GlyCosmos Portal

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **14876 - 14900** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:11162	respiratory failure Aliases: acute and chronic respiratory failure acute respiratory Failure acute-on-chronic respiratory failure chronic respiratory failure respiratory insufficiency/failure	Il15 Mbl2 Nup188 Sftpb	16168 17195 20388 227699	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060912	craniosynostosis 7 Aliases: CRS7	SMAD6	4091	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050964	spinocerebellar ataxia type 14	Prkcg	24681	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080177	hepatic veno-occlusive disease Aliases: veno-occlusive disease	ADAMTS13 HFE MMP9	11093 3077 4318	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050649	atransferrinemia Aliases: familial hypotransferrinemia	Tsf2	39435	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:9976	heroin dependence	drd2.L gdnf.L grin2a.L ngf.S	100127346 108709389 378584 779087	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0081124	craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1	TMCO1	54499	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081292	traumatic brain injury	Adam10 App Bad Drd2 Gria1 Lamp2 Lcn2 Mmp2 Nfe2l2 Ngf Nox1 Tgfb1 Tp53	114243 170496 24318 24842 24944 29650 310738 50592 54226 59086 64639 81686 83619	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080208	metabolic dysfunction-associated steatotic liver disease Aliases: MAFLD MASLD NAFLD metabolic dysfunction-associated fatty liver disease metabolic dysfunction-related steatotic liver disease metabolic-associated fatty liver disease non-alcoholic fatty liver disease nonalcoholic fatty liver disease	Abcc2 Abcc3 Abcg5 Abcg8 Acadm Acadvl Actb Adrb3 Akt1 Aldh2 Atp5f1a Ccl2 Col1a1 Dgat2 Fasn G6pd Hadha Hfe Hmgcr Hp Ifna5 Igf1r Il10 Il13 Il1rn Irs1 Krt18 Lep Lepr Lpl Mlxipl Nampt Nfe2l2 Pklr Pon2 Ppargc1a Samm50 Serpine1 Sidt2 Slc7a3 Sod2 Tfrc Tlr4 Tnf Ucp2	114628 116553 140668 155192 170670 171078 24158 24185 24377 24464 24536 24539 24617 24651 24770 24787 24835 252900 25303 25325 25363 25467 25608 25645 25675 25718 29199 29260 29393 29485 294853 29539 296851 297508 298210 300111 315617 50671 54315 60582 64678 65262 81822 83516 83619	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0112080	nuclear type mitochondrial complex I deficiency 32 Aliases: MC1DN32	NDUFB8	4714	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080559	congenital disorder of glycosylation Ig Aliases: ALG12-congenital disorder of glycosylation congenital disorder of glycosylation 1g	Alg12	223774	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5151	plexiform neurofibroma	Nf1	18015	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4415	fibrous histiocytoma Aliases: Fibroxanthoma benign fibrous histiocytoma	MFHAS1	9258	Homo sapiens (human)	Alliance of Genome Resources
DOID:12337	varicocele Aliases: Scrotal varices	CASP9 FAS HIF1A HSPD1 IL1A	3091 3329 355 3552 842	Homo sapiens (human)	Alliance of Genome Resources
DOID:13241	Behcet's disease Aliases: Adamantiades-Behcet disease Behcet syndrome Behet's syndrome triple symptom complex	ace pon1 vegfaa	30682 447803 565980	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0111153	congenital mirror movement disorder Aliases: familial congenital controlateral synkinesia familial congenital mirror movements hereditary congenital controlateral synkinesia hereditary congenital mirror movements isolated congenital controlateral synkinesia isolated congenital mirror movements	NetA NetB	32398 32400	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050437	Danon disease Aliases: ANTOPOL DISEASE PSEUDOGLYCOGENOSIS II	LAMP2	3920	Homo sapiens (human)	Alliance of Genome Resources
DOID:423	myopathy	HMG1 HMG2 VPS1	851171 853870 854900	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111756	Leber hereditary optic neuropathy with demyelinating disease of CNS	MECR	51102	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050466	Loeys-Dietz syndrome	daf-1 daf-4 sma-6	174044 175781 176829	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070462	mitochondrial complex V (ATP synthase) deficiency nuclear type 4B Aliases: MC5DN4B	ATP5F1A	498	Homo sapiens (human)	Alliance of Genome Resources
DOID:9775	diastolic heart failure	Ace Lepr	11421 16847	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080520	Tn polyagglutination syndrome Aliases: galactosyltransferase deficiency	C16D9.6	182687	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9667	placental abruption Aliases: abruptio placenta abruptio placentae	PROC	5624	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070489	classic dopamine transporter deficiency syndrome Aliases: PKDYS1 classic DTDS infantile parkinsonism-dystonia 1	dat-1	176304	Caenorhabditis elegans	Alliance of Genome Resources

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