

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

absent radius Gene Set

From HPO Gene-Disease Associations

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

absent fifth toenail Gene Set

From HPO Gene-Disease Associations

genes associated with the absent fifth toenail phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent lacrimal punctum Gene Set

From HPO Gene-Disease Associations

genes associated with the absent lacrimal punctum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent forearm Gene Set

From HPO Gene-Disease Associations

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

absent facial hair Gene Set

From HPO Gene-Disease Associations

genes associated with the absent facial hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent gallbladder Gene Set

From HPO Gene-Disease Associations

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

absent pubic hair Gene Set

From HPO Gene-Disease Associations

genes associated with the absent pubic hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent glenoid fossa Gene Set

From HPO Gene-Disease Associations

genes associated with the absent glenoid fossa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

genes associated with the absent retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent vas deferens Gene Set

From HPO Gene-Disease Associations

genes associated with the absent vas deferens phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplastic-absent sebaceous glands Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplastic-absent sebaceous glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent eyebrow Gene Set

From HPO Gene-Disease Associations

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

absent paranasal sinuses Gene Set

From HPO Gene-Disease Associations

genes associated with the absent paranasal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent microvilli on the surface of peripheral blood lymphocytes Gene Set

From HPO Gene-Disease Associations

genes associated with the absent microvilli on the surface of peripheral blood lymphocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent neutrophil specific granules Gene Set

From HPO Gene-Disease Associations

genes associated with the absent neutrophil specific granules phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent palmar crease Gene Set

From HPO Gene-Disease Associations

genes associated with the absent palmar crease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent pulmonary artery Gene Set

From HPO Gene-Disease Associations

genes associated with the absent pulmonary artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent in utero rib ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the absent in utero rib ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent toenail Gene Set

From HPO Gene-Disease Associations

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

absent distal interphalangeal creases Gene Set

From HPO Gene-Disease Associations

genes associated with the absent distal interphalangeal creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent septum pellucidum Gene Set

From HPO Gene-Disease Associations

genes associated with the absent septum pellucidum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent/shortened dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent/shortened dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent rod-and cone-mediated responses on erg Gene Set

From HPO Gene-Disease Associations

genes associated with the absent rod-and cone-mediated responses on erg phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent forearm bone Gene Set

From HPO Gene-Disease Associations

genes associated with the absent forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent hand Gene Set

From HPO Gene-Disease Associations

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

absent achilles reflex Gene Set

From HPO Gene-Disease Associations

genes associated with the absent achilles reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent proximal phalanx of thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the absent proximal phalanx of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent proximal finger flexion creases Gene Set

From HPO Gene-Disease Associations

genes associated with the absent proximal finger flexion creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent first metatarsal Gene Set

From HPO Gene-Disease Associations

genes associated with the absent first metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent axillary hair Gene Set

From HPO Gene-Disease Associations

genes associated with the absent axillary hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent brainstem auditory responses Gene Set

From HPO Gene-Disease Associations

genes associated with the absent brainstem auditory responses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent knee epiphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the absent knee epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sparse or absent eyelashes Gene Set

From HPO Gene-Disease Associations

genes associated with the sparse or absent eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent cellular immunity Gene Set

From HPO Gene-Disease Associations

genes associated with the absent cellular immunity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent patellar reflexes Gene Set

From HPO Gene-Disease Associations

genes associated with the absent patellar reflexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent nares Gene Set

From HPO Gene-Disease Associations

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

absent toe Gene Set

From HPO Gene-Disease Associations

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

absent/hypoplastic coccyx Gene Set

From HPO Gene-Disease Associations

genes associated with the absent/hypoplastic coccyx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent urinary urothione Gene Set

From HPO Gene-Disease Associations

genes associated with the absent urinary urothione phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased/absent ankle reflexes Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased/absent ankle reflexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent uvula Gene Set

From HPO Gene-Disease Associations

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

absent specific antibody response Gene Set

From HPO Gene-Disease Associations

genes associated with the absent specific antibody response phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent inner dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent inner dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent in utero ossification of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the absent in utero ossification of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent primary metaphyseal spongiosa Gene Set

