TRMT9B
geneOn this page
Also known as FLJ36980TRM9LhTRM9L
Summary
TRMT9B (tRNA methyltransferase 9B (putative), HGNC:26725) is a protein-coding gene on chromosome 8p22, encoding Probable tRNA methyltransferase 9B (Q9P272). May modify wobble uridines in specific arginine and glutamic acid tRNAs.
Enables tRNA methyltransferase activity. Predicted to be involved in tRNA methylation and tRNA wobble uridine modification. Predicted to be active in cytoplasm and nucleus.
Source: NCBI Gene 57604 — RefSeq curated summary.
At a glance
- GWAS associations: 4
- Clinical variants (ClinVar): 134 total
- MANE Select transcript:
NM_020844
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:26725 |
| Approved symbol | TRMT9B |
| Name | tRNA methyltransferase 9B (putative) |
| Location | 8p22 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | FLJ36980, TRM9L, hTRM9L |
| Ensembl gene | ENSG00000250305 |
| Ensembl biotype | protein_coding |
| OMIM | 615666 |
| Entrez | 57604 |
Gene structure
Transcript identifiers
Ensembl transcripts: 13 — 10 protein_coding, 2 retained_intron, 1 protein_coding_CDS_not_defined
ENST00000400069, ENST00000447063, ENST00000524591, ENST00000525249, ENST00000528335, ENST00000528753, ENST00000529706, ENST00000529978, ENST00000532376, ENST00000855797, ENST00000966194, ENST00000966195, ENST00000966196
RefSeq mRNA: 2 — MANE Select: NM_020844
NM_001099677, NM_020844
CCDS: CCDS47808
Canonical transcript exons
ENST00000524591 — 5 exons
| Exon | Start | End |
|---|---|---|
| ENSE00002147239 | 12945673 | 12945966 |
| ENSE00002193210 | 13021008 | 13029777 |
| ENSE00002294472 | 12990834 | 12991031 |
| ENSE00002300522 | 13006202 | 13006356 |
| ENSE00002305905 | 13012684 | 13012857 |
Expression profiles
Bgee: expression breadth ubiquitous, 226 present calls, max score 96.23.
FANTOM5 (CAGE): breadth broad, TPM avg 5.4941 / max 588.0670, expressed in 692 samples.
FANTOM5 promoters (25 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 87468 | 1.6210 | 532 |
| 87471 | 0.8445 | 181 |
| 87466 | 0.4312 | 161 |
| 87480 | 0.3564 | 80 |
| 87460 | 0.3391 | 60 |
| 87470 | 0.2680 | 84 |
| 87479 | 0.2551 | 69 |
| 87474 | 0.2413 | 104 |
| 87472 | 0.2384 | 50 |
| 87473 | 0.1426 | 30 |
Top tissues by expression
278 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| cerebellar vermis | UBERON:0004720 | 96.23 | gold quality |
| cerebellar cortex | UBERON:0002129 | 95.98 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 95.92 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 95.45 | gold quality |
| right lobe of thyroid gland | UBERON:0001119 | 95.42 | gold quality |
| cerebellum | UBERON:0002037 | 95.39 | gold quality |
| left lobe of thyroid gland | UBERON:0001120 | 95.21 | gold quality |
| thyroid gland | UBERON:0002046 | 94.94 | gold quality |
| endothelial cell | CL:0000115 | 89.32 | gold quality |
| pons | UBERON:0000988 | 89.29 | gold quality |
| Brodmann (1909) area 23 | UBERON:0013554 | 89.29 | gold quality |
| buccal mucosa cell | CL:0002336 | 89.14 | gold quality |
| middle temporal gyrus | UBERON:0002771 | 87.63 | gold quality |
| cortical plate | UBERON:0005343 | 87.25 | gold quality |
| primary visual cortex | UBERON:0002436 | 87.22 | gold quality |
| postcentral gyrus | UBERON:0002581 | 87.16 | gold quality |
| right uterine tube | UBERON:0001302 | 86.80 | gold quality |
| parietal lobe | UBERON:0001872 | 84.67 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 84.08 | gold quality |
