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), 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 **3751 - 3775** of **7942** in total

« First

‹ Prev

…

147

148

149

150

151

152

153

154

155

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▼
DOID:11257	social phobia	ABO CAT COMT GAD1 MANEA NANS PSAP	1312 2571 28 54187 5660 79694 847	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:9562	primary ciliary dyskinesia Aliases: ciliary motility disorder immotile ciliary syndrome	AKR1C4 CEL ICAM1 INPP5E MBL2 NCAM1 NT5E NTM PARP9 PNPLA2 SCD5 SDC1 SLC27A5	1056 10998 1109 3383 4153 4684 4907 50863 56623 57104 6382 79966 83666	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:0050144	Kartagener syndrome Aliases: Kartagener's syndrome	INPP5E MBL2 NTM	4153 50863 56623	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:3049	Churg-Strauss syndrome Aliases: Allergic Granulomatous Angiitis Allergic granulomatosis angiitis Churg-Strauss vasculitis	CMAS GFRA1 TNFRSF10C VCAM1	2674 55907 7412 8794	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
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)	DisGeNET DisGeNET
DOID:1562	chromoblastomycosis Aliases: Chromomycosis Mossy foot disease	CLEC7A	64581	Homo sapiens (human)	DisGeNET
DOID:12259	hemophilia B Aliases: Congenital factor IX deficiency Congenital factor IX disorder deficiency, functional factor IX factor IX deficiency	AMT CD38 DCXR EBP G6PD GAD1 SACM1L SMUG1	10682 22908 23583 2539 2571 275 51181 952	Homo sapiens (human)	DisGeNET
DOID:9821	choroideremia Aliases: progressive Choroidal Atrophy	IL1RL1 RPE	6120 9173	Homo sapiens (human)	DisGeNET
DOID:2021	placenta cancer Aliases: Placental tumors malignant Placental tumor malignant neoplasm of placenta neoplasm of placenta placental cancer primary malignant neoplasm of placenta	ABO AKR1C3 ALPI ALPP ANXA5 APRT ATRNL1 CAT CD1D CD44 CHST3 CYP11A1 CYP19A1 CYP1B1 CYP4F3 DHRS11 DLD EBP ENPP3 HMMR HPRT1 HPSE HSD11B2 HSD17B1 HSD17B7 HSD3B1 IL1R1 KLRC1 LGALS1 MCAT MRC1 OLR1 PIK3CA PIK3CB PIK3CD PIK3CG PKM PTEN SDC1 SDHC SLC2A3 VCAN	10682 10855 1462 1545 1583 1588 1738 248 250 26033 27349 28 308 3161 3251 3283 3291 3292 353 3554 3821 3956 4051 4360 4973 51478 5169 5290 5291 5293 5294 5315 5728 6382 6391 6515 79154 847 8644 912 9469 960	Homo sapiens (human)	DisGeNET
DOID:0050697	chorioamnionitis	ACAN CBR1 CD14 CYP1A1 IL1RL1 LGALS3 MBL2 PGP PTGS1 PTGS2 RECK STS TNF	1543 176 283871 3958 412 4153 5742 5743 7124 8434 873 9173 929	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:3594	choriocarcinoma Aliases: Chorioepithelioma	ABO AKR1C3 ALPI ALPP ANXA5 APRT ATRNL1 CAT CD1D CD44 CHST3 CYP11A1 CYP19A1 CYP1B1 CYP4F3 DHRS11 DLD EBP ENPP3 HMMR HPRT1 HPSE HSD11B2 HSD17B1 HSD17B7 HSD3B1 IGF2 IL1R1 KLRC1 LGALS1 MCAT MRC1 OLR1 PIK3CA PIK3CB PIK3CD PIK3CG PKM PTEN SDC1 SDHC SLC2A3 SMUG1 VCAN	10682 10855 1462 1545 1583 1588 1738 23583 248 250 26033 27349 28 308 3161 3251 3283 3291 3292 3481 353 3554 3821 3956 4051 4360 4973 51478 5169 5290 5291 5293 5294 5315 5728 6382 6391 6515 79154 847 8644 912 9469 960	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:0060810	syndromic X-linked intellectual disability type 10 Aliases: HSD10 deficiency, atypical type HSD10 disease, atypical type MRXS10 X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome mental retardation, X-linked syndromic 10	ACADSB ACAT2 ALG13 ARSA B3GALNT2 CACNA2D2 DHCR7 GM2A LMAN2L MAN1B1 MBOAT7 MECR MYORG NDST1 NGLY1 PGAP1 PIGC PLA2G6 PRNP PSAP SMUG1 ST3GAL3 TECR TUSC3	11253 148789 1717 23583 2760 3340 36 39 410 51102 5279 55768 5621 5660 57462 6487 79143 79868 7991 80055 81562 8398 9254 9524	Homo sapiens (human)	DisGeNET DisGeNET
