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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 6 - 9 of 9 in total
GO Term Evidence Code PMID
forebrain regionalization
endoplasmic reticulum to Golgi vesicle-mediated transport
protein transport
attachment of GPI anchor to protein
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 11 - 20 of 65 in total
HPO ID HPO Term
HP:0000556 Retinal dystrophy
HP:0000582 Upslanted palpebral fissure
HP:0000639 Nystagmus
HP:0000733 Motor stereotypy
HP:0000748 Inappropriate laughter
HP:0000750 Delayed speech and language development
HP:0001249 Intellectual disability
HP:0001250 Seizure
HP:0001252 Hypotonia
HP:0001256 Intellectual disability, mild
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
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: August 19, 2024