GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Source

Display
results per page.

Clear

Submissions

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 **10076 - 10100** of **15957** in total

« First

‹ Prev

…

400

401

402

403

404

405

406

407

408

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼	Source
DOID:288	endometriosis of uterus Aliases: Endometriosis interna Endometriosis of myometrium Endometriosis, myometrium adenomyosis uterine Adenomyosis	DNMT1	1786	Homo sapiens (human)	Alliance of Genome Resources
DOID:3317	hepatic angiomyolipoma	TSC2	7249	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070062	Arboleda-Tham syndrome Aliases: ARTHS MRD32 autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome autosomal dominant mental retardation 32 autosomal dominant non-syndromic intellectual disability 32	KAT6A	7994	Homo sapiens (human)	Alliance of Genome Resources
DOID:3069	malignant astrocytoma Aliases: Astrocytic tumor astrocytoma of Cerebrum astrocytoma of brain astroglioma cerebral astrocytoma	ADGRB1 AKT1 AKT2 AKT3 ANXA1 ATRX BRD7 BST2 CADM2 CAMK2G FUBP1 HRAS IL16 KRAS MAP2K3 MRE11 NF1 PCMT1 SLC7A5	10000 207 208 253559 29117 301 3265 3603 3845 4361 4763 5110 546 5606 575 684 8140 818 8880	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060532	latex allergy	HLA-DQB1 HLA-DRB1	3119 3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050429	Hailey-Hailey disease Aliases: BENIGN CHRONIC PEMPHIGUS Pemphigus, Benign Familial	ATP2B4	493	Homo sapiens (human)	Alliance of Genome Resources
DOID:5614	eye disease	COL2A1 EYA3 EYA4 F2 MYRF RP1L1 TLR2 TLR3 TLR4 TNF	1280 2070 2140 2147 7097 7098 7099 7124 745 94137	Homo sapiens (human)	Alliance of Genome Resources
DOID:12140	Chagas disease Aliases: Chagas' disease chagas' disease with digestive system involvement chagas' disease with nervous system involvement chagas' disease with other organ involvement	CCL2 CCL5 CHRM2 F2 HLA-DRB1 HSPA4 IFNG PRG2 SOAT1 VIM	1129 2147 3123 3308 3458 5553 6347 6352 6646 7431	Homo sapiens (human)	Alliance of Genome Resources
DOID:4428	dyslexia	DNAAF4 DRD4 FOXP2	161582 1815 93986	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110557	autosomal dominant nonsyndromic deafness 28 Aliases: DFNA28 autosomal dominant deafness 28	GRHL2	79977	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050816	urofacial syndrome Aliases: Ochoa syndrome hydronephrosis with peculiar facial expression	HPSE2 LRIG2	60495 9860	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110919	hereditary spherocytosis type 4 Aliases: HS4 SPH4 hereditary spherocytosis 4	SLC4A1	6521	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050563	nonsyndromic deafness Aliases: nonsyndromic hearing loss nonsyndromic hereditary hearing loss	ALG10 ALG10B DYNC2H1 KLC2 LRP5 MTO1 PPIP5K2 USH2A WFS1	144245 23262 25821 4041 64837 7399 7466 79659 84920	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111729	familial episodic pain syndrome 1 Aliases: FEPS1	TRPA1	8989	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070281	primary autosomal recessive microcephaly 19 Aliases: MCPH19	COPB2	9276	Homo sapiens (human)	Alliance of Genome Resources
DOID:10286	prostate carcinoma Aliases: cancer of prostate carcinoma of prostate	AKT2 ANGPT1 ATF4 AZGP1 BAD BAX BMP2 BMP4 CASP6 CDK13 CGA CHI3L1 CRKL EIF3H HDAC2 HDAC3 IGF1R INHA JUN MET MKI67 NME1 PDGFD PLK1 PRKCA SARS1 SKP2 SPINT1 SPP1 STAT3 STAT6 TMBIM6	1081 1116 1399 208 284 3066 3480 3623 3725 4233 4288 468 4830 5347 5578 563 572 581 6301 650 6502 652 6692 6696 6774 6778 7009 80310 839 8621 8667 8841	Homo sapiens (human)	Alliance of Genome Resources
DOID:3827	congenital diaphragmatic hernia Aliases: Diaphragmatic Hernia	ACE AGTR2 ALDH1A2 ATP7A BMP4 CBL ELN EP300 FREM1 GATA4 HTR2A IGF2 IGFBP3 IGFBP5 LCN2 LRP1 MYRF NDST1 NOS3 NR2F2 PDGFRA PLS3 SFTPA1 SFTPA2 SFTPB SLC6A4 SLIT2 SLIT3 SOD1 SOD2 SOX7 TNF VEGFA	158326 1636 186 2006 2033 2626 3340 3356 3481 3486 3488 3934 4035 4846 5156 5358 538 6439 652 6532 653509 6586 6647 6648 7026 7124 729238 7422 745 83595 867 8854 9353	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111994	immunodeficiency 45 Aliases: IMD45	IFNAR2	3455	Homo sapiens (human)	Alliance of Genome Resources
DOID:11695	portal vein thrombosis	F2 IGF1R SERPINE1	2147 3480 5054	Homo sapiens (human)	Alliance of Genome Resources
DOID:8986	narcolepsy Aliases: Narcolepsy, without cataplexy paroxysmal sleep	CD40LG CHKB HCRTR2 HLA-DPB1 HLA-DQA1 HLA-DQB1 HLA-DRB1 MOG	1120 3062 3115 3117 3119 3123 4340 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111744	cerebellar ataxia type 41 Aliases: SCA41	TRPC3	7222	Homo sapiens (human)	Alliance of Genome Resources
DOID:2280	hidradenitis suppurativa Aliases: Acne inversa, familial	CD163 LCN2 NCSTN TNF	23385 3934 7124 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050835	generalized dystonia Aliases: familial dystonia fragments of torsion dystonia	CACNA1A	773	Homo sapiens (human)	Alliance of Genome Resources
DOID:4306	radiculopathy Aliases: pinched nerve	ERBB4 SPP1 TNF	2066 6696 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081153	common variable immunodeficiency 11	IL21	59067	Homo sapiens (human)	Alliance of Genome Resources

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements