GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Source

Display
results per page.

Clear

Submissions

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 **6701 - 6725** of **15957** in total

« First

‹ Prev

…

265

266

267

268

269

270

271

272

273

…

Next ›

Last »
Disease ID	Disease Name ▼	Gene Symbol	Gene ID	Organism	Source
DOID:0110919	hereditary spherocytosis type 4 Aliases: HS4 SPH4 hereditary spherocytosis 4	abts-4	180943	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110919	hereditary spherocytosis type 4 Aliases: HS4 SPH4 hereditary spherocytosis 4	Slc4a1	20533	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110918	hereditary spherocytosis type 3 Aliases: HS3 SPH3 hereditary spherocytosis 3	SPTA1	6708	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110918	hereditary spherocytosis type 3 Aliases: HS3 SPH3 hereditary spherocytosis 3	Spta1	20739	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110917	hereditary spherocytosis type 2 Aliases: HS2 SPH2 hereditary spherocytosis 2	SPTB	6710	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110916	hereditary spherocytosis type 1 Aliases: HS1 SPH1 hereditary spherocytosis 1	Spta1	20739	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110916	hereditary spherocytosis type 1 Aliases: HS1 SPH1 hereditary spherocytosis 1	ADD2 ANK1 EPB42 SPTA1	119 2038 286 6708	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	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	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	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	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	Bscl2 Dnm1 Erlin2 Hspd1 Sec23ip	140694 290823 309010 361722 63868	Rattus norvegicus (Norway rat)	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	NTE1 SEY1 VPS1	853870 854336 854943	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110825	hereditary spastic paraplegia 9B Aliases: SPG9B autosomal recessive complex spastic paraplegia type 9B autosomal recessive spastic paraplegia 9B	ALDH18A1	5832	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110825	hereditary spastic paraplegia 9B Aliases: SPG9B autosomal recessive complex spastic paraplegia type 9B autosomal recessive spastic paraplegia 9B	Aldh18a1	56454	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110824	hereditary spastic paraplegia 9A Aliases: AD-SPG9A Cataracts motor neuropathy-short stature-skeletal anomalies syndrome SPG9A autosomal dominant complex spastic paraplegia type 9A autosomal dominant spastic paraplegia 9A cataracts with motor neuronopathy, short stature and skeletal abnormalities spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome	ALDH18A1	5832	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110824	hereditary spastic paraplegia 9A Aliases: AD-SPG9A Cataracts motor neuropathy-short stature-skeletal anomalies syndrome SPG9A autosomal dominant complex spastic paraplegia type 9A autosomal dominant spastic paraplegia 9A cataracts with motor neuronopathy, short stature and skeletal abnormalities spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome	Aldh18a1	56454	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070460	hereditary spastic paraplegia 90B Aliases: SPG90B autosomal recessive spastic paraplegia 90B	SPTSSA	171546	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070459	hereditary spastic paraplegia 90A Aliases: SPG90A autosomal dominant spastic paraplegia 90A	SPTSSA	171546	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070458	hereditary spastic paraplegia 89 Aliases: SPG89 autosomal recessive spastic paraplegia 89	hrdl-1	172833	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070456	hereditary spastic paraplegia 87 Aliases: SPG87 autosomal recessive spastic paraplegia 87	CSC1	850942	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070456	hereditary spastic paraplegia 87 Aliases: SPG87 autosomal recessive spastic paraplegia 87	TMEM63C	57156	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112347	hereditary spastic paraplegia 84 Aliases: SPG84 spastic paraplegia 84 autosomal recessive	Pi4ka	224020	Mus musculus (house mouse)	Alliance of Genome Resources

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements