Adrenocortical dysplasia protein homolog

Summary
UniProt ID
Q96AP0
Gene Symbol
ACD PIP1 PTOP TINT1 TPP1
Gene ID
65057
Organism
Homo sapiens (human)
PubChem
Q96AP0
The O-GlcNAc Database
Q96AP0
Re-Glyco
Q96AP0
Annotation
Keyword
3D-structure Alternative splicing DNA-binding Disease variant Dyskeratosis congenita Isopeptide bond Nucleus Phosphoprotein Proteomics identification Reference proteome Telomere Ubl conjugation
Gene Ontology (GO)
GO Hierarchy
Sequence
MAGSGRLVLRPWIRELILGSETPSSPRAGQLLEVLQDAEAAVAGPSHAPDTSDVGATLLVSDGTHSVRCLVTREALDTSDWEEKEFGFRGTEGRLLLLQDCGVHVQVAEGGAPAEFYLQVDRFSLLPTEQPRLRVPGCNQDLDVQKKLYDCLEEHLSESTSSNAGLSLSQLLDEMREDQEHQGALVCLAESCLTLEGPCTAPPVTHWAASRCKATGEAVYTVPSSMLCISENDQLILSSLGPCQRTQGPELPPPDPALQDLSLTLIASPPSSPSSSGTPALPGHMSSEESGTSISLLPALSLAAPDPGQRSSSQPSPAICSAPATLTPRSPHASRTPSSPLQSCTPSLSPRSHVPSPHQALVTRPQKPSLEFKEFVGLPCKNRPPFPRTGATRGAQEPCSVWEPPKRHRDGSAFQYEYEPPCTSLCARVQAVRLPPQLMAWALHFLMDAQPGSEPTPM
Glycosylation Sites
Displaying 1 entry
Position Description PubMed ID GlyTouCan ID Source
313
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Disease
Displaying 1 entry
DO ID Disease Name Source
DOID:0070023 autosomal dominant dyskeratosis congenita 6

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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: April 6, 2026