| occipital lobe | UBERON:0002021 | 83.87 | gold quality |
| right atrium auricular region | UBERON:0006631 | 82.84 | gold quality |
| mucosa of paranasal sinus | UBERON:0005030 | 82.53 | gold quality |
| cardiac atrium | UBERON:0002081 | 81.08 | gold quality |
| ganglionic eminence | UBERON:0004023 | 81.01 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 80.92 | gold quality |
| metanephros cortex | UBERON:0010533 | 80.82 | gold quality |
| heart | UBERON:0000948 | 79.46 | gold quality |
| heart left ventricle | UBERON:0002084 | 79.36 | gold quality |
| entorhinal cortex | UBERON:0002728 | 79.22 | gold quality |
| cardiac ventricle | UBERON:0002082 | 79.17 | gold quality |
Single-cell (SCXA)
Detected in 4 experiment(s), a significant marker in 2.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-GEOD-75367 | yes | 104.58 |
| E-GEOD-93593 | yes | 7.82 |
| E-GEOD-125970 | no | 3.53 |
| E-ANND-3 | no | 2.43 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
291 targeting TRMT9B, 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-4795-3P | 100.00 | 74.62 | 4024 |
| HSA-MIR-126-5P | 100.00 | 72.71 | 3180 |
| HSA-MIR-5011-5P | 100.00 | 83.46 | 5820 |
| HSA-MIR-190A-3P | 100.00 | 80.35 | 5520 |
| HSA-MIR-200B-3P | 100.00 | 73.31 | 2693 |
| HSA-MIR-200C-3P | 100.00 | 73.35 | 2685 |
| HSA-MIR-429 | 100.00 | 73.44 | 2698 |
| HSA-MIR-3613-3P | 100.00 | 76.36 | 7965 |
| HSA-MIR-5692A | 100.00 | 74.40 | 6850 |
| HSA-MIR-340-5P | 100.00 | 72.50 | 4437 |
| HSA-MIR-3646 | 100.00 | 73.56 | 5283 |
| HSA-MIR-4533 | 100.00 | 69.48 | 2758 |
| HSA-MIR-1277-5P | 100.00 | 73.95 | 5056 |
| HSA-MIR-6867-5P | 100.00 | 82.21 | 3464 |
| HSA-MIR-1252-5P | 100.00 | 69.80 | 2774 |
| HSA-LET-7A-3P | 100.00 | 74.03 | 3932 |
| HSA-LET-7B-3P | 100.00 | 74.08 | 3913 |
| HSA-LET-7F-1-3P | 100.00 | 74.02 | 3928 |
| HSA-MIR-98-3P | 100.00 | 74.08 | 3907 |
| HSA-MIR-3163 | 100.00 | 77.23 | 8605 |
| HSA-MIR-4668-3P | 100.00 | 68.74 | 2635 |
| HSA-MIR-6833-3P | 100.00 | 70.63 | 3197 |
| HSA-MIR-4768-5P | 100.00 | 69.49 | 2861 |
| HSA-MIR-371B-5P | 99.99 | 75.34 | 4759 |
| HSA-MIR-4531 | 99.99 | 69.70 | 3181 |
| HSA-MIR-548C-3P | 99.99 | 74.01 | 7587 |
| HSA-MIR-511-3P | 99.99 | 68.85 | 1467 |
| HSA-MIR-3662 | 99.99 | 73.82 | 5684 |
| HSA-MIR-186-5P | 99.99 | 70.83 | 3707 |
| HSA-MIR-373-5P | 99.98 | 75.36 | 4753 |
Literature-anchored findings (GeneRIF, showing 2)
- Study links hTRM9L and tRNA modifications to inhibition of tumour growth via LIN9 and HIF1-alpha-dependent mechanisms. (PMID:23381944)
- Over-expression of KIAA1456 inhibits the proliferation of HO8910PM ovarian cancer cells and arrests the cell cycle in G1 phase. (PMID:27609572)
Cross-species orthologs
2 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Trmt9b | ENSMUSG00000039620 |
| rattus_norvegicus | Trmt9b | ENSRNOG00000011253 |
Paralogs (2): ALKBH8 (ENSG00000137760), ALKBH6 (ENSG00000239382)
Protein
Protein identifiers
Probable tRNA methyltransferase 9B — Q9P272 (reviewed: Q9P272)
Alternative names: Probable tRNA methyltransferase 9-like protein
All UniProt accessions (4): A0AAA9YHN1, E9PK20, Q9P272, F6XBY7
UniProt curated annotations — full annotation on UniProt →
Function. May modify wobble uridines in specific arginine and glutamic acid tRNAs. Acts as a tumor suppressor by promoting the expression of LIN9.
Tissue specificity. Down-regulated in breast, bladder, colorectal, cervix and testicular carcinomas.
Similarity. Belongs to the methyltransferase superfamily.