From HPO Gene-Disease Associations

genes associated with the absent primary metaphyseal spongiosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent/hypoplastic paranasal sinuses Gene Set

From HPO Gene-Disease Associations

genes associated with the absent/hypoplastic paranasal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent vertebral body mineralization Gene Set

From HPO Gene-Disease Associations

genes associated with the absent vertebral body mineralization phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent distal phalanges Gene Set

From HPO Gene-Disease Associations

genes associated with the absent distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent eyelashes Gene Set

From HPO Gene-Disease Associations

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

absent styloid process of ulna Gene Set

From HPO Gene-Disease Associations

genes associated with the absent styloid process of ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent epiphyses Gene Set

From HPO Gene-Disease Associations

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

absent nipple Gene Set

From HPO Gene-Disease Associations

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

absent pigmentation of the ventral chest Gene Set

From HPO Gene-Disease Associations

genes associated with the absent pigmentation of the ventral chest phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent frontal sinuses Gene Set

From HPO Gene-Disease Associations

genes associated with the absent frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent vestibular function Gene Set

From HPO Gene-Disease Associations

genes associated with the absent vestibular function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent skin pigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the absent skin pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent speech Gene Set

From HPO Gene-Disease Associations

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

absent hair Gene Set

From HPO Gene-Disease Associations

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

absent metatarsal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the absent metatarsal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent anterior eye chamber Gene Set

From HPO Gene-Disease Associations

genes associated with the absent anterior eye chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent fourth finger distal interphalangeal crease Gene Set

From HPO Gene-Disease Associations

genes associated with the absent fourth finger distal interphalangeal crease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Eyes absent homologue 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Eyes absent homologue 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Eyes absent homologue 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Eyes absent homologue 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Eyes absent homologue 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Eyes absent homologue 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Eyes absent homologue 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Eyes absent homologue 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Eyes absent family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Eyes absent family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

absent metencephalon Gene Set

From MPO Gene-Phenotype Associations

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

absent cervical lymph nodes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cervical lymph nodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent prechordal plate Gene Set

From MPO Gene-Phenotype Associations

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

absent tibia Gene Set

From MPO Gene-Phenotype Associations

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

absent endoderm Gene Set

From MPO Gene-Phenotype Associations

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

absent b cells Gene Set

From MPO Gene-Phenotype Associations

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

absent acromion Gene Set

From MPO Gene-Phenotype Associations

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

absent nodal flow Gene Set

From MPO Gene-Phenotype Associations

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

absent cochlear hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent rathke's pouch Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent rathke's pouch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent pineal gland Gene Set

From MPO Gene-Phenotype Associations

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

absent caveolae Gene Set

From MPO Gene-Phenotype Associations

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

absent neutrophils Gene Set

From MPO Gene-Phenotype Associations

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

absent mesencephalic trigeminal nucleus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent mesencephalic trigeminal nucleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent trophectoderm Gene Set

From MPO Gene-Phenotype Associations

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

absent lamina terminalis Gene Set

From MPO Gene-Phenotype Associations

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

absent presphenoid bone Gene Set

From MPO Gene-Phenotype Associations

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

absent right lung accessory lobe Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent right lung accessory lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent circulating noradrenaline Gene Set

From MPO Gene-Phenotype Associations

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

absent long term depression Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent thymus cortex Gene Set

From MPO Gene-Phenotype Associations

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

absent tooth primordium Gene Set

From MPO Gene-Phenotype Associations

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

absent cartilage Gene Set

From MPO Gene-Phenotype Associations

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

absent molar root Gene Set

From MPO Gene-Phenotype Associations

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

absent maxillary shelf Gene Set

From MPO Gene-Phenotype Associations

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

absent hair follicle pheomelanosome pheomelanin Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicle pheomelanosome pheomelanin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent thyroid gland Gene Set

From MPO Gene-Phenotype Associations

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

absent cerebellum fissure Gene Set

From MPO Gene-Phenotype Associations

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

absent optic tract Gene Set

From MPO Gene-Phenotype Associations

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

absent immature b cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent immature b cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hair follicle inner root sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicle inner root sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent dorsal root ganglion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent dorsal root ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent digestive secretion Gene Set

From MPO Gene-Phenotype Associations

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

absent visual evoked potential Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent visual evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent horizontal cells Gene Set

