Gene ID | Gene Symbol | Description | Source |
---|---|---|---|
12 | SERPINA3 | serpin family A member 3 | |
2581 | GALC | galactosylceramidase | |
3119 | HLA-DQB1 | major histocompatibility complex, class II, DQ beta 1 | |
4137 | MAPT | microtubule associated protein tau | |
4744 | NEFH | neurofilament heavy chain | |
4747 | NEFL | neurofilament light chain | |
5621 | PRNP | prion protein (Kanno blood group) | |
5742 | PTGS1 | prostaglandin-endoperoxide synthase 1 | |
5743 | PTGS2 | prostaglandin-endoperoxide synthase 2 | |
6622 | SNCA | synuclein alpha |
Gene ID | Gene Symbol | Description | Source |
---|---|---|---|
20716 | Serpina3n | serine (or cysteine) peptidase inhibitor, clade A, member 3N | |
20717 | Serpina3m | serine (or cysteine) peptidase inhibitor, clade A, member 3M | |
20907 | Stx1a | syntaxin 1A (brain) | |
22628 | Ywhag | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma polypeptide | |
74069 | Serpina3a | serine (or cysteine) peptidase inhibitor, clade A, member 3A | |
238393 | Serpina3f | serine (or cysteine) peptidase inhibitor, clade A, member 3F | |
238395 | Serpina3j | serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 3J | |
271047 | Serpina3b | serine (or cysteine) peptidase inhibitor, clade A, member 3B | |
380684 | Nefh | neurofilament, heavy polypeptide |
Gene ID | Gene Symbol | Description | Source |
---|---|---|---|
24686 | Prnp | prion protein | |
24794 | Serpina3c | serine (or cysteine) proteinase inhibitor, clade A, member 3C | |
24795 | Serpina3n | serpin family A member 3N | |
29219 | Snca | synuclein alpha | |
29527 | Ptgs2 | prostaglandin-endoperoxide synthase 2 | |
83613 | Nefl | neurofilament light chain |
HPO ID | HPO Term |
---|---|
HP:0003487 | Babinski sign |
HP:0005327 | Loss of facial expression |
HP:0006943 | Diffuse spongiform leukoencephalopathy |
HP:0007009 | Central nervous system degeneration |
HP:0007017 | Progressive forgetfulness |
HP:0007158 | Progressive extrapyramidal muscular rigidity |
HP:0007183 | Focal T2 hyperintense basal ganglia lesion |
HP:0007256 | Abnormal pyramidal sign |
HP:0007686 | Abnormal pupillary function |
HP:0010542 | Vestibular nystagmus |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024