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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **1651 - 1675** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism
DOID:13912	acquired color blindness Aliases: acquired color vision deficiencies acquired color vision deficiency acquired colour blindness acquired colour vision deficiencies acquired colour vision deficiency	ACO2 CA4 CACNA2D4 ELOVL4 G6PD HS6ST1 MBD4 NYX PCYT1A SDHC STS	2539 412 50 5130 60506 6391 6785 762 8930 93589 9394	Homo sapiens (human)
DOID:13911	achromatopsia Aliases: ACHM Monochromatism	ACO2 CA4 CACNA2D4 ELOVL4 G6PD HS6ST1 MBD4 NYX PCYT1A SDHC STS	2539 412 50 5130 60506 6391 6785 762 8930 93589 9394	Homo sapiens (human)
DOID:11661	blue color blindness Aliases: Tritan defect Tritanopia	ACO2 CA4 CACNA2D4 ELOVL4 G6PD HS6ST1 MBD4 NYX PCYT1A SDHC STS	2539 412 50 5130 60506 6391 6785 762 8930 93589 9394	Homo sapiens (human)
DOID:13399	color blindness Aliases: BLINDNESS COLOR Colour blindness Colour vision deficiency	ACO2 CA4 CACNA2D4 ELOVL4 G6PD HS6ST1 MBD4 NYX PCYT1A SDHC STS	2539 412 50 5130 60506 6391 6785 762 8930 93589 9394	Homo sapiens (human)
DOID:12705	Friedreich ataxia Aliases: Friedreich's ataxia Friedreich's tabes	ACO2 CAT COG5 DLD GAA GPAA1 GPX1 HPGDS HSD17B4 ICAM1 LPL PIP5K1B PRKAA2 PRNP PTGS2 VCAM1	10466 1738 2548 27306 2876 3295 3383 4023 50 5563 5621 5743 7412 8395 847 8733	Homo sapiens (human)
DOID:0111218	Friedreich ataxia 1 Aliases: FA1 FRDA1	ACO2 CAT GAA GPAA1 GPX1 HPGDS ICAM1 LPL PIP5K1B PRKAA2 VCAM1	2548 27306 2876 3383 4023 50 5563 7412 8395 847 8733	Homo sapiens (human)
DOID:0070329	mitochondrial DNA depletion syndrome Aliases: mtDNA depletion syndrome	ACO2 CD44 CS DGKB DGKE PARP1 PIK3CA PIK3CB PIK3CD PIK3CG SLC25A10 SUCLA2 SUCLG1	142 1431 1468 1607 50 5290 5291 5293 5294 8526 8802 8803 960	Homo sapiens (human)
DOID:0111441	optic atrophy 1 Aliases: OPA1	ACO2 CYP1B1 DGKG PKLR PRKAA2 SDHA SLC5A1 TMED9 TREH	11181 1545 1608 50 5313 54732 5563 6389 6523	Homo sapiens (human)
DOID:0111261	fumarase deficiency Aliases: FMRD fumaric aciduria	ACO2 FH	2271 50	Homo sapiens (human)
DOID:0111340	dominant optic atrophy plus syndrome Aliases: DOA+ optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy	ACO2	50	Homo sapiens (human)
DOID:0111442	optic atrophy 9 Aliases: OPA9	ACO2	50	Homo sapiens (human)
DOID:0050883	infantile cerebellar-retinal degeneration	ACO2	50	Homo sapiens (human)
DOID:0060868	leukoencephalopathy with vanishing white matter Aliases: CACH CACH/VWM childhood ataxia with central nervous system hypomyelination vanishing white matter leukodystrophy	ACOT12 APRT CHST11 GBA1 HAS2 MICA SCP2 SOAT1	100507436 134526 2629 3037 353 50515 6342 6646	Homo sapiens (human)
DOID:1019	osteomyelitis	ACOT7 ACYP2 CHI3L1 DHCR24 EBP IL18R1 LCT LPIN2 MBD4 NANS PGM3 PTGS2 SMUG1 SPTLC2	10682 1116 11332 1718 23583 3938 5238 54187 5743 8809 8930 9517 9663 98	Homo sapiens (human)
