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
11951 to 11960 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

11951
Sirtuin 7
SIR2L7
Fatty liver, Fatty liver, alcoholic, Scleroderma, Systemic sclerosis

11952
Signaling threshold regulating transmembrane adaptor 1
SIT, SIT-R
Alzheimer disease

11953
SIX homeobox 1
BOS3, DFNA23, TIP39
Isolated sensorineural deafness, Nonsyndromic hearing loss, Bor syndrome, Branchiootic syndrome, Branchiootorenal syndrome, Congenital abnormalities, Craniofacial abnormalities, Deafness, Endometrial neoplasms, Hearing impairment, Hereditary hearing loss, Prostate cancer, Hearing loss, Wilms tumor

11954
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, Wilms tumor

11955
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

11956
SIX homeobox 4
AREC3
Prostate cancer, Diabetes mellitus type 2

11957
SIX homeobox 5
BOR2, DMAHP
Asthma, Bor syndrome, Branchiootorenal syndrome, Endometriosis, Open angle glaucoma

11958
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

11959
Spindle and kinetochore associated complex subunit 1
C18orf24
Hepatocellular carcinoma

11960
Spindle and kinetochore associated complex subunit 3
C13orf3, RAMA1
Hepatocellular carcinoma, Oligodendroglioma