| Name |
|---|
TAM GeneMyeloproliferative syndrome, transient (transient abnormal |
ASPM Geneasp (abnormal spindle) homolog, microcephaly associated (Drosophila) This gene is the human ortholog of the Drosophila melanogaster 'abnormal spindle' gene (asp), which is essential for normal mitotic spindle function in embryonic neuroblasts. Studies in mouse also suggest a role of this gene in mitotic spindle regulation, with a preferential role in regulating neurogenesis. Mutations in this gene are associated with microcephaly primary type 5. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011] |
SFPQP1 Genesplicing factor proline/glutamine-rich (polypyrimidine tract binding protein associated) pseudogene 1 |
PTBP3 Genepolypyrimidine tract binding protein 3 The protein encoded by this gene binds RNA and is a regulator of cell differentiation. The encoded protein preferentially binds to poly(G) and poly(U) sequences in vitro. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011] |
PTBP2 Genepolypyrimidine tract binding protein 2 The protein encoded by this gene binds to intronic polypyrimidine clusters in pre-mRNA molecules and is implicated in controlling the assembly of other splicing-regulatory proteins. This protein is very similar to the polypyrimidine tract binding protein (PTB) but most of its isoforms are expressed primarily in the brain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
PTBP1 Genepolypyrimidine tract binding protein 1 This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA-binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has four repeats of quasi-RNA recognition motif (RRM) domains that bind RNAs. This protein binds to the intronic polypyrimidine tracts that requires pre-mRNA splicing and acts via the protein degradation ubiquitin-proteasome pathway. It may also promote the binding of U2 snRNP to pre-mRNAs. This protein is localized in the nucleoplasm and it is also detected in the perinucleolar structure. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008] |
PTBP1P Genepolypyrimidine tract binding protein 1 pseudogene |
LOC100422623 Genecarcinoembryonic antigen-related cell adhesion molecule 1 (biliary glycoprotein) pseudogene |
PBC3 GeneBiliary cirrhosis, primary, 3 |
PBC2 GeneBiliary cirrhosis, primary, 2 |
PBC5 GeneBiliary cirrhosis, primary, 5 |
PBC4 GeneBiliary cirrhosis, primary, 4 |
CEACAM1 Genecarcinoembryonic antigen-related cell adhesion molecule 1 (biliary glycoprotein) This gene encodes a member of the carcinoembryonic antigen (CEA) gene family, which belongs to the immunoglobulin superfamily. Two subgroups of the CEA family, the CEA cell adhesion molecules and the pregnancy-specific glycoproteins, are located within a 1.2 Mb cluster on the long arm of chromosome 19. Eleven pseudogenes of the CEA cell adhesion molecule subgroup are also found in the cluster. The encoded protein was originally described in bile ducts of liver as biliary glycoprotein. Subsequently, it was found to be a cell-cell adhesion molecule detected on leukocytes, epithelia, and endothelia. The encoded protein mediates cell adhesion via homophilic as well as heterophilic binding to other proteins of the subgroup. Multiple cellular activities have been attributed to the encoded protein, including roles in the differentiation and arrangement of tissue three-dimensional structure, angiogenesis, apoptosis, tumor suppression, metastasis, and the modulation of innate and adaptive immune responses. Multiple transcript variants encoding different isoforms have been reported, but the full-length nature of all variants has not been defined. [provided by RefSeq, May 2010] |
abnormal biliary tract physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal biliary tract physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
biliary calculi; biliary tract neoplasm; biliary tract neoplasms; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary calculi; biliary tract neoplasm; biliary tract neoplasms; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; biliary tract neoplasm; biliary tract neoplasms; chromosome deletion; diabetes complications; pancreatic neoplasm; pancreatic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; biliary tract neoplasm; biliary tract neoplasms; chromosome deletion; diabetes complications; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary tract neoplasm; biliary tract neoplasms; digestive system neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary tract neoplasm; biliary tract neoplasms; digestive system neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary tract neoplasm; biliary tract neoplasms; cholangiocarcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary tract neoplasm; biliary tract neoplasms; cholangiocarcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary duct stones; biliary tract cancer; gallbladder cancer; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary duct stones; biliary tract cancer; gallbladder cancer; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal biliary tract morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal biliary tract morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal biliary tract morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal biliary tract morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal biliary tract morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal biliary tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Abnormal Biliary Tract Morphology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Biliary Tract Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal biliary tract morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal biliary tract morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
autoimmune diseases; biliary cirrhosis; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; biliary cirrhosis; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary cirrhosis; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary cirrhosis; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary cirrhosis; liver cirrhosis, biliary; osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary cirrhosis; liver cirrhosis, biliary; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary cirrhosis; hepatitis, autoimmune; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary cirrhosis; hepatitis, autoimmune; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary tract disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease biliary tract disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
biliary tract disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease biliary tract disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
biliary tract cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease biliary tract cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
biliary tract cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease biliary tract cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
biliary tract neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease biliary tract neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
biliary tract disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease biliary tract disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
biliary tract neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary tract neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary tract neoplasms; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary tract neoplasms; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pancreaticobiliary maljunction-associated biliary tract tumors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pancreaticobiliary maljunction-associated biliary tract tumors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary tract diseases; ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary tract diseases; ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary tract neoplasms; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary tract neoplasms; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary tract neoplasms; carcinoma, hepatocellular; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary tract neoplasms; carcinoma, hepatocellular; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary tract cancer; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary tract cancer; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary tract neoplasms; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary tract neoplasms; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary tract disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease biliary tract disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
biliary tract cancer Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease biliary tract cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
biliary tract abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the biliary tract abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
biliary tract neoplasm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the biliary tract neoplasm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
biliary tract abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the biliary tract abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
biliary tract neoplasm Gene SetFrom HPO Gene-Disease Associations genes associated with the biliary tract neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Biliary Tract Neoplasms Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Biliary Tract Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Biliary Tract Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Biliary Tract Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Liver And Intrahepatic Biliary Tract Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Liver And Intrahepatic Biliary Tract Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Cholangiocarcinoma Of Intrahepatic Biliary Tract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Cholangiocarcinoma Of Intrahepatic Biliary Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Tract Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Tract Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cyst Of Biliary Tract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cyst Of Biliary Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Tract Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Tract Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Tract Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Tract Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Biliary Tract Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Biliary Tract Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Tract Abnormality Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Biliary Tract Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Biliary tract disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Biliary tract disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Biliary tract cancer Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Biliary tract cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Biliary tract disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Biliary tract disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Biliary tract cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Biliary tract cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Biliary tract cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Biliary tract cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Biliary tract disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Biliary tract disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Biliary tract benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Biliary tract benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Biliary tract abnormality Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Biliary tract abnormality phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
bacteriuria; urinary tract infection; urinary tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bacteriuria; urinary tract infection; urinary tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
urinary tract infection; urinary tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease urinary tract infection; urinary tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cicatrix; pyelonephritis; urinary tract infection; urinary tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cicatrix; pyelonephritis; urinary tract infection; urinary tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cicatrization; escherichia coli infections; pyelonephritis; urinary tract infection; urinary tract infections; vesico-ureteral reflux; vesicoureteral reflux Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cicatrization; escherichia coli infections; pyelonephritis; urinary tract infection; urinary tract infections; vesico-ureteral reflux; vesicoureteral reflux in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cicatrization; kidney diseases; recurrence; urinary tract infection; urinary tract infections; vesico-ureteral reflux; vesicoureteral reflux Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cicatrization; kidney diseases; recurrence; urinary tract infection; urinary tract infections; vesico-ureteral reflux; vesicoureteral reflux in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bacterial infections; urinary tract infection; urinary tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bacterial infections; urinary tract infection; urinary tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal biliary ductule morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal biliary ductule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal optic tract morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal optic tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart ventricle outflow tract morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart ventricle outflow tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal olfactory tract morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal anterior corticospinal tract morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal anterior corticospinal tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart left ventricle outflow tract morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart left ventricle outflow tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart right ventricle outflow tract morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart right ventricle outflow tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal corticospinal tract morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal corticospinal tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nervous system tract morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nervous system tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lateral corticospinal tract morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lateral corticospinal tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal outflow tract development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal outflow tract development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
abnormal cardiac outflow tract development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cardiac outflow tract development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal heart ventricle outflow tract morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal heart ventricle outflow tract morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal heart right ventricle outflow tract morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal heart right ventricle outflow tract morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal anterior corticospinal tract morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal anterior corticospinal tract morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lateral corticospinal tract morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lateral corticospinal tract morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal corticospinal tract morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal corticospinal tract morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal nervous system tract morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal nervous system tract morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal heart left ventricle outflow tract morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal heart left ventricle outflow tract morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal olfactory tract morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal olfactory tract morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal optic tract morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic tract morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sperm migration in female genital tract Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sperm migration in female genital tract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
