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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:1474	aggressive periodontitis Aliases: juvenile periodontitis	BRINP3 CCL2 CCR2 COL1A1 CTSC IL10 IL1R2 IL2 IL6 POSTN PPIA	10631 1075 1277 339479 3558 3569 3586 5478 6347 729230 7850	Homo sapiens (human)	Alliance of Genome Resources
DOID:3388	periodontal disease Aliases: disease of supporting structures of teeth periodontium disorder	BRINP3 CD40LG CD80 DSPP IL15 IL16 IL17A IL19 IL21 IL24 IL6 IL7	11009 1834 29949 339479 3569 3574 3600 3603 3605 59067 941 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:9562	primary ciliary dyskinesia Aliases: ciliary motility disorder immotile ciliary syndrome	BRWD1 CFAP74 DNAH5 DNAH7 ODAD3 PCSK5 SLIT2 SPEF2 TTLL1	115948 1767 25809 5125 54014 56171 79925 85452 9353	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112045	non-syndromic X-linked intellectual disability 93 Aliases: MRX93 X-linked mental retardation 93 X-linked mental retardation with macrocephaly	BRWD3	254065	Homo sapiens (human)	Alliance of Genome Resources
DOID:14227	azoospermia	BSCL2 CDC34 CDC42BPA CDC42BPB CDC42BPG ISYNA1 NDST1 NDST2 NDST3 NDST4 PTPRD PTPRF PTPRS RBBP4 SCAPER SNRPA1 UBE2R2	26580 3340 49855 51477 54926 55561 5789 5792 5802 5928 64579 6627 8476 8509 9348 9578 997	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050585	congenital generalized lipodystrophy	BSCL2 PCYT1A	26580 5130	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111136	congenital generalized lipodystrophy type 2 Aliases: Berardinelli-Seip congenital lipodystrophy type 2 Berardinelli-Seip syndrome Brunzell syndrome BSCL2-related CGL2 congenital lipoatrophic diabetes total lipodystrophy and acromegaloid gigantism	BSCL2 PPARG	26580 5468	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
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:4621	holoprosencephaly Aliases: Holoprosencephaly sequence	BST1 MCD4	850519 853690	Saccharomyces cerevisiae S288C	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: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: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:0050746	mantle cell lymphoma	BTK CCDC50 CD79B TNFRSF10A	152137 695 8797 974	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:1556	arthus reaction Aliases: Arthus phenomenon Arthus type urticaria	BTK FCGR2A	2212 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: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: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:10322	berylliosis Aliases: beryllium poisoning	BTNL2 CCR5 TGFB1	1234 56244 7040	Homo sapiens (human)	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: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

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