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 1 - 10 of 34 in total
DO ID Disease Name Source
DOID:0060284 paroxysmal nocturnal hemoglobinuria
DOID:0060308 autosomal recessive intellectual developmental disorder
DOID:0060810 syndromic X-linked intellectual disability type 10
DOID:0060823 syndromic X-linked intellectual disability 94
DOID:0110881 holoprosencephaly 1
DOID:1059 intellectual disability
DOID:10907 microcephaly
DOID:11832 visual epilepsy
DOID:12139 dysthymic disorder
DOID:12859 choreatic disease
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 61 - 70 of 70 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
101807207 FICAL03802
103217575 CHLSB01487
108527826 RHIBE07747
104676740 RHIRO12961
100603465 NOMLE21673
115061912 ECHNA12383
850519 SGD:S000001869
109095948 CYPCA51477
116446432 CORMO24214
115608075 STRHB03321
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