abnormal eye physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal renal physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal gallbladder physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal male reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal autonomic nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal female reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal female reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hypothalamus physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hypothalamus physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal natural killer cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal natural killer cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal autonomic nervous system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal large intestine physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal large intestine physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vascular physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vascular physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory motile cilium physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory motile cilium physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal keratinocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal keratinocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male reproductive gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelial cell primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelial cell primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown adipose tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basophil physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basophil physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal olfactory system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural crest cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural crest cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal osteoblast physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal osteoblast physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal submandibular gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal submandibular gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal testis physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal testis physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mammary gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male reproductive system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blood cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blood cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal platelet physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal platelet physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal schwann cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal schwann cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal adipose tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thymus physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thymus physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neuronal stem cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neuronal stem cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear inner hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear inner hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hearing physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hearing physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd4-positive, alpha-beta t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive, alpha-beta t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal olfactory epithelium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory epithelium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal memory t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal memory t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal oligodendrocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal oligodendrocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal liver physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal liver physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic endocrine progenitor cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic endocrine progenitor cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ear physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ear physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female reproductive system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female reproductive system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lacrimal gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lacrimal gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal t-helper 1 physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal t-helper 1 physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immune system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immune system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal adrenal gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal adrenal gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sex gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sex gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal professional antigen presenting cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal professional antigen presenting cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hematopoietic system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hematopoietic system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somatic nervous system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somatic nervous system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hippocampus physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hippocampus physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal motile primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal motile primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hematopoietic stem cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hematopoietic stem cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal autonomic nervous system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sweat gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sweat gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spleen physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spleen physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd8-positive, alpha-beta t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd8-positive, alpha-beta t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal digestive system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal digestive system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ependyma motile cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ependyma motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestine physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestine physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal extraembryonic tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal extraembryonic tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dendritic cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dendritic cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal reproductive system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal reproductive system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal harderian gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal harderian gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neuron physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neuron physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lysosome physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lysosome physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sympathetic nervous system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sympathetic nervous system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal astrocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal astrocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neutrophil physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neutrophil physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic delta cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic delta cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymphocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymphocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mammary gland epithelium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland epithelium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal muscle precursor cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal muscle precursor cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cytotoxic t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cytotoxic t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eosinophil physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eosinophil physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal skeleton physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal skeleton physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nonmotile primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nonmotile primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somatosensory cortex physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somatosensory cortex physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal visceral endoderm physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal visceral endoderm physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal germinal center b cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal germinal center b cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal enterocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal enterocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal motile cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bile duct physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bile duct physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal splenocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal splenocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cardiac valve physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cardiac valve physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear outer hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear outer hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal follicular dendritic cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal follicular dendritic cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal t follicular helper cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal t follicular helper cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hepatobiliary system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hepatobiliary system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal t-helper 2 physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal t-helper 2 physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immune cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immune cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal oval cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal oval cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal placenta physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal placenta physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prostate gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thyroid physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thyroid physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal langerhans cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal langerhans cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal carotid body physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal carotid body physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal podocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal podocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal salivary gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal salivary gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sensory neuron physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sensory neuron physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal skin adnexa physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal skin adnexa physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal uterine nk cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal uterine nk cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hepatocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hepatocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gustatory system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gustatory system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urinary bladder physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urinary bladder physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mitochondrial physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mitochondrial physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pineal gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pineal gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pituitary gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pituitary gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymphatic system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymphatic system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vascular endothelial cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vascular endothelial cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bone marrow cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bone marrow cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal small intestinal crypt cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal small intestinal crypt cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal macrophage physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal macrophage physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain ependyma motile cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain ependyma motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cardiovascular system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cardiovascular system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal microglial cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal microglial cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal white adipose tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal white adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parathyroid gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parathyroid gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mast cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mast cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immune serum protein physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immune serum protein physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal granulocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal granulocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nervous system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nervous system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal histamine physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal histamine physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endocrine pancreas physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endocrine pancreas physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal myocardial fiber physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal myocardial fiber physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blood vessel physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blood vessel physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal osteoclast physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal osteoclast physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glial cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glial cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal marginal zone b cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal marginal zone b cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parasympathetic nervous system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parasympathetic nervous system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal erythrocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal erythrocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sympathetic neuron physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sympathetic neuron physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pre-botzinger complex physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pre-botzinger complex physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal follicular b cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal follicular b cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sebaceous gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sebaceous gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal exocrine pancreas physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal exocrine pancreas physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal platelet dense granule physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal platelet dense granule physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sperm physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sperm physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal uterus physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal uterus physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal/urinary system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal/urinary system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female reproductive gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gabaergic neuron physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gabaergic neuron physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hepatoblast physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hepatoblast physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lung endothelial cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lung endothelial cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic beta cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic