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
8021 to 8030 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8021
Metallophosphoesterase domain containing 2
239FB, C11orf8
Atrial fibrillation, Dental caries, Gout, Metabolic syndrome, Migraine, Obesity, Obstructive sleep apnea syndrome, Peripheral arterial disease, Diabetes mellitus type 2, Uterine fibroid

8022
Myosin phosphatase Rho interacting protein
M-RIP, MRIP, RHOIP3, RIP3, p116Rip
Atrial fibrillation, Diabetic retinopathy, Obesity, Prostate cancer

8023
Mercaptopyruvate sulfurtransferase
MST, TST2, TUM1
Melanoma, Psychiatric disorders

8024
Mitochondrial inner membrane protein MPV17
CMT2EE, MTDPS6, SYM1
Charcot-marie-tooth disease, Cochlear diseases, Mitochondrial dna depletion syndrome, Focal glomerulosclerosis, Gout, Mitochondrial disease, Navajo neurohepatopathy, Proteinuria

8025
MPV17 mitochondrial inner membrane protein like 2
FKSG24
Multiple sclerosis

8026
Myelin protein zero
CHM, CHN2, CMT1, CMT1B, CMT2I, CMT2J, CMT4E, CMTDI3, CMTDID, DSS, HMSNIB, MPP, P0
Charcot-marie-tooth disease, Congenital pes cavus, Dejerine-sottas disease, Distal hereditary motor neuropathy, Hereditary motor and sensory neuropathies, Motor neuron disease, Hereditary sensory and motor neuropathy, Hyperalgesia, Hypertrophic neuropathy, Intellectual developmental disorder, Neuropathy, congenital hypomyelinating, Peripheral neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome, Sensory neuropathy

8027
Myelin protein zero like 1
MPZL1b, PZR, PZR1b, PZRa, PZRb
Alzheimer disease, Carcinoma, Major depressive disorder, Schizophrenia

8028
Myelin protein zero like 2
DFNB111, EVA, EVA1
Isolated sensorineural deafness, Crohn disease, Deafness, Hearing loss, Inflammatory bowel disease, Lung cancer, Squamous cell carcinoma

8029
Myelin protein zero like 3
-
Lung cancer, Non-small cell lung carcinoma

8030
Major histocompatibility complex, class I-related
HLALS
Insomnia