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Trait
Abdominal bloating
Clinical name: Abdominal distention
Distention of the abdomen.
Summary
- Also called
- Abdominal swelling, Belly bloating, Bloating, Abdominal distension, Distended abdomen
- Body system
- Abnormality of the digestive system
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This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/abdominal-distention.json"
page <- fromJSON(url)
page$trait$nameAbdominal bloatingHP:0003270
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Read the genes linked to Abdominal bloating, and the rest of your genome, with one test.
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Get my Genome Test135 genes linked to Abdominal bloating
Changes in these genes cause rare conditions in which Abdominal bloating is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ATP7BATPase copper transporting beta | Always | In 1 condition |
| CLMPCXADR like cell adhesion molecule | Always | In 1 condition |
| DHCR77-dehydrocholesterol reductase | Always | In 1 condition |
| LIPAlipase A, lysosomal acid type | Always | In 2 conditions |
| LMOD1leiomodin 1 | Always | In 2 conditions |
| MYH11myosin heavy chain 11 | Always | In 2 conditions |
| MYL9myosin light chain 9 | Always | In 1 condition |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Always | In 1 condition |
| PLD4phospholipase D family member 4 | Always | In 1 condition |
| POLG2DNA polymerase gamma 2, accessory subunit | Always | In 1 condition |
| SLC9A3solute carrier family 9 member A3 | Always | In 1 condition |
| STX3syntaxin 3 | Always | In 2 conditions |
| TRMUtRNA mitochondrial 2-thiouridylase | Always | In 1 condition |
| TXNDC15thioredoxin domain containing 15 | Always | In 1 condition |
| ACTG2actin gamma 2, smooth muscle | Very often (80–99%) | In 3 conditions |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Very often (80–99%) | In 2 conditions |
| BRCA1BRCA1 DNA repair associated | Very often (80–99%) | In 1 condition |
| COL2A1collagen type II alpha 1 chain | Very often (80–99%) | In 1 condition |
| DYNC2H1dynein cytoplasmic 2 heavy chain 1 | Very often (80–99%) | In 1 condition |
| DYNC2I1dynein 2 intermediate chain 1 | Very often (80–99%) | In 1 condition |
| DYNC2I2dynein 2 intermediate chain 2 | Very often (80–99%) | In 1 condition |
| EWSR1EWS RNA binding protein 1 | Very often (80–99%) | In 1 condition |
| FOXE1forkhead box E1 | Very often (80–99%) | In 1 condition |
| FSHRfollicle stimulating hormone receptor | Very often (80–99%) | In 1 condition |
| IFT80intraflagellar transport 80 | Very often (80–99%) | In 1 condition |
| ITGA6integrin subunit alpha 6 | Very often (80–99%) | In 1 condition |
| ITGB4integrin subunit beta 4 | Very often (80–99%) | In 2 conditions |
| LIG3DNA ligase 3 | Very often (80–99%) | In 1 condition |
| LRP5LDL receptor related protein 5 | Very often (80–99%) | In 1 condition |
| MYLKmyosin light chain kinase | Very often (80–99%) | In 1 condition |
| NKX2-1NK2 homeobox 1 | Very often (80–99%) | In 1 condition |
| NKX2-5NK2 homeobox 5 | Very often (80–99%) | In 2 conditions |
| PAX8paired box 8 | Very often (80–99%) | In 4 conditions |
| POLGDNA polymerase gamma, catalytic subunit | Very often (80–99%) | In 2 conditions |
| PRKCSHPRKCSH beta subunit of glucosidase II | Very often (80–99%) | In 2 conditions |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Very often (80–99%) | In 1 condition |
| SEC63SEC63 protein translocation regulator | Very often (80–99%) | In 1 condition |
| SLC26A4solute carrier family 26 member 4 | Very often (80–99%) | In 2 conditions |
| TRIP11thyroid hormone receptor interactor 11 | Very often (80–99%) | In 1 condition |