beta cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nk cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nk cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal muscle physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal muscle physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal leukocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal leukocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal respiratory motile cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal respiratory motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal regulatory t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal regulatory t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryonic tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryonic tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ovary physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ovary physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal baroreceptor physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal baroreceptor physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ureter physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ureter physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal memory b cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal memory b cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic alpha cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic alpha cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vascular smooth muscle physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vascular smooth muscle physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal surfactant physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal surfactant physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nk t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nk t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasmacytoid dendritic cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasmacytoid dendritic cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal oviduct physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal oviduct physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gallbladder physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gallbladder physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fetal cardiomyocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal cardiomyocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pp cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pp cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gastroesophageal sphincter physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gastroesophageal sphincter physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal t-helper 17 cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal t-helper 17 cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal skin physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal skin physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hypothalamus physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hypothalamus physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immune organ physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immune organ physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal chondrocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal chondrocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal respiratory system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal respiratory system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Abnormal Aortic Valve Physiology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Aortic Valve Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Eye Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Eye Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Mitral Valve Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Mitral Valve Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Large Intestine Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Large Intestine Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Bronchus Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Bronchus Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Lymphocyte Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Lymphocyte Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Hypothalamus Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Hypothalamus Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Natural Killer Cell Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Natural Killer Cell Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thymus physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thymus physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal digestive system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal digestive system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal immune system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal immune system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal nervous system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal nervous system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal muscle physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal muscle physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ear physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ear physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal adrenal gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal adrenal gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal osteoclast physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal osteoclast physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hearing physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hearing physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal skeleton physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal skeleton physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal salivary gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal salivary gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal macrophage physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal macrophage physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal T-helper 1 physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal T-helper 1 physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal T-helper 2 physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal T-helper 2 physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal adipose tissue physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal adipose tissue physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vascular smooth muscle physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vascular smooth muscle physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mitochondrial physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mitochondrial physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal neutrophil physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neutrophil physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cardiovascular system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cardiovascular system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal B cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal B cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal respiratory system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal respiratory system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal Langerhans cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Langerhans cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal blood vessel physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal blood vessel physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lymphocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lymphocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal follicular dendritic cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal follicular dendritic cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal immune cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal immune cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cytotoxic T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cytotoxic T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal prostate gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal prostate gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal bulbourethral gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bulbourethral gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sympathetic nervous system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sympathetic nervous system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatobiliary system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatobiliary system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal reproductive system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal reproductive system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal microglial cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal microglial cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hematopoietic stem cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hematopoietic stem cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal dendritic cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dendritic cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sperm physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sperm physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal CD4-positive, alpha-beta T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal CD4-positive, alpha-beta T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal platelet physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal platelet physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal liver physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal liver physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal erythrocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal erythrocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intestine physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intestine physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreas physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreas physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal small intestinal crypt cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal small intestinal crypt cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal keratinocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal keratinocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lacrimal gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lacrimal gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreatic beta cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreatic beta cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal extraembryonic tissue physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal extraembryonic tissue physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal glial cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal glial cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal astrocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal astrocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male reproductive system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male reproductive system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal NK cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal NK cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal neuron physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neuron physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal skin physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal skin physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal leukocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal leukocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibular system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear outer hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear outer hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal myocardial fiber physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal myocardial fiber physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear inner hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear inner hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal immune serum protein physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal immune serum protein physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal osteoblast physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal osteoblast physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal professional antigen presenting cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal professional antigen presenting cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female reproductive system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female reproductive system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mast cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mast cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal baroreceptor physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal baroreceptor physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hematopoietic system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hematopoietic system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal uterus physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal uterus physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal gallbladder physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal gallbladder physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal spleen physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spleen physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal somatic nervous system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal somatic nervous system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pre-Botzinger complex physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pre-Botzinger complex physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal gustatory system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal gustatory system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urinary bladder physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urinary bladder physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibular hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pituitary gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pituitary gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vascular endothelial cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vascular endothelial cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal uterine NK cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal uterine NK cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal motile primary cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motile primary cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hypothalamus physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hypothalamus physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal olfactory system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal olfactory system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal splenocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal splenocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thyroid gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thyroid gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sensory neuron physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sensory neuron physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal renal/urinary system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal renal/urinary system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal platelet dense granule physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal platelet dense granule physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eosinophil physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eosinophil physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ovary physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ovary physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal bone marrow cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bone marrow cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal autonomic nervous system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal autonomic nervous system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal chondrocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal chondrocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal white adipose tissue physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal white adipose tissue physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal somatosensory cortex physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal somatosensory cortex physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal oligodendrocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal oligodendrocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lysosome physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lysosome physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal enterocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal enterocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lymphatic system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lymphatic system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal memory T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal memory T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal