Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

UDP-GLYCOSYLTRANSFERASE 1 FAMILY, POLYPEPTIDE A1
Synonyms

UGT1A
ID

http://purl.bioontology.org/ontology/OMIM/191740
altLabel

UGT1A

CRIGLER-NAJJAR SYNDROME, TYPE II

HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATAL

URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASE 1

UGT1A1

UDP-GLYCOSYLTRANSFERASE 1 FAMILY, POLYPEPTIDE A GENE COMPLEX

CRIGLER-NAJJAR SYNDROME, TYPE I

UGT1A GENE COMPLEX

GILBERT SYNDROME, SUSCEPTIBILITY TO

UDP-GLYCOSYLTRANSFERASE 1

URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASE 1 FAMILY, POLYPEPTIDE A1

BILIRUBIN UDP-GLUCURONOSYLTRANSFERASE

URIDINE DIPHOSPHATE GLUCURONOSYLTRANSFERASE, BILIRUBIN

BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1

GILBERT SYNDROME

UGT1
cui

C0010324

C1866173

C2931132

C0017551

C0537026

C0270210

C4016425
Gene Locus

2q37
Gene Symbol

UGT1A1

GNT1

BILIQTL1

UGT1
Has allelic variant

http://purl.bioontology.org/ontology/OMIM/191740.0006

http://purl.bioontology.org/ontology/OMIM/191740.0008

http://purl.bioontology.org/ontology/OMIM/191740.0010

http://purl.bioontology.org/ontology/OMIM/191740.0023

http://purl.bioontology.org/ontology/OMIM/191740.0011

http://purl.bioontology.org/ontology/OMIM/191740.0003

http://purl.bioontology.org/ontology/OMIM/191740.0024

http://purl.bioontology.org/ontology/OMIM/191740.0022

http://purl.bioontology.org/ontology/OMIM/191740.0004

http://purl.bioontology.org/ontology/OMIM/191740.0017

http://purl.bioontology.org/ontology/OMIM/191740.0016

http://purl.bioontology.org/ontology/OMIM/191740.0018

http://purl.bioontology.org/ontology/OMIM/191740.0009

http://purl.bioontology.org/ontology/OMIM/191740.0005

http://purl.bioontology.org/ontology/OMIM/191740.0020

http://purl.bioontology.org/ontology/OMIM/191740.0021

http://purl.bioontology.org/ontology/OMIM/191740.0013

http://purl.bioontology.org/ontology/OMIM/191740.0012

http://purl.bioontology.org/ontology/OMIM/191740.0014

http://purl.bioontology.org/ontology/OMIM/191740.0025

http://purl.bioontology.org/ontology/OMIM/191740.0002

http://purl.bioontology.org/ontology/OMIM/191740.0001

http://purl.bioontology.org/ontology/OMIM/191740.0019

http://purl.bioontology.org/ontology/OMIM/191740.0015
MIMTYPEMEANING

Gene with known sequence
Moved from

191741

191742
notation

191740
OMIM Entry Type

1
OMIM MimType Value

star
prefLabel

UDP-GLYCOSYLTRANSFERASE 1 FAMILY, POLYPEPTIDE A1
tui

T028

T033

T047
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Delete Mapping To Ontology Source
http://purl.bmicc.cn/ontology/ICD10CN/E80.4 International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/ICD10/E80.5 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/MESH/C562692 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/D003414 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/ICD10CM/E80.5 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/ICD10/E80.4 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/LNC/LP31870-6 Logical Observation Identifier Names and Codes CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0017551 MedlinePlus Health Topics CUI
http://purl.bmicc.cn/ontology/ICD10CN/E80.5 International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/ICD10CM/E80.4 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/MESH/C536213 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/D005878 Medical Subject Headings CUI