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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **12701 - 12725** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:0080390	nephrotic syndrome type 1 Aliases: Finnish congenital nephrosis	CCL11 NPHS1	4868 6356	Homo sapiens (human)	Alliance of Genome Resources
DOID:12804	mucopolysaccharidosis IV Aliases: Mucopolysaccharidosis, MPS-IV deficiency of N-acetylgalactosamine-6-sulphatase deficiency of chondroitinsulphatase galactosamine-6-sulfatase deficiency	CCL11 GALNS GLB1	2588 2720 6356	Homo sapiens (human)	Glyco-Disease Genes Database Glyco-Disease Genes Database Alliance of Genome Resources
DOID:1063	interstitial nephritis Aliases: renal tubulo-interstitial disease	CCL11 CCL7	6354 6356	Homo sapiens (human)	Alliance of Genome Resources
DOID:11204	allergic conjunctivitis	CCL11 CCL5 CCL7 ICAM1 IFNG IL10 IL13 IL1RN IL4R MUC1 MUC2 MUC4 PLA2G2A TLR4 TLR9 TNC	3371 3383 3458 3557 3566 3586 3596 4582 4583 4585 5320 54106 6352 6354 6356 7099	Homo sapiens (human)	Alliance of Genome Resources
DOID:594	panic disorder Aliases: panic anxiety syndrome	CCKBR HTR1A MANEA MAOA MBL2	3350 4128 4153 79694 887	Homo sapiens (human)	Alliance of Genome Resources
DOID:4988	alcoholic pancreatitis	CCK CFTR UGT1A7	1080 54577 885	Homo sapiens (human)	Alliance of Genome Resources
DOID:2913	acute pancreatitis	CCK CD163 CX3CL1 F3 F7 IL10 KIT LEP MTNR1B REG3G SERPINA1 TREM1	130120 2152 2155 3586 3815 3952 4544 5265 54210 6376 885 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050986	spinocerebellar ataxia type 40	CCDC88C	440193	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110569	autosomal dominant nonsyndromic deafness 44 Aliases: DFNA44 autosomal dominant deafness 44	CCDC50	152137	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110598	primary ciliary dyskinesia 14 Aliases: CILD14 primary ciliary dyskinesia 14 with or without situs inversus	CCDC39	339829	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050144	Kartagener syndrome Aliases: Kartagener's syndrome	CCDC39 DNAAF3 DNAH11 DNAH5 DRC1 MBL2 ODAD2 ODAD3 SLIT2	115948 1767 339829 352909 4153 55130 8701 92749 9353	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060572	Ritscher-Schinzel syndrome 2	CCDC22	28952	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070267	congenital disorder of glycosylation type IIo Aliases: CCDC115-CDG CDG IIo CDG syndrome type IIo CDG2O CDGIIdo Carbohydrate deficient glycoprotein syndrome type IIo Congenital disorder of glycosylation type 2o	CCDC115	84317	Homo sapiens (human)	Alliance of Genome Resources
DOID:12716	newborn respiratory distress syndrome Aliases: HMD - Hyaline membrane disease Neonatal respiratory Distress syndrome hyaline membrane disease pulmonary hyaline membrane disease pulmonary hypoperfusion syndrome of newborn respiratory distress syndrome of newborn	CCAP-R Sod3 sfl	2768688 36232 38736	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:535	sleep disorder Aliases: Non-organic sleep disorder	CCAP-R InR Pdfr	2768688 31234 42549	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:7148	rheumatoid arthritis Aliases: Arthritis or polyarthritis, rheumatic atrophic Arthritis	CCAP-R Hsp110 Idgf1 Idgf2 Idgf3 Idgf4 Idgf5 Idgf6 Mvl Octbeta1R Octbeta2R Orct2 Orct Sema2a Sema2b nAChRalpha6	246538 2768688 31926 34304 34978 34979 34981 36846 36868 37104 39557 41549 42490 42652 42890 42891	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050589	inflammatory bowel disease	CCAP-R Egfr GlyT Mvl Sb Tace Tsf2 cora	2768688 37205 37455 37772 39435 41958 42490 43558	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:2560	morphine dependence	CCAP-R Dop2R Fas2 GluRIA	2768688 31364 33007 38742	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111004	Joubert syndrome 9 Aliases: JBTS9	CC2D2A	57545	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070120	Meckel syndrome 6 Aliases: MKS6 Meckel-Gruber syndrome, type 6	CC2D2A	57545	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050778	Meckel syndrome Aliases: Meckel-Gruber syndrome	CC2D2A KIF14 RPGRIP1L TBC1D32 TMEM231 TMEM67 TXNDC15	221322 23322 57545 79583 79770 91147 9928	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081179	autosomal recessive intellectual developmental disorder 3	CC2D1A	54862	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060340	ciliopathy	CC2D1A CC2D2A DNAI4 INVS PKD2 PRKG1 RPGRIP1L SPRY2 TEKT1 TMEM67 TTC8	10253 123016 23322 27130 5311 54862 5592 57545 79819 83659 91147	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111776	46,XY sex reversal 5 Aliases: 46,XY gonadal dysgenesis, complete, CBX2-related 46,XY sex reversal, CBX2-related SRXY5 disorder of sex development, 46,XY, CBX2-related sex reversal, XY, CBX2-related	CBX2	84733	Homo sapiens (human)	Alliance of Genome Resources
DOID:14447	gonadal dysgenesis Aliases: Gonadal dysgenesis syndrome	CBX2 DLC1 STARD13	10395 84733 90627	Homo sapiens (human)	Alliance of Genome Resources

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