Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12011 to 12020 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12011
SIX homeobox 2
-
Amyotrophic lateral sclerosis, Congenital anomalies of the kidney and urinary tract, Color vision deficiency, Congenital anomalies of kidney and urinary tract, Frontonasal dysplasia, Kidney disease, Motor neuron disease, Myocarditis, Wilms tumor

12012
SIX homeobox 3
HPE2
Anophthalmia/microphthalmia-esophageal atresia syndrome, Holoprosencephaly, Liver neoplasms, Lung cancer, Microform holoprosencephaly, Syntelencephaly, Schizencephaly, Schizophrenia, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Squamous cell carcinoma, Diabetes mellitus type 2

12013
SIX homeobox 4
AREC3
Prostate cancer, Diabetes mellitus type 2

12014
SIX homeobox 5
BOR2, DMAHP
Asthma, Bor syndrome, Branchiootorenal syndrome, Endometriosis, Open angle glaucoma

12015
SIX homeobox 6
MCOPCT2, ODRMD, OPTX2, Six9
Anophthalmia/microphthalmia-esophageal atresia syndrome, Colobomatous microphthalmia, Colobomatous optic disc macular atrophy chorioretinopathy syndrome, Congenital cataract, Glaucoma, Microphthalmia, Myopia, Nanophthalmos, Nystagmus, Open angle glaucoma, Retinitis pigmentosa

12016
Spindle and kinetochore associated complex subunit 1
C18orf24
Hepatocellular carcinoma

12017
Spindle and kinetochore associated complex subunit 3
C13orf3, RAMA1
Hepatocellular carcinoma, Oligodendroglioma

12018
Src kinase associated phosphoprotein 1
HEL-S-81p, SCAP1, SKAP55
Fatigue syndrome, Crohn disease, Differentiated thyroid carcinoma, Endometrial cancer, Endometrial neoplasms, Endometriosis, Generalized epilepsy, Inflammatory bowel disease, Irritable bowel syndrome, Keratoconus, Ovarian epithelial cancer, Metabolic syndrome, Osteoarthritis, Ovarian cancer, Ovarian neoplasms
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12019
Src kinase associated phosphoprotein 2
PRAP, RA70, SAPS, SCAP2, SKAP-HOM, SKAP55R
Androgenetic alopecia, Ankylosing spondylitis, Venous insufficiency, Crohn disease, Inflammatory bowel disease, Liver cirrhosis, Multiple sclerosis, Psoriasis, Sclerosing cholangitis, Small cell lung carcinoma, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis

12020
SKI proto-oncogene
SGS, SKV
1p36 deletion syndrome, Aortic aneurysm, Chromosome 1p36 deletion syndrome, Congenital contractural arachnodactyly, Congenital musculoskeletal anomalies, Coronary artery disease, Craniofacial abnormalities, Desbuquois syndrome, Thoracic aortic aneurysm and aortic dissection, Gastroesophageal reflux disease, Gout, Intellectual developmental disorder, Larsen syndrome, Metabolic syndrome, Migraine
View all (10 more)