PPIAL4F
gene geneOn this page
Summary
PPIAL4F (peptidylprolyl isomerase A like 4F, HGNC:33999) is a protein-coding gene on chromosome 1q21.1, encoding Peptidyl-prolyl cis-trans isomerase A-like 4F (P0DN26). PPIases accelerate the folding of proteins.
Predicted to enable cyclosporin A binding activity and peptidyl-prolyl cis-trans isomerase activity. Predicted to be involved in protein folding. Predicted to be active in cytoplasm.
Source: NCBI Gene 728945 — RefSeq curated summary.
At a glance
- MANE Select transcript:
NM_001164262
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:33999 |
| Approved symbol | PPIAL4F |
| Name | peptidylprolyl isomerase A like 4F |
| Location | 1q21.1 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000279782 |
| Ensembl biotype | protein_coding |
| Entrez | 728945 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000581138
RefSeq mRNA: 1 — MANE Select: NM_001164262
NM_001164262
CCDS: CCDS76202
Canonical transcript exons
ENST00000369222 — 0 exons
Expression profiles
Bgee: expression breadth ubiquitous, 102 present calls, max score 85.50.
Top tissues by expression
125 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 85.50 | gold quality |
| granulocyte | CL:0000094 | 58.96 | gold quality |
| sural nerve | UBERON:0015488 | 53.77 | silver quality |
| mucosa of transverse colon | UBERON:0004991 | 53.46 | gold quality |
| right uterine tube | UBERON:0001302 | 52.26 | gold quality |
| blood | UBERON:0000178 | 48.21 | gold quality |
| cerebellum | UBERON:0002037 | 48.09 | gold quality |
| cerebellar cortex | UBERON:0002129 | 48.03 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 47.41 | gold quality |
| caudate nucleus | UBERON:0001873 | 47.38 | gold quality |
| lower esophagus mucosa | UBERON:0035834 | 46.82 | silver quality |
| nucleus accumbens | UBERON:0001882 | 45.84 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 45.02 | gold quality |
| putamen | UBERON:0001874 | 44.46 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 43.60 | gold quality |
| bone marrow | UBERON:0002371 | 43.21 | silver quality |
| spleen | UBERON:0002106 | 43.04 | gold quality |
| stromal cell of endometrium | CL:0002255 | 42.74 | silver quality |
| ventricular zone | UBERON:0003053 | 41.65 | gold quality |
| bone marrow cell | CL:0002092 | 41.43 | gold quality |
| amygdala | UBERON:0001876 | 41.25 | gold quality |
| brain | UBERON:0000955 | 41.22 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 41.19 | gold quality |
| temporal lobe | UBERON:0001871 | 41.09 | gold quality |
| Ammon’s horn | UBERON:0001954 | 40.58 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 40.41 | gold quality |
| hypothalamus | UBERON:0001898 | 39.93 | gold quality |
| leukocyte | CL:0000738 | 39.56 | silver quality |
| cerebral cortex | UBERON:0000956 | 39.15 | gold quality |
| tonsil | UBERON:0002372 | 38.98 | silver quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 1.49 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
9 targeting PPIAL4F, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-1252-5P | 100.00 | 69.80 | 2774 |
| HSA-MIR-4802-3P | 99.72 | 70.13 | 1273 |
| HSA-MIR-3202 | 99.66 | 67.70 | 2737 |
| HSA-MIR-548V | 99.29 | 69.47 | 1157 |
| HSA-MIR-6830-5P | 99.01 | 68.73 | 1884 |
