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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 **15876 - 15900** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:11400	pyelonephritis	ACE AMBP B2M BMP7 CALCA CFB CXCR1 IL1RN IL3 PGF TLR1	1636 259 3557 3562 3577 5228 567 629 655 7096 796	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080322	polycystic kidney disease	Agt C9 Ctsh Dll4 Gpbar1 Myc Nos3 Pparg Ptgs2 Tnc Xylt2	116640 117512 24179 24577 24600 25425 25664 29527 311332 338443 64134	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111535	progressive osseous heteroplasia Aliases: POH ectopic ossification familial type familial ectopic ossification osteoma cutis	BMP4 CTNNB1 GNAS SPARC SPP1	1499 2778 652 6678 6696	Homo sapiens (human)	Alliance of Genome Resources
DOID:11569	neurocirculatory asthenia Aliases: Cardiovascular malfunction arising from mental factors Cardiovascular neurosis Da Costa's syndrome Krishaber's disease	dat-1	176304	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111649	ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome Aliases: EEM syndrome EEMS ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome	Cdh3	12560	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110864	congenital stationary night blindness 1F Aliases: CSNB1F congenital stationary night blindness 1F autosomal recessive	LRIT3	345193	Homo sapiens (human)	Alliance of Genome Resources
DOID:10579	leukodystrophy	Sdha	157074	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3981	pantothenate kinase-associated neurodegeneration Aliases: Hallervorden-Spatz disease Hallervorden-Spatz syndrome NBIA1 Pigmentary pallidal degeneration brain Iron Accumulation type I syndrome neurodegeneration with brain iron accumulation 1	Snca Sncb Sncg	104069 20617 20618	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome Aliases: ATR, nondeletion type ATR-X syndrome alpha-thalassemia/mental retardation syndrome nondeletion type	Atrx	22589	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111434	optic atrophy 10 Aliases: OPA10 optic atrophy 10 with or without ataxia, mental retardation, and seizures	RTN4IP1	84816	Homo sapiens (human)	Alliance of Genome Resources
DOID:11263	chlamydia Aliases: Chlamydia trachomatis infectious disease Chlamydial Infection chlamydial disease	Foxp3 Tgfb1	20371 21803	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050651	atrioventricular septal defect Aliases: AVCD AVSD ECD atrioventricular canal defect endocardial cushion defect	Creld1	312638	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0112245	focal segmental glomerulosclerosis 3 Aliases: FSGS3	Cd2ap	12488	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2475	chronic conjunctivitis	lmp-1	180912	Caenorhabditis elegans	Alliance of Genome Resources
DOID:5408	Paget's disease of bone Aliases: Paget disease of bone Paget's bone disease osseous Paget's disease osteitis deformans	Tnfrsf11b	25341	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050534	congenital stationary night blindness Aliases: congenital essential nyctalopia	cacna1fb	559964	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0110550	autosomal dominant nonsyndromic deafness 20 Aliases: DFNA20 DFNA26 autosomal dominant deafness 20	ACTA1 ACTA2 ACTB ACTBL2 ACTC1 ACTG1	345651 58 59 60 70 71	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110676	congenital myasthenic syndrome 13 Aliases: CMS13 CMSTA2 congenital myasthenic syndrome 13 with tubular aggregates congenital myasthenic syndrome with tubular aggregates 2	dpagt1	566539	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:12858	Huntington's disease Aliases: HD Huntington disease Huntington's chorea	ache mtnr1aa nog1 nog3 parp1 slc18a3a slc18a3b	114549 30173 30174 30667 394082 559347 560788	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:12297	Vogt-Koyanagi-Harada disease Aliases: Harada's disease Vogt-Koyanagi syndrome uveomeningoencephalitic syndrome	mys	44885	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0090109	autosomal dominant hypocalcemia Aliases: HYPOC	CASR	846	Homo sapiens (human)	Alliance of Genome Resources
DOID:5162	arteriolosclerosis	C3	24232	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:13533	osteopetrosis Aliases: Albers-Schonberg disease marble bone	Clcn3 Ghr Slc4a2	24780 25235 84360	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2513	basal cell carcinoma Aliases: Basal cell cancer Basal cell carcinoma of skin Basal cell neoplasm Basal cell tumor Epithelioma basal cell Rodent ulcer malignant Basal cell neoplasm malignant basal cell tumor	BAP1 CRNKL1 CTCF CTLA4 OCA2 OGG1 PTCH1 PTCH2 RASA1 SHH SMO TP53 XRCC5 XRCC6	10664 1493 2547 4948 4968 51340 5727 5921 6469 6608 7157 7520 8314 8643	Homo sapiens (human)	Alliance of Genome Resources
DOID:12506	Bell's palsy Aliases: Bell palsy Bell's (facial) palsy	PPIA	5478	Homo sapiens (human)	Alliance of Genome Resources

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