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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 **4001 - 4025** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▼
DOID:2508	Takayasu's arteritis Aliases: Aortic arch arteritis Idiopathic aortitis Takayasu arteritis Takayasu's disease aortic arch syndrome	Ager H2-D1 H2-Eb1 H2-K1 H2-M2 H2-Q10 H2-Q1 H2-Q2 H2-Q4 H2-Q6 H2-Q7 H2-T3 Il2 Mmp9	110557 11596 14964 14969 14972 14990 15006 15007 15013 15015 15018 15043 16183 17395	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2508	Takayasu's arteritis Aliases: Aortic arch arteritis Idiopathic aortitis Takayasu arteritis Takayasu's disease aortic arch syndrome	W01F3.2 zmp-3 zmp-4	178748 179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2491	sensory peripheral neuropathy Aliases: peripheral Sensory Neuropathy sensory neuropathy	BACE1	23621	Homo sapiens (human)	Alliance of Genome Resources
DOID:2491	sensory peripheral neuropathy Aliases: peripheral Sensory Neuropathy sensory neuropathy	Bace1	29392	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2491	sensory peripheral neuropathy Aliases: peripheral Sensory Neuropathy sensory neuropathy	Bace1	23821	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2490	congenital nervous system abnormality Aliases: congenital neurologic anomaly	TUBA1A	7846	Homo sapiens (human)	Alliance of Genome Resources
DOID:2490	congenital nervous system abnormality Aliases: congenital neurologic anomaly	Eml1 Tuba1a	22142 68519	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2477	motor peripheral neuropathy Aliases: HSMN HSMN - Hereditary sensory and motor neuropathy Hereditary motor and sensory neuropathy Peripheral Motor Neuropathy neuropathic muscular atrophy	EGR2 SLC12A6	1959 9990	Homo sapiens (human)	Alliance of Genome Resources
DOID:2477	motor peripheral neuropathy Aliases: HSMN HSMN - Hereditary sensory and motor neuropathy Hereditary motor and sensory neuropathy Peripheral Motor Neuropathy neuropathic muscular atrophy	Slc12a6	107723	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	NTE1 SEY1 VPS1	853870 854336 854943	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	Afg3l2 Aldh18a1 Atl3 Atp13a2 Atp13a3 Atp13a5 Bscl2 Dnm1 Dnm2 Dnm3 Erlin1 Erlin2 Hspd1 Kif5b Nipal1 Nipal4 Pnpla6 Rtn1 Rtn3 Rtn4	103967 104001 109168 13429 13430 14705 15510 16573 20168 214112 224088 226144 244373 268878 50767 56454 68585 69597 70701 74772	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	erl-1 hrdl-1	172833 178178	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	ALDH18A1 AP5Z1 ATL2 ATL3 ATP13A2 ATP13A3 ATP13A5 BSCL2 CAPN1 CAPN3 DNM1 DNM2 ERLIN1 ERLIN2 HSPD1 KIF5B L2HGDH NIPAL1 NIPAL4 PNPLA6 PNPLA7 PSMC4 RTN1 RTN2 RTN3 RTN4 SEC23IP SPAST	10313 10613 10908 11160 11196 152519 1759 1785 23400 25923 26580 3329 344905 348938 375775 3799 5704 57142 5832 6252 6253 64225 6683 79572 79944 823 825 9907	Homo sapiens (human)	Alliance of Genome Resources
DOID:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	L2HGDH	35156	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	erlin1 erlin2	549473 549646	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	erlin1 erlin2	100151163 541490	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	Bscl2 Dnm1 Erlin2 Hspd1 Sec23ip	140694 290823 309010 361722 63868	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2475	chronic conjunctivitis	Fas Lamp2	246097 24944	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2475	chronic conjunctivitis	lmp-1	180912	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2475	chronic conjunctivitis	FAS LAMP2	355 3920	Homo sapiens (human)	Alliance of Genome Resources
DOID:2475	chronic conjunctivitis	Fas Lamp2	14102 16784	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2468	psychotic disorder Aliases: mental or behavioural disorder	Gdi1	14567	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2468	psychotic disorder Aliases: mental or behavioural disorder	vn	38657	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:2468	psychotic disorder Aliases: mental or behavioural disorder	MT2A NRG1	3084 4502	Homo sapiens (human)	Alliance of Genome Resources
DOID:2452	thrombophilia Aliases: hypercoagulability state	CD46 F2 FGA HLA-DQA1 PLG PROC SERPINA10 THBD	2147 2243 3117 4179 51156 5340 5624 7056	Homo sapiens (human)	Alliance of Genome Resources

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