| Name |
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small distal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the small distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Small Distal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 <small>Dsmall>-Tic9]OT Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 <small>Dsmall>-Tic9]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
abnormality of the distal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
irregular distal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the irregular distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlargement of the distal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the enlargement of the distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Irregular Distal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Irregular Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Flat Distal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Flat Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Enlargement Of The Distal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlargement Of The Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO2H Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO2H ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7]OT Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 Aib9]OT Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 Aib9]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO2H Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO2H ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
abnormality of femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flat capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the flat capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flattened femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the flattened femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
irregular femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the irregular femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
irregular capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the irregular capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
avascular necrosis of the capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the avascular necrosis of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cone-shaped capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the cone-shaped capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlargement of the proximal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the enlargement of the proximal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Irregular Capital Femoral Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Irregular Capital Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia/Hypoplasia Of The Capital Femoral Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The Capital Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Femoral Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of The Epiphysis Of The Femoral Head Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Epiphysis Of The Femoral Head in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Flat Capital Femoral Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flat Capital Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Enlargement Of The Proximal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlargement Of The Proximal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Irregular Femoral Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Irregular Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Stippling Of The Epiphysis Of The Distal Phalanx Of The Thumb Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stippling Of The Epiphysis Of The Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
trapezoidal distal femoral condyles Gene SetFrom HPO Gene-Disease Associations genes associated with the trapezoidal distal femoral condyles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal femoral metaphyseal abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the distal femoral metaphyseal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
wide distal femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the wide distal femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal femoral bowing Gene SetFrom HPO Gene-Disease Associations genes associated with the distal femoral bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Distal Femoral Bowing Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Femoral Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Trapezoidal Distal Femoral Condyles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Trapezoidal Distal Femoral Condyles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Wide Distal Femoral Metaphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Distal Femoral Metaphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bracket epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the bracket epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cone-shaped epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the cone-shaped epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal tibial epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal tibial epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the 1st metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cone-shaped epiphysis of the 1st metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the cone-shaped epiphysis of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the humeral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the humeral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bracket epiphysis of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the bracket epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lower limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lower limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flattened epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the flattened epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of vertebral epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of vertebral epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal long bone epiphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thickened long bone epiphysis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thickened long bone epiphysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
epiphysis Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue epiphysis in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Cone-Shaped Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cone-Shaped Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Vertebral Epiphysis Morphology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Vertebral Epiphysis Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Triangular Epiphysis Of The Middle Phalanx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Triangular Epiphysis Of The Middle Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Triangular Epiphysis Of The Proximal Phalanx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Triangular Epiphysis Of The Proximal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Epiphysis Morphology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Epiphysis Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cone-Shaped Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cone-Shaped Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Flattened Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flattened Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal long bone epiphysis morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone epiphysis morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thickened long bone epiphysis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thickened long bone epiphysis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Epiphysis Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Epiphysis in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d[<small>Dsmall>-Phe2]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d[<small>Dsmall>-Phe2]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[125I]d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [125I]d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Phaa1 <small>Dsmall>-Tyr2 Val4 Arg6 Arg-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa1 <small>Dsmall>-Tyr2 Val4 Arg6 Arg-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[<small>Dsmall>-Bpa5 Ile13]motilin (human) Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [<small>Dsmall>-Bpa5 Ile13]motilin (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[tBaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Arg-NH28 des-Gly9]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [tBaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Arg-NH28 des-Gly9]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[His5 <small>Dsmall>-Tyr6]GnRH Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [His5 <small>Dsmall>-Tyr6]GnRH ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d(CH2)5[<small>Dsmall>-Ile2 Ile4]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH2)5[<small>Dsmall>-Ile2 Ile4]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[<small>Lsmall>-Bpa5 Ile13]motilin (human) Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [<small>Lsmall>-Bpa5 Ile13]motilin (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Phaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Tyr-NH28 des-Gly9]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Tyr-NH28 des-Gly9]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Sar <small>Dsmall>-Phe8 des-Arg9]bradykinin Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Sar <small>Dsmall>-Phe8 des-Arg9]bradykinin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d[<small>Dsmall>-Pal2]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d[<small>Dsmall>-Pal2]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH2]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH2]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Phaa1 <small>Dsmall>-Tyr(Me)2 Arg6 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa1 <small>Dsmall>-Tyr(Me)2 Arg6 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Ile4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Ile4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[<small>Dsmall>-Lys1 des-Arg10]kallidin Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [<small>Dsmall>-Lys1 des-Arg10]kallidin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[125I]d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [125I]d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
<small>Dsmall>-Lys0-[des-Arg10]kallidin Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the <small>Dsmall>-Lys0-[des-Arg10]kallidin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Phaa1 <small>Dsmall>-Tyr(Et)2 Lys6 des-Gly9]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa1 <small>Dsmall>-Tyr(Et)2 Lys6 des-Gly9]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[125I][des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [125I][des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
U1 small nuclear ribonucleoprotein A/U2 small nuclear ribonucleoprotein B'' Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U1 small nuclear ribonucleoprotein A/U2 small nuclear ribonucleoprotein B'' protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Femoral Fractures Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Femoral Fractures from the curated CTD Gene-Disease Associations dataset. |
femoral neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease femoral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
femoral neck geometry Gene SetFrom GAD Gene-Disease Associations genes associated with the disease femoral neck geometry in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
femoral neck fractures; fractures, stress Gene SetFrom GAD Gene-Disease Associations genes associated with the disease femoral neck fractures; fractures, stress in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
femoral neck fractures; osteoporosis; spinal injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease femoral neck fractures; osteoporosis; spinal injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carotid and femoral artery stiffness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carotid and femoral artery stiffness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
femoral Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term femoral in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Femoral neck bone geometry Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Femoral neck bone geometry phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Femoral neck bone geometry and menarche (age at onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Femoral neck bone geometry and menarche (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
abnormality of the femoral neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck or head region phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral neck or head region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
femoral hernia Gene SetFrom HPO Gene-Disease Associations genes associated with the femoral hernia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short femoral neck Gene SetFrom HPO Gene-Disease Associations genes associated with the short femoral neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad femoral neck Gene SetFrom HPO Gene-Disease Associations genes associated with the broad femoral neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multicentric ossification of proximal femoral epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the multicentric ossification of proximal femoral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
femoral bowing Gene SetFrom HPO Gene-Disease Associations genes associated with the femoral bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
narrow femoral neck Gene SetFrom HPO Gene-Disease Associations genes associated with the narrow femoral neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
delayed femoral head ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the delayed femoral head ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
disproportionate prominence of the femoral medial condyle Gene SetFrom HPO Gene-Disease Associations genes associated with the disproportionate prominence of the femoral medial condyle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hyperplasia of the femoral trochanters Gene SetFrom HPO Gene-Disease Associations genes associated with the hyperplasia of the femoral trochanters phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification involving the femoral head and neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lateral displacement of the femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the lateral displacement of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal femoral epiphysiolysis Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal femoral epiphysiolysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flared femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the flared femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flattened femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the flattened femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal femoral metaphyseal abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal femoral metaphyseal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lateral femoral bowing Gene SetFrom HPO Gene-Disease Associations genes associated with the lateral femoral bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