CD8-positive, alpha-beta T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal CD8-positive, alpha-beta T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal testis physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal testis physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male germ cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male germ cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal marginal zone B cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal marginal zone B cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal neural crest cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neural crest cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal surfactant physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal surfactant physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal embryonic tissue physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryonic tissue physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal carotid body physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal carotid body physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal granulocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal granulocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal NK T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal NK T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sebaceous gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sebaceous gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal peroxisome physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal peroxisome physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mammary gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hippocampus physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hippocampus physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal respiratory motile cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal respiratory motile cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal parotid gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal parotid gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lung endothelial cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lung endothelial cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal type I cell of carotid body physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal type I cell of carotid body physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney epithelial cell primary cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney epithelial cell primary cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal germinal center B cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal germinal center B cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sex gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sex gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal submandibular gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal submandibular gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal regulatory T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal regulatory T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal oval cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal oval cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal Schwann cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Schwann cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mammary gland epithelium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary gland epithelium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal histamine physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal histamine physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vomeronasal sensory neuron physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vomeronasal sensory neuron physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal gastroesophageal sphincter physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal gastroesophageal sphincter physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal T-helper 17 cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal T-helper 17 cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal basophil physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal basophil physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal parasympathetic nervous system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal parasympathetic nervous system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal GABAergic neuron physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal GABAergic neuron physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibular endolymph physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular endolymph physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal endolymph physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endolymph physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal follicular B cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal follicular B cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mammary gland myoepithelium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary gland myoepithelium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fibroblast physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fibroblast physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brown adipose tissue physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brown adipose tissue physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal synaptic physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal synaptic physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal endoplasmic reticulum physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endoplasmic reticulum physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal PP cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal PP cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal plasmacytoid dendritic cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal plasmacytoid dendritic cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain ependyma motile cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain ependyma motile cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal Meibomian gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Meibomian gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sympathetic neuron physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sympathetic neuron physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal perilymph physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal perilymph physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreatic endocrine progenitor cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreatic endocrine progenitor cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal endocrine pancreas physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endocrine pancreas physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal placenta physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal placenta physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal exocrine pancreas physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal exocrine pancreas physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal skin adnexa physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal skin adnexa physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal motile cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motile cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal T follicular helper cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal T follicular helper cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal Paneth cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Paneth cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal memory B cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal memory B cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal visceral endoderm physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visceral endoderm physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ureter physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ureter physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fetal cardiomyocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal cardiomyocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ependyma motile cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ependyma motile cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal olfactory epithelium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal olfactory epithelium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pineal gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pineal gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intracellular organelle physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intracellular organelle physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intestinal epithelium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intestinal epithelium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intestinal goblet cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intestinal goblet cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal epididymis physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal epididymis physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sweat gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sweat gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal neuronal stem cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neuronal stem cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreatic acinar cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreatic acinar cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal beige fat cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal beige fat cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal heart valve physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal heart valve physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal visceral yolk sac physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visceral yolk sac physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female germ cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female germ cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal primary cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal primary cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal neuroendocrine gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neuroendocrine gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cornea physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cornea physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mucous gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mucous gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal respiratory epithelium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal respiratory epithelium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cerebrospinal fluid physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebrospinal fluid physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal tear film physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tear film physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cartilage physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cartilage physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal olfactory sensory neuron physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal olfactory sensory neuron physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Biliary Cirrhosis, Primary, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Biliary Cirrhosis, Primary, 2 from the curated CTD Gene-Disease Associations dataset. |
Biliary Atresia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Biliary Atresia from the curated CTD Gene-Disease Associations dataset. |
Liver Cirrhosis, Biliary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Liver Cirrhosis, Biliary from the curated CTD Gene-Disease Associations dataset. |
Biliary Cirrhosis, Primary, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Biliary Cirrhosis, Primary, 3 from the curated CTD Gene-Disease Associations dataset. |
Liver Cirrhosis, Biliary Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Liver Cirrhosis, Biliary in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
primary biliary cirrhosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease primary biliary cirrhosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
biliary atresia Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease biliary atresia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
biliary dyskinesia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease biliary dyskinesia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
biliary papillomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease biliary papillomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
biliary atresia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease biliary atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary biliary cirrhosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary biliary cirrhosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
intrahepatic biliary papillomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intrahepatic biliary papillomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary biliary cirrhosis] Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary biliary cirrhosis] in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, primary biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, primary biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary calculi; gallstones; gilbert disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary calculi; gallstones; gilbert disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; liver disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; liver disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary biliary cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary biliary cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholelithiasis; biliary duct stone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholelithiasis; biliary duct stone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary calculi; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary calculi; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; cholangitis, sclerosing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholestasis; biliary atresia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholestasis; biliary atresia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cirrhosis, biliary; pruritus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cirrhosis, biliary; pruritus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary calculi; cholecystolithiasis; gallstones; lipid metabolism disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary calculi; cholecystolithiasis; gallstones; lipid metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary calculi; gallstones; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary calculi; gallstones; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary atresia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary atresia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; hepatitis type 1, autoimmune (aih-1) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; hepatitis type 1, autoimmune (aih-1) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary atresia; choledochal cyst; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary atresia; choledochal cyst; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary calculi; cholelithiasis; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary calculi; cholelithiasis; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary atresia; liver diseases; primary graft dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary atresia; liver diseases; primary graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholangitis, sclerosing; fatty liver; hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune; hepatitis, chronic; liver cirrhosis, alcoholic; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; fatty liver; hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune; hepatitis, chronic; liver cirrhosis, alcoholic; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary calculi; carcinoma; gallbladder neoplasm; gallbladder neoplasms; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary calculi; carcinoma; gallbladder neoplasm; gallbladder neoplasms; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
osteoporosis; cirrhosis, primary biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease osteoporosis; cirrhosis, primary biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary atresia; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary atresia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bile duct neoplasms; biliary calculi; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; biliary calculi; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; hepatitis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; hepatitis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; diabetes, gestational Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; diabetes, gestational in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary calculi; diseases in twins; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary calculi; diseases in twins; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term biliary in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Biliary atresia Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Biliary atresia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Primary biliary cirrhosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Primary biliary cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