From MPO Gene-Phenotype Associations

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

absent urinary bladder Gene Set

From MPO Gene-Phenotype Associations

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

absent heartbeat Gene Set

From MPO Gene-Phenotype Associations

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

absent retinal ganglion layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent estrous cycle Gene Set

From MPO Gene-Phenotype Associations

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

absent magnocellular neurosecretory cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent magnocellular neurosecretory cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cerebellum vermis Gene Set

From MPO Gene-Phenotype Associations

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

absent salivary gland Gene Set

From MPO Gene-Phenotype Associations

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

absent petrosal ganglion Gene Set

From MPO Gene-Phenotype Associations

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

absent transitional stage b cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent transitional stage b cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent metanephric mesenchyme Gene Set

From MPO Gene-Phenotype Associations

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

absent cochlear hair bundle ankle links Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear hair bundle ankle links phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent optic placodes Gene Set

From MPO Gene-Phenotype Associations

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

absent hyoid bone greater horns Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hyoid bone greater horns phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent z lines Gene Set

From MPO Gene-Phenotype Associations

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

absent anterior definitive endoderm Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent anterior definitive endoderm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent mandibular coronoid process Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent mandibular coronoid process phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent superior cervical ganglion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent superior cervical ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent eyelids Gene Set

From MPO Gene-Phenotype Associations

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

absent mature gamma-delta t cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent mature gamma-delta t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent respiratory motile cilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent respiratory motile cilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent limbs Gene Set

From MPO Gene-Phenotype Associations

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

absent epiglottis Gene Set

From MPO Gene-Phenotype Associations

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

absent visceral yolk sac Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent visceral yolk sac phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent pharyngeal arch arteries Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent pharyngeal arch arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cerebellum vermis lobule ix Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cerebellum vermis lobule ix phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent facial nuclei Gene Set

From MPO Gene-Phenotype Associations

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

absent trigeminal nerve Gene Set

From MPO Gene-Phenotype Associations

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

absent visceral yolk sac blood islands Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent visceral yolk sac blood islands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent inner cell mass proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent inner cell mass proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent amacrine cells Gene Set

From MPO Gene-Phenotype Associations

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

absent brain internal capsule Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent brain internal capsule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent leydig cells Gene Set

From MPO Gene-Phenotype Associations

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

absent b-1 b cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent b-1 b cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cochlear microphonics Gene Set

From MPO Gene-Phenotype Associations

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

absent rectum Gene Set

From MPO Gene-Phenotype Associations

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

absent vestibular ganglion Gene Set

From MPO Gene-Phenotype Associations

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

absent endolymphatic sac Gene Set

From MPO Gene-Phenotype Associations

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

absent hair follicle melanin granules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicle melanin granules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent glossopharyngeal nerve Gene Set

From MPO Gene-Phenotype Associations

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

absent p wave Gene Set

From MPO Gene-Phenotype Associations

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

absent retinal inner plexiform layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hypodermis muscle layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hypodermis muscle layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent mullerian ducts Gene Set

From MPO Gene-Phenotype Associations

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

absent brain ventricles Gene Set

From MPO Gene-Phenotype Associations

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

absent proximal rib Gene Set

From MPO Gene-Phenotype Associations

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

absent hard palate Gene Set

From MPO Gene-Phenotype Associations

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

absent diencephalon Gene Set

From MPO Gene-Phenotype Associations

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

absent retinal rod cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal rod cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent intervertebral disk Gene Set

From MPO Gene-Phenotype Associations

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

absent midgut Gene Set

From MPO Gene-Phenotype Associations

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

absent thyroid follicular cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent thyroid follicular cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent uterus Gene Set

From MPO Gene-Phenotype Associations

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

absent vagal neural crest cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vagal neural crest cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent platelets Gene Set

From MPO Gene-Phenotype Associations

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

absent metoptic pilar Gene Set

From MPO Gene-Phenotype Associations

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

absent schwann cell precursors Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent schwann cell precursors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hindlimb buds Gene Set

From MPO Gene-Phenotype Associations

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

absent interventricular septum membranous part Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent interventricular septum membranous part phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent sperm mitochondrial sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent sperm mitochondrial sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent incisors Gene Set

