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
12971 to 12980 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12971
Sperm-tail PG-rich repeat containing 4
C2orf61, GSE
Alzheimer disease, Color vision deficiency, Dementia

12972
Signaling receptor and transporter of retinol STRA6
MCOPCB8, MCOPS9, PP14296, SLC69A1
Anophthalmia, Anophthalmia/microphthalmia-esophageal atresia syndrome, Cardiovascular abnormalities, Central nervous system cancer, Colobomatous microphthalmia, Congenital heart disease, Craniofacial abnormalities, Glioblastoma, Glioma, Congenital heart defect, Intellectual developmental disorder, Lung disease, Microphthalmia, Microphthalmos

12973
Stimulated by retinoic acid 8
-
Male infertility single gene azoospermia

12974
STE20 related adaptor alpha
LYK5, NY-BR-96, PMSE, STRAD, STRAD alpha, Stlk
Alzheimer disease, Atrial fibrillation, Epilepsy, Rolandic epilepsy, Intellectual developmental disorder, Medulloblastoma

12975
STE20 related adaptor beta
ALS2CR2, CALS-21, ILPIP, ILPIPA, PAPK, PRO1038
Eczema

12976
Serine/threonine kinase receptor associated protein
MAWD, PT-WD, UNRIP
Colorectal neoplasms

12977
Spermatid perinuclear RNA binding protein
HEL162, ILF3L, SPNR, p74
Astrocytoma, Central nervous system cancer, Dementia, Glioblastoma, Glioma, Insomnia, Metabolic syndrome, Oligodendroglioma, Diabetes mellitus type 2

12978
Stereocilin
DFNB16
Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Deafness, sensorineural, and male infertility, Deafness-infertility syndrome, Hearing impairment, Hearing loss, Hereditary hearing loss, Spermatogenic failure, Diabetes mellitus type 2

12979
Striatin interacting protein 1
FAM40A, FAR11A
Ocular hypotension, Open angle glaucoma

12980
Striatin interacting protein 2
FAM40B, FAR11B
Tourette syndrome