Name

absent retinal ganglion cell Gene Set

From MPO Gene-Phenotype Associations

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

Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease 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.

regulation of retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

positive regulation of retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

negative regulation of retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

abnormal retinal ganglion cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased retinal ganglion cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased retinal ganglion cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal ganglion cell degeneration Gene Set

From MPO Gene-Phenotype Associations

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

decreased retinal ganglion cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased retinal ganglion cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal ganglion cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal ganglion cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

thick retinal ganglion layer Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal ganglion layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

thin retinal ganglion layer Gene Set

From MPO Gene-Phenotype Associations

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

disorganized retinal ganglion layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized retinal ganglion layer 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 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 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 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 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 nodose ganglion Gene Set

From MPO Gene-Phenotype Associations

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

absent vestibulocochlear ganglion Gene Set

From MPO Gene-Phenotype Associations

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

absent trigeminal ganglion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent trigeminal ganglion 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 retinal cone cells Gene Set

From MPO Gene-Phenotype Associations

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

activated protein c resistance; retinal neovascularization; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; retinal neovascularization; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; retinal artery occlusion; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal artery occlusion; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD 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 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.

ganglion mother cell fate determination Gene Set

From GO Biological Process Annotations

genes participating in the ganglion mother cell fate determination biological process from the curated GO Biological Process Annotations dataset.

ganglion cell layer Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

regulation of retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

ganglion Gene Set

From GeneRIF Biological Term Annotations

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

cranial ganglion development Gene Set

From GO Biological Process Annotations

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

ganglion morphogenesis Gene Set

From GO Biological Process Annotations

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

ganglion development Gene Set

From GO Biological Process Annotations

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

facioacoustic ganglion development Gene Set

From GO Biological Process Annotations

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

trigeminal ganglion development Gene Set

From GO Biological Process Annotations

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

sympathetic ganglion development Gene Set

From GO Biological Process Annotations

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

abnormal trigeminal ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal paravertebral ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal parasympathetic ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal superior vagus ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal lumbar dorsal root ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

fused dorsal root ganglion Gene Set

From MPO Gene-Phenotype Associations

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

small superior glossopharyngeal ganglion Gene Set

From MPO Gene-Phenotype Associations

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

small cochlear ganglion Gene Set

From MPO Gene-Phenotype Associations

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

abnormal stellate ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal prevertebral ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal vagus ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal geniculate ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal l5 dorsal root ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal l5 dorsal root ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cochlear ganglion hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

small geniculate ganglion Gene Set

From MPO Gene-Phenotype Associations

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

abnormal basal ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal sublingual ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal petrosal ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal superior cervical ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal sensory ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

small submandibular ganglion Gene Set

From MPO Gene-Phenotype Associations

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

abnormal l3 dorsal root ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal l3 dorsal root ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal superior glossopharyngeal ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

enlarged trigeminal ganglion Gene Set

From MPO Gene-Phenotype Associations

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

small l5 dorsal root ganglion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small l5 dorsal root ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small vestibular ganglion Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ciliary ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal vestibular ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

small petrosal ganglion Gene Set

From MPO Gene-Phenotype Associations

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

small superior cervical ganglion Gene Set

From MPO Gene-Phenotype Associations

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

disorganized dorsal root ganglion Gene Set

From MPO Gene-Phenotype Associations

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

abnormal dorsal root ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

vestibular ganglion degeneration Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cardiac ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal otic ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

dorsal root ganglion hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

dorsal root ganglion degeneration Gene Set

From MPO Gene-Phenotype Associations

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

small nodose ganglion Gene Set

From MPO Gene-Phenotype Associations

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

small l4 dorsal root ganglion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small l4 dorsal root ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small superior vagus ganglion Gene Set

From MPO Gene-Phenotype Associations

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

small trigeminal ganglion Gene Set

From MPO Gene-Phenotype Associations

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

vestibular ganglion hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

abnormal glossopharyngeal ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal submandibular ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal pterygopalatine ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal l4 dorsal root ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal l4 dorsal root ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cochlear ganglion degeneration Gene Set