wide capital femoral epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the wide capital femoral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
femoral bowing present at birth, straightening with time Gene SetFrom HPO Gene-Disease Associations genes associated with the femoral bowing present at birth, straightening with time phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the femoral head and neck Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal femoral metaphyseal irregularity Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal femoral metaphyseal irregularity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad femoral metaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the broad femoral metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multicentric femoral head ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the multicentric femoral head ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dysplasia of the femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the dysplasia of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Femoral Neck Fractures Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Femoral Neck Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Femoral Fractures Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Femoral Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
abnormal femoral fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal femoral fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased femoral fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased femoral fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
avascular necrosis of the femoral head Gene SetFrom OMIM Gene-Disease Associations genes associated with the avascular necrosis of the femoral head phenotype from the curated OMIM Gene-Disease Associations dataset. |
femoral artery Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue femoral artery from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
femoral artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue femoral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
femoral muscle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue femoral muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Slipped Capital Femoral Epiphyses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Slipped Capital Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Femoral Artery Occlusion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Femoral Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Superficial Femoral Artery Occlusion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Superficial Femoral Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of The Femoral Metaphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Femoral Metaphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proximal Femoral Metaphyseal Abnormality Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal Femoral Metaphyseal Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Avascular Necrosis Of Femoral Head Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Avascular Necrosis Of Femoral Head in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Flared Femoral Metaphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Flared Femoral Metaphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Femoral Hypoplasia - Unusual Facies Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Femoral Hypoplasia - Unusual Facies Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Wide Capital Femoral Epiphyses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Wide Capital Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Femoral Neck Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Femoral Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Excessive Femoral Anteversion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Excessive Femoral Anteversion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Delayed Proximal Femoral Epiphyseal Ossification Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Proximal Femoral Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Femoral Neck Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Femoral Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Femoral Bowing Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Femoral Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Femoral Metaphyseal Irregularity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Femoral Metaphyseal Irregularity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atypical Femoral Fracture Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atypical Femoral Fracture in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Femoral Bowing Present At Birth, Straightening With Time Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Femoral Bowing Present At Birth, Straightening With Time in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Flattened Femoral Head Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flattened Femoral Head in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Narrow Femoral Neck Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Narrow Femoral Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Early Ossification Of Capital Femoral Epiphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Ossification Of Capital Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Delayed Femoral Head Ossification Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Femoral Head Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multicentric Femoral Head Ossification Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multicentric Femoral Head Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multicentric Ossification Of Proximal Femoral Epiphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multicentric Ossification Of Proximal Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Femoral Metaphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Femoral Metaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lateral Femoral Bowing Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lateral Femoral Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Ossification Involving The Femoral Head And Neck Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Ossification Involving The Femoral Head And Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dysplasia Of The Femoral Head Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dysplasia Of The Femoral Head in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Disproportionate Prominence Of The Femoral Medial Condyle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Disproportionate Prominence Of The Femoral Medial Condyle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Femoral Neck Or Head Region Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Femoral Neck Or Head Region in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lateral Displacement Of The Femoral Head Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lateral Displacement Of The Femoral Head in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Wide Proximal Femoral Metaphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Proximal Femoral Metaphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
decreased femoral compact bone area Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased femoral compact bone area phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased femoral compact bone area Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased femoral compact bone area phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased femoral fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased femoral fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Femoral cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Femoral cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Femoral neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Femoral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Femoral vein thrombophlebitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Femoral vein thrombophlebitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Femoral artery Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Femoral artery from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Femoral artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Femoral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Femoral muscle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Femoral muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Avascular necrosis of femoral head Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Avascular necrosis of femoral head phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Nontraumatic osteonecrosis of the femoral head Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nontraumatic osteonecrosis of the femoral head phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Arterial stiffness (carotid-femoral pulse wave velocity) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Arterial stiffness (carotid-femoral pulse wave velocity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Arterial stiffness (brachial-femoral pulse wave velocity) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Arterial stiffness (brachial-femoral pulse wave velocity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bone mineral density (femoral neck) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (femoral neck) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric bone mineral content (femoral neck) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric bone mineral content (femoral neck) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric bone mineral density (femoral neck) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric bone mineral density (femoral neck) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Idiopathic osteonecrosis of the femoral head Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic osteonecrosis of the femoral head phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck bone mineral density Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck bone mineral density phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck bone mineral density and trunk fat mass adjusted by trunk lean mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck bone mineral density and trunk fat mass adjusted by trunk lean mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck length Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck length phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Narrowest width of the femoral neck Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Narrowest width of the femoral neck phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck section modulus Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck section modulus phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck bone geometry Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck bone geometry phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck bone geometry and menarche (age at onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck bone geometry and menarche (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bisphosphonate-associated atypical femoral fracture Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bisphosphonate-associated atypical femoral fracture phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Atypical femoral fracture in phosphonate treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Atypical femoral fracture in phosphonate treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bone mineral density (femoral neck) in inflammatory bowel disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (femoral neck) in inflammatory bowel disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Distal hereditary motor neuronopathy 2D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal spinal muscular atrophy, X-linked 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, with normal red cell morphology Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, with normal red cell morphology phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal myopathy Markesbery-Griggs type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal myopathy Markesbery-Griggs type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, distal, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 5B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal arthrogryposis type 1B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal arthrogryposis type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 7B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, with hemolytic anemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, with hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal arthrogryposis type 2B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal arthrogryposis type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, distal, type 5d Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, distal, type 5d phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, distal, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, distal, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal spinal muscular atrophy, autosomal recessive 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, Distal, with Anterior Tibial Onset Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Distal, with Anterior Tibial Onset from the curated CTD Gene-Disease Associations dataset. |
Welander distal myopathy, Swedish type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Welander distal myopathy, Swedish type from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Distal Hereditary Motor, Type IIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type IIA from the curated CTD Gene-Disease Associations dataset. |
Renal Tubular Acidosis, Distal, With Hemolytic Anemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, With Hemolytic Anemia from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type V Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type V from the curated CTD Gene-Disease Associations dataset. |
Jacobsen Distal 11q Deletion Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Jacobsen Distal 11q Deletion Syndrome from the curated CTD Gene-Disease Associations dataset. |
Renal tubular acidosis, distal, autosomal recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal tubular acidosis, distal, autosomal recessive from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type IIB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type IIB from the curated CTD Gene-Disease Associations dataset. |
Arthrogryposis, Distal, Type 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis, Distal, Type 4 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset. |
ARTHROGRYPOSIS, DISTAL, TYPE 1A Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ARTHROGRYPOSIS, DISTAL, TYPE 1A from the curated CTD Gene-Disease Associations dataset. |
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness from the curated CTD Gene-Disease Associations dataset. |
Distal myopathy, Nonaka type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Distal myopathy, Nonaka type from the curated CTD Gene-Disease Associations dataset. |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Distal Hereditary Motor, Type VIIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type VIIA from the curated CTD Gene-Disease Associations dataset. |
Arthrogryposis multiplex congenita, distal, X-linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis multiplex congenita, distal, X-linked from the curated CTD Gene-Disease Associations dataset. |
Distal Myopathies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Distal Myopathies from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type Viib Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type Viib from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, X-Linked 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset. |
