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
4321 to 4330 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

4321
Exosome component 2
RRP4, Rrp4p, SHRF, hRrp4p, p7
Color vision deficiency, Liver neoplasms, Retinitis pigmentosa, Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome, Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome

4322
Exosome component 3
CGI-102, PCH1B, RRP40, Rrp40p, bA3J10.7, hRrp-40, p10
Congenital myopathy, Congenital neurologic anomalies, Congenital pontocerebellar hypoplasia, Lissencephaly, Pena-shokeir syndrome , Pontocerebellar hypoplasia

4323
Exosome component 4
RRP41, RRP41A, Rrp41p, SKI6, Ski6p, hRrp41p, p12A
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

4324
Exosome component 5
CABAC, RRP41B, RRP46, Rrp46p, hRrp46p, p12B
Atrial fibrillation, Cerebellar ataxia, brain abnormalities, and cardiac conduction defects, Desbuquois syndrome, Neurodevelopmental disorder, Stomach neoplasms

4325
Exosome component 8
CIP3, EAP2, OIP2, PCH1C, RRP43, Rrp43p, bA421P11.3, p9
Congenital pontocerebellar hypoplasia, Pontocerebellar hypoplasia, Spastic ataxia

4326
Exosome component 9
PCH1D, PM/Scl-75, PMSCL1, RRP45, Rrp45p, p5, p6
Cerebral atrophy, Congenital pontocerebellar hypoplasia, Osteoarthritis, Pontocerebellar hypoplasia

4327
Exophilin 5
EBS4, SLAC2-B, SLAC2B
Alzheimer disease, Clear cell renal cell carcinoma, Dementia, Epidermolysis bullosa, Estrogen-receptor negative breast cancer, Orofacial cleft, Prostate cancer, Scoliosis, Uterine fibroid

4328
Exostosin glycosyltransferase 1
EXT, LGCR, LGS, TRPS2, TTV
Atrial fibrillation, Autism, Bone fracture, Breast cancer, Chondrosarcoma, Colorectal cancer, Desbuquois syndrome, Endometrial cancer, Epilepsy, Exostoses, Generalized epilepsy, Gestational diabetes, Insomnia, Major depressive disorder, Metabolic syndrome
View all (6 more)

4329
Exostosin glycosyltransferase 2
SOTV, SSMS
Androgenetic alopecia, 11p11.2 deletion syndrome, Desbuquois syndrome, Exostoses, Potocki-shaffer syndrome, Seizures, scoliosis, and macrocephaly/microcephaly syndrome

4330
Exostosin like glycosyltransferase 2
EXTR2
Multiple sclerosis, Prostate cancer, Schizophrenia