Gene2Function

Disease Annotation

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Disease_Term	Source	Rank	Other Values
Myopia 6, 608908 (3)	OMIM	high	Genome region : 22q13.33 OMIM_ID : 604272 OMIM gene ID OMIM_ID : 608908 OMIM phenotype ID
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1, 604377 (3)	OMIM	high	Genome region : 22q13.33 OMIM_ID : 604272 OMIM gene ID OMIM_ID : 604377 OMIM phenotype ID
Multiple sclerosis	GWAS	high	Pubmed_ID : 17660530 Pubmed_ID : 18941528 Pubmed_ID : 18997785 Pubmed_ID : 19010793 Pubmed_ID : 19525953 Pubmed_ID : 19525955 Pubmed_ID : 20159113 Pubmed_ID : 20453840 Pubmed_ID : 20598377 Pubmed_ID : 21244703 Pubmed_ID : 21654844 Pubmed_ID : 21833088 Pubmed_ID : 22190364 Pubmed_ID : 22457343 Pubmed_ID : 22570697 Pubmed_ID : 23412934 Pubmed_ID : 27386562
Red blood cell traits	GWAS	high	Pubmed_ID : 20927387 Pubmed_ID : 23222517 Pubmed_ID : 23446634 Pubmed_ID : 23696099 Pubmed_ID : 23935956
Mean corpuscular hemoglobin	GWAS	high	Pubmed_ID : 19862010 Pubmed_ID : 20139978 Pubmed_ID : 23263863