YY1AP1
YY1-associated protein 1
Also known as: HCCA2, YAP, YY1AP, YYAP1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H869
- Gene
- YY1AP1
- Ensembl
- ENSG00000163374
- Chromosome
- 1
- Canonical length
- 796 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoli fibrillar center
OverviewNCBI Gene
Involved in cell differentiation; cell population proliferation; and regulation of cell cycle. Located in Ino80 complex; fibrillar center; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
796 residues, UniProt reviewed canonical sequence.
>Q9H869|YY1AP1
1 MEEEASRSAA ATNPGSRLTR WPPPDKREGS AVDPGKRRSL AATPSSSLPC TLIALGLRHE
61 KEANELMEDL FETFQDEMGF SNMEDDGPEE EERVAEPQAN FNTPQALRFE ELLANLLNEQ
121 HQIAKELFEQ LKMKKPSAKQ QKEVEKVKPQ CKEVHQTLIL DPAQRKRLQQ QMQQHVQLLT
181 QIHLLATCNP NLNPEASSTR ICLKELGTFA QSSIALHHQY NPKFQTLFQP CNLMGAMQLI
241 EDFSTHVSID CSPHKTVKKT ANEFPCLPKQ VAWILATSKV FMYPELLPVC SLKAKNPQDK
301 ILFTKAEDNK YLLTCKTARQ LTVRIKNLNM NRAPDNIIKF YKKTKQLPVL GKCCEEIQPH
361 QWKPPIEREE HRLPFWLKAS LPSIQEELRH MADGAREVGN MTGTTEINSD QGLEKDNSEL
421 GSETRYPLLL PKGVVLKLKP VADRFPKKAW RQKRSSVLKP LLIQPSPSLQ PSFNPGKTPA
481 QSTHSEAPPS KMVLRIPHPI QPATVLQTVP GVPPLGVSGG ESFESPAALP AMPPEARTSF
541 PLSESQTLLS SAPVPKVMMP SPASSMFRKP YVRRRPSKRR GARAFRCIKP APVIHPASVI
601 FTVPATTVKI VSLGGGCNMI QPVNAAVAQS PQTIPIATLL VNPTSFPCPL NQPLVASSVS
661 PLIVSGNSVN LPIPSTPEDK AHMNVDIACA VADGENAFQG LEPKLEPQEL SPLSATVFPK
721 VEHSPGPPPV DKQCQEGLSE NSAYRWTVVK TEEGRQALEP LPQGIQESLN NSSPGDLEEV
781 VKMEPEDATE EISGFLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against YY1AP1 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)
- 0.58
- Highest tissue expression
- 108 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 108 nTPM
- bone marrow: 73 nTPM
- testis: 71 nTPM
- tongue: 68 nTPM
- blood vessel: 56 nTPM
- colon: 54 nTPM
Single-cell type
- neutrophils: 127 nCPM
- myonuclei: 122 nCPM
- neutrophil progenitors: 110 nCPM
- esophageal apical cells: 89 nCPM
- cone photoreceptor cells: 89 nCPM
- cardiomyocytes: 86 nCPM
Immune cell
- eosinophil: 51 nTPM
- NK-cell: 45 nTPM
- basophil: 40 nTPM
- T-reg: 40 nTPM
- MAIT T-cell: 37 nTPM
- memory CD8 T-cell: 36 nTPM
Brain region
- cerebellum: 93 nTPM
- cerebral cortex: 75 nTPM
- white matter: 72 nTPM
- thalamus: 70 nTPM
- basal ganglia: 66 nTPM
- midbrain: 62 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about YY1AP1.
Disease | AllUniProt
Conditions YY1AP1 is implicated in, by any mechanism.
- Grange syndrome (GRNG) MIM:602531
Disease | GeneticClinVar
15 pathogenic / likely-pathogenic of 219 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Grange syndrome
- YY1AP1-related disorder
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)
- 1.31
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.18
- DepMap mean gene effect
- -0.09
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 19% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of YY1AP1 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 YY1AP1 as an antibody target. Whether an autoantibody or antibody against YY1AP1 could matter depends on whether native YY1AP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
YY1AP1 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 YY1AP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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