Distal arthrogryposis type 2B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Distal arthrogryposis type 2B from the curated CTD Gene-Disease Associations dataset. |
distal muscular dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
distal hereditary motor neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal hereditary motor neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
distal arthrogryposis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal arthrogryposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial distal renal tubular acidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
proximal chromosome 9p to q and distal chromosome 9q Gene SetFrom GAD Gene-Disease Associations genes associated with the disease proximal chromosome 9p to q and distal chromosome 9q in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
distal myopathies; myositis, inclusion body Gene SetFrom GAD Gene-Disease Associations genes associated with the disease distal myopathies; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
distal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term distal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
proximal/distal pattern formation involved in nephron development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in nephron development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
proximal/distal pattern formation involved in metanephric nephron development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in metanephric nephron development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric distal tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric distal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
distal tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the distal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
lung proximal/distal axis specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lung proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
polarity specification of proximal/distal axis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the polarity specification of proximal/distal axis biological process from the curated GO Biological Process Annotations 2015 dataset. |
proximal/distal axis specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
proximal/distal pattern formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in positive regulation of transcription Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in positive regulation of transcription molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase ii distal enhancer sequence-specific dna binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in negative regulation of transcription Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in negative regulation of transcription molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
wide tufts of distal phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the wide tufts of distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tapering pointed ends of distal finger phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the tapering pointed ends of distal finger phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal upper limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the distal upper limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
osteolytic defects of the distal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the osteolytic defects of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal widening of metacarpals Gene SetFrom HPO Gene-Disease Associations genes associated with the distal widening of metacarpals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
late-onset distal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the late-onset distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
impaired distal vibration sensation Gene SetFrom HPO Gene-Disease Associations genes associated with the impaired distal vibration sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of distal phalanx of toe Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the distal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
impaired distal tactile sensation Gene SetFrom HPO Gene-Disease Associations genes associated with the impaired distal tactile sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of hand Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanges of all fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanges of all fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sclerosis of distal finger phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the sclerosis of distal finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dysplastic distal thumb phalanges with a central hole Gene SetFrom HPO Gene-Disease Associations genes associated with the dysplastic distal thumb phalanges with a central hole phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
widened distal phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the widened distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) Gene SetFrom HPO Gene-Disease Associations genes associated with the osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent distal interphalangeal creases Gene SetFrom HPO Gene-Disease Associations genes associated with the absent distal interphalangeal creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped distal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slender distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the slender distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal ulnar hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the distal ulnar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive distal muscular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal upper limb amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the distal upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bifid distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the bifid distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal lower limb amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the distal lower limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal lower limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the distal lower limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased distal sensory nerve action potential Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased distal sensory nerve action potential phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal tapering of metatarsals Gene SetFrom HPO Gene-Disease Associations genes associated with the distal tapering of metatarsals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal ileal atresia Gene SetFrom HPO Gene-Disease Associations genes associated with the distal ileal atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal tapering femur Gene SetFrom HPO Gene-Disease Associations genes associated with the distal tapering femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ivory epiphyses of the distal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the ivory epiphyses of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplastic distal humeri Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplastic distal humeri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
complete duplication of the distal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the complete duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanx of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanx of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the distal amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanx of the hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal shortening of limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the distal shortening of limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
osteolytic defects of the distal phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the osteolytic defects of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal sensory impairment of all modalities Gene SetFrom HPO Gene-Disease Associations genes associated with the distal sensory impairment of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fifth finger distal phalanx clinodactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the fifth finger distal phalanx clinodactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of the hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
club-shaped distal femur Gene SetFrom HPO Gene-Disease Associations genes associated with the club-shaped distal femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shortening of all distal phalanges of the fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the shortening of all distal phalanges of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal/middle symphalangism of 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the distal/middle symphalangism of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the long distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent distal phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the absent distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal symphalangism Gene SetFrom HPO Gene-Disease Associations genes associated with the distal symphalangism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized distal tubular acidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized distal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the distal phalanx of the hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bifid distal phalanx of toe Gene SetFrom HPO Gene-Disease Associations genes associated with the bifid distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypermobility of distal interphalangeal joints Gene SetFrom HPO Gene-Disease Associations genes associated with the hypermobility of distal interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of toe Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal renal tubular acidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the distal renal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal sensory impairment Gene SetFrom HPO Gene-Disease Associations genes associated with the distal sensory impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive distal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tapered distal phalanges of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the tapered distal phalanges of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal peripheral sensory neuropathy Gene SetFrom HPO Gene-Disease Associations genes associated with the distal peripheral sensory neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
complete duplication of distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the complete duplication of distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
acroosteolysis of distal phalanges (feet) Gene SetFrom HPO Gene-Disease Associations genes associated with the acroosteolysis of distal phalanges (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal tibial bowing Gene SetFrom HPO Gene-Disease Associations genes associated with the distal tibial bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal urethral duplication Gene SetFrom HPO Gene-Disease Associations genes associated with the distal urethral duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal sensory loss of all modalities Gene SetFrom HPO Gene-Disease Associations genes associated with the distal sensory loss of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal arthrogryposis Gene SetFrom HPO Gene-Disease Associations genes associated with the distal arthrogryposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal symphalangism (hands) Gene SetFrom HPO Gene-Disease Associations genes associated with the distal symphalangism (hands) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
impaired distal proprioception Gene SetFrom HPO Gene-Disease Associations genes associated with the impaired distal proprioception phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent fourth finger distal interphalangeal crease Gene SetFrom HPO Gene-Disease Associations genes associated with the absent fourth finger distal interphalangeal crease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Distal-less-like homeobox protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Distal-less-like homeobox protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
dilated distal convoluted tubules Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated distal convoluted tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal distal convoluted tubule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal distal convoluted tubule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal distal visceral endoderm morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal distal visceral endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal proximal-distal axis patterning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal proximal-distal axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent distal visceral endoderm Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent distal visceral endoderm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
chromosome 7q11.23 deletion syndrome, distal, 1.2mb Gene SetFrom OMIM Gene-Disease Associations genes associated with the chromosome 7q11.23 deletion syndrome, distal, 1.2mb phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type vi Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type vi phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, autosomal recessive, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, autosomal recessive, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type vb Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type vb phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type viia Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type viia phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, chronic distal, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type iid Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type iid phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthyrgryposis, distal, type 2b Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthyrgryposis, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset. |
chromosome 22q11.2 deletion syndrome, distal Gene SetFrom OMIM Gene-Disease Associations genes associated with the chromosome 22q11.2 deletion syndrome, distal phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, jerash type Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, jerash type phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 2b Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 2a Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset. |
welander distal myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the welander distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
renal tubular acidosis, distal, ar Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, distal, ar phenotype from the curated OMIM Gene-Disease Associations dataset. |
renal tubular acidosis, distal, ad Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, distal, ad phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
laing distal myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the laing distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
?neuronopathy, distal hereditary motor, type iic Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?neuronopathy, distal hereditary motor, type iic phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type va Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type va phenotype from the curated OMIM Gene-Disease Associations dataset. |
