GO Term | Evidence Code | PMID |
---|---|---|
heparin biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
extracellular space | ||
Golgi membrane |
GO Term | Evidence Code | PMID |
---|---|---|
protein xylosyltransferase activity | ||
magnesium ion binding | ||
manganese ion binding |
Species | Protein | mRNA |
---|---|---|
Rattus norvegicus | NP_071632 | NM_022296 |
Caenorhabditis elegans | AAO85277 | AY241928 |
Mus musculus | CAC185567 | AJ291751 |
DO ID | Disease Name | Source |
---|---|---|
DOID:1425 | pyoureter | |
DOID:1432 | blindness | |
DOID:0050427 | xeroderma pigmentosum | |
DOID:0050458 | juvenile myelomonocytic leukemia | |
DOID:0050569 | Seckel syndrome | |
DOID:0050778 | Meckel syndrome | |
DOID:0060254 | Robinow syndrome | |
DOID:0060262 | gallbladder disease | |
DOID:0060462 | Desbuquois dysplasia | |
DOID:0060578 | Noonan syndrome 1 |
HPO ID | HPO Term |
---|---|
HP:0000465 | Webbed neck |
HP:0000470 | Short neck |
HP:0000505 | Visual impairment |
HP:0000518 | Cataract |
HP:0000534 | Abnormal eyebrow morphology |
HP:0000541 | Retinal detachment |
HP:0000545 | Myopia |
HP:0000568 | Microphthalmia |
HP:0000572 | Visual loss |
HP:0000573 | Retinal hemorrhage |
Disease ID | Disease Name |
---|---|
ORPHA:85194 |
|
OMIM:605822 |
|
OMIM:264800 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
102440255 | MYOLU15916 | ||
117013516 | RHIFE08371 | ||
103242938 | CHLSB05585 | ||
108516436 | RHIBE12508 | ||
104680299 | RHIRO29253 | ||
100600245 | NOMLE08181 | ||
106826421 | EQUAS21325 | ||
105295404 | PTEVA08002 | ||
105824761 | PROCO10236 | ||
103738383 | NANGA01344 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024