From MPO Gene-Phenotype Associations

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

small dorsal root ganglion Gene Set

From MPO Gene-Phenotype Associations

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

l5 dorsal root ganglion hypertrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the l5 dorsal root ganglion hypertrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal nodose ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal sympathetic ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

superior cervical ganglion degeneration Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

enlarged superior cervical ganglion Gene Set

From MPO Gene-Phenotype Associations

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

abnormal vestibulocochlear ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

peripheral ganglion Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

sympathetic ganglion Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

spinal ganglion Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

basal ganglion Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

ganglion Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

peripheral ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

superior cervical ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

trigeminal ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

basal ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

cranial ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

sympathetic ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

cervical ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

spinal ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

cerebral ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

sympathetic ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

thoracic ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

superior cervical ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

abdominal ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

basal ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

thoracico-abdominal ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

pedal ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cervical ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

spinal ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

larval ventral ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

inferior cervical ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

pleural ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cochlear ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

optic ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

vertebral ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

ingluvial ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

subesophageal ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

submandibular ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

middle cervical ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

parietal ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

stellate ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

trigeminal ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

peripheral ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cranial ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

parasympathetic ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebellar purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation biological process from the curated GO Biological Process Annotations dataset.

retinal cell cancer Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease retinal cell cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

retinal cell cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal rod cell development Gene Set

From GO Biological Process Annotations

genes participating in the retinal rod cell development biological process from the curated GO Biological Process Annotations dataset.

retinal cell apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the retinal cell apoptotic process biological process from the curated GO Biological Process Annotations dataset.

retinal cone cell development Gene Set

From GO Biological Process Annotations

genes participating in the retinal cone cell development biological process from the curated GO Biological Process Annotations dataset.

retinal rod cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the retinal rod cell differentiation biological process from the curated GO Biological Process Annotations dataset.

abnormal retinal rod cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal cone cell inner segment morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal cone bipolar cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased retinal cone cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased retinal cone cell number 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 retinal bipolar cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal cone cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal progenitor cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased retinal photoreceptor cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased retinal photoreceptor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased retinal photoreceptor cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased retinal photoreceptor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal rod cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal rod cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal rod bipolar cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

retinal cone cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal cone cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased retinal rod cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased retinal rod cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal rod cell inner segment morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased retinal cone cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased retinal cone cell number 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.

retinal microvascular endothelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal pigment epithelium cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal pigment epithelium cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue retinal stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 adrenal chromaffin cells Gene Set

From MPO Gene-Phenotype Associations

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

absent respiratory mucosa goblet cells Gene Set

From MPO Gene-Phenotype Associations

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

absent interdental cells Gene Set

From MPO Gene-Phenotype Associations

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

absent cardiac neural crest cells Gene Set

From MPO Gene-Phenotype Associations

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

absent cochlear inner hair cells Gene Set

From MPO Gene-Phenotype Associations

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

absent b-1b cells Gene Set

From MPO Gene-Phenotype Associations

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

absent follicular b cells Gene Set

From MPO Gene-Phenotype Associations

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

absent strial marginal cells Gene Set

From MPO Gene-Phenotype Associations

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

absent germ cells Gene Set

From MPO Gene-Phenotype Associations

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

absent regulatory t cells Gene Set

From MPO Gene-Phenotype Associations

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

absent strial basal cell tight junctions Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent strial basal cell tight junctions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent t cells Gene Set

From MPO Gene-Phenotype Associations

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

absent pancreatic delta cells Gene Set

From MPO Gene-Phenotype Associations

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

absent primordial germ cells Gene Set

From MPO Gene-Phenotype Associations

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

absent pillar cells Gene Set

From MPO Gene-Phenotype Associations

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

absent pancreatic beta cells Gene Set

From MPO Gene-Phenotype Associations

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

absent enteric neural crest cell Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent enteric neural crest cell phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent neuronal precursor cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent neuronal precursor 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 cochlear hair cells Gene Set

From MPO Gene-Phenotype Associations

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

absent gamma-delta intraepithelial t cell Gene Set

From MPO Gene-Phenotype Associations

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

absent active-zone-anchored inner hair cell synaptic ribbon Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent active-zone-anchored inner hair cell synaptic ribbon phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent solitary pulmonary neuroendocrine cells Gene Set

From MPO Gene-Phenotype Associations

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

absent langerhans cell Gene Set

From MPO Gene-Phenotype Associations

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

absent cd4-positive, alpha beta t cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cd4-positive, alpha beta t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent schwann cells Gene Set

