Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4341 to 4350 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4341
Exosome component 4
RRP41, RRP41A, Rrp41p, SKI6, Ski6p, hRrp41p, p12A
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

4342
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

4343
Exosome component 8
CIP3, EAP2, OIP2, PCH1C, RRP43, Rrp43p, bA421P11.3, p9
Congenital pontocerebellar hypoplasia, Pontocerebellar hypoplasia, Spastic ataxia

4344
Exosome component 9
PCH1D, PM/Scl-75, PMSCL1, RRP45, Rrp45p, p5, p6
Cerebral atrophy, Congenital pontocerebellar hypoplasia, Osteoarthritis, Pontocerebellar hypoplasia

4345
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

4346
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, Leprosy, Major depressive disorder
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4347
Exostosin glycosyltransferase 2
SOTV, SSMS
Androgenetic alopecia, 11p11.2 deletion syndrome, Desbuquois syndrome, Exostoses, Potocki-shaffer syndrome, Seizures, scoliosis, and macrocephaly/microcephaly syndrome

4348
Exostosin like glycosyltransferase 1
EXTL
Liver cirrhosis

4349
Exostosin like glycosyltransferase 2
EXTR2
Multiple sclerosis, Prostate cancer, Schizophrenia

4350
Exostosin like glycosyltransferase 3
BOTV, EXTL1L, EXTR1, ISDNA, REGR, RPR
Atrial fibrillation, Desbuquois syndrome, Skeletal dysplasia