| HSA-MIR-4456 | 97.50 | 64.88 | 1678 |
| HSA-MIR-3622B-5P | 94.62 | 64.58 | 835 |
| HSA-MIR-6750-5P | 93.94 | 66.68 | 797 |
| HSA-MIR-6822-5P | 93.94 | 66.34 | 812 |
Cross-species orthologs
10 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| danio_rerio | ppifa | ENSDARG00000007409 |
| danio_rerio | ppiaa | ENSDARG00000009212 |
| danio_rerio | ppiab | ENSDARG00000103994 |
| drosophila_melanogaster | Cyp40 | FBGN0036020 |
| drosophila_melanogaster | Moca-cyp | FBGN0039581 |
| caenorhabditis_elegans | WBGENE00000877 | |
| caenorhabditis_elegans | WBGENE00000878 | |
| caenorhabditis_elegans | WBGENE00000879 | |
| caenorhabditis_elegans | WBGENE00000883 | |
| caenorhabditis_elegans | WBGENE00000885 |
Paralogs (22): PPIE (ENSG00000084072), PPIL2 (ENSG00000100023), PPIF (ENSG00000108179), PPWD1 (ENSG00000113593), NKTR (ENSG00000114857), PPIL4 (ENSG00000131013), PPIL1 (ENSG00000137168), PPIG (ENSG00000138398), CWC27 (ENSG00000153015), PPIB (ENSG00000166794), PPIC (ENSG00000168938), PPID (ENSG00000171497), PPIH (ENSG00000171960), PPIL6 (ENSG00000185250), PPIA (ENSG00000196262), PPIAL4G (ENSG00000236334), PPIL3 (ENSG00000240344), PPIAL4A (ENSG00000263353), PPIAL4H (ENSG00000270339), PPIAL4E (ENSG00000271567), PPIAL4C (ENSG00000288867), PPIAL4D (ENSG00000289549)
Protein
Protein identifiers
Peptidyl-prolyl cis-trans isomerase A-like 4F — P0DN26 (reviewed: P0DN26)
All UniProt accessions (1): P0DN26
UniProt curated annotations — full annotation on UniProt →
Function. PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides.
Subcellular location. Cytoplasm.
Miscellaneous. It is one of six related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 1.
Similarity. Belongs to the cyclophilin-type PPIase family. PPIase A subfamily.
RefSeq proteins (1): NP_001157734* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR002130 | Cyclophilin-type_PPIase_dom | Domain |
| IPR020892 | Cyclophilin-type_PPIase_CS | Conserved_site |
| IPR024936 | Cyclophilin-type_PPIase | Family |
| IPR029000 | Cyclophilin-like_dom_sf | Homologous_superfamily |
Pfam: PF00160
Catalyzed reactions (Rhea), 1 shown:
- [protein]-peptidylproline (omega=180) = [protein]-peptidylproline (omega=0) (RHEA:16237)
UniProt features (2 total): chain 1, domain 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-P0DN26-F1 | 96.65 | 0.98 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 10 (showing top):
GOBP_PROTEIN_MATURATION, GOBP_PROTEIN_FOLDING, chr1q21, GOMF_CIS_TRANS_ISOMERASE_ACTIVITY, GOMF_AMIDE_BINDING, GOMF_ISOMERASE_ACTIVITY, GOMF_CYCLOSPORIN_A_BINDING, MIR548V, MIR6750_5P, MIR6822_5P
GO Biological Process (2): protein folding (GO:0006457), protein peptidyl-prolyl isomerization (GO:0000413)
GO Molecular Function (3): peptidyl-prolyl cis-trans isomerase activity (GO:0003755), cyclosporin A binding (GO:0016018), isomerase activity (GO:0016853)
GO Cellular Component (1): cytoplasm (GO:0005737)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| cellular process | 1 |
| protein maturation | 1 |
| peptidyl-proline modification | 1 |
| cis-trans isomerase activity | 1 |
| catalytic activity, acting on a protein | 1 |
| binding | 1 |
| catalytic activity | 1 |
| intracellular anatomical structure | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
0 interactions, top by confidence (×1000):
