GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **15226 - 15250** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▼	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q5T7M9	Divergent protein kinase domain 1A	DIPK1A FAM69A	Homo sapiens (human)	3	1
Q9Y2E4	Disco-interacting protein 2 homolog C	DIP2C KIAA0934	Homo sapiens (human)	0	1
Q9P265	Disco-interacting protein 2 homolog B	DIP2B KIAA1463	Homo sapiens (human)	4	1
Q14689	Disco-interacting protein 2 homolog A	DIP2A C21orf106 DIP2 KIAA0184	Homo sapiens (human)	2	1
Q9UNQ2	Probable dimethyladenosine transferase	DIMT1 DIMT1L	Homo sapiens (human)	3	1
Q9BTC0	Death-inducer obliterator 1	DIDO1 C20orf158 DATF1 KIAA0333	Homo sapiens (human)	32	2
Q9UPY3	Endoribonuclease Dicer	DICER1 DICER HERNA KIAA0928	Homo sapiens (human)	1	2
Q9NSV4	Protein diaphanous homolog 3	DIAPH3 DIAP3	Homo sapiens (human)	2	2
O60610	Protein diaphanous homolog 1	DIAPH1 DIAP1	Homo sapiens (human)	6	2
Q9NR28	Diablo IAP-binding mitochondrial protein	DIABLO SMAC	Homo sapiens (human)	0	1
Q08211	ATP-dependent RNA helicase A	DHX9 DDX9 LKP NDH2	Homo sapiens (human)	5	2
Q14562	ATP-dependent RNA helicase DHX8	DHX8 DDX8	Homo sapiens (human)	1	1
Q6P158	Putative ATP-dependent RNA helicase DHX57	DHX57	Homo sapiens (human)	2	1
Q92620	Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16	DHX38 DDX38 KIAA0224 PRP16	Homo sapiens (human)	2	1
Q8IY37	Probable ATP-dependent RNA helicase DHX37	DHX37 DDX37 KIAA1517	Homo sapiens (human)	1	1
Q9H2U1	ATP-dependent DNA/RNA helicase DHX36	DHX36 DDX36 KIAA1488 MLEL1 RHAU	Homo sapiens (human)	1	2
Q9H5Z1	Probable ATP-dependent RNA helicase DHX35	DHX35 C20orf15 DDX35	Homo sapiens (human)	1	2
Q7L2E3	ATP-dependent RNA helicase DHX30	DHX30 DDX30 KIAA0890	Homo sapiens (human)	2	1
Q7Z478	ATP-dependent RNA helicase DHX29	DHX29 DDX29	Homo sapiens (human)	0	1
O60231	Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16	DHX16 DBP2 DDX16 KIAA0577 PRP2	Homo sapiens (human)	0	1
O43143	ATP-dependent RNA helicase DHX15	DHX15 DBP1 DDX15	Homo sapiens (human)	4	1
Q9Y394	Dehydrogenase/reductase SDR family member 7	DHRS7 DHRS7A RETSDR4 SDR34C1	Homo sapiens (human)	0	1
Q6PKH6	Dehydrogenase/reductase SDR family member 4-like 2	DHRS4L2 SDR25C3	Homo sapiens (human)	1	0
Q13268	Dehydrogenase/reductase SDR family member 2, mitochondrial	DHRS2 SDR25C1	Homo sapiens (human)	0	1
Q9UBM7	7-dehydrocholesterol reductase	DHCR7 D7SR	Homo sapiens (human)	0	1	3-methylglutaconic aciduria Behcet's disease Dandy-Walker syndrome Hailey-Hailey disease Laron syndrome Marfan syndrome Meckel syndrome Potter's syndrome Rapp-Hodgkin syndrome Rothmund-Thomson syndrome Smith-Lemli-Opitz syndrome X-linked ichthyosis achondroplasia ankyloblepharon-ectodermal defects-cleft lip/palate syndrome arteriosclerotic cardiovascular disease atherosclerosis atrioventricular septal defect autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal dominant polycystic kidney disease autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bilateral optic nerve hypoplasia bilateral renal aplasia cardiovascular system disease choanal atresia coloboma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc coronary artery disease cutis laxa dermatitis diabetes mellitus diabetic ketoacidosis fissured tongue glaucoma glycoproteinosis heart disease hepatitis C hepatocellular carcinoma hydrocephalus hypohidrotic ectodermal dysplasia hypospadias immune system disease intellectual disability interstitial nephritis large intestine cancer learning disability leukocyte adhesion deficiency 2 leukocyte adhesion deficiency lingual-facial-buccal dyskinesia liver cancer liver cirrhosis mal de Meleda microcephaly movement disease multiple sclerosis nutmeg liver obsolete type 1 diabetes mellitus 9 oligohydramnios osteomalacia periventricular nodular heterotopia photosensitive epilepsy photosensitivity disease placental insufficiency polycystic ovary syndrome polydactyly polyhydramnios pyelitis pyelonephritis restrictive dermopathy rheumatoid arthritis rickets scoliosis sensorineural hearing loss situs inversus syndromic X-linked intellectual disability type 10 tongue disease tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ventricular septal defect

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