Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7871 to 7880 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7871
Migration and invasion inhibitory protein
IIP45
Eczema

7872
Mast cell immunoglobulin like receptor 1
Allergin-1, C17orf60, MCA-32, MCA32
Asthma, Liver failure, Mitochondrial dna depletion syndrome, Respiratory system disease, Hereditary spastic paraplegia

7873
Membrane integral NOTCH2 associated receptor 1
KIAA1024, UBTOR
Color vision deficiency, Osteoarthritis

7874
Membrane integral NOTCH2 associated receptor 2
DFNB120, KIAA1024L
Isolated sensorineural deafness, Deafness, Hearing loss, Open angle glaucoma, Nonsyndromic hearing loss

7875
MINDY lysine 48 deubiquitinase 1
FAM63A, MINDY-1
Attention deficit hyperactivity disorder, Diabetes mellitus, Schizophrenia, Diabetes mellitus type 2

7876
MINDY lysine 48 deubiquitinase 2
FAM63B
Bipolar disorder, Major depressive disorder, Schizophrenia

7877
MINDY lysine 48 deubiquitinase 3
C10orf97, CARP, DERP5, FAM188A, MST126, MSTP126, my042
Metabolic syndrome, Orofacial cleft, Diabetes mellitus type 2

7878
MINDY lysine 48 deubiquitinase 4
AQP-1, AQP1, C7orf67, CHIP28, FAM188B
Gout, Huntington disease, Lung cancer, Nephrolithiasis, Urolithiasis

7879
Misshapen like kinase 1
B55, MAP4K6, MEKKK 6, MINK, YSK2, ZC3
Attention deficit hyperactivity disorder, Brain aneurysm, Multiple sclerosis, Myasthenic syndrome, Substance abuse

7880
Multiple inositol-polyphosphate phosphatase 1
HIPER1, MINPP2, MIPP, PCH16
Congenital pontocerebellar hypoplasia, Dermatologic disorder, Thyroid cancer, Migraine, Pontocerebellar hypoplasia, Skin disease, Follicular thyroid cancer, Nonmedullary thyroid cancer