Gene ID | Gene Symbol | Description | Source |
---|---|---|---|
44058 | Ugt36A1 | UDP-glycosyltransferase family 36 member A1 | |
53501 | Ugt304A1 | UDP-glycosyltransferase family 304 member A1 | |
53502 | Ugt302K1 | UDP-glycosyltransferase family 302 member K1 | |
53503 | Ugt303A1 | UDP-glycosyltransferase family 303 member A1 | |
53506 | Ugt35E2 | UDP-glycosyltransferase family 35 member E2 | |
53507 | Ugt35C1 | UDP-glycosyltransferase family 35 member C1 | |
53511 | Ugt37D1 | UDP-glycosyltransferase family 37 member D1 | |
53512 | Ugt37E1 | UDP-glycosyltransferase family 37 member E1 | |
53583 | Ugt37C1 | UDP-glycosyltransferase family 37 member C1 | |
53584 | Ugt37B1 | UDP-glycosyltransferase family 37 member B1 |
HPO ID | HPO Term |
---|---|
HP:0001392 | Abnormality of the liver |
HP:0001249 | Intellectual disability |
HP:0008282 | Unconjugated hyperbilirubinemia |
HP:0000750 | Delayed speech and language development |
HP:0003265 | Neonatal hyperbilirubinemia |
HP:0012246 | Oculomotor nerve palsy |
HP:0001337 | Tremor |
HP:0000365 | Hearing impairment |
HP:0001343 | Kernicterus |
HP:0006579 | Prolonged neonatal jaundice |
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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