PATL1
Protein PAT1 homolog 1
Also known as: FLJ36874, Pat1b, PATL1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86TB9
- Gene
- PATL1
- Ensembl
- ENSG00000166889
- Chromosome
- 11
- Canonical length
- 770 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytoplasmic bodies
OverviewNCBI Gene
Enables poly(G) binding activity and poly(U) RNA binding activity. Involved in P-body assembly and deadenylation-dependent decapping of nuclear-transcribed mRNA. Located in CCR4-NOT complex; P-body; and cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
770 residues, UniProt reviewed canonical sequence.
>Q86TB9|PATL1
1 MFRYESLEDC PLDEDEDAFQ GLGEEDEEID QFNDDTFGSG AVDDDWQEAH ERLAELEEKL
61 PVAVNEQTGN GERDEMDLLG DHEENLAERL SKMVIENELE DPAIMRAVQT RPVLQPQPGS
121 LNSSIWDGSE VLRRIRGPLL AQEMPTVSVL EYALPQRPPQ GPEDDRDLSE RALPRRSTSP
181 IIGSPPVRAV PIGTPPKQMA VPSFTQQILC PKPVHVRPPM PPRYPAPYGE RMSPNQLCSV
241 PNSSLLGHPF PPSVPPVLSP LQRAQLLGGA QLQPGRMSPS QFARVPGFVG SPLAAMNPKL
301 LQGRVGQMLP PAPGFRAFFS APPSATPPPQ QHPPGPGPHL QNLRSQAPMF RPDTTHLHPQ
361 HRRLLHQRQQ QNRSQHRNLN GAGDRGSHRS SHQDHLRKDP YANLMLQREK DWVSKIQMMQ
421 LQSTDPYLDD FYYQNYFEKL EKLSAAEEIQ GDGPKKERTK LITPQVAKLE HAYKPVQFEG
481 SLGKLTVSSV NNPRKMIDAV VTSRSEDDET KEKQVRDKRR KTLVIIEKTY SLLLDVEDYE
541 RRYLLSLEEE RPALMDDRKH KICSMYDNLR GKLPGQERPS DDHFVQIMCI RKGKRMVARI
601 LPFLSTEQAA DILMTTARNL PFLIKKDAQD EVLPCLLSPF SLLLYHLPSV SITSLLRQLM
661 NLPQSAATPA LSNPHLTAVL QNKFGLSLLL ILLSRGEDLQ SSDPATESTQ NNQWTEVMFM
721 ATRELLRIPQ AALAKPISIP TNLVSLFSRY VDRQKLNLLE TKLQLVQGIRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PATL1 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)
- 0.53
- Highest tissue expression
- 54 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 54 nTPM
- skeletal muscle: 38 nTPM
- liver: 31 nTPM
- tongue: 31 nTPM
- tonsil: 22 nTPM
- retina: 22 nTPM
Single-cell type
- neutrophils: 193 nCPM
- neutrophil progenitors: 89 nCPM
- kupffer cells: 70 nCPM
- endometrial glandular cells: 61 nCPM
- gastric progenitor cells: 55 nCPM
- endometrial stromal cells: 54 nCPM
Immune cell
- eosinophil: 3.4 nTPM
- neutrophil: 3.4 nTPM
- non-classical monocyte: 2.9 nTPM
- intermediate monocyte: 2.8 nTPM
- gdT-cell: 2.7 nTPM
- classical monocyte: 2.4 nTPM
Brain region
- white matter: 25 nTPM
- choroid plexus: 22 nTPM
- medulla oblongata: 22 nTPM
- thalamus: 22 nTPM
- pons: 21 nTPM
- cerebellum: 21 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)
- 0.32
- gnomAD pLI
- 0.96
- gnomAD missense Z
- 2.44
- DepMap mean gene effect
- -0.07
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PATL1 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 PATL1 as an antibody target. Whether an autoantibody or antibody against PATL1 could matter depends on whether native PATL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PATL1 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 PATL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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