DOID:12859	choreatic disease Aliases: chorea hereditary chorea	ACAT2 ALG13 ARSA B3GALNT2 CACNA2D2 GM2A LMAN2L MAN1B1 MBOAT7 MECR MYORG NDST1 NGLY1 PGAP1 PIGC PLA2G6 PRNP PSAP SMUG1 ST3GAL3 TECR TUSC3	11253 148789 23583 2760 3340 39 410 51102 5279 55768 5621 5660 57462 6487 79143 79868 7991 80055 81562 8398 9254 9524	Homo sapiens (human)	DisGeNET DisGeNET
DOID:3302	chordoma Aliases: notochordoma	ACAN CBR1 CSPG4 FCGR3B IDH1 LGALS9 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN SIGLEC7	142 1464 176 2215 27036 3417 3965 5290 5291 5293 5294 5728 873	Homo sapiens (human)	DisGeNET
DOID:3371	chondrosarcoma Aliases: Cartilaginous cancer chondrosarcoma of bone primary chondrosarcoma of the bone	ACAN AMACR ANXA5 APRT CD44 CDS1 CHI3L1 CSPG4 DCN EFNA5 EXT1 EXT2 GLB1 GPC3 HS3ST1 HSPG2 ICAM1 IDH1 IDH2 LDHA MTAP NAMPT PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PRKAA2 PRNP PTEN PTGS2 SDC2 SFTPC SLC2A10 SMUG1 SPHK2 TM7SF2 TUSC3 VCAM1 VCAN	10135 1040 1116 142 1462 1464 1634 176 1946 2131 2132 23583 23600 2719 2720 308 3339 3383 3417 3418 353 3939 4507 5290 5291 5293 5294 5563 5621 56848 5728 5743 6383 6440 7108 7412 7991 81031 960 9957	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:0110852	rhizomelic chondrodysplasia punctata type 2 Aliases: Chondrodysplasia Punctata, Rhizomelic, Due To Dihydroxyacetonephosphate Acyltransferase Deficiency Dhapat Deficiency Dihydroxyacetonephosphate Acyltransferase Deficiency Glyceronephosphate O-Acyltransferase Deficiency Gnpat Deficiency Peroxisomal Dihydroxyacetonephosphate Acyltransferase Deficiency Rcdp2	AGPS ARSH DHCR24 EBP GNPAT NSDHL STS SUMF1	10682 1718 285362 347527 412 50814 8443 8540	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:0060293	autosomal dominant chondrodysplasia punctata	AGPS ARSH DHCR24 EBP GNPAT NSDHL STS SUMF1	10682 1718 285362 347527 412 50814 8443 8540	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0110853	rhizomelic chondrodysplasia punctata type 3 Aliases: Agps Deficiency Alkyldihydroxyacetonephosphate Synthase Deficiency Alkylglycerone-Phosphate Synthase Deficiency Rcdp3	AGPS ARSH DHCR24 EBP GNPAT NSDHL STS SUMF1	10682 1718 285362 347527 412 50814 8443 8540	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:0110851	rhizomelic chondrodysplasia punctata type 1 Aliases: Pbd9 Peroxisome Biogenesis Disorder 9 Rcdp1	AGPS ARSH DHCR24 EBP FAR1 GNPAT HSD17B4 NSDHL STS SUMF1	10682 1718 285362 3295 347527 412 50814 84188 8443 8540	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:2581	chondrodysplasia punctata Aliases: Chondrodysplasia punctata congenita	AGPS ARSB ARSH B3GALT6 COL9A2 DHCR24 EBP EXTL3 FDFT1 GNPAT GUSB MSMO1 NEU1 NSDHL SLC26A2 STS SUMF1 TMEM165 XYLT1	10682 126792 1298 1718 1836 2137 2222 285362 2990 347527 411 412 4758 50814 55858 6307 64131 8443 8540	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0060292	X-linked chondrodysplasia punctata 1 Aliases: chondrodystrophia calcificans congenita	AGPS ARSH DHCR24 EBP FDFT1 GNPAT NSDHL STS SUMF1	10682 1718 2222 285362 347527 412 50814 8443 8540	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:2649	chondroblastoma Aliases: Chondroblastoma of bone	ACAN EXT1 IDH2 PTGS2	176 2131 3418 5743	Homo sapiens (human)	DisGeNET
DOID:8456	choline deficiency disease Aliases: choline deficiency	MLYCD PEMT	10400 23417	Homo sapiens (human)	DisGeNET
DOID:14502	cholesterol ester storage disease Aliases: CESD partial LAL deficiency partial LIPA deficiency partial cholesterol ester hydrolase deficiency partial lysosomal acid lipase deficiency	LIPA	3988	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:7439	polyp of middle ear Aliases: polyp - middle ear polyp of the middle ear	CLEC10A CLEC12B CLEC5A CLEC6A CLEC7A LY75 MGLL MRC1 PIK3CA PIK3CB PIK3CD PIK3CG PSMD10 PTGS2 STS	10462 11343 23601 387837 4065 412 4360 5290 5291 5293 5294 5716 5743 64581 93978	Homo sapiens (human)	DisGeNET

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

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements