Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6321 to 6330 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6321
Interphotoreceptor matrix proteoglycan 1
GP147, IPM150, RP91, SPACR, VMD4
Distal myopathy, Benign concentric annular macular dystrophy, Cone-rod dystrophy, Macular dystrophy, Retinitis pigmentosa, Vitelliform macular dystrophy

6322
Interphotoreceptor matrix proteoglycan 2
IPM200, RP56, SPACRCAN, VMD5
Distal myopathy, Atrial fibrillation, Retinitis pigmentosa, Cone-rod dystrophy, Crohn disease, Inflammatory bowel disease, Macular dystrophy, Ulcerative colitis, Vitelliform macular dystrophy

6323
Internexin neuronal intermediate filament protein alpha
NEF5, NF-66, NF66, TXBP-1
Amyotrophic lateral sclerosis, Anorexia nervosa, Motor neuron disease, Schizophrenia, Myopia, Uterine fibroid

6324
InaF motif containing 2
LINC00984, OGU1
Diabetes mellitus type 2

6325
Innate immunity activator
C1orf106
Androgenetic alopecia, Ankylosing spondylitis, Bipolar disorder, Celiac disease, Crohn disease, Inflammatory bowel disease, Multiple sclerosis, Psoriasis, Rheumatoid arthritis, Schizophrenia, Sclerosing cholangitis, Ulcerative colitis

6326
Inhibitor of CDK, cyclin A1 interacting protein 1
HSD45
Obesity, Oligodendroglioma

6327
Inner centromere protein
-
Basal cell carcinoma, Breast cancer, Clear cell renal cell carcinoma, Kidney cancer, Melanoma, Nephronophthisis, Ovarian cancer, Prostate cancer

6328
Inverted formin 2
C14orf151, C14orf173, CMTDIE, FSGS5, pp9484
Charcot-marie-tooth disease, Dejerine-sottas disease, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Glomerulonephritis, Hereditary motor and sensory neuropathies, Hereditary steroid-resistant nephrotic syndrome, Hypertension, Hypertrophic neuropathy, Kidney disease, Nephrotic syndrome, Hereditary motor and sensory neuropathy, Peroneal muscle atrophy
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6329
Inhibitor of growth family member 1
p24ING1c, p33, p33ING1, p33ING1b, p47, p47ING1a
Atrial fibrillation, Contact dermatitis, Coronary artery disease, Parkinson disease, Squamous cell carcinoma, Stomach neoplasms

6330
Inhibitor of growth family member 2
ING1L, p33ING2
Alzheimer disease