DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 46751 - 46775 of 62743 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Gene Name UniProt ID
C1306503 Congenital exomphalos LFNG 3955 LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase Q8NES3
C1306503 Congenital exomphalos PIGQ 9091 phosphatidylinositol glycan anchor biosynthesis class Q Q9BRB3
C1306503 Congenital exomphalos PIGS 94005 phosphatidylinositol glycan anchor biosynthesis class S Q96S52
C1306503 Congenital exomphalos AGA 175 aspartylglucosaminidase P20933
C1306503 Congenital exomphalos SLC26A2 1836 solute carrier family 26 member 2 P50443
C1306503 Congenital exomphalos ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C1306503 Congenital exomphalos GUSB 2990 glucuronidase beta P08236
C1306503 Congenital exomphalos IDS 3423 iduronate 2-sulfatase P22304
C1306503 Congenital exomphalos ARSB 411 arylsulfatase B P15848
C1306503 Congenital exomphalos GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C1306503 Congenital exomphalos GPC6 10082 glypican 6 Q9Y625
C1306503 Congenital exomphalos COMT 1312 catechol-O-methyltransferase P21964
C1306503 Congenital exomphalos AGPAT2 10555 1-acylglycerol-3-phosphate O-acyltransferase 2 O15120
C1306503 Congenital exomphalos COLEC10 10584 collectin subfamily member 10 Q9Y6Z7
C1306503 Congenital exomphalos PLA2G15 23659 phospholipase A2 group XV Q8NCC3
C1306503 Congenital exomphalos ACSS2 55902 acyl-CoA synthetase short chain family member 2 Q9NR19
C1306503 Congenital exomphalos SLC2A10 81031 solute carrier family 2 member 10 O95528
C1306503 Congenital exomphalos PIGP 51227 phosphatidylinositol glycan anchor biosynthesis class P P57054
C1306503 Congenital exomphalos GPC3 2719 glypican 3 P51654
C1306503 Congenital exomphalos TGDS 23483 TDP-glucose 4,6-dehydratase O95455
C1306503 Congenital exomphalos OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C1306503 Congenital exomphalos NSDHL 50814 NAD(P) dependent steroid dehydrogenase-like Q15738
C1306503 Congenital exomphalos MASP1 5648 mannan binding lectin serine peptidase 1 P48740
C1306503 Congenital exomphalos COLEC11 78989 collectin subfamily member 11 Q9BWP8
C1306589 Congenital dyserythropoietic anemia, type II MGAT2 4247 alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Q10469

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024