| TSHRthyroid stimulating hormone receptor | Very often (80–99%) | In 2 conditions |
Show 95 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| TYMPthymidine phosphorylase | Very often (80–99%) | In 1 condition |
| WDR35WD repeat domain 35 | Very often (80–99%) | In 1 condition |
| WT1WT1 transcription factor | Very often (80–99%) | In 1 condition |
| ABCD1ATP binding cassette subfamily D member 1 | Often (30–79%) | In 1 condition |
| ALKALK receptor tyrosine kinase | Often (30–79%) | In 1 condition |
| ANO1anoctamin 1 | Often (30–79%) | In 1 condition |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Often (30–79%) | In 1 condition |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Often (30–79%) | In 1 condition |
| ATP7AATPase copper transporting alpha | Often (30–79%) | In 1 condition |
| C2orf69chromosome 2 open reading frame 69 | Often (30–79%) | In 1 condition |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Often (30–79%) | In 1 condition |
| COX11cytochrome c oxidase copper chaperone COX11 | Often (30–79%) | In 1 condition |
| DYMdymeclin | Often (30–79%) | In 1 condition |
| ECE1endothelin converting enzyme 1 | Often (30–79%) | In 1 condition |
| EDN3endothelin 3 | Often (30–79%) | In 1 condition |
| EDNRBendothelin receptor type B | Often (30–79%) | In 1 condition |
| EPCAMepithelial cell adhesion molecule | Often (30–79%) | In 1 condition |
| ERBB2erb-b2 receptor tyrosine kinase 2 | Often (30–79%) | In 1 condition |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Often (30–79%) | In 1 condition |
| FOCADfocadhesin | Often (30–79%) | In 1 condition |
| GDNFglial cell derived neurotrophic factor | Often (30–79%) | In 1 condition |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Often (30–79%) | In 1 condition |
| INSRinsulin receptor | Often (30–79%) | In 2 conditions |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | Often (30–79%) | In 1 condition |
| LMO1LIM domain only 1 | Often (30–79%) | In 1 condition |
| MNX1motor neuron and pancreas homeobox 1 | Often (30–79%) | In 2 conditions |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Often (30–79%) | In 1 condition |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Often (30–79%) | In 1 condition |
| MYO5Bmyosin VB | Often (30–79%) | In 1 condition |
| NRTNneurturin | Often (30–79%) | In 1 condition |
| PHOX2Bpaired like homeobox 2B | Often (30–79%) | In 1 condition |
| PI4KAphosphatidylinositol 4-kinase alpha | Often (30–79%) | In 1 condition |
| PLECplectin | Often (30–79%) | In 1 condition |
| RETret proto-oncogene | Often (30–79%) | In 2 conditions |
| RHOBTB2Rho related BTB domain containing 2 | Often (30–79%) | In 1 condition |
| SAR1Bsecretion associated Ras related GTPase 1B | Often (30–79%) | In 1 condition |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Often (30–79%) | In 1 condition |
| SEMA3Csemaphorin 3C | Often (30–79%) | In 1 condition |
| SEMA3Dsemaphorin 3D | Often (30–79%) | In 1 condition |
| SLC1A3solute carrier family 1 member 3 | Often (30–79%) | In 1 condition |
| SLC2A1solute carrier family 2 member 1 | Often (30–79%) | In 1 condition |
| SLC2A2solute carrier family 2 member 2 | Often (30–79%) | In 2 conditions |
| SLC5A1solute carrier family 5 member 1 | Often (30–79%) | In 2 conditions |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | Often (30–79%) | In 1 condition |
| SMOsmoothened, frizzled class receptor | Often (30–79%) | In 1 condition |
| SMPD1sphingomyelin phosphodiesterase 1 | Often (30–79%) | In 2 conditions |
| SREBF1sterol regulatory element binding transcription factor 1 | Often (30–79%) | In 1 condition |
| TCTN2tectonic family member 2 | Often (30–79%) | In 1 condition |
