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
7681 to 7690 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7681
Minichromosome maintenance 10 replication initiation factor
CNA43, DNA43, IMD80, PRO2249
Hepatocellular carcinoma, Immunodeficiency

7682
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

7683
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

7684
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

7685
Minichromosome maintenance complex component 4
CDC21, CDC54, IMD54, NKCD, NKGCD, P1-CDC21, hCdc21
Immunodeficiency, Natural killer cell deficiency

7686
Minichromosome maintenance complex component 5
CDC46, MGORS8, P1-CDC46
Androgenetic alopecia, Desbuquois syndrome, Meier-gorlin syndrome

7687
Minichromosome maintenance complex component 6
MCG40308, Mis5, P105MCM
Gout, Obesity, Neurodevelopmental disorder

7688
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

7689
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

7690
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