From MPO Gene-Phenotype Associations

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

absent cajal-retzius cell Gene Set

From MPO Gene-Phenotype Associations

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

absent oval cells Gene Set

From MPO Gene-Phenotype Associations

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

absent inner cell mass Gene Set

From MPO Gene-Phenotype Associations

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

absent mesangial cell Gene Set

From MPO Gene-Phenotype Associations

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

absent mast cells Gene Set

From MPO Gene-Phenotype Associations

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

absent trophoblast giant cells Gene Set

From MPO Gene-Phenotype Associations

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

absent nk cells Gene Set

From MPO Gene-Phenotype Associations

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

absent gamma-delta t cells Gene Set

From MPO Gene-Phenotype Associations

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

absent follicular dendritic cells Gene Set

From MPO Gene-Phenotype Associations

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

absent germinal center b cells Gene Set

From MPO Gene-Phenotype Associations

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

absent adrenergic chromaffin cells Gene Set

From MPO Gene-Phenotype Associations

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

absent b-1a cells Gene Set

From MPO Gene-Phenotype Associations

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

absent organ of corti supporting cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent organ of corti supporting cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent common myeloid progenitor cells Gene Set

From MPO Gene-Phenotype Associations

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

absent late pro-b cells Gene Set

From MPO Gene-Phenotype Associations

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

absent cd8-positive, alpha-beta t cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cd8-positive, alpha-beta t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

b-cell lymphomas; lymphoma, b-cell; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse Gene Set

From GAD Gene-Disease Associations

genes associated with the disease b-cell lymphomas; lymphoma, b-cell; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, giant cell; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, giant cell; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cell-cell signaling involved in cell-cell junction organization Gene Set

From GO Biological Process Annotations

genes participating in the cell-cell signaling involved in cell-cell junction organization biological process from the curated GO Biological Process Annotations dataset.

non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Patterned dystrophy of retinal pigment epithelium Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Patterned dystrophy of retinal pigment epithelium phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rhegmatogenous retinal detachment, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rhegmatogenous retinal detachment, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal degeneration, autosomal recessive, clumped pigment type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal degeneration, autosomal recessive, clumped pigment type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal cone dystrophy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal cone dystrophy 3B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal cone dystrophy 3B 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.

Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

retinal dimer Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical retinal dimer from the curated CTD Gene-Chemical Interactions dataset.

9-cis-retinal Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 9-cis-retinal from the curated CTD Gene-Chemical Interactions dataset.

13-cis-retinal Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 13-cis-retinal from the curated CTD Gene-Chemical Interactions dataset.

Retinal Cone Dystrophy 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Cone Dystrophy 1 from the curated CTD Gene-Disease Associations dataset.

Retinal Detachment Gene Set

From CTD Gene-Disease Associations

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

Retinal Cone Dystrophy 3A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Cone Dystrophy 3A from the curated CTD Gene-Disease Associations dataset.

Macular dystrophy, retinal, 1, North Carolina type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular dystrophy, retinal, 1, North Carolina type from the curated CTD Gene-Disease Associations dataset.

Retinal Cone Dystrophy 3B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Cone Dystrophy 3B from the curated CTD Gene-Disease Associations dataset.

Retinal Artery Occlusion Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Artery Occlusion from the curated CTD Gene-Disease Associations dataset.

Vasculopathy, Retinal, With Cerebral Leukodystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Vasculopathy, Retinal, With Cerebral Leukodystrophy from the curated CTD Gene-Disease Associations dataset.

Macular Dystrophy, Retinal, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular Dystrophy, Retinal, 2 from the curated CTD Gene-Disease Associations dataset.

Retinal Dystrophies Gene Set

From CTD Gene-Disease Associations

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

Patterned dystrophy of retinal pigment epithelium Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Patterned dystrophy of retinal pigment epithelium from the curated CTD Gene-Disease Associations dataset.

Retinal Diseases Gene Set

From CTD Gene-Disease Associations

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

MACULAR DYSTROPHY, RETINAL, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MACULAR DYSTROPHY, RETINAL, 3 from the curated CTD Gene-Disease Associations dataset.

Bothnia Retinal Dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bothnia Retinal Dystrophy from the curated CTD Gene-Disease Associations dataset.

