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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM00398KIF5AbrainMESH:D005234Fatty Liver
HM00398KIF5AbrainMESH:D015658HIV Infections
HM00398KIF5AbrainMESH:D001008Anxiety Disorders
HM00398KIF5AbrainMESH:D007248Infertility, Male
HM00398KIF5AbrainMESH:D001932Brain Neoplasmsbrain
HM00398KIF5AbrainMESH:D005832Genital Diseases, Maletestis
HM00398KIF5AbrainMESH:D005832Genital Diseases, Maleprostate
HM00398KIF5AbrainMESH:D005832Genital Diseases, Maleblood vessel
HM00398KIF5AbrainMESH:D004362Drug Toxicity
HM00398KIF5AbrainMESH:D003456Cryptorchidism
HM00398KIF5AbrainMESH:D011472Prostatitisprostate
HM00398KIF5AbrainMESH:D007984Leydig Cell Tumor
HM00398KIF5AbrainMESH:D009437Neuralgia
HM00398KIF5AbrainMESH:D030342Genetic Diseases, Inborn
HM00398KIF5AbrainMESH:D009374Neoplasms, Experimental
HM00398KIF5AbrainMESH:D009202Cardiomyopathies
HM00398KIF5AbrainMESH:D005909Glioblastomabone
HM00398KIF5AbrainMESH:D005909Glioblastomabrain
HM00398KIF5AbrainMESH:D005909Glioblastomabone
HM00398KIF5AbrainMESH:D010523Peripheral Nervous System Diseasesnerve
HM00398KIF5AbrainMESH:D008545Melanomaeye
HM00398KIF5AbrainMESH:D008545Melanomacervix
HM00398KIF5AbrainMESH:D008545Melanomabone
HM00398KIF5AbrainMESH:C537482Spastic paraplegia 10, autosomal dominant
HM00398KIF5AbrainMESH:D011469Prostatic Diseasesureter
HM00398KIF5AbrainMESH:D011469Prostatic Diseasesprostate
HM00398KIF5AbrainMESH:D011297Prenatal Exposure Delayed Effects
HM00398KIF5AbrainMESH:D008223Lymphoma