GlyCosmos Portal

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **5601 - 5625** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:687	hepatoblastoma	Axn dally smo	33196 39013 43565	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:9282	ocular hypertension	Sod3 Tpi smo	33196 36232 43582	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:2512	nevoid basal cell carcinoma syndrome Aliases: Gorlin syndrome NBCCS basal cell nevus syndrome	ptc smo	33196 35851	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:7474	malignant pleural mesothelioma Aliases: malignant mesothelioma of pleura	nAChRalpha6 smo	33196 34304	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0060071	pre-malignant neoplasm	Acer Ance InR smo	33196 34189 34805 42549	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:4989	pancreatitis	CtsL1 Spn28Dc TkR99D Tl smo	33196 34091 36546 43222 43551	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:5082	liver cirrhosis Aliases: Cirrhosis cirrhosis of liver	Acer Ance Atg6 Axn Egfr InR Mdr49 Mdr65 Parp1 Pxn Sb SerT Snmp2 Spn28Dc Tl btl dally htl mys smo	33196 3355109 34091 34189 34805 36428 37455 37895 38326 38726 38868 39013 39564 41958 42160 42549 42850 43222 43565 44885	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050338	primary bacterial infectious disease	Duox smo	33196 33477	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0090084	hypogonadotropic hypogonadism 5 with or without anosmia	kis	33185	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111207	autosomal dominant distal hereditary motor neuronopathy 3 Aliases: HMN IIB HMN2B distal hereditary motor neuronopathy type 2B distal hereditary motor neuropathy type IIB	HSPB1	3315	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110163	Charcot-Marie-Tooth disease axonal type 2F Aliases: CMT2F Charcot-Marie-Tooth neuronal type 2F Charcot-Marie-Tooth neuropathy type 2F autosomal dominant Charcot-Marie-Tooth disease type 2F	HSPB1	3315	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112022	non-syndromic X-linked intellectual disability 21 Aliases: MRX21 MRX34 X-linked mental retardation 21 X-linked mental retardation 21/34 X-linked mental retardation 34	Il1rapl1	331461	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112056	X-linked intellectual disability-short stature-overweight syndrome Aliases: MRX12 MRX35 X-linked mental retardation 12 X-linked mental retardation 35	Thoc2	331401	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060335	autosomal dominant sideroblastic anemia 4	HSPA9	3313	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060706	X-linked lymphoproliferative syndrome 2 Aliases: XIAP deficiency XLP2	XIAP	331	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110225	Brugada syndrome 8 Aliases: BRGDA8	Hcn4	330953	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080697	Opitz GBBB syndrome Aliases: Opitz G/BBB Syndrome Opitz GBBB syndrome type I	Trim67	330863	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080572	congenital disorder of glycosylation Iw Aliases: congenital disorder of glycosylation 1w	Stt3A Stt3B	33082 43005	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0070113	Niemann-Pick disease type C1 Aliases: NPC1	Npc1b	33072	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:14504	Niemann-Pick disease Aliases: Sphingomyelinase Deficiency Disease lipoid histiocytosis sphingomyelin lipidosis	Npc1b Npc2a	33072 33374	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111636	autosomal recessive nonsyndromic deafness 113 Aliases: DFNB113 autosomal recessive deafness 113	Ceacam16	330483	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110573	autosomal dominant nonsyndromic deafness 4A Aliases: DFNA4A autosomal dominant deafness 4A	Ceacam16	330483	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110574	autosomal dominant nonsyndromic deafness 4B Aliases: DFNA4B autosomal dominant deafness 4B	Ceacam16	330483	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080205	CAKUT Aliases: Congenital anomalies of the kidney and urinary tract Renal or urinary tract malformation	BMP4 HSPA1B LIFR NRIP1	3304 3977 652 8204	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080784	urinary tract infection Aliases: UTI	CXCR1 HSPA1B IL1A LCN2 TLR2 TLR4	3304 3552 3577 3934 7097 7099	Homo sapiens (human)	Alliance of Genome Resources

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