GlyCosmos Portal

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

Displaying entries **13551 - 13575** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:0090056	dystonia 12	Atp1a3	24213	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070385	developmental and epileptic encephalopathy 99 Aliases: DEE99 early infantile epileptic encephalopathy 99	Atp1a3	24213	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070385	developmental and epileptic encephalopathy 99 Aliases: DEE99 early infantile epileptic encephalopathy 99	Atp1a3	232975	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090056	dystonia 12	Atp1a3 Pla2g6	232975 53357	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070384	developmental and epileptic encephalopathy 98 Aliases: DEE98 early infantile epileptic encephalopathy 98	Atp1a2	98660	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111182	familial hemiplegic migraine 2 Aliases: FHM2 Familial hemiplegic migraine-2 MHP2	Atp1a2	98660	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14264	benign neonatal seizures Aliases: benign familial neonatal seizures benign neonatal convulsions	Atp1a2 Kcnq2 Kcnq3	110862 16536 98660	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10024	migraine with aura Aliases: classic migraine	Atp1a2 Cacna1a Dbh Drd2	12286 13166 13489 98660	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050635	alternating hemiplegia of childhood Aliases: AHC	Atp1a2 Atp1a3	232975 98660	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070384	developmental and epileptic encephalopathy 98 Aliases: DEE98 early infantile epileptic encephalopathy 98	Atp1a2	24212	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111182	familial hemiplegic migraine 2 Aliases: FHM2 Familial hemiplegic migraine-2 MHP2	Atp1a2	24212	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:14264	benign neonatal seizures Aliases: benign familial neonatal seizures benign neonatal convulsions	Atp1a2	24212	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9279	hyperhomocysteinemia	Atp1a2 Ccl2 Ednra F10 F12 G6pd Gria1 Grin2a Grin2b Icam1 Ngf Sod2	24212 24326 24377 24409 24410 24770 24787 25464 29243 306761 310738 50592	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10024	migraine with aura Aliases: classic migraine	Atp1a2 Cacna1a Dbh Drd2	24212 24318 25398 25699	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:863	nervous system disease	Atp1a2 Atp1a3	24212 24213	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050635	alternating hemiplegia of childhood Aliases: AHC	Atp1a2 Atp1a3	24212 24213	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111558	Charcot-Marie-Tooth disease type 2DD Aliases: ATP1A1-related CMT2 ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2 CMT2DD Charcot-Marie-Tooth disease, axonal, type 2DD Charcot-Marie-Tooth neuropathy, type 2DD	Atp1a2 Atp1a3	24212 24213	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060178	familial hemiplegic migraine	Atp1a2 Atp1a3 Cacna1a	24212 24213 25398	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10003	sensorineural hearing loss Aliases: High Frequency Hearing Loss High frequency deafness Perceptive deafness Perceptive hearing loss Perceptive hearing loss or deafness Sensorineural Deafness Sensory hearing loss central hearing loss high-frequency hearing loss	Atp1a1 Atp1b1 Clcnka Clcnkb Ednrb Eya4 F2 F5 H2-D1 H2-Eb1 H2-K1 H2-M2 H2-Q10 H2-Q1 H2-Q2 H2-Q4 H2-Q6 H2-Q7 H2-T3 Ifng Il2 Itga2 Lnx1 Mbl2 Myh9 Myo1a Myo6 Ngf Opn4 Ptgds Scarb1 Slc12a2 Slc44a4 Slc7a14 Sod2 Strc Tecta Tmprss3 Tnf Wfs1	110557 11928 11931 12733 13618 140476 14051 14061 14067 140765 14964 14969 14972 14990 15006 15007 15013 15015 15018 15043 15978 16183 16398 16924 17195 17886 17920 18049 19215 20496 20656 20778 21683 21926 22393 241919 30044 432516 56365 70129	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111558	Charcot-Marie-Tooth disease type 2DD Aliases: ATP1A1-related CMT2 ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2 CMT2DD Charcot-Marie-Tooth disease, axonal, type 2DD Charcot-Marie-Tooth neuropathy, type 2DD	Atp1a1 Atp1a2 Atp1a3 Atp4a	11928 11944 232975 98660	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060178	familial hemiplegic migraine	Atp1a1 Atp1a2 Atp1a3 Atp4a Cacna1a	11928 11944 12286 232975 98660	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112348	hereditary spastic paraplegia 78 Aliases: SPG78 spastic paraplegia 78 autosomal recessive	Atp13a2	74772	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060556	Kufor-Rakeb syndrome Aliases: autosomal recessive Parkinson disease 9 autosomal recessive juvenile onset Parkinson disease 9	Atp13a2 Atp13a3 Atp13a5	224088 268878 74772	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060893	juvenile-onset Parkinson's disease Aliases: juvenile-onset Parkinson disease	Atp13a2 Atp13a3 Atp13a5	224088 268878 74772	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14503	neuronal ceroid lipofuscinosis Aliases: hereditary ceroid lipofuscinosis	Atp13a2 Atp13a3 Atp13a5 Cln3 Ctsd Ppt1 Ppt2 Sod2	12752 13033 19063 20656 224088 268878 54397 74772	Mus musculus (house mouse)	Alliance of Genome Resources

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