biliary atresia Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease biliary atresia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
primary biliary cirrhosis Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease primary biliary cirrhosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
biliary atresia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the biliary atresia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the biliary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the biliary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
biliary cirrhosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the biliary cirrhosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
biliary atresia Gene SetFrom HPO Gene-Disease Associations genes associated with the biliary atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the biliary system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the biliary system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
intrahepatic biliary dysgenesis Gene SetFrom HPO Gene-Disease Associations genes associated with the intrahepatic biliary dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
biliary cirrhosis Gene SetFrom HPO Gene-Disease Associations genes associated with the biliary cirrhosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Biliary Atresia Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Biliary Atresia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Liver Cirrhosis, Biliary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Liver Cirrhosis, Biliary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
biliary cyst Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the biliary cyst phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
liver/biliary system phenotype Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the liver/biliary system phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
biliary cirrhosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the biliary cirrhosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{biliary cirrhosis, primary, 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {biliary cirrhosis, primary, 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
biliary cirrhosis, primary, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the biliary cirrhosis, primary, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
biliary cirrhosis, primary, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the biliary cirrhosis, primary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{biliary cirrhosis, primary, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {biliary cirrhosis, primary, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
biliary epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue biliary epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
biliary epithelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue biliary epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Primary Biliary Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Biliary Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Atresia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Cirrhosis, Primary, 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Cirrhosis, Primary, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Intraepithelial Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Biliary Cholangitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Biliary Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Obstruction Of Biliary Tree Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Obstruction Of Biliary Tree in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Papillomatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Papillomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Hamartoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Hamartoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary System Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary System Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Stricture Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Stricture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Biliary Hamartomas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Biliary Hamartomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Adenoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Adenoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Atresia With Splenic Malformation Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Atresia With Splenic Malformation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Hyperplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Sludge Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Sludge in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Extrahepatic Biliary Atresia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Extrahepatic Biliary Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Idiopathic Extrahepatic Biliary Atresia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Extrahepatic Biliary Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Biliary Obstruction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Biliary Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Postoperative Biliary Stricture Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Postoperative Biliary Stricture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Acute Pancreatitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Acute Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pancreatitis Biliary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pancreatitis Biliary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Calculi Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Biliary Calculi in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intrahepatic Biliary Atresia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intrahepatic Biliary Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intrahepatic Biliary Dysgenesis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intrahepatic Biliary Dysgenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
biliary cirrhosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the biliary cirrhosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
biliary cyst Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the biliary cyst phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
biliary atresia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the biliary atresia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Biliary epithelial cell_Intestine_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Biliary epithelial cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Biliary cell_Liver_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Biliary cell_Liver_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Biliary cell_Bile duct_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Biliary cell_Bile duct_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Biliary epithelial cell_Liver_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Biliary epithelial cell_Liver_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Biliary cell_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Biliary cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Disorders of bile acid synthesis and biliary transport Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Disorders of bile acid synthesis and biliary transport pathway from the WikiPathways Pathways 2024 dataset. |
Primary biliary cholangitis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Primary biliary cholangitis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary biliary cholangitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary biliary cholangitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Biliary atresia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Biliary atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Biliary dyskinesia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Biliary dyskinesia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary biliary cholangitis 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary biliary cholangitis 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary biliary cholangitis 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary biliary cholangitis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary biliary cholangitis 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary biliary cholangitis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary biliary cholangitis 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary biliary cholangitis 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Biliary papillomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Biliary papillomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary biliary cholangitis 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary biliary cholangitis 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intrahepatic biliary papillomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrahepatic biliary papillomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Biliary epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Biliary epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Biliary epithelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Biliary epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Biliary Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Biliary phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Primary biliary cholangitis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Primary biliary cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Primary biliary cirrhosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Primary biliary cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Biliary atresia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Biliary atresia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Nucleus of the solitary tract, medial part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Nucleus of the solitary tract, medial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
lateral terminal nucleus of the accessory optic tract, lateral part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in lateral terminal nucleus of the accessory optic tract, lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Nucleus of the lateral olfactory tract, layer 3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Nucleus of the lateral olfactory tract, layer 3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
nucleus of the lateral olfactory tract Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in nucleus of the lateral olfactory tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Nucleus of the lateral olfactory tract, molecular layer Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Nucleus of the lateral olfactory tract, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
lateral terminal nucleus of the accessory optic tract, ventral part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in lateral terminal nucleus of the accessory optic tract, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Nucleus of the lateral olfactory tract, pyramidal layer Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Nucleus of the lateral olfactory tract, pyramidal layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
dorsal terminal nucleus of the accessory optic tract Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in dorsal terminal nucleus of the accessory optic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Bed nucleus of the accessory olfactory tract Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nucleus of the accessory olfactory tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Nucleus of the optic tract Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Nucleus of the optic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Lateral terminal nucleus of the accessory optic tract Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Lateral terminal nucleus of the accessory optic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Nucleus of the solitary tract Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Nucleus of the solitary tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Nucleus of the solitary tract, lateral part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Nucleus of the solitary tract, lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Nucleus of the solitary tract, commissural part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Nucleus of the solitary tract, commissural part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Nucleus of the solitary tract, gelatinous part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Nucleus of the solitary tract, gelatinous part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
nucleus of the central acoustic tract Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in nucleus of the central acoustic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Respiratory Tract Infections Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Respiratory Tract Infections from the curated CTD Gene-Disease Associations dataset. |
Respiratory Tract Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Respiratory Tract Diseases from the curated CTD Gene-Disease Associations dataset. |
Granuloma, Respiratory Tract Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Granuloma, Respiratory Tract from the curated CTD Gene-Disease Associations dataset. |
Urinary Tract Infections Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Urinary Tract Infections from the curated CTD Gene-Disease Associations dataset. |
autoimmune disease of gastrointestinal tract Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease autoimmune disease of gastrointestinal tract from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
lower respiratory tract disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease lower respiratory tract disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
autoimmune disease of gastrointestinal tract Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease autoimmune disease of gastrointestinal tract in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
autoimmune disease of urogenital tract Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease autoimmune disease of urogenital tract in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
lower respiratory tract disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease lower respiratory tract disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
upper respiratory tract disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease upper respiratory tract disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
lower respiratory tract disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lower respiratory tract disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
upper respiratory tract disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease upper respiratory tract disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
urinary tract papillary transitional cell benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urinary tract papillary transitional cell benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
urinary tract obstruction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urinary tract obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lower urinary tract calculus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lower urinary tract calculus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
autoimmune disease of gastrointestinal tract Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autoimmune disease of gastrointestinal tract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
autoimmune disease of urogenital tract Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autoimmune disease of urogenital tract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastrointestinal hemorrhage; haematuria; hematuria; henoch-schoenlein purpura; purpura, schoenlein-henoch; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gastrointestinal hemorrhage; haematuria; hematuria; henoch-schoenlein purpura; purpura, schoenlein-henoch; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases; hypersensitivity; respiratory tract diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases; hypersensitivity; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma of the upper gastrointestinal tract. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma of the upper gastrointestinal tract. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; hypersensitivity; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; hypersensitivity; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
prenatal exposure delayed effects; respiratory tract diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease prenatal exposure delayed effects; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
respiratory syncytial virus infections; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease respiratory syncytial virus infections; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
respiratory tract diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tumours of the upper aerodigestive tract Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tumours of the upper aerodigestive tract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, sickle cell; ischemia; recurrence; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; ischemia; recurrence; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