Retinal Degeneration Gene Set

From CTD Gene-Disease Associations

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

Retinal Vein Occlusion Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Vein Occlusion from the curated CTD Gene-Disease Associations dataset.

Doyne honeycomb retinal dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Doyne honeycomb retinal dystrophy from the curated CTD Gene-Disease Associations dataset.

RETINAL DYSPLASIA, PRIMARY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETINAL DYSPLASIA, PRIMARY from the curated CTD Gene-Disease Associations dataset.

Retinal cone dystrophy 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal cone dystrophy 2 from the curated CTD Gene-Disease Associations dataset.

Retinal Telangiectasis Gene Set

From CTD Gene-Disease Associations

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

Retinal Nonattachment, Nonsyndromic Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Nonattachment, Nonsyndromic Congenital from the curated CTD Gene-Disease Associations dataset.

Retinal Hemorrhage Gene Set

From CTD Gene-Disease Associations

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

Retinal Cone Dystrophy 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Cone Dystrophy 4 from the curated CTD Gene-Disease Associations dataset.

Late-Onset Retinal Degeneration Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Late-Onset Retinal Degeneration from the curated CTD Gene-Disease Associations dataset.

Retinal Vein Gene Set

From dbGAP Gene-Trait Associations

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

retinal cancer Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease retinal cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

retinal degeneration Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease retinal degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

retinal disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease retinal disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

retinal vascular disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease retinal vascular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

retinal degeneration Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

retinal disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

retinal artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal vein occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal microaneurysm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

peripheral retinal degeneration Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal telangiectasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal vasculitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal degeneration Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

macular retinal edema Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hereditary retinal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal drusen Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal vascular occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal edema Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

abnormal retinal correspondence Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal perforation Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

acute retinal necrosis syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal ischemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal vascular disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

branch retinal artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease branch retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

retinal cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

central retinal artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease central retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

retinal hemangioblastoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

central retinal vein occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease central retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

retinal detachment Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

diabetes complications; retinal artery occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye diseases; retinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

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

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, renal; hypertrophy, left ventricular; retinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, renal; hypertrophy, left ventricular; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blind vision; blindness; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blind vision; blindness; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

branch retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease branch retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriosclerosis; hyperhomocysteinemia; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriosclerosis; hyperhomocysteinemia; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye diseases, hereditary; macular degeneration; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases, hereditary; macular degeneration; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal function Gene Set

From GAD Gene-Disease Associations

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

adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vein Gene Set

From GAD Gene-Disease Associations

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

geographic atrophy; macular degeneration; retinal drusen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease geographic atrophy; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal degeneration Gene Set

From GAD Gene-Disease Associations

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

hearing loss/deafness; retinal disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss/deafness; retinal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blindness; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blindness; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; retinal vein occlusion; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; retinal vein occlusion; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; retinal vein occlusion; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroidal neovascularization; macular degeneration; retinal drusen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroidal neovascularization; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; retinal vascular occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; retinal vascular occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal detachment; vitreoretinopathy, proliferative Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal detachment; vitreoretinopathy, proliferative in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vascular occlusion Gene Set

From GAD Gene-Disease Associations

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

retinal detachment Gene Set

From GAD Gene-Disease Associations

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

hyperhomocysteinemia; retinal artery occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal degeneration; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal degeneration; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

night blindness; retinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease night blindness; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; retinal artery occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; retinal vasculitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; retinal vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

color vision defects; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease color vision defects; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vein occlusion; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vein thrombosis Gene Set

From GAD Gene-Disease Associations

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

behcet's disease; retinal vasculitis; uveitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet's disease; retinal vasculitis; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal artery occlusion Gene Set

From GAD Gene-Disease Associations

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

retinal diseases Gene Set

From GAD Gene-Disease Associations

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

retinal neoplasms; retinoblastoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal neoplasms; retinoblastoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vascular occlusive disease Gene Set

From GAD Gene-Disease Associations

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

blind vision; blindness; retinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blind vision; blindness; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diseases in twins; macular degeneration; retinal drusen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diseases in twins; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neovascularization, pathologic; retinal vasculitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neovascularization, pathologic; retinal vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vein occlusion; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; retinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; inflammation; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; inflammation; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroidal neovascularization; retinal drusen; wet macular degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroidal neovascularization; retinal drusen; wet macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal dystrophies; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal dystrophies; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blind vision; blindness; retinal diseases; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blind vision; blindness; retinal diseases; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal Gene Set

