Gene ID | Gene Symbol | Description | Source |
---|---|---|---|
1836 | SLC26A2 | solute carrier family 26 member 2 | |
2135 | EXTL2 | exostosin like glycosyltransferase 2 | |
2137 | EXTL3 | exostosin like glycosyltransferase 3 | |
2517 | FUCA1 | alpha-L-fucosidase 1 | |
2523 | FUT1 | fucosyltransferase 1 (H blood group) | |
2588 | GALNS | galactosamine (N-acetyl)-6-sulfatase | |
2720 | GLB1 | galactosidase beta 1 | |
2799 | GNS | glucosamine (N-acetyl)-6-sulfatase | |
2990 | GUSB | glucuronidase beta | |
3373 | HYAL1 | hyaluronidase 1 |
UniProt ID | Protein Name | Source |
---|---|---|
P15813 | Antigen-presenting glycoprotein CD1d | |
P15848 | Arylsulfatase B | |
P16112 | Aggrecan core protein | |
P16278 | Beta-galactosidase | |
P16444 | Dipeptidase 1 | |
P19526 | Galactoside alpha-(1,2)-fucosyltransferase 1 | |
P20933 | N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase | |
P21589 | 5'-nucleotidase | |
P22304 | Iduronate 2-sulfatase | |
P27824 | Calnexin |
HPO ID | HPO Term |
---|---|
HP:0000431 | Wide nasal bridge |
HP:0000445 | Wide nose |
HP:0000488 | Retinopathy |
HP:0000493 | Abnormal foveal morphology |
HP:0000505 | Visual impairment |
HP:0000553 | Abnormal uvea morphology |
HP:0000648 | Optic atrophy |
HP:0000654 | Decreased light- and dark-adapted electroretinogram amplitude |
HP:0000662 | Nyctalopia |
HP:0000707 | Abnormality of the nervous system |
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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