From MPO Gene-Phenotype Associations

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

absent visceral endoderm Gene Set

From MPO Gene-Phenotype Associations

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

absent hair follicle dermal papilla Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicle dermal papilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent ectoplacental cone Gene Set

From MPO Gene-Phenotype Associations

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

absent alisphenoid bone Gene Set

From MPO Gene-Phenotype Associations

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

absent guard hair Gene Set

From MPO Gene-Phenotype Associations

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

absent muscle spindles Gene Set

From MPO Gene-Phenotype Associations

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

absent vertebral spinous process Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vertebral spinous process phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent ribs Gene Set

From MPO Gene-Phenotype Associations

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

absent ovary capsule Gene Set

From MPO Gene-Phenotype Associations

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

absent patella Gene Set

From MPO Gene-Phenotype Associations

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

absent ulna Gene Set

From MPO Gene-Phenotype Associations

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

absent neural folds Gene Set

From MPO Gene-Phenotype Associations

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

absent gametes Gene Set

From MPO Gene-Phenotype Associations

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

absent fourth pharyngeal arch Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent fourth pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent subplate Gene Set

From MPO Gene-Phenotype Associations

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

absent podocytes Gene Set

From MPO Gene-Phenotype Associations

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

absent mature b cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent mature b cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent pulmonary alveoli Gene Set

From MPO Gene-Phenotype Associations

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

absent vestibular hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vestibular hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent zygomatic bone Gene Set

From MPO Gene-Phenotype Associations

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

absent marginal zone b cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent marginal zone b cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent malleus manubrium Gene Set

From MPO Gene-Phenotype Associations

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

absent retina Gene Set

From MPO Gene-Phenotype Associations

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

absent axillary lymph nodes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent axillary lymph nodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent myocardial trabeculae Gene Set

From MPO Gene-Phenotype Associations

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

absent vertebrae Gene Set

From MPO Gene-Phenotype Associations

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

absent thyrotrophs Gene Set

From MPO Gene-Phenotype Associations

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

absent adrenal gland Gene Set

From MPO Gene-Phenotype Associations

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

absent nk t cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent nk t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent stapes Gene Set

From MPO Gene-Phenotype Associations

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

absent corpus luteum Gene Set

From MPO Gene-Phenotype Associations

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

absent eye pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

absent subcutaneous adipose tissue Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent subcutaneous adipose tissue phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent testis cords Gene Set

From MPO Gene-Phenotype Associations

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

absent allantois Gene Set

From MPO Gene-Phenotype Associations

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

absent modiolus Gene Set

From MPO Gene-Phenotype Associations

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

absent olfactory bulb Gene Set

From MPO Gene-Phenotype Associations

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

absent aorticopulmonary septum Gene Set

From MPO Gene-Phenotype Associations

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

absent forelimb Gene Set

From MPO Gene-Phenotype Associations

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

absent deiters cells Gene Set

From MPO Gene-Phenotype Associations

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

absent scala media Gene Set

From MPO Gene-Phenotype Associations

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

absent nephron Gene Set

From MPO Gene-Phenotype Associations

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

absent malleus processus brevis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent malleus processus brevis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cochlear ganglion Gene Set

From MPO Gene-Phenotype Associations

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

absent vibrissae Gene Set

From MPO Gene-Phenotype Associations

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

absent palatine gland Gene Set

From MPO Gene-Phenotype Associations

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

absent pulmonary neuroendocrine bodies Gene Set

From MPO Gene-Phenotype Associations

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

absent cerebellar foliation Gene Set

From MPO Gene-Phenotype Associations

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

absent seminal vesicle Gene Set

From MPO Gene-Phenotype Associations

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

absent vestibuloocular reflex Gene Set

From MPO Gene-Phenotype Associations

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

absent ureter Gene Set

From MPO Gene-Phenotype Associations

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

absent cerebellar granule cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cerebellar granule cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent nasal bone Gene Set

From MPO Gene-Phenotype Associations

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

absent hindlimb Gene Set

From MPO Gene-Phenotype Associations

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

absent ethmoidal bone Gene Set

From MPO Gene-Phenotype Associations

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

absent pancreatic acinar cell zymogen granule Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent pancreatic acinar cell zymogen granule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent superior semicircular canal Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent superior semicircular canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent heart tube Gene Set