renal tubular acidosis, distal, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis multiplex congenita, distal, type 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis multiplex congenita, distal, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis multiplex congenita, distal, type 2b Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis multiplex congenita, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal, with anterior tibial onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal, with anterior tibial onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, x-linked 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type viib Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type viib phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 1b Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, congenital nonprogressive Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 5d Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 5d phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal, tateyama type Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal, tateyama type phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type iib Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iib phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type iia Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iia phenotype from the curated OMIM Gene-Disease Associations dataset. |
distal tip Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue distal tip in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
distal tubular epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue distal tubular epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
renal distal tubule Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue renal distal tubule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
distal tip cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue distal tip cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Distal Amyotrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Arthrogryposis Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Arthrogryposis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Lower Limb Amyotrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Lower Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Jacobsen Distal 11Q Deletion Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Jacobsen Distal 11Q Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Renal Tubular Acidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Renal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Distal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Distal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Monosomy 3P Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 3P Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periodic Paralysis With Later-Onset Distal Motor Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Periodic Paralysis With Later-Onset Distal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Distal Phalanges Of All Fingers Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Broad Distal Phalanges Of All Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chromosome 22Q11.2 Deletion Syndrome, Distal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 22Q11.2 Deletion Syndrome, Distal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complete Duplication Of Distal Phalanx Of The Thumb Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Distal Phalanx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fifth Finger Distal Phalanx Clinodactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fifth Finger Distal Phalanx Clinodactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Welander Distal Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Welander Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Upper Limb Amyotrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Upper Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Ileal Obstruction Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Ileal Obstruction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Intestinal Obstruction Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Intestinal Obstruction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Tibial Bowing Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Tibial Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Bile Duct Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Bile Duct Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tapering Pointed Ends Of Distal Finger Phalanges Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tapering Pointed Ends Of Distal Finger Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Hereditary Motor Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Hereditary Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Triangular Shaped Distal Phalanx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Triangular Shaped Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Peripheral Sensory Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Peripheral Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bifid Distal Phalanx Of Toe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bifid Distal Phalanx Of Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Arthrogryposis Type 5D Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Arthrogryposis Type 5D in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Monosomy 12P Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 12P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Partial Duplication Of The Distal Phalanx Of The 2Nd Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Partial Duplication Of The Distal Phalanx Of The 3Rd Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Tapering Femur Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Tapering Femur in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Generalized Distal Tubular Acidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Generalized Distal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Colitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Colitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Urethral Duplication Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Urethral Duplication in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dysplastic Distal Thumb Phalanges With A Central Hole Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dysplastic Distal Thumb Phalanges With A Central Hole in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Distal Phalanx Of The Hallux Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Broad Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Distal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Klhl9-Related Early-Onset Distal Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Klhl9-Related Early-Onset Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Bile Duct Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Bile Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complete Duplication Of The Distal Phalanges Of The Hand Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acroosteolysis Of Distal Phalanges (Feet) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acroosteolysis Of Distal Phalanges (Feet) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Curved Distal Phalanges Of The Hand Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Curved Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Myopathy 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Myopathy 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Tapering Of Metatarsals Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Tapering Of Metatarsals in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Trisomy 10Q Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Trisomy 10Q Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Absent Fourth Finger Distal Interphalangeal Crease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Absent Fourth Finger Distal Interphalangeal Crease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyperkalemic Distal Renal Tubular Acidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyperkalemic Distal Renal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal-Type Epithelioid Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal-Type Epithelioid Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bullet-Shaped Distal Phalanx Of The Hallux Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bullet-Shaped Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ivory Epiphyses Of The Distal Phalanges Of The Hand Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ivory Epiphyses Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal 17P13.3 Microdeletion Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal 17P13.3 Microdeletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Monosomy 1Q Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 1Q in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Monosomy 13Q Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 13Q Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chromosome 19Q13.11 Deletion Syndrome, Distal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 19Q13.11 Deletion Syndrome, Distal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Sensory Impairment Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Sensory Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Distal Phalanx Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Impaired Distal Proprioception Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Distal Proprioception in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Muscle Atrophy Due To Neurologic Disease Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Atrophy Due To Neurologic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Shortening Of All Distal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Shortening Of All Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Distal Limb Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Distal Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Late-Onset Distal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Late-Onset Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Lower Limb Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Lower Limb Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Upper Limb Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Upper Limb Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Distal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Club-Shaped Distal Femur Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Club-Shaped Distal Femur in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Sensory Impairment Of All Modalities Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Sensory Impairment Of All Modalities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Renal Tubular Acidosis Co-Occurrent With Sensorineural Deafness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Renal Tubular Acidosis Co-Occurrent With Sensorineural Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Osteolytic Defects Of The Distal Phalanges Of The Hand Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Osteolytic Defects Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Bifid Distal Phalanx Of The Thumb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bifid Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Partial Duplication Of The Distal Phalanx Of The Hallux Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Duplication Of The Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Impaired Distal Vibration Sensation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Distal Vibration Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Distal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Wide Tufts Of Distal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Tufts Of Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hypermobility Of Distal Interphalangeal Joints Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypermobility Of Distal Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Joint Laxity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Joint Laxity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Distal Phalanx Of The Thumb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Impaired Distal Tactile Sensation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Distal Tactile Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Ileal Atresia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Ileal Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tapered Distal Phalanges Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tapered Distal Phalanges Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Duplication Of The Distal Phalanx Of Hand Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duplication Of The Distal Phalanx Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Distal Hallux Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Distal Phalanx Of The Thumb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Widened Distal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Widened Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Shortening Of Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Shortening Of Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Distal Interphalangeal Creases Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Distal Interphalangeal Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Slender Distal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slender Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Acroosteolysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Acroosteolysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Distal Sensory Nerve Action Potential Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Distal Sensory Nerve Action Potential in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Ulnar Hypoplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Ulnar Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Widening Of Metacarpals Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Widening Of Metacarpals in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Distal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal/Middle Symphalangism Of 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal/Middle Symphalangism Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
proximal/distal pattern formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
proximal/distal axis specification Gene SetFrom GO Biological Process Annotations 2023 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2023 dataset. |
metanephric distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
metanephric distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
metanephric distal tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric distal tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
distal tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the distal tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
distal dendrite Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the distal dendrite cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
apical distal dendrite Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the apical distal dendrite cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