IntAct
2 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| PPIAL4F | PNN | psi-mi:“MI:0915”(physical association) | 0.400 |
ESM2 similar proteins: A0A075B759, A0A075B767, A0A0B4J2A2, F5H284, O00060, O43447, O74729, O94273, P0C1I0, P0C1I3, P0C1I5, P0C1I8, P0CP82, P0CP83, P0DN26, P0DN37, P17742, P23285, P24525, P25719, P52010, P52018, P62940, P84343, Q0P5D0, Q0ZQK7, Q0ZQK8, Q0ZQL0, Q0ZQL1, Q26516, Q26551, Q26565, Q27774, Q2TZ33, Q38867, Q38900, Q42406, Q4IPH4, Q4P6X6, Q4WCM6
Diamond homologs: A0A075B759, A0A075B767, A0A0B4J2A2, A0A0R0H9T5, A4FV72, D4AY02, F5H284, H2QII6, O00060, O49886, O93826, P0C1H7, P0C1H8, P0C1I2, P0C1I7, P0C1I8, P0C1I9, P0CP78, P0CP79, P0DN26, P0DN37, P10111, P10255, P14088, P14832, P14851, P17742, P18253, P21568, P21569, P22011, P24367, P24525, P25007, P25719, P29117, P30404, P30405, P34790, P34791
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
0 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
273 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 1:144593068:A:T | donor_gain | 0.7700 |
| 1:144593076:G:GT | donor_gain | 0.7700 |
| 1:144593164:TGAC:T | donor_gain | 0.7600 |
| 1:144593611:T:G | donor_gain | 0.7200 |
| 1:144592982:G:A | donor_gain | 0.7000 |
| 1:144593118:GGTT:G | donor_gain | 0.7000 |
| 1:144593119:GTT:G | donor_gain | 0.7000 |
| 1:144593120:TTT:T | donor_gain | 0.7000 |
| 1:144593165:GACA:G | donor_gain | 0.6900 |
| 1:144593166:ACAA:A | donor_gain | 0.6900 |
| 1:144593095:C:G | donor_gain | 0.6800 |
| 1:144592977:C:A | donor_gain | 0.6700 |
| 1:144592929:CAGGG:C | donor_gain | 0.6600 |
| 1:144593092:T:TA | donor_gain | 0.6200 |
| 1:144593297:AGT:A | donor_gain | 0.6100 |
| 1:144593093:T:A | donor_gain | 0.6000 |
| 1:144593135:G:GA | donor_gain | 0.6000 |
| 1:144593297:A:AC | donor_gain | 0.6000 |
| 1:144593312:G:A | donor_gain | 0.6000 |
| 1:144593072:A:T | donor_gain | 0.5900 |
| 1:144593090:GGT:G | donor_gain | 0.5800 |
| 1:144593303:C:CT | donor_gain | 0.5800 |
| 1:144593054:GCTC:G | donor_gain | 0.5700 |
| 1:144593091:G:T | donor_gain | 0.5700 |
| 1:144593106:G:GT | donor_gain | 0.5700 |
| 1:144593270:TCCC:T | donor_gain | 0.5700 |
| 1:144593616:T:G | donor_gain | 0.5600 |
| 1:144593089:GG:G | donor_gain | 0.5500 |
| 1:144593042:G:GT | donor_gain | 0.5400 |
| 1:144593043:A:T | donor_gain | 0.5400 |
AlphaMissense
0 scored. Top likely-pathogenic:
dbSNP variants (sampled 300 via entrez): RS1157397692 (1:144592919 G>A,T), RS1163135638 (1:144592794 G>T), RS1166096024 (1:144592718 A>G,T), RS1171183906 (1:144592551 T>A,C), RS1171451718 (1:144592650 C>A,T), RS1174199359 (1:144592610 A>T), RS1176854744 (1:144592821 G>A,T), RS1185649839 (1:144592558 CAAAAAAA>C,CA,CAA,CAAAA,CAAAAA,CAAAAAA,CAAAAAAAA,CAAAAAAAAA,CAAAAAAAAAA), RS1186159036 (1:144592558 C>A,T), RS1187281439 (1:144592431 A>C), RS1187466363 (1:144592730 T>C,G), RS1189210512 (1:144592660 G>A), RS1195550100 (1:144592300 G>A), RS1195685603 (1:144592947 T>C), RS1196882220 (1:144592739 C>T)
Disease associations
OMIM: gene `` | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
0 associations (top):
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
1 total (human), top 1 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Caffeine | decreases expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.