From MPO Gene-Phenotype Associations

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

absent maternal crouching Gene Set

From MPO Gene-Phenotype Associations

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

absent cochlear nerve Gene Set

From MPO Gene-Phenotype Associations

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

absent parathyroid glands Gene Set

From MPO Gene-Phenotype Associations

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

absent erythroid progenitor cell Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent erythroid progenitor cell phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vertebral arch Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vertebral arch 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.

absent optic nerve Gene Set

From MPO Gene-Phenotype Associations

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

absent pro-b cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent pro-b cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent external male genitalia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent external male genitalia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent gonadotrophs Gene Set

From MPO Gene-Phenotype Associations

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

absent inner hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent endolymphatic duct Gene Set

From MPO Gene-Phenotype Associations

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

absent rosenthal canal Gene Set

From MPO Gene-Phenotype Associations

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

absent type i pneumocytes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent type i pneumocytes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hyoid bone lesser horns Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hyoid bone lesser horns phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent spleen Gene Set

From MPO Gene-Phenotype Associations

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

absent zygomatic arch Gene Set

From MPO Gene-Phenotype Associations

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

absent sternum body Gene Set

From MPO Gene-Phenotype Associations

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

absent intersomitic vessels Gene Set

From MPO Gene-Phenotype Associations

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

absent nasal placodes Gene Set

From MPO Gene-Phenotype Associations

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

absent masseter muscle Gene Set

From MPO Gene-Phenotype Associations

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

absent odontoid process Gene Set

From MPO Gene-Phenotype Associations

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

absent purkinje cell layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent purkinje cell layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent megakaryocytes Gene Set

From MPO Gene-Phenotype Associations

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

absent cerebral aqueduct Gene Set

From MPO Gene-Phenotype Associations

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

absent pp cells Gene Set

From MPO Gene-Phenotype Associations

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

absent pubis Gene Set

From MPO Gene-Phenotype Associations

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

absent palatal shelf Gene Set

From MPO Gene-Phenotype Associations

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

absent atrioventricular cushions Gene Set

From MPO Gene-Phenotype Associations

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

absent gallbladder Gene Set

From MPO Gene-Phenotype Associations

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

absent clavicle Gene Set

From MPO Gene-Phenotype Associations

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

absent enamel Gene Set

From MPO Gene-Phenotype Associations

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

absent linear vestibular evoked potential Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent linear vestibular evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent facial nerve Gene Set

From MPO Gene-Phenotype Associations

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

absent barrels in primary somatosensory cortex Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent barrels in primary somatosensory cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent upper incisors Gene Set

From MPO Gene-Phenotype Associations

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

absent craniofacial bones Gene Set

From MPO Gene-Phenotype Associations

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

absent epidermis stratum granulosum Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent epidermis stratum granulosum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent anterior lingual gland Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent anterior lingual gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent pharyngeal arches Gene Set

From MPO Gene-Phenotype Associations

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

absent somites Gene Set

From MPO Gene-Phenotype Associations

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

absent placenta hemotrichorial membrane Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent placenta hemotrichorial membrane phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vas deferens Gene Set

From MPO Gene-Phenotype Associations

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

absent pre-b cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent pre-b cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent bulbourethral gland Gene Set

From MPO Gene-Phenotype Associations

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

absent male inguinal canal Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent male inguinal canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent uterine nk cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent uterine nk cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent gonial bone Gene Set

From MPO Gene-Phenotype Associations

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

absent palatine bone horizontal plate Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent palatine bone horizontal plate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent auchene hairs Gene Set

From MPO Gene-Phenotype Associations

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

absent cardiac jelly Gene Set

From MPO Gene-Phenotype Associations

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

absent fibroblast proliferation Gene Set

From MPO Gene-Phenotype Associations

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

absent epididymis Gene Set

From MPO Gene-Phenotype Associations

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

absent primitive node Gene Set

From MPO Gene-Phenotype Associations

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

absent strial intermediate cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent strial intermediate cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent plasma cells Gene Set

From MPO Gene-Phenotype Associations

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

absent epidermis stratum spinosum Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent epidermis stratum spinosum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent spleen germinal center Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent spleen germinal center phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent skeletal muscle Gene Set