dilated distal convoluted tubule Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated distal convoluted tubule phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal distal convoluted tubule morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal distal convoluted tubule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal proximal-distal axis patterning Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal proximal-distal axis patterning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal distal visceral endoderm morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal distal visceral endoderm morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent distal visceral endoderm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent distal visceral endoderm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased distal limb length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased distal limb length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - Kidney - L1 - Distal Convoluted Tubule Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L1 - Distal Convoluted Tubule cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Distal Convoluted Tubule Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Distal Convoluted Tubule cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Distal Convoluted Tubule Type 1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Distal Convoluted Tubule Type 1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Distal Convoluted Tubule Type 2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Distal Convoluted Tubule Type 2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Distal epithelial cell_Distal airway_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal epithelial cell_Distal airway_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal Proliferative Progenitor cell_Bone_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal Proliferative Progenitor cell_Bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal limb bud cell_Limb bud_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal limb bud cell_Limb bud_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Enterocyte distal cell_Intestine_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Enterocyte distal cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal cell_Epithelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal stem cell_Epithelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal stem cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal convoluted tubular cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal convoluted tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal tubule & loop of Henle cell_Fetal kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal tubule & loop of Henle cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal tubular cell_Fetal kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal tubular cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Medial and distal segment cell_Fetal kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Medial and distal segment cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal tubular cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal tubular cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal convoluted tubular cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal convoluted tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal cell_Blood vessel_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal cell_Blood vessel_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal lung progenitor cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal lung progenitor cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal epithelial cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal epithelial cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal cell_Prostate_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal cell_Prostate_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal convoluted tubular cell_Epithelium_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal convoluted tubular cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
16p11 2 distal deletion syndrome Gene SetFrom WikiPathways Pathways 2024 proteins participating in the 16p11 2 distal deletion syndrome pathway from the WikiPathways Pathways 2024 dataset. |
7q11 23 distal copy number variation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the 7q11 23 distal copy number variation pathway from the WikiPathways Pathways 2024 dataset. |
Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) Gene Setproteins participating in the Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) pathway from the Reactome Pathways 2024 dataset. |
Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5619114 Gene Setproteins participating in the Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5619114 pathway from the Reactome Pathways 2024 dataset. |
Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5658471 Gene Setproteins participating in the Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5658471 pathway from the Reactome Pathways 2024 dataset. |
proximal/distal pattern formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
proximal/distal axis specification Gene SetFrom GO Biological Process Annotations 2025 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2025 dataset. |
metanephric distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
metanephric distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
metanephric distal tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric distal tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
distal tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the distal tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
distal dendrite Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the distal dendrite cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
apical distal dendrite Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the apical distal dendrite cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Distal arthrogryposis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant distal hereditary motor neuronopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 5 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant distal hereditary motor neuronopathy 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis type 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive distal hereditary motor neuronopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive distal hereditary motor neuronopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis type 2B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal 10q deletion syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal 10q deletion syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal myopathy 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal arthrogryposis type 5D Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 5D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy with rimmed vacuoles Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with rimmed vacuoles in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy with anterior tibial onset Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with anterior tibial onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 14 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Chromosome 22q11.2 deletion syndrome, distal Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 22q11.2 deletion syndrome, distal in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 9 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
X-linked distal spinal muscular atrophy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked distal spinal muscular atrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 10 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1C Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Partial trisomy distal 4q Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial trisomy distal 4q in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal 10q deletion syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal 10q deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Renal distal tubule Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal distal tubule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Distal tip cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Distal tip cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Distal tip Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Distal tip in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Distal tubular epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Distal tubular epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Distal axon Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Distal axon cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Distal portion of axoneme Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Distal portion of axoneme cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Distal dendrite Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Distal dendrite cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Apical distal dendrite Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Apical distal dendrite cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Photoreceptor distal connecting cilium Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Photoreceptor distal connecting cilium cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Distal axon Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Distal axon cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Distal dendrite Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Distal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Photoreceptor distal connecting cilium Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Photoreceptor distal connecting cilium cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Distal portion of axoneme Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Distal portion of axoneme cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Basal distal dendrite Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Basal distal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Apical distal dendrite Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Apical distal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
bacterial-type flagellum basal body, distal rod, L ring Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the bacterial-type flagellum basal body, distal rod, L ring cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
bacterial-type flagellum basal body, distal rod Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the bacterial-type flagellum basal body, distal rod cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Distal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive distal renal tubular acidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive distal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive distal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive distal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked distal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal renal tubular acidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal arthrogryposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal arthrogryposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal lower limb muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal lower limb muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal lower limb amyotrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal lower limb amyotrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal hereditary motor neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal hereditary motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant distal renal tubular acidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant distal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive scapulohumeroperoneal distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive scapulohumeroperoneal distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Arthrogryposis multiplex congenita distal Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Arthrogryposis multiplex congenita distal phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Welander distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Welander distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal shortening of limbs Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal shortening of limbs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Finnish upper limb-onset distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Finnish upper limb-onset distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal/Left-sided colorectal cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Distal/Left-sided colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Distal colorectal cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Distal colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
PMC8104016-hcg-12-e002353-s006.xlsx-mTHP-1-LPS_Prom-Distal-RefSeq_Name_IRF6 Gene SetFrom Rummagene Transcription Factor Associations 2026 target genes of the PMC8104016-hcg-12-e002353-s006.xlsx-mTHP-1-LPS_Prom-Distal-RefSeq_Name_IRF6 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset. |
Non-small cell lung cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Non-small cell lung cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brain small vessel disease with hemorrhage Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital sensory neuropathy with selective loss of small myelinated fibers Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
mitochondrial small ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
preribosome, small subunit precursor Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the preribosome, small subunit precursor cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
small nuclear ribonucleoprotein complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small nuclear ribonucleoprotein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
small nucleolar ribonucleoprotein complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small nucleolar ribonucleoprotein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
organellar small ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the organellar small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
small ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
gamma-tubulin small complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the gamma-tubulin small complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cytosolic small ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cytosolic small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
small-subunit processome Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small-subunit processome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mitochondrial small ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
preribosome, small subunit precursor Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the preribosome, small subunit precursor cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
small nuclear ribonucleoprotein complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the small nuclear ribonucleoprotein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
small nucleolar ribonucleoprotein complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the small nucleolar ribonucleoprotein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
chloroplast small ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the chloroplast small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
organellar small ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the organellar small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
small ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
gamma-tubulin small complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the gamma-tubulin small complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cytosolic small ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cytosolic small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