occupational diseases; respiratory tract diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease occupational diseases; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bacterial infections; recurrence; respiratory tract infections; tuberculosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bacterial infections; recurrence; respiratory tract infections; tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mycobacterium avium-intracellulare infection; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mycobacterium avium-intracellulare infection; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
otitis media; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease otitis media; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; head and neck neoplasms; respiratory tract neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; head and neck neoplasms; respiratory tract neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; respiratory tract diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bronchiectasis; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bronchiectasis; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
upper aerodigestive tract cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease upper aerodigestive tract cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bacterial infections; burkholderia infections; cystic fibrosis; pseudomonas infections; recurrence; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bacterial infections; burkholderia infections; cystic fibrosis; pseudomonas infections; recurrence; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
urinary tract symptoms, prostate volume, uroflow and psa Gene SetFrom GAD Gene-Disease Associations genes associated with the disease urinary tract symptoms, prostate volume, uroflow and psa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mouth neoplasms; respiratory tract neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mouth neoplasms; respiratory tract neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
urinary tract infections after renal transplantation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease urinary tract infections after renal transplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aerodigestive tract cancers Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aerodigestive tract cancers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
urinary tract infection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease urinary tract infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystitis; pyelonephritis; urinary tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystitis; pyelonephritis; urinary tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
common variable immunodeficiency; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease common variable immunodeficiency; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
upper aerodigestive tract cancers Gene SetFrom GAD Gene-Disease Associations genes associated with the disease upper aerodigestive tract cancers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney diseases; urinary tract infections; vesico-ureteral reflux Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney diseases; urinary tract infections; vesico-ureteral reflux in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrence; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrence; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
disorders of excessive somnolence; fatigue; gastrointestinal diseases; respiratory tract infections; rhinitis; urticaria; xerostomia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disorders of excessive somnolence; fatigue; gastrointestinal diseases; respiratory tract infections; rhinitis; urticaria; xerostomia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; infant, premature, diseases; respiratory tract diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; infant, premature, diseases; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tract Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term tract in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
negative regulation of apoptotic process involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of apoptotic process involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic ectodermal digestive tract development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic ectodermal digestive tract development biological process from the curated GO Biological Process Annotations 2015 dataset. |
corticospinal tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the corticospinal tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of semaphorin-plexin signaling pathway involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of semaphorin-plexin signaling pathway involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cell proliferation involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cell proliferation involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
digestive tract development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the digestive tract development biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cell proliferation involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cell proliferation involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
planar cell polarity pathway involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the planar cell polarity pathway involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of apoptotic process involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of apoptotic process involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
endodermal digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the endodermal digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of wnt signaling pathway involved in digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of wnt signaling pathway involved in digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cardiac neural crest cell migration involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cardiac neural crest cell migration involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of planar cell polarity pathway involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of planar cell polarity pathway involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
mammillothalamic axonal tract development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mammillothalamic axonal tract development biological process from the curated GO Biological Process Annotations 2015 dataset. |
digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
canonical wnt signaling pathway involved in positive regulation of cardiac outflow tract cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the canonical wnt signaling pathway involved in positive regulation of cardiac outflow tract cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
post-embryonic digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the post-embryonic digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of wnt signaling pathway involved in digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of wnt signaling pathway involved in digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of planar cell polarity pathway involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of planar cell polarity pathway involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
outflow tract septum morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the outflow tract septum morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cardiac neural crest cell development involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cardiac neural crest cell development involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic digestive tract development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic digestive tract development biological process from the curated GO Biological Process Annotations 2015 dataset. |
determination of digestive tract left/right asymmetry Gene SetFrom GO Biological Process Annotations 2015 genes participating in the determination of digestive tract left/right asymmetry biological process from the curated GO Biological Process Annotations 2015 dataset. |
urinary tract smooth muscle contraction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the urinary tract smooth muscle contraction biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic ectodermal digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic ectodermal digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
poly-pyrimidine tract binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the poly-pyrimidine tract binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
poly-purine tract binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the poly-purine tract binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
poly-glutamine tract binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the poly-glutamine tract binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Upper aerodigestive tract cancers Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Upper aerodigestive tract cancers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
autoimmune disease of gastrointestinal tract Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease autoimmune disease of gastrointestinal tract in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
autoimmune disease of urogenital tract Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease autoimmune disease of urogenital tract in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
lower respiratory tract disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease lower respiratory tract disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
upper respiratory tract disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease upper respiratory tract disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormality of the upper urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
malignant gastrointestinal tract tumors Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the malignant gastrointestinal tract tumors phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
neoplasm of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the neoplasm of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
urinary tract neoplasm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the urinary tract neoplasm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
recurrent infection of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the recurrent infection of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
neoplasm of the genitourinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the neoplasm of the genitourinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricular outflow tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricular outflow tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinocerebellar tract disease in lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the spinocerebellar tract disease in lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
urinary tract neoplasm Gene SetFrom HPO Gene-Disease Associations genes associated with the urinary tract neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the pyramidal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neoplasm of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent infection of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent infection of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the corticospinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the corticospinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
genital tract atresia Gene SetFrom HPO Gene-Disease Associations genes associated with the genital tract atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
benign genitourinary tract neoplasm Gene SetFrom HPO Gene-Disease Associations genes associated with the benign genitourinary tract neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent lower respiratory tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent lower respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
respiratory tract infection Gene SetFrom HPO Gene-Disease Associations genes associated with the respiratory tract infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinocerebellar tract degeneration Gene SetFrom HPO Gene-Disease Associations genes associated with the spinocerebellar tract degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corticospinal tract hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the corticospinal tract hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the left ventricular outflow tract Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the left ventricular outflow tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent urinary tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent urinary tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent upper and lower respiratory tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent upper and lower respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the optic tract Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
malignant gastrointestinal tract tumors Gene SetFrom HPO Gene-Disease Associations genes associated with the malignant gastrointestinal tract tumors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long-tract signs Gene SetFrom HPO Gene-Disease Associations genes associated with the long-tract signs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper respiratory tract Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper respiratory tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the optic tract Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
functional abnormality of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the functional abnormality of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
acute respiratory tract infection Gene SetFrom HPO Gene-Disease Associations genes associated with the acute respiratory tract infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lower urinary tract Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lower urinary tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent upper respiratory tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent upper respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
benign gastrointestinal tract tumors Gene SetFrom HPO Gene-Disease Associations genes associated with the benign gastrointestinal tract tumors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neoplasm of the genitourinary tract Gene SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the genitourinary tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the pyramidal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper urinary tract Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper urinary tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the pyramidal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
malignant genitourinary tract tumor Gene SetFrom HPO Gene-Disease Associations genes associated with the malignant genitourinary tract tumor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Respiratory Tract Neoplasms Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Respiratory Tract Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Respiratory Tract Infections Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Respiratory Tract Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Respiratory Tract Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Respiratory Tract Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Urinary Tract Infections Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Urinary Tract Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
absent optic tract Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent optic tract phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased corticospinal tract size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased corticospinal tract size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
gastrointestinal tract polyps Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the gastrointestinal tract polyps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
heart right ventricle outflow tract stenosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the heart right ventricle outflow tract stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
heart left ventricle outflow tract stenosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the heart left ventricle outflow tract stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{aerodigestive tract cancer, squamous cell, alcohol-related, protection against} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {aerodigestive tract cancer, squamous cell, alcohol-related, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{congenital anomalies of kidney and urinary tract, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {congenital anomalies of kidney and urinary tract, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
urinary tract Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue urinary tract from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
gastrointestinal tract Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue gastrointestinal tract from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
urinary tract Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue urinary tract in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
gastrointestinal tract Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue gastrointestinal tract in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
fibre tract Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue fibre tract in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
