DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 16676 - 16700 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0009806 Constipation CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0032326 Pneumothorax CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0010417 Cryptorchidism CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0017601 Glaucoma CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0000768 Congenital Abnormality CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C1306503 Congenital exomphalos CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0033578 Prostatic Neoplasms CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0026848 Myopathy CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0520947 Clumsiness - motor delay CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0036439 Scoliosis, unspecified CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C1301937 Talipes CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0027092 Myopia CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0221356 Brachycephaly CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0266544 Microcornea CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0376358 Malignant neoplasm of prostate CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0018817 Atrial Septal Defects CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C1384666 hearing impairment CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0022410 Joint Instability CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C3489393 Hiatal Hernia CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C1531647 Cerebral ventriculomegaly CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0027726 Nephrotic Syndrome CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0035305 Retinal Detachment CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0038379 Strabismus CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C0265213 Distal arthrogryposis syndrome CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0
C4551497 Ehlers-Danlos syndrome kyphoscoliotic type CHST14 113189 carbohydrate sulfotransferase 14 Q8NCH0

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Last updated: August 19, 2024