arylsulfatase G
| GO Term | Evidence Code | PMID |
|---|---|---|
| sulfur compound metabolic process | ||
| lysosome organization | ||
| glial cell differentiation | ||
| gene expression | ||
| homeostasis of number of cells |
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular space | ||
| lysosome | ||
| endoplasmic reticulum | ||
| endoplasmic reticulum lumen |
| GO Term | Evidence Code | PMID |
|---|---|---|
| arylsulfatase activity | ||
| arylsulfatase activity | ||
| arylsulfatase activity | ||
| arylsulfatase activity | ||
| N-sulfoglucosamine-3-sulfatase activity |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050439 | Usher syndrome |
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000375 | Abnormal cochlea morphology |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000408 | Progressive sensorineural hearing impairment |
| HP:0000483 | Astigmatism |
| HP:0000512 | Abnormal electroretinogram |
| HP:0000518 | Cataract |
| HP:0000546 | Retinal degeneration |
| HP:0000572 | Visual loss |
| HP:0000575 | Scotoma |
| Disease ID | Disease Name |
|---|---|
| ORPHA:231183 |
|
| OMIM:618144 |
|
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 6, 2026