From MPO Gene-Phenotype Associations

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

absent embryonic epiblast Gene Set

From MPO Gene-Phenotype Associations

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

absent trophectoderm cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent trophectoderm cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent trabeculae carneae Gene Set

From MPO Gene-Phenotype Associations

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

absent cerebellum Gene Set

From MPO Gene-Phenotype Associations

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

absent arcus anterior Gene Set

From MPO Gene-Phenotype Associations

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

absent superior olivary complex Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent superior olivary complex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent memory b cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent memory b cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent myotome Gene Set

From MPO Gene-Phenotype Associations

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

absent pulmonary artery Gene Set

From MPO Gene-Phenotype Associations

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

absent stapedial artery Gene Set

From MPO Gene-Phenotype Associations

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

absent carpal bone Gene Set

From MPO Gene-Phenotype Associations

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

absent circulating adrenaline Gene Set

From MPO Gene-Phenotype Associations

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

absent b-2 b cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent b-2 b cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent oviduct Gene Set

From MPO Gene-Phenotype Associations

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

absent vestibular hair cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vestibular hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hair-down neurons Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair-down neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent pr interval Gene Set

From MPO Gene-Phenotype Associations

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

absent theca folliculi Gene Set

From MPO Gene-Phenotype Associations

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

absent kidney cortex Gene Set

From MPO Gene-Phenotype Associations

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

absent radius Gene Set

From MPO Gene-Phenotype Associations

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

absent tympanic membrane Gene Set

From MPO Gene-Phenotype Associations

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

absent embryonic cilia Gene Set

From MPO Gene-Phenotype Associations

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

absent nucleus pulposus Gene Set

From MPO Gene-Phenotype Associations

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

absent enterocytes Gene Set

From MPO Gene-Phenotype Associations

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

absent male preputial gland Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent male preputial gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent mandibular angle Gene Set

From MPO Gene-Phenotype Associations

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

increased or absent threshold for auditory brainstem response Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased or absent threshold for auditory brainstem response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent harderian gland Gene Set

From MPO Gene-Phenotype Associations

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

absent anus Gene Set

From MPO Gene-Phenotype Associations

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

absent lateral semicircular canal Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent lateral semicircular canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vertebral body Gene Set

From MPO Gene-Phenotype Associations

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

absent oviduct epithelium motile cilium Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent oviduct epithelium motile cilium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent pulmonary vein Gene Set

From MPO Gene-Phenotype Associations

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

absent pancreatic alpha cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent pancreatic alpha cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent primordial ovarian follicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent primordial ovarian follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent apical ectodermal ridge Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent apical ectodermal ridge phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent prostate gland Gene Set

From MPO Gene-Phenotype Associations

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

absent hassall's corpuscle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hassall's corpuscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent podocyte foot process Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent podocyte foot process phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent liver Gene Set

From MPO Gene-Phenotype Associations

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

absent pinna reflex Gene Set

From MPO Gene-Phenotype Associations

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

absent rhombomere 3 Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent rhombomere 3 phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent rhombomere 5 Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent rhombomere 5 phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent limb buds Gene Set

From MPO Gene-Phenotype Associations

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

absent zona pellucida Gene Set

From MPO Gene-Phenotype Associations

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

absent inner hair cell kinocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent inner hair cell kinocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent bone marrow cell Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent bone marrow cell phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent neurocranium Gene Set

From MPO Gene-Phenotype Associations

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

absent humerus Gene Set

From MPO Gene-Phenotype Associations

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

absent pterygoid muscle Gene Set

From MPO Gene-Phenotype Associations

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

absent dermatome Gene Set

From MPO Gene-Phenotype Associations

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

absent cerebellar lobules Gene Set

From MPO Gene-Phenotype Associations

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

absent sternum Gene Set

From MPO Gene-Phenotype Associations

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

absent basisphenoid bone Gene Set

From MPO Gene-Phenotype Associations

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

absent nasal septum Gene Set

From MPO Gene-Phenotype Associations

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

absent pulmonary valve cusps Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent pulmonary valve cusps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent sexual maturation Gene Set

From MPO Gene-Phenotype Associations

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