| TFAMtranscription factor A, mitochondrial | Often (30–79%) | In 1 condition |
| TTC7Atetratricopeptide repeat domain 7A | Often (30–79%) | In 1 condition |
| AGR2anterior gradient 2, protein disulphide isomerase family member | Sometimes (5–29%) | In 1 condition |
| ALADaminolevulinate dehydratase | Sometimes (5–29%) | In 1 condition |
| ALDOBaldolase, fructose-bisphosphate B | Sometimes (5–29%) | In 1 condition |
| ARSAarylsulfatase A | Sometimes (5–29%) | In 3 conditions |
| CHD8chromodomain helicase DNA binding protein 8 | Sometimes (5–29%) | In 1 condition |
| DDRGK1DDRGK domain containing 1 | Sometimes (5–29%) | In 2 conditions |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Sometimes (5–29%) | In 1 condition |
| HMBShydroxymethylbilane synthase | Sometimes (5–29%) | In 1 condition |
| IFT56intraflagellar transport 56 | Sometimes (5–29%) | In 1 condition |
| IL12Ainterleukin 12A | Sometimes (5–29%) | In 1 condition |
| IL12RB1interleukin 12 receptor subunit beta 1 | Sometimes (5–29%) | In 1 condition |
| IPO8importin 8 | Sometimes (5–29%) | In 1 condition |
| IRAK1interleukin 1 receptor associated kinase 1 | Sometimes (5–29%) | In 1 condition |
| IRF5interferon regulatory factor 5 | Sometimes (5–29%) | In 1 condition |
| MMEL1membrane metalloendopeptidase like 1 | Sometimes (5–29%) | In 1 condition |
| MPV17mitochondrial inner membrane protein MPV17 | Sometimes (5–29%) | In 1 condition |
| POU2AF1POU class 2 homeobox associating factor 1 | Sometimes (5–29%) | In 1 condition |
| PSAPprosaposin | Sometimes (5–29%) | In 3 conditions |
| PYGLglycogen phosphorylase L | Sometimes (5–29%) | In 1 condition |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| SIsucrase-isomaltase | Sometimes (5–29%) | In 1 condition |
| SPIBSpi-B transcription factor | Sometimes (5–29%) | In 1 condition |
| SPP1secreted phosphoprotein 1 | Sometimes (5–29%) | In 1 condition |
| STAT4signal transducer and activator of transcription 4 | Sometimes (5–29%) | In 1 condition |
| TNFSF15TNF superfamily member 15 | Sometimes (5–29%) | In 1 condition |
| TNPO3transportin 3 | Sometimes (5–29%) | In 1 condition |
| TREHtrehalase | Sometimes (5–29%) | In 1 condition |
| ANK1ankyrin 1 | Rarely (1–4%) | In 1 condition |
| EPB42erythrocyte membrane protein band 4.2 | Rarely (1–4%) | In 1 condition |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Rarely (1–4%) | In 1 condition |
| SPTA1spectrin alpha, erythrocytic 1 | Rarely (1–4%) | In 1 condition |
| SPTBspectrin beta, erythrocytic | Rarely (1–4%) | In 1 condition |
| DLL3delta like canonical Notch ligand 3 | Not recorded | In 1 condition |
| EPHB4EPH receptor B4 | Not recorded | In 1 condition |
| FLNAfilamin A | Not recorded | In 1 condition |
| FREM2FRAS1 related extracellular matrix 2 | Not recorded | In 1 condition |
| HLA-DQA1major histocompatibility complex, class II, DQ alpha 1 | Not recorded | In 1 condition |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Not recorded | In 1 condition |
| KRT18keratin 18 | Not recorded | In 1 condition |
| MESP2mesoderm posterior bHLH transcription factor 2 | Not recorded | In 1 condition |
| NPHS1NPHS1 adhesion molecule, nephrin | Not recorded | In 1 condition |
| SLC26A2solute carrier family 26 member 2 | Not recorded | In 1 condition |
| SLC26A3solute carrier family 26 member 3 | Not recorded | In 1 condition |
| SPINT2serine peptidase inhibitor, Kunitz type 2 | Not recorded | In 1 condition |
| ZEB2zinc finger E-box binding homeobox 2 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Narrower traits
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Who We HelpOur ScienceProductsOutcomes
Log InAskGet Startedfrom $449
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks