Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7901 to 7910 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7901
Mohawk homeobox
C10orf48, IFRX, IRXL1
Alzheimer disease, Asthma, Carpal tunnel syndrome, Heart disease

7902
Melan-A
MART-1, MART1
Contact dermatitis, Melanoma, Mesothelioma, Multiple sclerosis, Peritoneal neoplasms

7903
Modulator of VRAC current 1
LVM, MLC, VL
Biliary tract cancer, Bipolar disorder, Breast cancer, Cancer, Adenoid cystic carcinoma, Central nervous system demyelinating disease, Cerebellar ataxia, Cervical cancer, Schizophrenia, Colorectal cancer, Congenital neurologic anomalies, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer
View all (11 more)

7904
Myeloid leukemia factor 1
-
Dilated cardiomyopathy, Heart failure, Stomach neoplasms

7905
Myeloid leukemia factor 2
NTN4
Insomnia, Willis-ekbom disease, Schizophrenia

7906
MutL homolog 1
COCA2, FCC2, HNPCC, HNPCC2, LYNCH2, MLH-1, MMRCS1, hMLH1
Colonic neoplasms, Colorectal cancer, Lynch syndrome, Colorectal neoplasms, Constitutional mismatch repair deficiency syndrome, Hereditary breast cancer, Lymphoma, Pancreatic neoplasms, Constitutional mismatch repair deficiency, Muir-torre syndrome, Ovarian cancer, Ovarian neoplasms, Prostate cancer, Prostatic neoplasms, Rhabdomyosarcoma
View all (1 more)

7907
MutL homolog 3
HNPCC7
Colorectal cancer, Lynch syndrome, Colorectal neoplasms, Endometrial cancer, Endometrial neoplasms, Esophageal neoplasms, Intestinal polyposis, Premature ovarian failure

7908
Muscular LMNA interacting protein
C6orf142, CIP, MMCKR
Amblyopia, Attention deficit hyperactivity disorder, Diabetic ketoacidosis, Heart failure, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Diabetes mellitus type 1, Diabetes mellitus type 2

7909
Mixed lineage kinase domain like pseudokinase
hMLKL
Multifocal osteomyelitis, Maturity-onset diabetes of the young (mody), Scoliosis

7910
MLLT1 super elongation complex subunit
ENL, LTG19, YEATS1
Cerebral atrophy, Global developmental delay, Wilms tumor