Trait
Gap between large left and right abdominal muscles
Clinical name: Diastasis recti
A separation of the rectus abdominis muscle into right and left halves (which are normally joined at the midline at the linea alba).
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test27 genes linked to Gap between large left and right abdominal muscles
Changes in these genes cause rare conditions in which Gap between large left and right abdominal muscles 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 |
|---|---|---|
| ELMO2engulfment and cell motility 2 | Always | In 1 condition |
| GUSBglucuronidase beta | Always | In 1 condition |
| MTORmechanistic target of rapamycin kinase | Always | In 2 conditions |
| PIGQphosphatidylinositol glycan anchor biosynthesis class Q | Always | In 1 condition |
| CHAMP1chromosome alignment maintaining phosphoprotein 1 | Often (30–79%) | In 1 condition |
| COLEC10collectin subfamily member 10 | Often (30–79%) | In 2 conditions |
| COLEC11collectin subfamily member 11 | Often (30–79%) | In 2 conditions |
| DLK1delta like non-canonical Notch ligand 1 | Often (30–79%) | In 3 conditions |
| GPC3glypican 3 | Often (30–79%) | In 1 condition |
| MASP1MBL associated serine protease 1 | Often (30–79%) | In 1 condition |
| MEG3maternally expressed 3 | Often (30–79%) | In 3 conditions |
| RTL1retrotransposon Gag like 1 | Often (30–79%) | In 3 conditions |
| SHPKsedoheptulokinase | Often (30–79%) | In 1 condition |
| FOXF1forkhead box F1 | Sometimes (5–29%) | In 1 condition |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Sometimes (5–29%) | In 3 conditions |
| H19H19 imprinted maternally expressed transcript | Sometimes (5–29%) | In 1 condition |
| IGF2insulin like growth factor 2 | Sometimes (5–29%) | In 2 conditions |
| PPP2R3Cprotein phosphatase 2 regulatory subunit B''gamma | Sometimes (5–29%) | In 1 condition |
| SOX6SRY-box transcription factor 6 | Sometimes (5–29%) | In 1 condition |
| TBCKTBC1 domain containing kinase | Rarely (1–4%) | In 1 condition |
| B3GLCTbeta 3-glucosyltransferase | Not recorded | In 1 condition |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Not recorded | In 1 condition |
| CHST14carbohydrate sulfotransferase 14 | Not recorded | In 1 condition |
| EZH2enhancer of zeste 2 polycomb repressive complex 2 subunit | Not recorded | In 1 condition |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Not recorded | In 1 condition |
| KCNQ1OT1KCNQ1 opposite strand/antisense transcript 1 | Not recorded | In 1 condition |
| PORCNporcupine O-acyltransferase | 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.
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.
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