urinary tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue urinary tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
spinal trigeminal tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue spinal trigeminal tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
gastrointestinal tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue gastrointestinal tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
fibre tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue fibre tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
olfactory tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue olfactory tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Gastrointestinal Tract Vascular Insufficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gastrointestinal Tract Vascular Insufficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Febrile Urinary Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Febrile Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Urinary Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cancer Of Urinary Tract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cancer Of Urinary Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Urinary Tract Obstruction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Urinary Tract Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Lower Respiratory Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Lower Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Upper Respiratory Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Upper Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Respiratory Tract Infection Viral Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Respiratory Tract Infection Viral in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Morphological Abnormality Of The Pyramidal Tract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Morphological Abnormality Of The Pyramidal Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Urinary Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Respiratory Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Urinary Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Spinocerebellar Tract Degeneration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Spinocerebellar Tract Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reproductive Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reproductive Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Enteropathogenic Escherichia Coli Gastrointestinal Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Enteropathogenic Escherichia Coli Gastrointestinal Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Upper Urinary Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Upper Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Left Ventricular Outflow Tract Obstruction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Left Ventricular Outflow Tract Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Verotoxigenic Escherichia Coli Gastrointestinal Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Verotoxigenic Escherichia Coli Gastrointestinal Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Urinary Tract Obstruction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Urinary Tract Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lower Respiratory Tract Inflammation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lower Respiratory Tract Inflammation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complicated Urinary Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complicated Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Respiratory Tract Infections Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Respiratory Tract Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fistula Of Genitourinary Tract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fistula Of Genitourinary Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Enterotoxigenic Escherichia Coli Gastrointestinal Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Enterotoxigenic Escherichia Coli Gastrointestinal Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pyramidal Tract Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pyramidal Tract Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gastrointestinal Stromal Tumor Of The Gastrointestinal Tract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gastrointestinal Stromal Tumor Of The Gastrointestinal Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Spinocerebellar Tract Disease In Lower Limbs Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Spinocerebellar Tract Disease In Lower Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Genitourinary Tract Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Genitourinary Tract Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Genitourinary Tract Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Genitourinary Tract Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Brain Malformations With Or Without Urinary Tract Defects Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Brain Malformations With Or Without Urinary Tract Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gastrointestinal Tract Adenoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gastrointestinal Tract Adenoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Urinary Tract Inflammation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Urinary Tract Inflammation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long-Tract Signs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long-Tract Signs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lower Urinary Tract Symptoms Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lower Urinary Tract Symptoms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Infection Of The Gastrointestinal Tract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infection Of The Gastrointestinal Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Upper And Lower Respiratory Tract Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Upper And Lower Respiratory Tract Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Lower Respiratory Tract Infection Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Lower Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Corticospinal Tract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Corticospinal Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Gastrointestinal Tract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Gastrointestinal Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corticospinal Tract Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corticospinal Tract Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aerodigestive Tract Cancer, Squamous Cell, Alcohol-Related, Protection Against Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aerodigestive Tract Cancer, Squamous Cell, Alcohol-Related, Protection Against in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Functional Abnormality Of The Gastrointestinal Tract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Abnormality Of The Gastrointestinal Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Granuloma, Respiratory Tract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Granuloma, Respiratory Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Morphological Abnormality Of The Gastrointestinal Tract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Morphological Abnormality Of The Gastrointestinal Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corticospinal Tract Hypoplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corticospinal Tract Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Upper Urinary Tract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Upper Urinary Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
digestive tract development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the digestive tract development biological process from the curated GO Biological Process Annotations 2023 dataset. |
outflow tract septum morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the outflow tract septum morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
embryonic digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryonic digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
determination of digestive tract left/right asymmetry Gene SetFrom GO Biological Process Annotations 2023 genes participating in the determination of digestive tract left/right asymmetry biological process from the curated GO Biological Process Annotations 2023 dataset. |
embryonic digestive tract development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryonic digestive tract development biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of cell proliferation involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of cell proliferation involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
cardiac neural crest cell migration involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cardiac neural crest cell migration involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cardiac neural crest cell migration involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cardiac neural crest cell migration involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
canonical Wnt signaling pathway involved in positive regulation of cardiac outflow tract cell proliferation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the canonical Wnt signaling pathway involved in positive regulation of cardiac outflow tract cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset. |
corticospinal tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the corticospinal tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
cardiac neural crest cell development involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cardiac neural crest cell development involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of semaphorin-plexin signaling pathway involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of semaphorin-plexin signaling pathway involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of apoptotic process involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of apoptotic process involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
endodermal digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the endodermal digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
embryonic ectodermal digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryonic ectodermal digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of Wnt signaling pathway involved in digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of Wnt signaling pathway involved in digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
cell proliferation involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cell proliferation involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of cardiac neural crest cell migration involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of cardiac neural crest cell migration involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cell proliferation involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cell proliferation involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
urinary tract smooth muscle contraction Gene SetFrom GO Biological Process Annotations 2023 genes participating in the urinary tract smooth muscle contraction biological process from the curated GO Biological Process Annotations 2023 dataset. |
ectodermal digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the ectodermal digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
embryonic ectodermal digestive tract development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryonic ectodermal digestive tract development biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of Wnt signaling pathway involved in digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of Wnt signaling pathway involved in digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
poly-pyrimidine tract binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the poly-pyrimidine tract binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
poly-purine tract binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the poly-purine tract binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
heart right ventricle outflow tract stenosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the heart right ventricle outflow tract stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
impaired sperm migration in female genital tract Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired sperm migration in female genital tract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased corticospinal tract size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased corticospinal tract size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent optic tract Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent optic tract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent cardiac outflow tract Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cardiac outflow tract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
gastrointestinal tract polyps Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the gastrointestinal tract polyps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased mammillothalamic tract size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased mammillothalamic tract size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Outflow tract(OFT) cell_Outflow tract_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Outflow tract(OFT) cell_Outflow tract_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
digestive tract development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the digestive tract development biological process from the curated GO Biological Process Annotations 2025 dataset. |
outflow tract septum morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the outflow tract septum morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
embryonic digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryonic digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
determination of digestive tract left/right asymmetry Gene SetFrom GO Biological Process Annotations 2025 genes participating in the determination of digestive tract left/right asymmetry biological process from the curated GO Biological Process Annotations 2025 dataset. |
embryonic digestive tract development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryonic digestive tract development biological process from the curated GO Biological Process Annotations 2025 dataset. |
cardiac neural crest cell migration involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cardiac neural crest cell migration involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cardiac neural crest cell migration involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cardiac neural crest cell migration involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
corticospinal tract morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the corticospinal tract morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
cardiac neural crest cell development involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cardiac neural crest cell development involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of apoptotic process involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of apoptotic process involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
endodermal digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the endodermal digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
embryonic ectodermal digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryonic ectodermal digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of cardiac neural crest cell migration involved in outflow tract morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of cardiac neural crest cell migration involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
urinary tract smooth muscle contraction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the urinary tract smooth muscle contraction biological process from the curated GO Biological Process Annotations 2025 dataset. |
ectodermal digestive tract morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the ectodermal digestive tract morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
embryonic ectodermal digestive tract development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryonic ectodermal digestive tract development biological process from the curated GO Biological Process Annotations 2025 dataset. |
poly-pyrimidine tract binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the poly-pyrimidine tract binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