plastid small ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the plastid small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
small-subunit processome Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the small-subunit processome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
SNAPc (small nuclear RNA-activating protein) complex Gene Setproteins in the SNAPc (small nuclear RNA-activating protein) complex protein complex from the CORUM Protein Complexes dataset. |
Carcinoma, Small Cell Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, Small Cell from the curated CTD Gene-Disease Associations dataset. |
Brain Small Vessel Disease with Hemorrhage Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Small Vessel Disease with Hemorrhage from the curated CTD Gene-Disease Associations dataset. |
Carcinoma, Non-Small-Cell Lung Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, Non-Small-Cell Lung from the curated CTD Gene-Disease Associations dataset. |
Small Cell Lung Carcinoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Small Cell Lung Carcinoma from the curated CTD Gene-Disease Associations dataset. |
Desmoplastic Small Round Cell Tumor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Desmoplastic Small Round Cell Tumor from the curated CTD Gene-Disease Associations dataset. |
Carcinoma, Non-Small-Cell Lung Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Carcinoma, Non-Small-Cell Lung in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
non-small cell lung carcinoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease non-small cell lung carcinoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
small intestine cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease small intestine cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
ureter small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ureter small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small cell osteogenic sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small cell osteogenic sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine neuroendocrine neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine neuroendocrine neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
prostate small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease prostate small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gallbladder small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gallbladder small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine leiomyoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine leiomyoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lung combined type small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung combined type small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
laryngeal small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease laryngeal small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lung mixed small cell and squamous cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung mixed small cell and squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine leiomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine leiomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hypercalcemic type ovarian small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypercalcemic type ovarian small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastric small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastric small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small cell sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small cell sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
non-small cell lung carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease non-small cell lung carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovarian small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestinal sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestinal sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cervix small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cervix small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lung small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
urinary bladder small cell neuroendocrine carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urinary bladder small cell neuroendocrine carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small for gestational age infant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease small for gestational age infant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; exanthema; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; exanthema; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; head and neck neoplasms; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; head and neck neoplasms; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms; lymphatic metastasis; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms; lymphatic metastasis; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; lung neoplasms; neoplasm metastasis; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm metastasis; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
non-small-cell lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease non-small-cell lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; colorectal neoplasms; genitourinary neoplasms; lung neoplasms; neoplasm of lung ; neutropenia; urogenital neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; colorectal neoplasms; genitourinary neoplasms; lung neoplasms; neoplasm of lung ; neutropenia; urogenital neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral small-vessel disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral small-vessel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
non-small cell lung carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease non-small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stroke, lacunar; small-vessel disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stroke, lacunar; small-vessel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
small artery compliance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease small artery compliance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; colorectal neoplasms; head and neck neoplasms; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; colorectal neoplasms; head and neck neoplasms; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cachexia; carcinoma, non-small-cell lung; gastrointestinal neoplasms; lung neoplasms; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cachexia; carcinoma, non-small-cell lung; gastrointestinal neoplasms; lung neoplasms; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
non-small cell lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease non-small cell lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; esophageal neoplasms; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; esophageal neoplasms; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; diarrhea; exanthema; head and neck neoplasms; lung neoplasms; neoplasms, squamous cell; ovarian neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; diarrhea; exanthema; head and neck neoplasms; lung neoplasms; neoplasms, squamous cell; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neuropathy, small fiber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neuropathy, small fiber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; lung neoplasms; pleural effusion, malignant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; pleural effusion, malignant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, giant cell; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, giant cell; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
vasculitis, antineutrophil cytoplasmic; antibodies-associated small vessel Gene SetFrom GAD Gene-Disease Associations genes associated with the disease vasculitis, antineutrophil cytoplasmic; antibodies-associated small vessel in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
small for gestational age Gene SetFrom GAD Gene-Disease Associations genes associated with the disease small for gestational age in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
differential expansion rates of small abdominal aortic aneurysms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease differential expansion rates of small abdominal aortic aneurysms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenocarcinoma, mucinous; carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenocarcinoma, mucinous; carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
small Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term small in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Adenoma of small intestine_Intestinal Epithelium_GSE422 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Adenoma of small intestine_Intestinal Epithelium_GSE422 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
B-cell chronic lymphocytic leukaemia-small lymphocytic lymphoma_Peripheral blood mononuclear cell_GSE8835 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during B-cell chronic lymphocytic leukaemia-small lymphocytic lymphoma_Peripheral blood mononuclear cell_GSE8835 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
PLAGL2_deficiency_GDS3010_139_mouse_embryonic small intestine Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PLAGL2_deficiency_GDS3010_139_mouse_embryonic small intestine gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
PDX1_KO_GDS4348_360_mouse_Proximal small intestine Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PDX1_KO_GDS4348_360_mouse_Proximal small intestine gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
PTEN_KD_GDS2958_100_human_HCC827 - NON-SMALL CELL LUNG carcinoma cell line Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PTEN_KD_GDS2958_100_human_HCC827 - NON-SMALL CELL LUNG carcinoma cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
amoxicillin_rattus norvegicus_gpl341_distal small intestine_gds1273 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the amoxicillin_rattus norvegicus_gpl341_distal small intestine_gds1273 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset. |
amoxicillin_rattus norvegicus_gpl341_proximal small intestine_gds1273 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the amoxicillin_rattus norvegicus_gpl341_proximal small intestine_gds1273 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset. |
regulation of small gtpase mediated signal transduction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of small gtpase mediated signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of small gtpase mediated signal transduction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of small gtpase mediated signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset. |
small molecule catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the small molecule catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein conjugation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2015 dataset. |
ribosomal small subunit biogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ribosomal small subunit biogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of small gtpase mediated signal transduction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of small gtpase mediated signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset. |
production of small rna involved in gene silencing by rna Gene SetFrom GO Biological Process Annotations 2015 genes participating in the production of small rna involved in gene silencing by rna biological process from the curated GO Biological Process Annotations 2015 dataset. |
nucleobase-containing small molecule catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nucleobase-containing small molecule catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of production of small rna involved in gene silencing by rna Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of production of small rna involved in gene silencing by rna biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
small gtpase mediated signal transduction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the small gtpase mediated signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset. |
small molecule biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the small molecule biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
nucleobase-containing small molecule interconversion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nucleobase-containing small molecule interconversion biological process from the curated GO Biological Process Annotations 2015 dataset. |
small rna loading onto risc Gene SetFrom GO Biological Process Annotations 2015 genes participating in the small rna loading onto risc biological process from the curated GO Biological Process Annotations 2015 dataset. |
ribosomal small subunit export from nucleus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ribosomal small subunit export from nucleus biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
small nucleolar ribonucleoprotein complex assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the small nucleolar ribonucleoprotein complex assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
nucleobase-containing small molecule metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nucleobase-containing small molecule metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
small molecule metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the small molecule metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
ribosomal small subunit assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ribosomal small subunit assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
mitochondrial small ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the mitochondrial small ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
preribosome, small subunit precursor Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the preribosome, small subunit precursor cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
small nuclear ribonucleoprotein complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the small nuclear ribonucleoprotein complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
small nucleolar ribonucleoprotein complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the small nucleolar ribonucleoprotein complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
organellar small ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the organellar small ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
small ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the small ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
gamma-tubulin small complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the gamma-tubulin small complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
cytosolic small ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the cytosolic small ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
small-subunit processome Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the small-subunit processome cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
small molecule binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small molecule binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small gtpase binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small gtpase binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small conductance calcium-activated potassium channel activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small conductance calcium-activated potassium channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small protein activating enzyme binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small protein activating enzyme binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small gtpase regulator activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small gtpase regulator activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ribosomal small subunit binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ribosomal small subunit binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small protein activating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small protein activating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small ribosomal subunit rrna binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small ribosomal subunit rrna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small intestine Gene SetFrom GTEx Tissue Gene Expression Profiles genes with high or low expression in small intestine relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. |
Response to irinotecan in non-small-cell lung cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to irinotecan in non-small-cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Non-small cell lung cancer (survival) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Non-small cell lung cancer (survival) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Non-small cell lung cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Non-small cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Response to platinum-based chemotherapy in non-small-cell lung cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to platinum-based chemotherapy in non-small-cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Response to irinotecan and platinum-based chemotherapy in non-small-cell lung cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to irinotecan and platinum-based chemotherapy in non-small-cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
non-small cell lung carcinoma Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease non-small cell lung carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
small intestine neoplasm Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease small intestine neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
lung small cell carcinoma Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease lung small cell carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormality of the small intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the small intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
small intestine Gene SetFrom HPA Tissue Gene Expression Profiles genes with high or low expression in small intestine relative to other tissues from the HPA Tissue Gene Expression Profiles dataset. |
small intestine Gene SetFrom HPA Tissue Protein Expression Profiles proteins with high or low expression in small intestine relative to other tissues from the HPA Tissue Protein Expression Profiles dataset. |
small cerebral cortex Gene SetFrom HPO Gene-Disease Associations genes associated with the small cerebral cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small nail Gene SetFrom HPO Gene-Disease Associations genes associated with the small nail phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small pituitary gland Gene SetFrom HPO Gene-Disease Associations genes associated with the small pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small proximal tibial epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the small proximal tibial epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small sella turcica Gene SetFrom HPO Gene-Disease Associations genes associated with the small sella turcica phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypotrophy of the small hand muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the hypotrophy of the small hand muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neoplasm of the small intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the small intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small foramen magnum Gene SetFrom HPO Gene-Disease Associations genes associated with the small foramen magnum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small anterior fontanelle Gene SetFrom HPO Gene-Disease Associations genes associated with the small anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the small epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased number of small peripheral myelinated nerve fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased number of small peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
arteriosclerosis of small cerebral arteries Gene SetFrom HPO Gene-Disease Associations genes associated with the arteriosclerosis of small cerebral arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small, conical teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the small, conical teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small earlobe Gene SetFrom HPO Gene-Disease Associations genes associated with the small earlobe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small forehead Gene SetFrom HPO Gene-Disease Associations genes associated with the small forehead phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple small vertebral fractures Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple small vertebral fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small cervical vertebral bodies Gene SetFrom HPO Gene-Disease Associations genes associated with the small cervical vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small intestine carcinoid Gene SetFrom HPO Gene-Disease Associations genes associated with the small intestine carcinoid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small intestinal polyposis Gene SetFrom HPO Gene-Disease Associations genes associated with the small intestinal polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small hypothenar eminence Gene SetFrom HPO Gene-Disease Associations genes associated with the small hypothenar eminence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of small intestinal villus morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of small intestinal villus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small vessel vasculitis Gene SetFrom HPO Gene-Disease Associations genes associated with the small vessel vasculitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small intestinal stenosis Gene SetFrom HPO Gene-Disease Associations genes associated with the small intestinal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small thenar eminence Gene SetFrom HPO Gene-Disease Associations genes associated with the small thenar eminence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small placenta Gene SetFrom HPO Gene-Disease Associations genes associated with the small placenta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ankylosis of feet small joints Gene SetFrom HPO Gene-Disease Associations genes associated with the ankylosis of feet small joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small hand Gene SetFrom HPO Gene-Disease Associations genes associated with the small hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the small intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the small intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple small medullary renal cysts Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple small medullary renal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
brain very small Gene SetFrom HPO Gene-Disease Associations genes associated with the brain very small phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small face Gene SetFrom HPO Gene-Disease Associations genes associated with the small face phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small for gestational age Gene SetFrom HPO Gene-Disease Associations genes associated with the small for gestational age phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
calcification of the small brain vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the calcification of the small brain vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small abnormally formed scapulae Gene SetFrom HPO Gene-Disease Associations genes associated with the small abnormally formed scapulae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Carcinoma, Small Cell Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Carcinoma, Small Cell phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Carcinoma, Non-Small-Cell Lung Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Carcinoma, Non-Small-Cell Lung phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Small Cell Lung Carcinoma Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Small Cell Lung Carcinoma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Desmoplastic Small Round Cell Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Desmoplastic Small Round Cell Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Large neutral amino acids transporter small subunit 4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Large neutral amino acids transporter small subunit 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small-subunit processome, Utp21 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp21 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
GyrI-like small molecule binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the GyrI-like small molecule binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U2 auxiliary factor small subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U2 auxiliary factor small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small proline-rich protein/late cornified envelope protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small proline-rich protein/late cornified envelope protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, Ras type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, Ras type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U3 small nucleolar ribonucleoprotein complex, subunit Mpp10 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar ribonucleoprotein complex, subunit Mpp10 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, Rho type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, Rho type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U1 small nuclear ribonucleoprotein of 70kDa N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U1 small nuclear ribonucleoprotein of 70kDa N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U6 snRNA-associated Sm-like protein LSm4/Small nuclear ribonucleoprotein Sm D1/D3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U6 snRNA-associated Sm-like protein LSm4/Small nuclear ribonucleoprotein Sm D1/D3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, mitochondrial Rho Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, mitochondrial Rho protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTP-binding protein domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTP-binding protein domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U4/U6 small nuclear ribonucleoprotein Prp31 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U4/U6 small nuclear ribonucleoprotein Prp31 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small nuclear RNA activating complex subunit 2-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small nuclear RNA activating complex subunit 2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small acidic protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small acidic protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U1 small nuclear ribonucleoprotein C Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U1 small nuclear ribonucleoprotein C protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Clathrin adaptor complex, small chain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Clathrin adaptor complex, small chain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small nuclear RNA activating complex (SNAPc), subunit SNAP43 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small nuclear RNA activating complex (SNAPc), subunit SNAP43 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U3 small nucleolar RNA-associated protein 10 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar RNA-associated protein 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal RNA small subunit methyltransferase H Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal RNA small subunit methyltransferase H protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small membrane A-kinase anchor protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small membrane A-kinase anchor protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small nuclear ribonucleoprotein Sm D2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small nuclear ribonucleoprotein Sm D2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, GEM/REM/Rad Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, GEM/REM/Rad protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA polymerase delta/II small subunit family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA polymerase delta/II small subunit family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U3 small nucleolar RNA-associated protein 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar RNA-associated protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small proline-rich protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small proline-rich protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small-subunit processome, Utp13 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp13 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small-subunit processome, Utp12 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp12 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small-subunit processome, Utp11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small-subunit processome, Utp14 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp14 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Carbamoyl-phosphate synthase, small subunit N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Carbamoyl-phosphate synthase, small subunit N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small ribonucleoprotein associated, SmB/SmN Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small ribonucleoprotein associated, SmB/SmN protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribonucleotide reductase small subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribonucleotide reductase small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Methyltransferase small domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Methyltransferase small domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small nuclear ribonucleoprotein E Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small nuclear ribonucleoprotein E protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Iron hydrogenase, small subunit-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron hydrogenase, small subunit-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U3 small nucleolar RNA-associated protein 15, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar RNA-associated protein 15, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Xanthine dehydrogenase, small subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Xanthine dehydrogenase, small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U4/U6 small nuclear ribonucleoprotein Prp4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U4/U6 small nuclear ribonucleoprotein Prp4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U4/U6 small nuclear ribonucleoprotein Prp3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U4/U6 small nuclear ribonucleoprotein Prp3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, CybS Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, CybS protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Aconitase A/isopropylmalate dehydratase small subunit, swivel Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Aconitase A/isopropylmalate dehydratase small subunit, swivel protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small integral membrane protein 15 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small integral membrane protein 15 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Citrate synthase-like, small alpha subdomain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Citrate synthase-like, small alpha subdomain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small leucine-rich proteoglycan, class I, decorin/asporin/byglycan Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small leucine-rich proteoglycan, class I, decorin/asporin/byglycan protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small ubiquitin-related modifier, chordates Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small ubiquitin-related modifier, chordates protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small subunit of serine palmitoyltransferase-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small subunit of serine palmitoyltransferase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small integral membrane protein 19 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small integral membrane protein 19 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small integral membrane protein 10 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small integral membrane protein 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA primase, small subunit, eukaryotic/archaeal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA primase, small subunit, eukaryotic/archaeal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, ARF type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, ARF type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small muscular protein Chisel Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small muscular protein Chisel protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, SAR1-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, SAR1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small acidic protein-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small acidic protein-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, ARF/SAR type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, ARF/SAR type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA primase, small subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA primase, small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Calpain small subunit 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Calpain small subunit 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, Rab type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, Rab type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Carbamoyl-phosphate synthase, small subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Carbamoyl-phosphate synthase, small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Sirtuin family, catalytic core small domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Sirtuin family, catalytic core small domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
non small cell lung cancer Gene SetFrom KEGG Pathways proteins participating in the non small cell lung cancer pathway from the KEGG Pathways dataset. |
small cell lung cancer Gene SetFrom KEGG Pathways proteins participating in the small cell lung cancer pathway from the KEGG Pathways dataset. |
small endolymphatic duct Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small endolymphatic duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small sebaceous gland Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small sebaceous gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pharynx Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pharynx phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small vagina Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small vagina phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small nasal bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small nasal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small alisphenoid bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small alisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small trigeminal motor nucleus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small trigeminal motor nucleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pituitary gland Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pituitary gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small alveolar lamellar bodies Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small alveolar lamellar bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small basioccipital bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small basioccipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small floor plate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small floor plate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small epididymis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small epididymis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased small intestinal microvillus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased small intestinal microvillus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal small intestine crypts of lieberkuhn morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal small intestine crypts of lieberkuhn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small premaxilla Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small premaxilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small superior glossopharyngeal ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small superior glossopharyngeal ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small proamniotic cavity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small proamniotic cavity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small gallbladder Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small gallbladder phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small cochlear ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small cochlear ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small malleus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small malleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small esophagus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small esophagus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small otic capsule Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small otic capsule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small lymph nodes Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small lymph nodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small ischium Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small ischium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small molars Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small molars phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small cecum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small cecum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small seminal vesicle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small seminal vesicle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small sacral vertebrae Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small sacral vertebrae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small penile bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small penile bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small spleen Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small spleen phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased small intestinal villus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased small intestinal villus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small olfactory bulb Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small olfactory bulb phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small inner medullary pyramid Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small inner medullary pyramid phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small male preputial glands Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small male preputial glands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small geniculate ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small geniculate ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small popliteal lymph nodes Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small popliteal lymph nodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small visceral yolk sac Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small visceral yolk sac phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased small intestine adenocarcinoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased small intestine adenocarcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pterygoid bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pterygoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal small intestinal crypt cell proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal small intestinal crypt cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small second pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small second pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small lung saccule Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small lung saccule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small ears Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small ears phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small caput epididymis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small caput epididymis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small caudal vertebrae Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small caudal vertebrae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small submandibular ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small submandibular ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small trachea Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small trachea phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small exoccipital bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small exoccipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small limb buds Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small limb buds phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small myocardial fiber Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small myocardial fiber phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased lung non-small cell carcinoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased lung non-small cell carcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small l5 dorsal root ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small l5 dorsal root ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small clavicle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small clavicle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small uterus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small uterus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small vestibular ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small vestibular ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal small intestine placement Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal small intestine placement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small petrosal ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small petrosal ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small superior cervical ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small superior cervical ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small ectoplacental cone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small ectoplacental cone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small vulva Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small vulva phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pancreatic islets Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pancreatic islets phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small thyroid gland Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small thyroid gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small lymphoid organs Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small lymphoid organs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small interparietal bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small interparietal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small prostate gland ventral lobe Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small prostate gland ventral lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small peyer's patches Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small peyer's patches phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small scrotum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small scrotum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small vertebrae Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small vertebrae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small ureteric bud Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small ureteric bud phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small seminiferous tubules Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small seminiferous tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small maxilla Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small maxilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small testis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small testis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small perianal sebaceous gland Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small perianal sebaceous gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small basisphenoid bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small basisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pancreas Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pancreas phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small lens Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small lens phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small inguinal lymph nodes Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small inguinal lymph nodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small endometrial glands Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small endometrial glands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pubis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pubis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small thymus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small thymus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pituitary intermediate lobe Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pituitary intermediate lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small parietal bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small parietal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small adenohypophysis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small adenohypophysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small kidney Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small kidney phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small xiphoid process Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small xiphoid process phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |