Gene ID | Gene Symbol | Description | Source |
---|---|---|---|
8692 | HYAL2 | hyaluronidase 2 | |
10020 | GNE | glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | |
10724 | OGA | O-GlcNAcase | |
22901 | ARSG | arylsulfatase G | |
79158 | GNPTAB | N-acetylglucosamine-1-phosphate transferase subunits alpha and beta | |
84572 | GNPTG | N-acetylglucosamine-1-phosphate transferase subunit gamma | |
138050 | HGSNAT | heparan-alpha-glucosaminide N-acetyltransferase | |
159371 | SLC35G1 | solute carrier family 35 member G1 | |
285362 | SUMF1 | sulfatase modifying factor 1 | |
347527 | ARSH | arylsulfatase family member H |
UniProt ID | Protein Name | Source |
---|---|---|
Q3T906 | N-acetylglucosamine-1-phosphotransferase subunits alpha/beta | |
Q68CP4 | Heparan-alpha-glucosaminide N-acetyltransferase | |
Q8NBK3 | Formylglycine-generating enzyme | |
Q96EG1 | Arylsulfatase G | |
Q99519 | Sialidase-1 | |
Q9UBQ6 | Exostosin-like 2 | |
Q9UJJ9 | N-acetylglucosamine-1-phosphotransferase subunit gamma |
HPO ID | HPO Term |
---|---|
HP:0000023 | Inguinal hernia |
HP:0000158 | Macroglossia |
HP:0000212 | Gingival overgrowth |
HP:0000256 | Macrocephaly |
HP:0000280 | Coarse facial features |
HP:0000293 | Full cheeks |
HP:0000336 | Prominent supraorbital ridges |
HP:0000362 | Otosclerosis |
HP:0000405 | Conductive hearing impairment |
HP:0000407 | Sensorineural hearing impairment |
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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