poly-purine tract binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the poly-purine tract binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Lower respiratory tract disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Lower respiratory tract disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autoimmune disease of gastrointestinal tract Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autoimmune disease of gastrointestinal tract from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autoimmune disease of gastrointestinal tract Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Autoimmune disease of gastrointestinal tract in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lower respiratory tract disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Lower respiratory tract disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Upper respiratory tract disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Upper respiratory tract disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lower respiratory tract disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lower respiratory tract disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Upper respiratory tract disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Upper respiratory tract disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autoimmune disease of gastrointestinal tract Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune disease of gastrointestinal tract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Urinary tract infection Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Urinary tract infection in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Urinary tract obstruction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Urinary tract obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autoimmune disease of urogenital tract Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune disease of urogenital tract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lower urinary tract calculus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lower urinary tract calculus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Urinary tract papillary transitional cell benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Urinary tract papillary transitional cell benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Gastrointestinal tract Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Gastrointestinal tract from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Urinary tract Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Urinary tract from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Gastrointestinal tract Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Gastrointestinal tract in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Urinary tract Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Urinary tract in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Fibre tract Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Fibre tract in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Gastrointestinal tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Gastrointestinal tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Urinary tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Urinary tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Corticospinal tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Corticospinal tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Spinothalamic tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Spinothalamic tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Fibre tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Fibre tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Olfactory tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Olfactory tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Rubrospinal tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Rubrospinal tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Spinal trigeminal tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Spinal trigeminal tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Lateral spinothalamic tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Lateral spinothalamic tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Anterior spinothalamic tract Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Anterior spinothalamic tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Congenital anomaly of kidney and urinary tract Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital anomaly of kidney and urinary tract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital anomalies of kidney and urinary tract Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital anomalies of kidney and urinary tract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lower urinary tract obstruction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lower urinary tract obstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital anomalies of kidney and urinary tract syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital anomalies of kidney and urinary tract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Non-syndromic renal or urinary tract malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-syndromic renal or urinary tract malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Common Congenital Anomalies of the Kidney and Urinary Tract Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Common Congenital Anomalies of the Kidney and Urinary Tract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
DCHS1-related congenital anomalies of the kidney and urinary tract Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the DCHS1-related congenital anomalies of the kidney and urinary tract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SLIT3-related anomalies of the kidney and urinary tract Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SLIT3-related anomalies of the kidney and urinary tract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Urinary tract infection frequency Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Urinary tract infection frequency phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Left ventricular obstructive tract defect (inherited effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular obstructive tract defect (inherited effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Left ventricular obstructive tract defect (maternal effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular obstructive tract defect (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Benign prostatic hyperplasia and lower urinary tract symptoms Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign prostatic hyperplasia and lower urinary tract symptoms phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Benign prostatic hyperplasia and/or lower urinary tract symptoms Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign prostatic hyperplasia and/or lower urinary tract symptoms phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
physiology Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term physiology in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
modification of morphology or physiology of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modification of morphology or physiology of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
modification of morphology or physiology of other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modification of morphology or physiology of other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
modification by host of symbiont morphology or physiology Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modification by host of symbiont morphology or physiology biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation by virus of host morphology or physiology Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation by virus of host morphology or physiology biological process from the curated GO Biological Process Annotations 2015 dataset. |
modification by symbiont of host morphology or physiology Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modification by symbiont of host morphology or physiology biological process from the curated GO Biological Process Annotations 2015 dataset. |
abnormality of immune serum protein physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune serum protein physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pancreas physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pancreas physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiovascular system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiovascular system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of muscle physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the parathyroid physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the parathyroid physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pancreas physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pancreas physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of neutrophil physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of neutrophil physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of nervous system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of nervous system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of exocrine pancreas physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of exocrine pancreas physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiovascular system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiovascular system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thyroid physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thyroid physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of adrenal physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of adrenal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of t cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of t cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of endocrine pancreas physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of endocrine pancreas physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of skin physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of skin physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of skeletal physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of skeletal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of immune system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of immune system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the urinary system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the urinary system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of The Parathyroid Physiology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Parathyroid Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Nervous System Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Nervous System Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Immune System Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Immune System Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Exocrine Pancreas Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Exocrine Pancreas Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Thyroid Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Thyroid Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of T Cell Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of T Cell Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Endocrine Pancreas Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Endocrine Pancreas Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of B Cell Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of B Cell Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Neutrophil Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Neutrophil Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Reproductive System Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Reproductive System Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality of immune system physiology Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of immune system physiology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thyroid hormone metabolism, abnormal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone metabolism, abnormal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Reflex, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Reflex, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Neutrophil Chemotactic Response, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutrophil Chemotactic Response, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Thyroid Hormone Metabolism, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Metabolism, Abnormal from the curated CTD Gene-Disease Associations dataset. |
abnormal retinal correspondence Gene SetFrom DISEASES Text-mining Gene-Disease Association 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. |
abnormal splicing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal splicing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal; brugada syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal; brugada syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal urogenital development Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal urogenital development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal fibrin polymerization and thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal fibrin polymerization and thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormal cannabidiol Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the abnormal cannabidiol ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
abnormal gallbladder morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal intraocular pressure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal intraocular pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eating behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eating behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal thrombosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal thrombosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal leukocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal leukocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal iris pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal iris pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bone structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bone structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal serum iron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal serum iron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal emotion/affect behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal emotion/affect behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bleeding Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bleeding phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal atrioventricular conduction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal atrioventricular conduction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair quantity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair quantity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal ekg Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal ekg phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal axial skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal axial skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal immunoglobulin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal immunoglobulin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal monocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal monocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neutrophil cell number Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neutrophil cell number phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal facial shape Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal facial shape phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal aggressive, impulsive or violent behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal aggressive, impulsive or violent behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
acquired abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glomerular filtration rate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glomerular filtration rate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eye morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal testosterone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal testosterone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal joint morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal joint morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal motor neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal motor neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal genital system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal genital system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal appendicular skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal appendicular skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal cortical bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal cortical bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal electrophysiology of sinoatrial node origin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal respiratory system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal respiratory system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal number of teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal circulating creatinine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal circulating creatinine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal peripheral nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal muscle tone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal muscle tone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal diaphysis morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal diaphysis morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal spermatogenesis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal spermatogenesis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hemoglobin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hemoglobin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glucose homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glucose homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal renal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal dermatoglyphics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification of hand bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone structure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone structure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |