Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
Resources Genes Glycoproteins Lectins Glycolipids Glycans Pathways Diseases Organisms
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Other Information
Release Statistics Download
Tools
SugarDrawer GlycanBuilder Glycan Converters GlycoMaple GlycomeAtlas LM-GlycomeAtlas GALAXY MCAW GlycoSim GRable
Search Tools
Cross Search Glycan Search Publication Search Programmatic Access
Standards Ontologies Notations
post-GPI attachment to proteins inositol deacylase 1

Summary
Gene Symbol
  • PGAP1
Aliases
  • Bst1
  • FLJ12377
  • GPI inositol-deacylase
  • SPG67
Organism
Homo sapiens (human)
External Links
NCBI Gene
80055
HGNC
25712
KEGG Gene ID
hsa:80055
PubChem
80055
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Disease variant
  • Endoplasmic reticulum
  • Glycoprotein
  • Hydrolase
  • Intellectual disability
  • Protein transport
  • Reference proteome
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
Q75T13
  • Post-GPI attachment to proteins factor 1
Annotation information from UniProt.
Gene Ontology (GO)
Displaying entries 1 - 5 of 9 in total
GO Term Evidence Code PMID
positive regulation of ER to Golgi vesicle-mediated transport
embryonic pattern specification
sensory perception of sound
GPI anchor metabolic process
anterior/posterior axis specification
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
KEGG BRITE Database
Orthology
K05294
Name
GPI inositol-deacylase [EC:3.-.-.-]
References
Disease
Disease Ontology
Displaying entries 11 - 20 of 34 in total
DO ID Disease Name Source
DOID:1443 cerebral degeneration
DOID:1470 major depressive disorder
DOID:1595 melancholic depression
DOID:1596 depressive disorder
DOID:1826 epilepsy
DOID:2231 factor XII deficiency
DOID:2234 focal epilepsy
DOID:2303 stereotypic movement disorder
DOID:2481 obsolete infantile epileptic encephalopathy
DOID:2848 obsolete melancholia
The Human Phenotype Ontology
Displaying entries 1 - 10 of 65 in total
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000154 Wide mouth
HP:0000164 Abnormality of the dentition
HP:0000193 Bifid uvula
HP:0000252 Microcephaly
HP:0000294 Low anterior hairline
HP:0000395 Prominent antihelix
HP:0000400 Macrotia
HP:0000470 Short neck
HP:0000490 Deeply set eye
Displaying all 2 entries
Disease ID Disease Name
OMIM:615802
  • intellectual disability, autosomal recessive 42
ORPHA:401820
  • autosomal recessive spastic paraplegia type 67
PubChem Disease
MedGen Diseases
OMIM Phenotypes
KEGG Diseases
Gene-Disease-Co-Occurrences-in-Literature (PubChem)
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP006714
Gene Name
post-GPI attachment to proteins 1
Ortholog
Displaying entries 1 - 10 of 70 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
179556 WB:WBGene00011835
31487 FB:FBgn0029789
103176553 CALMI10750
100147850 ZFIN:ZDB-GENE-090313-216
108266695 ICTPU31399
115160628 SALTR15051
103461932 POERE23482
101174236 ORYLA10048
100692117 ORENI23358
102306148 HAPBU22755
About Release Notes Help Feedback
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