GO Term | Evidence Code | PMID |
---|---|---|
basement membrane assembly | ||
hydroxylysine biosynthetic process | ||
protein O-linked glycosylation | ||
lung morphogenesis | ||
protein localization |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum lumen | ||
endoplasmic reticulum | ||
trans-Golgi network | ||
endoplasmic reticulum membrane | ||
collagen-containing extracellular matrix |
GO Term | Evidence Code | PMID |
---|---|---|
small molecule binding | ||
procollagen glucosyltransferase activity | ||
iron ion binding | ||
procollagen galactosyltransferase activity | ||
metal ion binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050328 | congenital hypothyroidism | |
DOID:0060058 | lymphoma | |
DOID:0060249 | scoliosis | |
DOID:0060735 | epidermolysis bullosa simplex Dowling-Meara type | |
DOID:0060736 | epidermolysis bullosa simplex Ogna type | |
DOID:0080001 | bone disease | |
DOID:0080087 | nonsyndromic congenital nail disorder 9 | |
DOID:0090017 | epidermolysis bullosa simplex with muscular dystrophy | |
DOID:0111257 | gamma-glutamyl transpeptidase deficiency | |
DOID:10003 | sensorineural hearing loss |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000164 | Abnormality of the dentition |
HP:0000272 | Malar flattening |
HP:0000307 | Pointed chin |
HP:0000369 | Low-set ears |
HP:0000407 | Sensorineural hearing impairment |
HP:0000463 | Anteverted nares |
HP:0000518 | Cataract |
HP:0000545 | Myopia |
HP:0000586 | Shallow orbits |
Disease ID | Disease Name |
---|---|
OMIM:612394 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
174564 | WB:WBGene00002497 | ||
39265 | FB:FBgn0036147 | ||
556077 | ZFIN:ZDB-GENE-021031-4 | DANRE24743 | |
108275691 | ICTPU07525 | ||
115183238 | SALTR50777 | ||
115529392 | GADMO20708 | ||
100697420 | ORENI49600 | ||
115589962 | SPAAU07491 | ||
380138 | Xenbase:XB-GENE-5916727 | ||
495489 | Xenbase:XB-GENE-17339835 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
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