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
8221 to 8230 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8221
Mucin 3A, cell surface associated
MUC-3A, MUC3
Non-small cell lung carcinoma

8222
Mucin 4, cell surface associated
ASGP, HSA276359, MUC-4
Aortic stenosis, Aortic valve disease, Renal cell carcinoma, Central nervous system cancer, Cystic fibrosis, Glioblastoma, Glioma, Lung disease, Prostatic neoplasms

8223
Mucin 5AC, oligomeric mucus/gel-forming
MUC5, TBM, leB, mucin
Asthma, Central nervous system cancer, Cholecystolithiasis, Dry eye syndrome, Gallstones, Gastric ulcer, Glioblastoma, Glioma, Idiopathic pulmonary fibrosis, Interstitial lung disease, Keratoconus, Pulmonary fibrosis, Respiratory system disease

8224
Mucin 5B, oligomeric mucus/gel-forming
MG1, MUC-5B, MUC5, MUC9
Anorectal malformation, Antithrombin deficiency, Bronchiolitis, Diffuse panbronchiolitis, Extrinsic allergic alveolitis, Idiopathic pulmonary fibrosis, Interstitial lung disease, Major depressive disorder, Pulmonary fibrosis, Respiratory system disease

8225
Mucin 6, oligomeric mucus/gel-forming (gene/pseudogene)
MUC-6
Alzheimer disease, Hypertrophic cardiomyopathy, Peptic ulcer disease, Stomach neoplasms

8226
Mucin 7, secreted
MG2
Asthma, Diabetic neuropathy, Esophageal squamous cell carcinoma, Sarcoidosis, Scoliosis, Uterine fibroid

8227
Mucin like 1
SBEM
Blood coagulation disorder, Dementia

8228
Mucin like 3
C6orf37, DPCR1, PBLT
Attention deficit hyperactivity disorder, Autism, Bell's palsy, Bipolar disorder, Interstitial cystitis, Diffuse panbronchiolitis, Major depressive disorder, Membranous glomerulonephritis, Psoriasis, Rheumatoid arthritis, Schizophrenia

8229
MUS81 structure-specific endonuclease subunit
SLX3
Cutis laxa

8230
Muscle associated receptor tyrosine kinase
CMS9, FADS, FADS1
Ptosis, Color vision deficiency, Congenital myasthenic syndrome, Dementia, Fetal akinesia deformation sequence, Gross motor development delay, Lung cancer, Myasthenia gravis, Myasthenic syndrome, Non-small cell lung carcinoma, Pena-shokeir syndrome , Postsynaptic congenital myasthenic syndrome, Diabetes mellitus type 2