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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	January 28, 2025
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **751 - 775** of **5716** in total

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Disease ID	Disease Name ▲	Gene Symbol	Gene ID	Organism	Source
DOID:0060371	Parkinson's disease 8 Aliases: autosomal dominant Parkinson disease 8 autosomal dominant Parkinson's disease 8	LRRK2	120892	Homo sapiens (human)	Alliance of Genome Resources
DOID:14330	Parkinson's disease Aliases: Parkinson disease paralysis agitans	A2M AKT1 ATM ATP13A2 CASP9 CAST CHRNB3 CREB1 CYP1A1 DBH DNAJC13 EIF2AK2 EPO FBXO7 GBA1 GDF5 GIGYF2 GSTO1 GSTO2 HLA-DRA HLA-DRB1 HMGCR HSPA8 HSPA9 HTT KLK6 LRRK2 MAPT NAT2 ND3 NOS1 PARK7 PARP1 PHACTR2 PINK1 PLA2G6 PPARGC1A PTGIS SLC11A2 SLC18A2 SNCA SNCB SOD1 SYNJ1 TARDBP TFAM	10 10891 11315 1142 119391 120892 1385 142 1543 1621 2 2056 207 23317 23400 23435 25793 26058 2629 3064 3122 3123 3156 3312 3313 4137 4537 472 4842 4891 5610 5653 5740 65018 6571 6620 6622 6647 7019 8200 831 8398 842 8867 9446 9749	Homo sapiens (human)	Alliance of Genome Resources
DOID:14330	Parkinson's disease Aliases: Parkinson disease paralysis agitans	daf-2 dop-2 glit-1 ida-1 ptc-1	174274 175410 175807 179347 180747	Caenorhabditis elegans	Alliance of Genome Resources
DOID:14330	Parkinson's disease Aliases: Parkinson disease paralysis agitans	Gsk3b Htr1a Igf1r Lep Nox1 Slc18a2 Snca Th	114243 24473 25085 25549 25608 25718 29219 84027	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:14330	Parkinson's disease Aliases: Parkinson disease paralysis agitans	Adcy5 Adh7 Atg7 Drd2 Kcnn2 Minar2 Ppargc1a	11529 13489 140492 19017 224129 225583 74244	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14330	Parkinson's disease Aliases: Parkinson disease paralysis agitans	PSD1 TIF4631	853071 855552	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:14330	Parkinson's disease Aliases: Parkinson disease paralysis agitans	Pgk	33461	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080855	Parkinsonism	Bad Cnr1 Comt Csf2 Drd2 Drd3 Esr1 Gdnf Gfra1 Grm8 Ntrk1 Ptgs2 Shh Slc11a2 Vip	116630 117064 24267 24318 24890 25248 25453 25454 25715 29238 29499 29527 59109 60590 64639	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080855	Parkinsonism	BDNF GBA1 GDNF HSPA1A LRRK2 PARK7 TNFRSF1B	11315 120892 2629 2668 3303 627 7133	Homo sapiens (human)	Alliance of Genome Resources
DOID:14744	Partington syndrome Aliases: X-linked Russell-Silver syndrome	ARX	170302	Homo sapiens (human)	Alliance of Genome Resources
DOID:9631	Pelger-Huet anomaly	Lbr	98386	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9631	Pelger-Huet anomaly	LBR	3930	Homo sapiens (human)	Alliance of Genome Resources
DOID:3210	Pelizaeus-Merzbacher disease Aliases: HLD1 Leukodystrophy, sudanophilic PMD Pelizaeus Merzbacher brain sclerosis Pelizaeus-Merzbacher brain sclerosis diffuse familial brain sclerosis hypomyelinating leukodystrophy 1 sudanophilic leukodystrophy, Paelizeus-Merzbacher type	PLP1	5354	Homo sapiens (human)	Alliance of Genome Resources
DOID:3210	Pelizaeus-Merzbacher disease Aliases: HLD1 Leukodystrophy, sudanophilic PMD Pelizaeus Merzbacher brain sclerosis Pelizaeus-Merzbacher brain sclerosis diffuse familial brain sclerosis hypomyelinating leukodystrophy 1 sudanophilic leukodystrophy, Paelizeus-Merzbacher type	Plp1	18823	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081440	Peroxisome biogenesis disorder 10B	PEX3	8504	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050857	Perrault syndrome	HSD17B4 LARS2	23395 3295	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060486	Perry syndrome Aliases: parkinsonism with alveolar hypoventilation and mental depression	DCTN1	1639	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060673	Peters anomaly	CYP1B1	1545	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080201	Peters plus syndrome Aliases: Krause-Kivlin syndrome Peters anomaly-short limb dwarfism syndrome Peters-plus syndrome	B3GLCT	145173	Homo sapiens (human)	Glyco-Disease Genes Database Alliance of Genome Resources
DOID:0080201	Peters plus syndrome Aliases: Krause-Kivlin syndrome Peters anomaly-short limb dwarfism syndrome Peters-plus syndrome	B3glct	381694	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14705	Pfeiffer syndrome Aliases: acrocephalosyndactylia type V	Fgfr1 Fgfr2	14182 14183	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14705	Pfeiffer syndrome Aliases: acrocephalosyndactylia type V	FGFR1 FGFR2	2260 2263	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080354	Phelan-McDermid syndrome Aliases: 22q13.3 deletion syndrome monosomy 22q13 syndrome	Shank3 Tcf20	21411 58234	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11870	Pick's disease Aliases: Dementia in Pick's disease LOBAR ATROPHY OF BRAIN PICK DISEASE OF BRAIN Pick disease	MAP2K6 MAPT	4137 5608	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060852	Pierson syndrome Aliases: microcoria-congenital nephrosis syndrome	LAMB2	3913	Homo sapiens (human)	Alliance of Genome Resources

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