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Trait
Rocker bottom foot
The presence of both a prominent heel and a convex contour of the sole.
Summary
- Also called
- Rocker bottom feet, Rocker-bottom feet, Rockerbottom feet, Congenital vertical talus
Rocker bottom footHP:0001838
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Read the genes linked to Rocker bottom foot, and the rest of your genome, with one test.
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Get my Genome Test71 genes linked to Rocker bottom foot
Changes in these genes cause rare conditions in which Rocker bottom foot 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 |
|---|---|---|
| AARS1alanyl-tRNA synthetase 1 | Always | In 1 condition |
| ATPAF2ATP synthase mitochondrial F1 complex assembly factor 2 | Always | In 1 condition |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Always | In 1 condition |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Always | In 1 condition |
| MYH3myosin heavy chain 3 | Always | In 2 conditions |
| NUP188nucleoporin 188 | Always | In 1 condition |
| PSAT1phosphoserine aminotransferase 1 | Always | In 1 condition |
| SCYL2SCY1 like pseudokinase 2 | Always | In 2 conditions |
| THOC2THO complex subunit 2 | Always | In 1 condition |
| TOR1Atorsin family 1 member A | Always | In 1 condition |
| CCDC8coiled-coil domain containing 8 subunit of 3M complex | Very often (80–99%) | In 1 condition |
| CHRNGcholinergic receptor nicotinic gamma subunit | Very often (80–99%) | In 1 condition |
| CUL7cullin 7 | Very often (80–99%) | In 1 condition |
| LMNAlamin A/C | Very often (80–99%) | In 1 condition |
| OBSL1obscurin like cytoskeletal adaptor 1 | Very often (80–99%) | In 1 condition |
| EMG1EMG1 N1-specific pseudouridine methyltransferase | Often (30–79%) | In 2 conditions |
| ERCC5ERCC excision repair 5, endonuclease | Often (30–79%) | In 1 condition |
| FIG4FIG4 phosphoinositide 5-phosphatase | Often (30–79%) | In 1 condition |
| H4C9H4 clustered histone 9 | Often (30–79%) | In 1 condition |
| KIF14kinesin family member 14 | Often (30–79%) | In 1 condition |
| MAFMAF bZIP transcription factor | Often (30–79%) | In 1 condition |
| MYL11myosin light chain 11 | Often (30–79%) | In 1 condition |
| PHGDHphosphoglycerate dehydrogenase | Often (30–79%) | In 1 condition |
| PLAAphospholipase A2 activating protein | Often (30–79%) | In 2 conditions |
| PORcytochrome p450 oxidoreductase | Often (30–79%) | In 3 conditions |
| RBM10RNA binding motif protein 10 | Often (30–79%) | In 2 conditions |
| RSPRY1ring finger and SPRY domain containing 1 | Often (30–79%) | In 1 condition |
| TPM2tropomyosin 2 | Often (30–79%) | In 2 conditions |
| VAC14VAC14 component of PIKFYVE complex | Often (30–79%) | In 1 condition |
| WRNWRN RecQ like helicase | Often (30–79%) | In 1 condition |
| ADAT3adenosine deaminase tRNA specific 3 | Sometimes (5–29%) | In 1 condition |
| ARID1BAT-rich interaction domain 1B | Sometimes (5–29%) | In 1 condition |
| BAP1BRCA1 associated deubiquitinase 1 | Sometimes (5–29%) | In 1 condition |
| CLTCL1clathrin heavy chain like 1 | Sometimes (5–29%) | In 1 condition |
| COASYCoenzyme A synthase | Sometimes (5–29%) | In 1 condition |
| COL25A1collagen type XXV alpha 1 chain | Sometimes (5–29%) | In 1 condition |
| DPH5diphthamide biosynthesis 5 | Sometimes (5–29%) | In 1 condition |
| ERGIC1endoplasmic reticulum-golgi intermediate compartment 1 | Sometimes (5–29%) | In 1 condition |
| EXOC7exocyst complex component 7 | Sometimes (5–29%) | In 1 condition |
| FILIP1filamin A interacting protein 1 | Sometimes (5–29%) | In 1 condition |
Show 31 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| IPO8importin 8 | Sometimes (5–29%) | In 1 condition |
| KATNB1katanin regulatory subunit B1 | Sometimes (5–29%) | In 1 condition |
| KCNK3potassium two pore domain channel subfamily K member 3 | Sometimes (5–29%) | In 1 condition |
| MUSKmuscle associated receptor tyrosine kinase | Sometimes (5–29%) | In 1 condition |
| MYBPC1myosin binding protein C1 | Sometimes (5–29%) | In 2 conditions |
| NALCNsodium leak channel, non-selective | Sometimes (5–29%) | In 1 condition |
| NDE1nudE neurodevelopment protein 1 | Sometimes (5–29%) | In 1 condition |
| NUP88nucleoporin 88 | Sometimes (5–29%) | In 1 condition |
| OTUD5OTU deubiquitinase 5 | Sometimes (5–29%) | In 1 condition |
| PUF60poly(U) binding splicing factor 60 | Sometimes (5–29%) | In 1 condition |
| RBMXRNA binding motif protein X-linked | Sometimes (5–29%) | In 1 condition |
| RELNreelin | Sometimes (5–29%) | In 1 condition |
| SAMD9sterile alpha motif domain containing 9 | Sometimes (5–29%) | In 1 condition |
| SLC29A3solute carrier family 29 member 3 | Sometimes (5–29%) | In 1 condition |
| SLC2A10solute carrier family 2 member 10 | Sometimes (5–29%) | In 1 condition |
| SMPD4sphingomyelin phosphodiesterase 4 | Sometimes (5–29%) | In 1 condition |
| SOX4SRY-box transcription factor 4 | Sometimes (5–29%) | In 1 condition |
| TBC1D32TBC1 domain family member 32 | Sometimes (5–29%) | In 1 condition |
| TELO2telomere maintenance 2 | Sometimes (5–29%) | In 1 condition |
| TNNI2troponin I2, fast skeletal type | Sometimes (5–29%) | In 2 conditions |
| TNNT3troponin T3, fast skeletal type | Sometimes (5–29%) | In 1 condition |
| DOK7docking protein 7 | Not recorded | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Not recorded | In 1 condition |
| FGFR2fibroblast growth factor receptor 2 | Not recorded | In 1 condition |
| FLNAfilamin A | Not recorded | In 1 condition |
| GLE1GLE1 RNA export mediator | Not recorded | In 1 condition |
| HOXD10homeobox D10 | Not recorded | In 1 condition |
| MAGEL2MAGE family member L2 | Not recorded | In 1 condition |
| PEX1peroxisomal biogenesis factor 1 | Not recorded | In 1 condition |
| ZC4H2zinc finger C4H2-type containing | Not recorded | In 1 condition |
| ZMPSTE24zinc metallopeptidase STE24 | 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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