Isoforms (2)
| UniProt ID | Names | Canonical? |
|---|---|---|
| Q9P272-1 | 1 | yes |
| Q9P272-3 | 2 |
RefSeq proteins (2): NP_001093147, NP_065895* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR013216 | Methyltransf_11 | Domain |
| IPR029063 | SAM-dependent_MTases_sf | Homologous_superfamily |
| IPR051422 | AlkB_tRNA_MeTrf/Diox | Family |
Pfam: PF08241
UniProt features (12 total): sequence variant 8, splice variant 2, chain 1, modified residue 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q9P272-F1 | 62.21 | 0.39 |
Functional residue map
Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.
Post-translational modifications (1): 214
Function
Pathways and Gene Ontology
Reactome pathways
1 pathways
| ID | Pathway |
|---|---|
| R-HSA-6782315 | tRNA modification in the nucleus and cytosol |
MSigDB gene sets: 127 (showing top):
GOBP_TRNA_METABOLIC_PROCESS, GOBP_RNA_METHYLATION, GOBP_RNA_MODIFICATION, GRE_C, SCHAEFFER_PROSTATE_DEVELOPMENT_48HR_UP, GOBP_TRNA_METHYLATION, SCHAEFFER_SOX9_TARGETS_IN_PROSTATE_DEVELOPMENT_UP, AACTTT_UNKNOWN, RFX1_02, GOBP_METHYLATION, RIGGI_EWING_SARCOMA_PROGENITOR_UP, CAGCCTC_MIR4855P, GOBP_TRNA_PROCESSING, REACTOME_METABOLISM_OF_RNA, GOBP_TRNA_MODIFICATION
GO Biological Process (5): tRNA wobble uridine modification (GO:0002098), tRNA modification (GO:0006400), tRNA methylation (GO:0030488), tRNA processing (GO:0008033), methylation (GO:0032259)
GO Molecular Function (6): tRNA binding (GO:0000049), tRNA methyltransferase activity (GO:0008175), S-adenosylmethionine-dependent methyltransferase activity (GO:0008757), tRNA (5-carboxymethyluridine(34)-5-O)-methyltransferase activity (GO:0106335), methyltransferase activity (GO:0008168), transferase activity (GO:0016740)
GO Cellular Component (2): nucleus (GO:0005634), cytoplasm (GO:0005737)
Reactome top-level categories
Rollup of top-1 pathways:
| Category | Pathways |
|---|---|
| tRNA processing | 1 |
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| tRNA wobble base modification | 1 |
| tRNA processing | 1 |
| RNA modification | 1 |
| RNA methylation | 1 |
| tRNA modification | 1 |
| RNA processing | 1 |
| tRNA metabolic process | 1 |
| metabolic process | 1 |
| RNA binding | 1 |
| RNA methyltransferase activity | 1 |
| catalytic activity, acting on a tRNA | 1 |
| methyltransferase activity | 1 |
| tRNA (uridine) methyltransferase activity | 1 |
| transferase activity, transferring one-carbon groups | 1 |
| catalytic activity | 1 |
| intracellular membrane-bounded organelle | 1 |
| intracellular anatomical structure | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
1164 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| TRMT9B | TRMT112 | Q9UI30 | 690 |
| TRMT9B | TRMT11 | Q7Z4G4 | 607 |
| TRMT9B | CTU1 | Q7Z7A3 | 607 |
| TRMT9B | ELP3 | Q9H9T3 | 606 |
| TRMT9B | TYW2 | Q53H54 | 550 |
| TRMT9B | NSUN2 | Q08J23 | 516 |
| TRMT9B | ALKBH1 | Q13686 | 510 |
| TRMT9B | LIN9 | Q5TKA1 | 486 |
| TRMT9B | TRMT13 | Q9NUP7 | 482 |
| TRMT9B | OR10H2 | O60403 | 474 |
| TRMT9B | FTSJ1 | Q9UET6 | 448 |
| TRMT9B | URM1 | Q9BTM9 | 435 |
| TRMT9B | C8orf48 | Q96LL4 | 434 |
| TRMT9B | LONRF1 | Q17RB8 | 432 |
| TRMT9B | PURG | Q9UJV8 | 414 |
IntAct
3 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| TRMT9B | RPS6KA3 | psi-mi:“MI:0914”(association) | 0.350 |
