PYGO1
Pygopus homolog 1
Also known as: PYGO1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y3Y4
- Gene
- PYGO1
- Ensembl
- ENSG00000171016
- Chromosome
- 15
- Canonical length
- 419 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Enables methylated histone binding activity. Predicted to be involved in kidney development and spermatid nucleus differentiation. Predicted to act upstream of or within several processes, including hematopoietic progenitor cell differentiation; positive regulation of transcription by RNA polymerase II; and spermatid development. Predicted to be located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
419 residues, UniProt reviewed canonical sequence.
>Q9Y3Y4|PYGO1
1 MPAENSPAPA YKVSSHGGDS GLDGLGGPGV QLGSPDKKKR KANTQGPSFP PLSEYAPPPN
61 PNSDHLVAAN PFDDNYNTIS YKPLPSSNPY LGPGYPGFGG YSTFRMPPHV PPRMSSPYCG
121 PYSLRNQPHP FPQNPLGMGF NRPHAFNFGP HDNSSFGNPS YNNALSQNVN MPNQHFRQNP
181 AENFSQIPPQ NASQVSNPDL ASNFVPGNNS NFTSPLESNH SFIPPPNTFG QAKAPPPKQD
241 FTQGATKNTN QNSSAHPPHL NMDDTVNQSN IELKNVNRNN AVNQENSRSS STEATNNNPA
301 NGTQNKPRQP RGAADACTTE KSNKSSLHPN RHGHSSSDPV YPCGICTNEV NDDQDAILCE
361 ASCQKWFHRI CTGMTETAYG LLTAEASAVW GCDTCMADKD VQLMRTRETF GPSAVGSDALocalizationUniProt · AlphaFold · HPA
Whether an antibody against PYGO1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.67
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- parathyroid gland: 12 nTPM
- skeletal muscle: 11 nTPM
- tongue: 8.4 nTPM
- thyroid gland: 6.4 nTPM
- endometrium: 5.2 nTPM
- ovary: 5.2 nTPM
Single-cell type
- myonuclei: 142 nCPM
- somatotrophs: 122 nCPM
- oligodendrocyte progenitor cells: 94 nCPM
- gonadotrophs: 79 nCPM
- pituitary stem cells: 56 nCPM
- pituicytes/fscs: 54 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 19 nTPM
- hypothalamus: 14 nTPM
- midbrain: 13 nTPM
- medulla oblongata: 11 nTPM
- spinal cord: 10 nTPM
- pons: 9.8 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.23
- gnomAD pLI
- 0.99
- gnomAD missense Z
- -0.11
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- canonical Wnt signaling pathway
- hematopoietic progenitor cell differentiation
- kidney development
- positive regulation of transcription by RNA polymerase II
- protein localization to nucleus
- spermatid nucleus differentiation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PYGO1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PYGO1 as an antibody target. Whether an autoantibody or antibody against PYGO1 could matter depends on whether native PYGO1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PYGO1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label PYGO1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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