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
7761 to 7770 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

7761
Meiosis specific with OB-fold
C16orf73, POF23, SPGF22, gs129
Azoospermia, Male infertility single gene azoospermia, Premature ovarian failure, Spermatogenic failure

7762
Meiosis initiator
BHMG1, HMGDC
Alzheimer disease, Mitral valve prolapse, Open angle glaucoma, Diabetes mellitus type 2

7763
Meis homeobox 1
-
Breast neoplasms, Clonal hematopoiesis, Colorectal cancer, Endometriosis, Insomnia, Movement disorder, Periodic limb movement disorder, Willis-ekbom disease, Sleep apnea, Sleep disorder, Diabetes mellitus type 2

7764
Meis homeobox 2
CPCMR, HsT18361, MRG1
15q24 microdeletion, Atrial fibrillation, Breast cancer, Cardiac, facial, and digital anomalies with developmental delay, Cleft palate, Cleft palate cardiac defects impaired intellectual development, Cleft palate congenital heart defect intellectual disability syndrome due to 15q14 microdeletion, Glaucoma, Learning disorders, Neurodevelopmental disorder, Orofacial cleft, Preeclampsia, Scoliosis, Uranostaphyloschisis

7765
Maternal embryonic leucine zipper kinase
HPK38
Alzheimer disease, Hepatocellular carcinoma, Colorectal cancer

7766
Melanotransferrin
CD228, MAP97, MFI2, MTF1, MTf
Melanoma, Diabetes mellitus type 2

7767
Mediator of cell motility 1
C2orf4, CGI-27, MEMO, NS5ATP7
Androgenetic alopecia, Central nervous system cancer, Diabetic ketoacidosis, Glioblastoma, Glioma, Diabetes mellitus type 1

7768
Menin 1
MEAI, SCG2
Diabetes mellitus, Hyperparathyroidism, Gout, Hypertension, Pancreatic neoplasms, Pituitary gigantism, Post-traumatic stress disorder, Vipoma

7769
Mesenchyme homeobox 1
KFS2, MOX1
Non-small-cell lung carcinoma, Allergic contact dermatitis, Desbuquois syndrome, Dupuytren contracture, Klippel-feil syndrome, Mitral valve prolapse

7770
Mesenchyme homeobox 2
GAX, MOX2
Behcet disease, Myocardial ischemia, Scoliosis