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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 **13226 - 13250** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:1324	lung cancer	BUD2 GIS1 IDP2 IDP3 MLP1 MLP2 NFT1 PBS2 RNY1	850871 851670 853313 853770 853970 853978 854657 855723 855980	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1574	alcohol use disorder Aliases: Ethanol abuse alcohol abuse	BUD2 CYC8 GAC1 GIP2 GIS1 KEX2 KIC1 PIG1 PKH3 SNF12 SNF2 SYT1	850979 851670 852077 852410 853770 854350 854465 855483 855757 856210 856502 856781	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3748	esophagus squamous cell carcinoma Aliases: SCC of esophagus SCC of oesophagus oesophagus squamous cell carcinoma	BUD2 CYC8 DAP2 ENV9 GIS1 IDP2 IDP3 MCH4 MCH5 SET3 STE13	850871 851670 852410 853770 853900 854030 854394 854420 854483 855723 856423	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5419	schizophrenia Aliases: schizophrenia-1	BUD2 CTS2 PBS2 SMY2 STE20 SYH1	851977 852470 853313 853770 855999 856382	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10591	pre-eclampsia Aliases: gestational hypertension hypertension induced by pregnancy pre-eclamptic toxaemia preeclampsia preeclampsia/eclampsia pregnancy associated hypertension pregnancy toxemia proteinuric hypertension of pregnancy toxaemia of pregnancy	BUD2 CTS2 GCY1 GPX1 GPX2 OGG1 VVS1 YPR1	851974 851977 852543 852546 853770 853842 854287 854942	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5844	myocardial infarction Aliases: Myocardial infarct heart attack	BUD2 CIT1 CIT2 CIT3 CTS2 CYC8 GLR1 LRO1 MDH1 MDH2 MDH3 PEP4 YLR001C ZWF1	850361 850687 851481 851977 852410 853770 853777 853994 855480 855732 855742 855949 856014 856107	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060041	autism spectrum disorder	BUD2 CHD1 NHX1 SEC12 STE20 YAK1	852066 853300 853770 855760 856382 856911	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10283	prostate cancer Aliases: NGP - new growth of prostate hereditary prostate cancer malignant tumor of the prostate prostate cancer, familial prostate neoplasm prostatic cancer prostatic neoplasm tumor of the prostate	BUD2 CDC25 CHD1 CYC8 ENO1 ENO2 GCY1 GIS1 OGG1 OST3 PBS2 PKH3 SCP160 SET3 SNF2 TRE1 TRE2 VPS1 VPS70 YPR1	851019 851670 851974 852077 852410 853169 853313 853365 853590 853770 853870 853900 854252 854287 854430 854465 854942 855927 856579 856911	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080141	mosaic variegated aneuploidy syndrome 1	BUB1B	701	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080641	tongue carcinoma	BUB1B	701	Homo sapiens (human)	Alliance of Genome Resources
DOID:10322	berylliosis Aliases: beryllium poisoning	BTNL2 CCR5 TGFB1	1234 56244 7040	Homo sapiens (human)	Alliance of Genome Resources
DOID:399	tuberculosis	BTNL2 CCL1 CD209 CD274 CYP2B6 CYP2C19 EREG HLA-A HLA-B HLA-DQB1 HLA-DRB1 IFNG IFNGR1 IL22 IRAK3 KIR3DL1 KIR3DS1 KLRK1 NFE2L2 NRG1 PDCD1 SLC11A1 SPP1 TLR1 TLR2 TLR6 TNF TNFRSF1B	10333 11213 1555 1557 2069 22914 29126 30835 3084 3105 3106 3119 3123 3458 3459 3811 3813 4780 50616 5133 56244 6346 6556 6696 7096 7097 7124 7133	Homo sapiens (human)	Alliance of Genome Resources
DOID:14179	X-linked agammaglobulinemia Aliases: BTK deficiency Bruton agammaglobulinemia tyrosine kinase deficiency Bruton disease Bruton's Sex-Linked Agammaglobulinemia Bruton's agammaglobulinaemia Bruton's type agammaglobulinemia Bruton-type agammaglobulinemia	BTK	695	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060875	isolated growth hormone deficiency type III Aliases: Fleisher syndrome IGHD III X-linked IGHD X-linked agammaglobulinemia and isolated growth hormone deficiency X-linked hypogammaglobulinemia and isolated growth hormone deficiency X-linked isolated growth hormone deficiency congenital IGHD type III congenital isolated GH deficiency type III congenital isolated growth hormone deficiency type III growth hormone deficiency with hypogammaglobulinemia	BTK	695	Homo sapiens (human)	Alliance of Genome Resources
DOID:2583	agammaglobulinemia Aliases: IGHM hypogammaglobulinemia mu heavy chain deficiency	BTK LRRC8A	56262 695	Homo sapiens (human)	Alliance of Genome Resources
DOID:1556	arthus reaction Aliases: Arthus phenomenon Arthus type urticaria	BTK FCGR2A	2212 695	Homo sapiens (human)	Alliance of Genome Resources
DOID:3234	central nervous system lymphoma Aliases: Microglioma primary CNS lymphoma	BTK CD79B IL10 MYD88	3586 4615 695 974	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050746	mantle cell lymphoma	BTK CCDC50 CD79B TNFRSF10A	152137 695 8797 974	Homo sapiens (human)	Alliance of Genome Resources
DOID:8584	Burkitt lymphoma Aliases: Burkitt lymphoma/leukaemia Burkitt's Lymphoma Burkitt's tumor Burkitt's tumor or lymphoma malignant lymphoma, Burkitt's type small Non-Cleaved cell Lymphoma, Burkitt's type	BTK CALR CD40 CD79B MYC	4609 695 811 958 974	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080998	acute necrotizing pancreatitis	BTG2 CALCA CCL2 CD46 CD59 CTSB ICAM1 IL17A IL1RN IL6 MIF MMP2 NOS1 NOS2 PDX1 RELA SELP SERPINE1 SERPINF2 SERPING1 TACR1 TBXAS1 TLR2 TLR4 TLR9	1508 3383 3557 3569 3605 3651 4179 4282 4313 4842 4843 5054 5345 54106 5970 6347 6403 6869 6916 7097 7099 710 7832 796 966	Homo sapiens (human)	Alliance of Genome Resources
DOID:856	biotinidase deficiency Aliases: BTD deficiency Juvenile-onset multiple carboxylase deficiency Late-onset multiple carboxylase deficiency deficiency of biotinidase	BTD	686	Homo sapiens (human)	Alliance of Genome Resources
DOID:4621	holoprosencephaly Aliases: Holoprosencephaly sequence	BST1 MCD4	850519 853690	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5744	ovary serous adenocarcinoma Aliases: malignant ovarian serous tumor serous carcinoma of Ovary	BSG TP53	682 7157	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081401	autosomal dominant distal hereditary motor neuronopathy 13	BSCL2	26580	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110770	hereditary spastic paraplegia 17 Aliases: SPG17 Silver spastic paraplegia syndrome Silver syndrome autosomal dominant spastic paraplegia 17 autosomal dominant spastic paraplegia type 17 dHMN5B distal hereditary motor neuropathy type 5B spastic paraplegia with amyotrophy of hands and feet spastic paraplegia-amyotrophy of hands and feet	BSCL2	26580	Homo sapiens (human)	Alliance of Genome Resources

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