Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
8301 to 8310 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8301
Myosin XIX
MYOHD1
Anorexia nervosa, Attention deficit hyperactivity disorder, Bipolar disorder, Kidney disease, Global developmental delay, Glycosylphosphatidylinositol biosynthesis defect, Obesity, Schizophrenia, Tourette syndrome, Diabetes mellitus type 2, Uranostaphyloschisis

8302
Myosin IA
BBMI, DFNA48, DIAR15, MIHC, MYHL
Asthma, Nonsyndromic hearing loss, Congenital chloride diarrhea, Deafness, Hereditary hearing loss, Insomnia, Migraine, Hearing loss

8303
Myosin IB
MMI-alpha, MMIa, MYH-1c, myr1
Esophageal squamous cell carcinoma, Hepatomegaly, Obesity, Oligodendroglioma, Open angle glaucoma, Pancreatic cancer, Scoliosis, Hypertension

8304
Myosin IC
MMI-beta, MMIb, MyoIC, NMI, myr2
Alzheimer disease, Atrial fibrillation, Isolated sensorineural deafness, Nonsyndromic hearing loss, Heart failure, Meniere disease, Miller-dieker syndrome

8305
Myosin ID
PPP1R108, myr4
Anorexia nervosa, Autism, Dupuytren contracture, Eating disorder, Hypertension, Metabolic syndrome, Pancreatic cancer

8306
Myosin IE
FSGS6, HuncM-IC, MYO1C
Alzheimer disease, Anorexia nervosa, Attention deficit hyperactivity disorder, Dementia, Dupuytren contracture, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Major depressive disorder, Metabolic syndrome, Nephrotic syndrome, Nephrotic syndrome, focal segmental type, Schizophrenia
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8307
Myosin IF
-
Metabolic syndrome, Nonsyndromic hearing loss, Diabetes mellitus type 2

8308
Myosin IG
HA2, HLA-HA2, MHAG
Bipolar disorder, Major depressive disorder, Schizoaffective disorder, Squamous cell carcinoma

8309
Myosin IH
CCHS2
Bipolar disorder, Haddad syndrome, Central hypoventilation syndrome, Color vision deficiency, Congenital central hypoventilation syndrome, Insomnia, Major depressive disorder, Migraine, Mood disorder, Neurotic disorder, Schizophrenia

8310
Myosin IIIA
DFNA90, DFNB30
Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss, Obesity, Diabetes mellitus type 2