| TRMT9B | RUFY3 | psi-mi:“MI:0914”(association) | 0.350 |
BioGRID (10): TTC19 (Affinity Capture-MS), ZDHHC17 (Affinity Capture-MS), RUFY3 (Affinity Capture-MS), RPS6KA3 (Affinity Capture-MS), RPS6KA3 (Affinity Capture-MS), RUFY3 (Affinity Capture-MS), KIAA1456 (Affinity Capture-RNA), C9orf156 (Affinity Capture-MS), RUFY3 (Affinity Capture-MS), KIAA1456 (Affinity Capture-RNA)
ESM2 similar proteins: A2AUU0, A3KMI0, E7F654, F1MAB7, P33279, P59114, Q08DH3, Q0P5B2, Q13686, Q28H30, Q3T131, Q3T9Z9, Q49AR2, Q4R8E0, Q5R5W9, Q5R6T6, Q5U2S3, Q5ZLL7, Q62240, Q63185, Q6DTM3, Q6NXH8, Q6NZP1, Q6P1Q9, Q6PAE6, Q6PD74, Q6ZUJ8, Q7SZF1, Q7TNN8, Q7Z3E5, Q8BGC1, Q8BMD7, Q8BMK1, Q8CHK4, Q8K3E5, Q8N6Q8, Q8TE76, Q8W5R2, Q92993, Q96IZ6
Diamond homologs: A0A075D5I4, A0A075D654, A0A075D657, A0A075D6M1, A0A0E0SMA3, A0A1D6NER6, A0A8X8M4T9, A0A8X8M4W6, A0A8X8M501, A0A8X8M505, A1RGE6, A4Y9Y4, A5U866, A9L1I5, B8E5Q5, C3SBU5, C8YTM5, H2E7T7, P0A9H7, P0A9H8, P31049, P46326, P9WPB6, P9WPB7, Q08DH3, Q108P1, Q22993, Q24W96, Q31P90, Q39227, Q4W9V1, Q5N4X9, Q6C2D9, Q6CYB3, Q6ZIK0, Q72HI4, Q7NZ91, Q80WQ4, Q875K1, Q8KZ94
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
134 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 111 |
| Likely benign | 6 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
1485 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 8:12945966:GGTA:G | donor_loss | 0.9900 |
| 8:12988304:A:G | donor_gain | 0.9900 |
| 8:12990830:ATAGG:A | acceptor_loss | 0.9900 |
| 8:12990831:TA:T | acceptor_loss | 0.9900 |
| 8:12990832:A:AC | acceptor_loss | 0.9900 |
| 8:12990832:AG:A | acceptor_gain | 0.9900 |
| 8:12990833:GG:G | acceptor_gain | 0.9900 |
| 8:13006353:ATAGG:A | donor_loss | 0.9900 |
| 8:13006354:TAGGT:T | donor_loss | 0.9900 |
| 8:13006355:AG:A | donor_loss | 0.9900 |
| 8:13006356:G:T | donor_loss | 0.9900 |
| 8:13006357:G:A | donor_loss | 0.9900 |
| 8:13006640:GCAA:G | donor_gain | 0.9900 |
| 8:13006641:C:T | donor_gain | 0.9900 |
| 8:13012678:TTATA:T | acceptor_loss | 0.9900 |
| 8:13012679:TATA:T | acceptor_loss | 0.9900 |
| 8:13012680:ATAG:A | acceptor_loss | 0.9900 |
| 8:13012681:TA:T | acceptor_loss | 0.9900 |
| 8:13012682:A:AC | acceptor_loss | 0.9900 |
| 8:13012683:G:A | acceptor_loss | 0.9900 |
| 8:13012683:GGTT:G | acceptor_gain | 0.9900 |
| 8:13021006:A:AG | acceptor_gain | 0.9900 |
| 8:13021007:G:GG | acceptor_gain | 0.9900 |
| 8:12963934:A:AG | donor_gain | 0.9800 |
| 8:12977376:G:GT | donor_gain | 0.9800 |
| 8:12990828:T:A | acceptor_gain | 0.9800 |
| 8:13006200:AGGAT:A | acceptor_gain | 0.9800 |
| 8:13006201:GGATG:G | acceptor_gain | 0.9800 |
| 8:13006644:G:GG | donor_gain | 0.9800 |
| 8:13021007:GTC:G | acceptor_gain | 0.9800 |
AlphaMissense
3029 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 8:13021103:T:A | W142R | 0.999 |
| 8:13021103:T:C | W142R | 0.999 |
| 8:13021039:A:C | R120S | 0.998 |
| 8:13021039:A:T | R120S | 0.998 |
| 8:13021105:G:C | W142C | 0.998 |
| 8:13021105:G:T | W142C | 0.998 |
| 8:13006296:T:A | W32R | 0.997 |
| 8:13006296:T:C | W32R | 0.997 |
| 8:13006315:T:C | F38S | 0.997 |
| 8:13006348:C:A | A49D | 0.997 |
| 8:13012848:T:C | S107P | 0.997 |
| 8:13021011:T:A | I111K | 0.997 |
| 8:13021016:C:G | H113D | 0.997 |
| 8:13021038:G:C | R120T | 0.997 |
| 8:13021922:T:C | F415L | 0.997 |
| 8:13021923:T:C | F415S | 0.997 |
| 8:13021924:T:A | F415L | 0.997 |