DOID:1247	blood coagulation disease Aliases: coagulation protein disease postpartum coagulation defect postpartum coagulation defect with delivery	ACOT7 AKR1D1 ALDOB AMACR ARSA BAAT CAT CD14 CLEC1B COG4 COG6 CYP7B1 DDOST ENO1 ENPP2 G6PC1 GALT GOLPH3 HPSE HSD3B7 LGALS3 LMAN1 MCFD2 MPI NAAA PC PIGA PIK3CA PLA2G4A PLB1 PTGS1 RFT1 SDC1 SELP TMTC3	10855 11332 151056 160418 1650 2023 229 23600 2538 25839 2592 27163 3958 3998 410 4351 5091 51266 5168 5277 5290 5321 570 5742 57511 6382 6403 64083 6718 80270 847 90411 91869 929 9420	Homo sapiens (human)
DOID:2214	obsolete inherited blood coagulation disease	ACOT7 AKR1D1 ALDOB AMACR ARSA BAAT CAT CD14 CLEC1B COG4 CYP7B1 DDOST ENO1 ENPP2 GOLPH3 HPSE HSD3B7 LGALS3 LMAN1 MCFD2 MPI NAAA PC PIK3CA PLA2G4A PLB1 PTGS1 RFT1 SDC1 SELP	10855 11332 151056 1650 2023 229 23600 25839 27163 3958 3998 410 4351 5091 51266 5168 5290 5321 570 5742 6382 6403 64083 6718 80270 847 90411 91869 929 9420	Homo sapiens (human)
DOID:2320	obstructive lung disease Aliases: respiratory airway obstruction	ACOT7 ALPI ALPP CAT GLA LTC4S MBL2 SFTPA1 SFTPA2 SFTPC SFTPD SLC2A10	11332 248 250 2717 4056 4153 6440 6441 653509 729238 81031 847	Homo sapiens (human)
DOID:12241	beta thalassemia	ACOT7 ANXA5 CAT CD177 CD38 CD55 CHIT1 CHPT1 CPT1A CPT2 CRYL1 CYP2E1 CYP3A4 FUT1 FUT4 G6PD H6PD HACD1 HJV HPGDS KL LPCAT3 OGA PC PGD PRKCSH SCD SELP SLC35A2 TNF UGDH UGGT1 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UMPS	10162 10724 1118 11332 1374 1376 148738 1571 1576 1604 2523 2526 2539 27306 308 5091 51084 5226 54575 54576 54577 54578 54579 54600 54657 54658 54659 5589 56886 56994 57126 6319 6403 7124 7355 7358 7372 847 9200 9365 952 9563	Homo sapiens (human)
DOID:12384	dysentery Aliases: Infectious diarrhea	ACOT7 APRT IL18R1 LCT LYZ SULT1E1	11332 353 3938 4069 6783 8809	Homo sapiens (human)
DOID:724	female stress incontinence Aliases: Stress incontinence - female female urinary stress incontinence	ACOT7 ARSA CAT DCN FMOD GBA1 GPI	11332 1634 2331 2629 2821 410 847	Homo sapiens (human)
DOID:8670	eating disorder	ACOT7 ARSD COMT DBT GPCPD1 SIGLEC7	11332 1312 1629 27036 414 56261	Homo sapiens (human)
DOID:11996	spermatic cord torsion Aliases: Torsion of testicle Torsion of testis testicular Torsion	ACOT7 B4GALT7 GPX3 HSPG2 SMUG1	11285 11332 23583 2878 3339	Homo sapiens (human)
DOID:999	hypereosinophilic syndrome Aliases: Eosinophilic leukocytosis eosinophilia	ACOT7 CD1D CEL CLEC10A CYP2C19 ETNK1 EXTL3 HPGDS HS2ST1 HSPG2 ICAM1 IL18R1 IL1RL1 LGALS9 LPCAT1 MBL2 NDST1 PARP1 PARP9 PGM3 PLA2G5 PTEN PTGDS PTGS2 SDC2 SELL SFTPA2 SFTPD SIGLEC8 SLC27A5 TNFRSF10C VCAM1	10462 1056 10998 11332 142 1557 2137 27181 27306 3339 3340 3383 3965 4153 5238 5322 55500 5728 5730 5743 6383 6402 6441 729238 7412 79888 83666 8794 8809 912 9173 9653	Homo sapiens (human)
DOID:1116	pertussis Aliases: WC - Whooping cough bordetella infection whooping cough	ACOT7 PIK3CG UMOD	11332 5294 7369	Homo sapiens (human)
DOID:13461	urethral intrinsic sphincter deficiency Aliases: Intrinsic (urethral) sphincter deficiency [ISD]	ACOT7	11332	Homo sapiens (human)

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