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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 **2701 - 2725** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:365	bladder disease Aliases: Urinary Bladder Disease	Chrm3	12671	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081216	autosomal recessive intellectual developmental disorder 54	TNIK	23043	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060692	platelet-type bleeding disorder 8 Aliases: ADP platelet receptor P2Y12 defect P2Y12 defect	P2ry12	64803	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:8466	retinal degeneration Aliases: degeneration of retina	Bdnf C3 Clu Cs Hgf Inhba Kcnh8 Lcn2 Mertk Nos3 Opn4 Pdha1 Pdha2 Pf4 Prom2 Prph2 Ptprc Vdac1 Vdac2	117098 170496 170587 192211 192223 24225 24232 24446 24600 246325 24699 24854 25534 29200 29554 360918 65037 83529 83531	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070162	hereditary sensory and autonomic neuropathy type 1 Aliases: HSAN1 hereditary sensory and autonomic neuropathy type I	SPTLC1 SPTLC2 SPTLC3	10558 55304 9517	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050814	temtamy preaxial brachydactyly syndrome Aliases: PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE	sqv-5	172851	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080207	CAKUT2 Aliases: Congenital anomalies of the kidney and urinary tract 2	Mmp9 Timp1	116510 81687	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:13241	Behcet's disease Aliases: Adamantiades-Behcet disease Behcet syndrome Behet's syndrome triple symptom complex	Abcb1a Abcb1b Ace Adipoq Ccl2 Ccr5 Cd40lg Cfb Cpb2 Ctla4 Cyp1a1 Fas Fcgr4 H2-Ab1 H2-D1 H2-Eb1 H2-K1 H2-M2 H2-Q10 H2-Q1 H2-Q2 H2-Q4 H2-Q6 H2-Q7 H2-T3 Icam1 Ifng Il10 Il17a Il1rn Il21r Il23r Il2 Il4 Itga2 Itgam Mbl2 Mmp2 Mmp9 Nos3 Pon1 Proz Slc11a1 Sod1 Stat3 Tgfb1 Tlr2 Tlr3 Tlr4 Tnf Tnfrsf1a Vegfa Vim Vwf	110557 11421 11450 12477 12774 13076 14102 142980 14961 14962 14964 14969 14972 14990 15006 15007 15013 15015 15018 15043 15894 15978 16153 16171 16181 16183 16189 16398 16409 17195 17390 17395 18127 18173 18669 18671 18979 20296 20655 20848 209590 21803 21898 21926 21937 21947 22339 22352 22371 24088 246256 56373 60504 66901	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080453	developmental and epileptic encephalopathy 25 Aliases: DEE25 developmental and epileptic encephalopathy 25, with amelogenesis imperfecta early infantile epileptic encephalopathy 25	Slc13a5	237831	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111334	congenital leptin deficiency Aliases: LEPD leptin deficiency or dysfunction obesity due to congenital leptin deficiency	Lep	16846	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110820	hereditary spastic paraplegia 75 Aliases: SPG75 autosomal recessive spastic paraplegia 75 autosomal recessive spastic paraplegia type 75	Mag	17136	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4621	holoprosencephaly Aliases: Holoprosencephaly sequence	NOSIP PGAP1 PIGN PLCH1 PTCH1 SHH TGIF1 ZIC4	23007 23556 51070 5727 6469 7050 80055 84107	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070004	myeloid neoplasm	Snmp2 htl	38868 42160	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050563	nonsyndromic deafness Aliases: nonsyndromic hearing loss nonsyndromic hereditary hearing loss	Alg10b Dync2h1 Lrp5 Mto1 Ush2a Wfs1	110350 16973 22283 22393 380959 68291	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:6652	diffuse idiopathic skeletal hyperostosis Aliases: Ankylosing vertebral hyperostosis DISH Disseminated idiopathic skeletal hyperostosis	Slc29a1	63997	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:4033	bacterial gastritis	TREM1	54210	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081075	Marsili syndrome Aliases: congenital analgesia congenital insensitivity to pain	Zfhx2	239102	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:848	arthritis Aliases: Inflammatory disorder of joint	parp-1	266823	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110438	dilated cardiomyopathy 1JJ Aliases: CMD1JJ	Lama4	16775	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9362	status asthmaticus Aliases: Asthma with status asthmaticus Severe asthma attack	Pxn	38326	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:3426	vestibular disease Aliases: Vertigo, vestibular disorder	Sh	32780	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080939	hereditary angioedema type I	Serping1	12258	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050452	mevalonic aciduria Aliases: Mevalonate Kinase Deficiency	MVK TNF	4598 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080563	congenital disorder of glycosylation Ik Aliases: congenital disorder of glycosylation 1k	Alg1	42146	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110751	type 1 diabetes mellitus 12 Aliases: IDDM12 Insulin-Dependent Diabetes Mellitus 12	Ctla4	12477	Mus musculus (house mouse)	Alliance of Genome Resources

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