Gene ID | Gene Symbol | Description | Source |
---|---|---|---|
6120 | RPE | ribulose-5-phosphate-3-epimerase | |
6476 | SI | sucrase-isomaltase | |
6785 | ELOVL4 | ELOVL fatty acid elongase 4 | |
8972 | MGAM | maltase-glucoamylase | |
8987 | STBD1 | starch binding domain 1 | |
10159 | ATP6AP2 | ATPase H+ transporting accessory protein 2 | |
10327 | AKR1A1 | aldo-keto reductase family 1 member A1 | |
26503 | SLC17A5 | solute carrier family 17 member 5 | |
27306 | HPGDS | hematopoietic prostaglandin D synthase | |
54575 | UGT1A10 | UDP glucuronosyltransferase family 1 member A10 |
UniProt ID | Protein Name | Source |
---|---|---|
Q04446 | 1,4-alpha-glucan-branching enzyme | |
Q96AD5 | Patatin-like phospholipase domain-containing protein 2 | |
Q96AT9 | Ribulose-phosphate 3-epimerase | |
Q9GZR5 | Very long chain fatty acid elongase 4 | |
Q9HAW7 | UDP-glucuronosyltransferase 1A7 | |
Q9HAW8 | UDP-glucuronosyltransferase 1A10 | |
Q9HAW9 | UDP-glucuronosyltransferase 1A8 | |
Q9NRA2 | Sialin |
HPO ID | HPO Term |
---|---|
HP:0002878 | Respiratory failure |
HP:0011947 | Respiratory tract infection |
HP:0002240 | Hepatomegaly |
HP:0001284 | Areflexia |
HP:0008872 | Feeding difficulties in infancy |
HP:0000297 | Facial hypotonia |
HP:0003324 | Generalized muscle weakness |
HP:0001640 | Cardiomegaly |
HP:0002202 | Pleural effusion |
HP:0011462 | Young adult onset |
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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