From GeneRIF Biological Term Annotations

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

retinal bipolar neuron differentiation Gene Set

From GO Biological Process Annotations

genes participating in the retinal bipolar neuron differentiation biological process from the curated GO Biological Process Annotations dataset.

retinal pigment epithelium development Gene Set

From GO Biological Process Annotations

genes participating in the retinal pigment epithelium development biological process from the curated GO Biological Process Annotations dataset.

retinal blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the retinal blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

retinal metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the retinal metabolic process biological process from the curated GO Biological Process Annotations dataset.

retinal dehydrogenase activity Gene Set

From GO Molecular Function Annotations

genes performing the retinal dehydrogenase activity molecular function from the curated GO Molecular Function Annotations dataset.

retinal isomerase activity Gene Set

From GO Molecular Function Annotations

genes performing the retinal isomerase activity molecular function from the curated GO Molecular Function Annotations dataset.

all-trans retinal binding Gene Set

From GO Molecular Function Annotations

genes performing the all-trans retinal binding molecular function from the curated GO Molecular Function Annotations dataset.

11-cis retinal binding Gene Set

From GO Molecular Function Annotations

genes performing the 11-cis retinal binding molecular function from the curated GO Molecular Function Annotations dataset.

retinal binding Gene Set

From GO Molecular Function Annotations

genes performing the retinal binding molecular function from the curated GO Molecular Function Annotations dataset.

all-trans-retinal Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the all-trans-retinal ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Retinal vascular caliber Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Retinal vascular caliber phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Rhegmatogenous retinal detachment Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

retinal degeneration Gene Set

From GWASdb SNP-Disease Associations

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

retinal disease Gene Set

From GWASdb SNP-Disease Associations

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

retinal detachment Gene Set

From GWASdb SNP-Disease Associations

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

retinal vascular disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormality of retinal arteries Gene Set

From GWASdb SNP-Phenotype Associations

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

retinal coloboma Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the retinal coloboma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

rhegmatogenous retinal detachment Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

retinal detachment Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the retinal detachment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the retinal vasculature Gene Set

From GWASdb SNP-Phenotype Associations

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

4-OH-Retinal Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 4-OH-Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.

Retinal Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.

9-cis-Retinal Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 9-cis-Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.

retinal hypoplasia Gene Set

From HPO Gene-Disease Associations

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

retinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

retinal dysplasia Gene Set

From HPO Gene-Disease Associations

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

retinal striation Gene Set

From HPO Gene-Disease Associations

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

peripheral retinal atrophy Gene Set

From HPO Gene-Disease Associations

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

lacunar retinal depigmentation Gene Set

From HPO Gene-Disease Associations

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

abnormality of the retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

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

focal retinal infarction Gene Set

From HPO Gene-Disease Associations

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

exudative retinal detachment Gene Set

From HPO Gene-Disease Associations

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

tractional retinal detachment Gene Set

From HPO Gene-Disease Associations

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

macroreticular retinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

rarefaction of retinal pigmentation Gene Set

From HPO Gene-Disease Associations

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

retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

abnormal retinal folds Gene Set

From HPO Gene-Disease Associations

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

large hyperpigmented retinal spots Gene Set

From HPO Gene-Disease Associations

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

retinal telangiectasia Gene Set

From HPO Gene-Disease Associations

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

peripheral retinal pigmentation abnormalities Gene Set

From HPO Gene-Disease Associations

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

depigmented lesions of the retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

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

achromatic retinal patches Gene Set

From HPO Gene-Disease Associations

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

retinal calcification Gene Set

From HPO Gene-Disease Associations

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

retinal vascular malformation Gene Set

From HPO Gene-Disease Associations

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

retinal neoplasm Gene Set

From HPO Gene-Disease Associations

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

retinal vascular tortuosity Gene Set

From HPO Gene-Disease Associations

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

retinal detachment Gene Set

From HPO Gene-Disease Associations

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

retinal flecks Gene Set

From HPO Gene-Disease Associations

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

retinal arteriolar constriction Gene Set

From HPO Gene-Disease Associations

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

peripheral retinal avascularization Gene Set

From HPO Gene-Disease Associations

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

retinal pigment epithelial atrophy Gene Set

From HPO Gene-Disease Associations

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

retinal nonattachment Gene Set

From HPO Gene-Disease Associations

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

decreased retinal pigmentation with dispersion Gene Set

From HPO Gene-Disease Associations

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

retinal malformation Gene Set

From HPO Gene-Disease Associations

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

nonprogressive congenital retinal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the nonprogressive congenital retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

falciform retinal fold Gene Set

From HPO Gene-Disease Associations

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

congenital hypertrophy of retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

