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
Showing genes starting with "M"
231 to 240 of 893 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

231
Minichromosome maintenance complex component 2
BM28, CCNL1, CDCL1, D3S3194, DFNA70, MITOTIN, cdc19
Alzheimer disease, Isolated sensorineural deafness, Nonsyndromic hearing loss, Hepatocellular carcinoma, Colonic neoplasms, Deafness

232
Minichromosome maintenance complex component 3
HCC5, P1-MCM3, P1.h, RLFB
Obstructive pulmonary disease, Color vision deficiency, Ear, patella, short stature syndrome, Peripheral arterial disease

233
Minichromosome maintenance complex component 3 associated protein
GANP, MAP80, PNRIID, SAC3
Autism, Charcot-marie-tooth disease, Congenital fibrosis of extraocular muscles, Major depressive disorder, Periodontitis, Peripheral neuropathy, Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development, Psychotic disorders, Testicular carcinoma, Testicular germ cell tumor, Depression

234
Minichromosome maintenance complex component 4
CDC21, CDC54, IMD54, NKCD, NKGCD, P1-CDC21, hCdc21
Immunodeficiency, Natural killer cell deficiency

235
Minichromosome maintenance complex component 5
CDC46, MGORS8, P1-CDC46
Androgenetic alopecia, Desbuquois syndrome, Meier-gorlin syndrome

236
Minichromosome maintenance complex component 6
MCG40308, Mis5, P105MCM
Gout, Obesity, Neurodevelopmental disorder

237
Minichromosome maintenance complex component 7
CDC47, MCM2, P1.1-MCM3, P1CDC47, P85MCM, PNAS146, PPP1R104
Anisometropia, Astigmatism, Primary microcephaly, Ear, patella, short stature syndrome, Hyperopia, Microphthalmos, Trichiasis

238
Minichromosome maintenance 8 homologous recombination repair factor
C20orf154, POF10, dJ967N21.5
Azoospermia, Breast cancer, Colorectal cancer, Estrogen-receptor negative breast cancer, Preeclampsia, Premature ovarian failure, Uterine fibroid

239
Minichromosome maintenance 9 homologous recombination repair factor
C6orf61, MCMDC1, ODG4, dJ329L24.1, dJ329L24.3
46,xx ovotesticular disorder of sex development, Attention deficit hyperactivity disorder, Cardiomyopathy, Major depressive disorder, Male infertility, Ovarian dysgenesis, Premature ovarian failure, Testicular azoospermia

240
Minichromosome maintenance complex binding protein
C10orf119, MCM-BP
Major depressive disorder