Results for "[axillary odor, variation in]": 108 gene sets

Name

[axillary odor, variation in] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [axillary odor, variation in] phenotype from the curated OMIM Gene-Disease Associations dataset.

odor Gene Set

From GeneRIF Biological Term Annotations

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

abnormal response to novel odor Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal response to novel odor phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal odor adaptation Gene Set

From MPO Gene-Phenotype Associations

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

[cinnamon odor, pleasantness of] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [cinnamon odor, pleasantness of] phenotype from the curated OMIM Gene-Disease Associations dataset.

Body Odor Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Body Odor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Body Odor, Ctcae Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Body Odor, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Fish Odor Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Fish Odor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

abnormal odor adaptation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal odor adaptation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal response to novel odor Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal response to novel odor phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal habituation to a novel odor Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal habituation to a novel odor phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

axillary lipoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

axillary adenitis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

axillary Gene Set

From GeneRIF Biological Term Annotations

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

axillary freckling Gene Set

From HPO Gene-Disease Associations

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

absent axillary hair Gene Set

From HPO Gene-Disease Associations

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

axillary pterygia Gene Set

From HPO Gene-Disease Associations

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

abnormality of the axillary hair Gene Set

From HPO Gene-Disease Associations

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

sparse axillary hair Gene Set

From HPO Gene-Disease Associations

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

axillary apocrine gland hypoplasia Gene Set

From HPO Gene-Disease Associations

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

abnormal axillary lymph node morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent axillary lymph nodes Gene Set

From MPO Gene-Phenotype Associations

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

enlarged axillary lymph nodes Gene Set

From MPO Gene-Phenotype Associations

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

small axillary lymph nodes Gene Set

From MPO Gene-Phenotype Associations

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

axillary bud Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Axillary Web Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Axillary Web Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Axillary Vein Thrombosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Axillary Vein Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Sparse Axillary Hair Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Sparse Axillary Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Absent Axillary Hair Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Absent Axillary Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Axillary Pterygium Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Axillary Pterygium in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Axillary Freckling Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Axillary Freckling in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Axillary Apocrine Gland Hypoplasia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Axillary Apocrine Gland Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

enlarged axillary lymph nodes Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the enlarged axillary lymph nodes phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

absent axillary lymph nodes Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the absent axillary lymph nodes phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

small axillary lymph nodes Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the small axillary lymph nodes phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal axillary lymph node morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal axillary lymph node morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Axillary adenitis Gene Set

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

genes co-occuring with the disease Axillary adenitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Axillary lipoma Gene Set

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

genes co-occuring with the disease Axillary lipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Axillary bud meristem Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Axillary bud meristem in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Axillary bud Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Axillary bud in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Axillary bud primordium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Axillary bud primordium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Axillary freckling Gene Set

From ClinVar Gene-Phenotype Associations 2025

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

Impdh2 enzyme activity, variation in Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Impdh2 enzyme activity, variation in phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Apocrine gland secretion, variation in Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Apocrine gland secretion, variation in phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

QT INTERVAL, VARIATION IN Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease QT INTERVAL, VARIATION IN from the curated CTD Gene-Disease Associations dataset.

quantitative variation in lipid and lipoprotein traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease quantitative variation in lipid and lipoprotein traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

normmal variation Gene Set

From GAD Gene-Disease Associations

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

normal variation in leptin levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease normal variation in leptin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nomal variation Gene Set

From GAD Gene-Disease Associations

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

pharmacogenetic variation Gene Set

From GAD Gene-Disease Associations

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

dyslexia; reading; normal variation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyslexia; reading; normal variation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

variation in platelet integrin alpha 2 beta 1 density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease variation in platelet integrin alpha 2 beta 1 density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

variation in plasma lipoproteins Gene Set

From GAD Gene-Disease Associations

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

quantitative variation in plasma high-density lipoproteins and triacylglycerides Gene Set

From GAD Gene-Disease Associations

genes associated with the disease quantitative variation in plasma high-density lipoproteins and triacylglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

normal variation Gene Set

From GAD Gene-Disease Associations

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

variation Gene Set

From GeneRIF Biological Term Annotations

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

DNA methylation (variation) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the DNA methylation (variation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

patchy variation in bone mineral density Gene Set

From HPO Gene-Disease Associations

genes associated with the patchy variation in bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

[skin/hair/eye pigmentation, variation in, 8] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation, variation in, 8] phenotype from the curated OMIM Gene-Disease Associations dataset.

[colostrum secretion, variation in] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [colostrum secretion, variation in] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] phenotype from the curated OMIM Gene-Disease Associations dataset.

[qt interval, variation in] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [qt interval, variation in] phenotype from the curated OMIM Gene-Disease Associations dataset.

{gene expression, variation in, qtl} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {gene expression, variation in, qtl} phenotype from the curated OMIM Gene-Disease Associations dataset.

[impdh2 enzyme activity, variation in] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [impdh2 enzyme activity, variation in] phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density variation qtl] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density variation qtl] phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, variation in} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, variation in} phenotype from the curated OMIM Gene-Disease Associations dataset.

Impdh2 Enzyme Activity, Variation In Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Impdh2 Enzyme Activity, Variation In in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Patchy Variation In Bone Mineral Density Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Patchy Variation In Bone Mineral Density in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

22q11 2 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 22q11 2 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

1q21 1 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 1q21 1 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

3q29 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 3q29 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

7q11 23 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 7q11 23 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

15q11 2 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 15q11 2 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

15q13 3 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 15q13 3 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

2q11 2 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 2q11 2 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

2q13 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 2q13 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

2q21 1 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 2q21 1 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

2q37 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 2q37 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

17q12 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 17q12 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

1p36 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 1p36 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

8p23 1 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 8p23 1 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

11p11 2 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 11p11 2 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

10q11 21q11 23 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the 10q11 21q11 23 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

4p16 3 copy number variation Gene Set

From WikiPathways Pathways 2024

proteins participating in the 4p16 3 copy number variation pathway from the WikiPathways Pathways 2024 dataset.

NF1 copy number variation syndrome Gene Set

From WikiPathways Pathways 2024

proteins participating in the NF1 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

17p13 3 YWHAE copy number variation Gene Set

From WikiPathways Pathways 2024

proteins participating in the 17p13 3 YWHAE copy number variation pathway from the WikiPathways Pathways 2024 dataset.

5q35 copy number variation Gene Set

From WikiPathways Pathways 2024

proteins participating in the 5q35 copy number variation pathway from the WikiPathways Pathways 2024 dataset.

Smith Magenis and Potocki Lupski syndrome copy number variation Gene Set

From WikiPathways Pathways 2024

proteins participating in the Smith Magenis and Potocki Lupski syndrome copy number variation pathway from the WikiPathways Pathways 2024 dataset.

6q16 copy number variation Gene Set

From WikiPathways Pathways 2024

proteins participating in the 6q16 copy number variation pathway from the WikiPathways Pathways 2024 dataset.

7q11 23 distal copy number variation Gene Set

From WikiPathways Pathways 2024

proteins participating in the 7q11 23 distal copy number variation pathway from the WikiPathways Pathways 2024 dataset.

10q22q23 copy number variation Gene Set

From WikiPathways Pathways 2024

proteins participating in the 10q22q23 copy number variation pathway from the WikiPathways Pathways 2024 dataset.

13q12 or CRYL1 copy number variation Gene Set

From WikiPathways Pathways 2024

proteins participating in the 13q12 or CRYL1 copy number variation pathway from the WikiPathways Pathways 2024 dataset.

13q12 12 copy number variation Gene Set

From WikiPathways Pathways 2024

proteins participating in the 13q12 12 copy number variation pathway from the WikiPathways Pathways 2024 dataset.

15q11q13 copy number variation Gene Set

From WikiPathways Pathways 2024

proteins participating in the 15q11q13 copy number variation pathway from the WikiPathways Pathways 2024 dataset.

15q25 copy number variation Gene Set

From WikiPathways Pathways 2024

proteins participating in the 15q25 copy number variation pathway from the WikiPathways Pathways 2024 dataset.

PAFAH1B1 copy number variation Gene Set

From WikiPathways Pathways 2024

proteins participating in the PAFAH1B1 copy number variation pathway from the WikiPathways Pathways 2024 dataset.

8q11 23 RB1CC1 copy number variation Gene Set

From WikiPathways Pathways 2024

proteins participating in the 8q11 23 RB1CC1 copy number variation pathway from the WikiPathways Pathways 2024 dataset.

Myopathy caused by variation in F Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Myopathy caused by variation in F phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Myopathy caused by variation in POMG Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Myopathy caused by variation in POMG phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Myopathy caused by variation in PO Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Myopathy caused by variation in PO phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

DNA methylation (variation) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the DNA methylation (variation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.