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

retinal hemorrhage Gene Set

From HPO Gene-Disease Associations

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

pigmentary retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

loss of retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

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

pigmentary retinal deposits Gene Set

From HPO Gene-Disease Associations

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

abnormality of the retinal vasculature Gene Set

From HPO Gene-Disease Associations

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

macular retinal pigment epithelial mottling Gene Set

From HPO Gene-Disease Associations

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

retinal arteriolar tortuosity Gene Set

From HPO Gene-Disease Associations

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

abnormal retinal pigmentation Gene Set

From HPO Gene-Disease Associations

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

retinal arteriolar occlusion Gene Set

From HPO Gene-Disease Associations

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

reticular retinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

abnormality of retinal arteries Gene Set

From HPO Gene-Disease Associations

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

rhegmatogenous retinal detachment Gene Set

From HPO Gene-Disease Associations

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

honeycomb retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

hypermyelinated retinal fibers Gene Set

From HPO Gene-Disease Associations

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

retinal coloboma Gene Set

From HPO Gene-Disease Associations

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

retinal exudate Gene Set

From HPO Gene-Disease Associations

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

retinal hamartoma Gene Set

From HPO Gene-Disease Associations

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

cystic retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

progressive retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

retinal vascular proliferation Gene Set

From HPO Gene-Disease Associations

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

attenuation of retinal blood vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the attenuation of retinal blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral traction retinal detachment Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral traction retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

retinal hemangioblastoma Gene Set

From HPO Gene-Disease Associations

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

retinal atrophy Gene Set

From HPO Gene-Disease Associations

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

Retinal Detachment Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Artery Occlusion Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Retinal Artery Occlusion phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Retinal Dystrophies Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Degeneration Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Vein Occlusion Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Retinal Vein Occlusion phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Retinal Drusen Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Vasculitis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Neovascularization Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Perforations Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Hemorrhage Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal pigment epithelium GPCR Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal pigment epithelium GPCR protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal-specific ATP-binding cassette transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal-specific ATP-binding cassette transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal protein C2orf71 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal protein C2orf71 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal rod rhodopsin-sensitive cGMP 3', 5'-cyclic phosphodiesterase, delta subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal rod rhodopsin-sensitive cGMP 3', 5'-cyclic phosphodiesterase, delta subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal cGMP phosphodiesterase, gamma subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal cGMP phosphodiesterase, gamma subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Visual pigments (opsins) retinal binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Visual pigments (opsins) retinal binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal degeneration protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal degeneration protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal retinal photoreceptor layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

retinal fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal inner nuclear layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal melanocyte morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal neuronal layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal neuronal layer morphology 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.

retinal degeneration Gene Set

From MPO Gene-Phenotype Associations

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

retinal pigment epithelium atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal pigment epithelium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized retinal layers Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal photoreceptor morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

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

retinal pigment epithelium hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal pigment epithelium hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal deposits Gene Set

From MPO Gene-Phenotype Associations

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

abnormal induced retinal neovascularization Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal induced retinal neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal development Gene Set

From MPO Gene-Phenotype Associations

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

retinal ischemia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal ischemia 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.

retinal detachment Gene Set

From MPO Gene-Phenotype Associations

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

retinal gliosis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal apoptosis Gene Set

From MPO Gene-Phenotype Associations

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

thin retinal inner nuclear layer Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal vasculature morphology Gene Set

From MPO Gene-Phenotype Associations

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

retinal hemorrhage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal hemorrhage 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 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.

retinal spots Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal blood vessel pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal blood vessel pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin retinal inner plexiform layer Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

decreased susceptibility to induced retinal damage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced retinal damage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal nerve fiber layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

retinal photoreceptor degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal photoreceptor degeneration 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.

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.

abnormal retinal pigment epithelium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal pigment epithelium morphology 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.

abnormal retinal inner plexiform layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal inner nuclear layer thickness Gene Set

From MPO Gene-Phenotype Associations

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

disorganized retinal inner nuclear layer Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

retinal neovascularization Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal melanin granule morphology Gene Set

From MPO Gene-Phenotype Associations

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

{retinal disease in usher syndrome type iia, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {retinal disease in usher syndrome type iia, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

bothnia retinal dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the bothnia retinal dystrophy 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.

retinal degeneration, late-onset, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal degeneration, late-onset, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, truncal obesity, retinal dystrophy, and micropenis Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, truncal obesity, retinal dystrophy, and micropenis phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod retinal dystrophy-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod retinal dystrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod retinal dystrophy-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod retinal dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, retinal, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, retinal, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, retinal, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, retinal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

retinal nonattachment, nonsyndromic congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal nonattachment, nonsyndromic congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal cone dystrophy 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal cone dystrophy 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal cone dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal arterial macroaneurysm with supravalvular pulmonic stenosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal arterial macroaneurysm with supravalvular pulmonic stenosis 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.

infantile cerebellar-retinal degeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the infantile cerebellar-retinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal degeneration, autosomal recessive, clumped pigment type Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal degeneration, autosomal recessive, clumped pigment type phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinal cone dystrophy-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal cone dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal cone dystrophy 3b Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal cone dystrophy 3b phenotype from the curated OMIM Gene-Disease Associations dataset.

vasculopathy, retinal, with cerebral leukodystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the vasculopathy, retinal, with cerebral leukodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

Biosynthesis of A2E, implicated in retinal degradation Gene Set

From Reactome Pathways

proteins participating in the Biosynthesis of A2E, implicated in retinal degradation pathway from the Reactome Pathways dataset.

retinal rod Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

retinal pigment epithelium Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

retinal cone Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

retinal pigment epithelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal cone Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal rod Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Neural retinal development(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Neural retinal development(Mus musculus) pathway from the Wikipathways Pathways 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 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 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 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 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/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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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.