| 8:13021924:T:G | F415L | 0.997 |
| 8:13006229:G:C | E9D | 0.996 |
| 8:13006229:G:T | E9D | 0.996 |
| 8:13006314:T:C | F38L | 0.996 |
| 8:13006316:C:A | F38L | 0.996 |
| 8:13006316:C:G | F38L | 0.996 |
| 8:13021011:T:G | I111R | 0.996 |
| 8:13021013:C:G | H112D | 0.996 |
| 8:13021018:T:A | H113Q | 0.996 |
| 8:13021018:T:G | H113Q | 0.996 |
| 8:13021916:C:G | H413D | 0.996 |
| 8:13012684:G:A | G52D | 0.995 |
| 8:13012849:C:T | S107F | 0.995 |
dbSNP variants (sampled 300 via entrez): RS1000039370 (8:12986967 T>C,G), RS1000041825 (8:13010522 C>G,T), RS1000057903 (8:12986150 C>G), RS1000108633 (8:12983455 A>G), RS1000151298 (8:12957793 C>A), RS1000169668 (8:13008651 C>G), RS1000170611 (8:12990522 T>G), RS1000193155 (8:13018189 C>T), RS1000200713 (8:13013827 T>C,G), RS1000221864 (8:12965075 T>A,C), RS1000244713 (8:12995061 T>A), RS1000277704 (8:12952452 G>A), RS1000301550 (8:12998843 G>C), RS1000354895 (8:12982515 A>T), RS1000356234 (8:13028348 T>G)
Disease associations
OMIM: gene MIM:615666 | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
4 associations (top):
| Study | Trait | p-value |
|---|---|---|
| GCST002401_4 | Post-traumatic stress disorder | 5.000000e-06 |
| GCST002415_1 | Colorectal cancer (diet interaction) | 2.000000e-06 |
| GCST003400_24 | Type 2 diabetes | 4.000000e-06 |
| GCST004744_44 | Lung adenocarcinoma | 6.000000e-06 |
EFO canonical traits (1, from GWAS)
| EFO ID | Trait name |
|---|---|
| EFO:0008111 | diet measurement |
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
31 total (human), top 30 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Valproic Acid | affects cotreatment, increases expression | 4 |
| trichostatin A | affects cotreatment, increases expression | 2 |
| sodium arsenite | affects methylation, decreases expression | 2 |
| Benzo(a)pyrene | affects methylation, increases methylation | 2 |
| Aflatoxin B1 | decreases expression, decreases methylation | 2 |
| fluorene-9-bisphenol | increases expression | 1 |
| sotorasib | affects cotreatment, increases expression | 1 |
| bufotalin | decreases expression | 1 |
| aflatoxin B2 | decreases methylation | 1 |
| 4-nonylphenol | affects cotreatment, increases expression | 1 |
| 4-tert-octylphenol | affects cotreatment, increases expression | 1 |
| 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide | affects cotreatment, increases expression | 1 |
| abrine | decreases expression | 1 |
| dorsomorphin | increases expression, affects cotreatment | 1 |
| trametinib | affects cotreatment, increases expression | 1 |
| MT19c compound | decreases expression | 1 |
| NVP-BKM120 | affects cotreatment, increases expression | 1 |
| Acetaminophen | decreases expression | 1 |
| Arsenic | affects methylation | 1 |
| Carbamazepine | affects expression | 1 |
| Diethylhexyl Phthalate | decreases expression | 1 |
| Doxorubicin | decreases expression | 1 |
| Phthalic Acids | increases methylation | 1 |
| Thiram | decreases expression | 1 |
| Tobacco Smoke Pollution | decreases expression | 1 |
| Tretinoin | increases expression | 1 |
| Triclosan | decreases expression | 1 |
| Antirheumatic Agents | increases expression | 1 |
| Okadaic Acid | decreases expression | 1 |
| Acrylamide | decreases expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): post-traumatic stress disorder