absent gastric milk in neonates Gene Set

From MPO Gene-Phenotype Associations

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

absent awl hair Gene Set

From MPO Gene-Phenotype Associations

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

absent placental labyrinth Gene Set

From MPO Gene-Phenotype Associations

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

absent uterine horn Gene Set

From MPO Gene-Phenotype Associations

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

absent chiasmata formation Gene Set

From MPO Gene-Phenotype Associations

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

absent cochlea Gene Set

From MPO Gene-Phenotype Associations

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

absent meckel's cartilage Gene Set

From MPO Gene-Phenotype Associations

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

absent lactotrophs Gene Set

From MPO Gene-Phenotype Associations

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

absent vagina Gene Set

From MPO Gene-Phenotype Associations

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

absent lymphocyte Gene Set

From MPO Gene-Phenotype Associations

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

absent vertebral pedicles Gene Set

From MPO Gene-Phenotype Associations

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

absent heart valves Gene Set

From MPO Gene-Phenotype Associations

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

absent photoreceptor inner segment Gene Set

From MPO Gene-Phenotype Associations

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

absent scrotum Gene Set

From MPO Gene-Phenotype Associations

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

absent ilium Gene Set

From MPO Gene-Phenotype Associations

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

absent epidermis stratum corneum Gene Set

From MPO Gene-Phenotype Associations

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

absent lymph nodes Gene Set

From MPO Gene-Phenotype Associations

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

absent peritoneal vaginal process Gene Set

From MPO Gene-Phenotype Associations

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

absent podocyte slit diaphragm Gene Set

From MPO Gene-Phenotype Associations

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

absent forelimb buds Gene Set

From MPO Gene-Phenotype Associations

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

absent mesoderm Gene Set

From MPO Gene-Phenotype Associations

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

absent estrus Gene Set

From MPO Gene-Phenotype Associations

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

absent cranial vagina Gene Set

From MPO Gene-Phenotype Associations

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

absent prostate gland anterior lobe Gene Set

From MPO Gene-Phenotype Associations

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

absent adenohypophysis Gene Set

From MPO Gene-Phenotype Associations

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

absent premaxilla Gene Set

From MPO Gene-Phenotype Associations

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

absent optic vesicle Gene Set

From MPO Gene-Phenotype Associations

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

absent tympanic ring Gene Set

From MPO Gene-Phenotype Associations

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

absent tongue Gene Set

From MPO Gene-Phenotype Associations

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

absent oocytes Gene Set

From MPO Gene-Phenotype Associations

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

absent posterior semicircular canal Gene Set

From MPO Gene-Phenotype Associations

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

absent ovary Gene Set

From MPO Gene-Phenotype Associations

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

absent reichert cartilage Gene Set

From MPO Gene-Phenotype Associations

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

absent molars Gene Set

From MPO Gene-Phenotype Associations

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

absent hallux Gene Set

From MPO Gene-Phenotype Associations

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

absent hippocampal fimbria Gene Set

From MPO Gene-Phenotype Associations

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

absent lungs Gene Set

From MPO Gene-Phenotype Associations

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

absent hippocampus ca3 region Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hippocampus ca3 region phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent ovarian follicles Gene Set

From MPO Gene-Phenotype Associations

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

absent endocochlear potential Gene Set

From MPO Gene-Phenotype Associations

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

absent styloid process Gene Set

From MPO Gene-Phenotype Associations

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

absent kidney medulla Gene Set

From MPO Gene-Phenotype Associations

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

absent brain ependyma motile cilia Gene Set

From MPO Gene-Phenotype Associations

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

absent dentate gyrus Gene Set

From MPO Gene-Phenotype Associations

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

absent epidermis Gene Set

From MPO Gene-Phenotype Associations

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

absent tarsus bones Gene Set

From MPO Gene-Phenotype Associations

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

absent extraembryonic ectoderm Gene Set

From MPO Gene-Phenotype Associations

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

absent paraxial mesoderm Gene Set

From MPO Gene-Phenotype Associations

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

absent hair follicles Gene Set

From MPO Gene-Phenotype Associations

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

absent third pharyngeal arch Gene Set

From MPO Gene-Phenotype Associations

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

absent nasolacrimal duct Gene Set

From MPO Gene-Phenotype Associations

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

absent spiral limbus Gene Set

From MPO Gene-Phenotype Associations

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

absent sacral vertebrae Gene Set

From MPO Gene-Phenotype Associations

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

absent semicircular canal ampulla Gene Set

From MPO Gene-Phenotype Associations

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

absent squamosal bone Gene Set

From MPO Gene-Phenotype Associations

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

absent diaphragm Gene Set

From MPO Gene-Phenotype Associations

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

absent oculomotor nerve Gene Set

From MPO Gene-Phenotype Associations

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

absent cardiogenic plate Gene Set

From MPO Gene-Phenotype Associations

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

absent spongiotrophoblast Gene Set

From MPO Gene-Phenotype Associations

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

absent schlemm's canal Gene Set

From MPO Gene-Phenotype Associations

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

absent enteric neurons Gene Set

From MPO Gene-Phenotype Associations

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

absent optic disc Gene Set

From MPO Gene-Phenotype Associations

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

absent anterior visceral endoderm Gene Set

From MPO Gene-Phenotype Associations

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

absent occipital bone Gene Set

From MPO Gene-Phenotype Associations

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

absent endometrium Gene Set

From MPO Gene-Phenotype Associations

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

absent vestibular nerve Gene Set

From MPO Gene-Phenotype Associations

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

absent right subclavian artery Gene Set

From MPO Gene-Phenotype Associations

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

absent ectoderm Gene Set

From MPO Gene-Phenotype Associations

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

absent proprioceptive neurons Gene Set

From MPO Gene-Phenotype Associations

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

absent floor plate Gene Set

From MPO Gene-Phenotype Associations

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

absent sperm annulus Gene Set

From MPO Gene-Phenotype Associations

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

absent deltoid tuberosity Gene Set

From MPO Gene-Phenotype Associations

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

absent red nucleus Gene Set

From MPO Gene-Phenotype Associations

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

absent type ii pneumocytes Gene Set

From MPO Gene-Phenotype Associations

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

absent interparietal bone Gene Set

From MPO Gene-Phenotype Associations

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

absent hyoid bone Gene Set

From MPO Gene-Phenotype Associations

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

absent semicircular canals Gene Set

From MPO Gene-Phenotype Associations

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

absent epididymal fat pad Gene Set

From MPO Gene-Phenotype Associations

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

absent mandible Gene Set

From MPO Gene-Phenotype Associations

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

absent otic vesicle Gene Set