Trait
Short palm
Short palm.
Summary
- Also called
- Short hands, Short palms
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test120 genes linked to Short palm
Changes in these genes cause rare conditions in which Short palm 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 |
|---|---|---|
| ANKRD11ankyrin repeat domain 11 | Always | In 1 condition |
| B3GLCTbeta 3-glucosyltransferase | Always | In 1 condition |
| BRD4bromodomain containing 4 | Always | In 1 condition |
| CAMK2Gcalcium/calmodulin dependent protein kinase II gamma | Always | In 1 condition |
| DDR2discoidin domain receptor tyrosine kinase 2 | Always | In 1 condition |
| DYNC1H1dynein cytoplasmic 1 heavy chain 1 | Always | In 1 condition |
| ERI1exoribonuclease 1 | Always | In 1 condition |
| FBN1fibrillin 1 | Always | In 4 conditions |
| FGD1FYVE, RhoGEF and PH domain containing 1 | Always | In 2 conditions |
| INPPL1inositol polyphosphate phosphatase like 1 | Always | In 1 condition |
| KDM6Blysine demethylase 6B | Always | In 1 condition |
| KLHL15kelch like family member 15 | Always | In 1 condition |
| MRPS28mitochondrial ribosomal protein S28 | Always | In 1 condition |
| PPP2R3Cprotein phosphatase 2 regulatory subunit B''gamma | Always | In 1 condition |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Always | In 1 condition |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Always | In 3 conditions |
| SMAD4SMAD family member 4 | Always | In 2 conditions |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Always | In 1 condition |
| ANTXR2ANTXR cell adhesion molecule 2 | Very often (80–99%) | In 1 condition |
| BHLHA9basic helix-loop-helix family member a9 | Very often (80–99%) | In 1 condition |
| COG4component of oligomeric golgi complex 4 | Very often (80–99%) | In 1 condition |
| COL2A1collagen type II alpha 1 chain | Very often (80–99%) | In 1 condition |
| CUL4Bcullin 4B | Very often (80–99%) | In 1 condition |
| DVL1dishevelled segment polarity protein 1 | Very often (80–99%) | In 2 conditions |
| DVL3dishevelled segment polarity protein 3 | 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 |
| FGF9fibroblast growth factor 9 | Very often (80–99%) | In 1 condition |
| FZD2frizzled class receptor 2 | Very often (80–99%) | In 2 conditions |
| GDF5growth differentiation factor 5 | Very often (80–99%) | In 1 condition |
| GDF6growth differentiation factor 6 | Very often (80–99%) | In 1 condition |
| GPX4glutathione peroxidase 4 | Very often (80–99%) | In 1 condition |
| HDAC6histone deacetylase 6 | Very often (80–99%) | In 1 condition |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Very often (80–99%) | In 1 condition |
| IFT80intraflagellar transport 80 | Very often (80–99%) | In 1 condition |
| IHHIndian hedgehog signaling molecule | Very often (80–99%) | In 3 conditions |
| KAT6Blysine acetyltransferase 6B | Very often (80–99%) | In 1 condition |
| LMNAlamin A/C | Very often (80–99%) | In 1 condition |
| LTBP3latent transforming growth factor beta binding protein 3 | Very often (80–99%) | In 2 conditions |
Show 80 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| MAGEL2MAGE family member L2 | Very often (80–99%) | In 1 condition |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Very often (80–99%) | In 1 condition |
| MEGF8multiple EGF like domains 8 | Very often (80–99%) | In 1 condition |
| MKRN3makorin ring finger protein 3 | Very often (80–99%) | In 1 condition |
| NOGnoggin | Very often (80–99%) | In 1 condition |
| NPAP1nuclear pore associated protein 1 | Very often (80–99%) | In 1 condition |
| PTDSS1phosphatidylserine synthase 1 | Very often (80–99%) | In 1 condition |
| PWAR1Prader Willi/Angelman region RNA 1 | Very often (80–99%) | In 1 condition |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Very often (80–99%) | In 1 condition |
| RAB23RAB23, member RAS oncogene family | Very often (80–99%) | In 1 condition |
| RNU4ATACRNA, U4atac small nuclear | Very often (80–99%) | In 1 condition |
| ROR2ROR family WNT receptor 2 | Very often (80–99%) | In 1 condition |
| SCUBE3signal peptide, CUB domain and EGF like domain containing 3 | Very often (80–99%) | In 1 condition |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Very often (80–99%) | In 1 condition |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Very often (80–99%) | In 1 condition |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Very often (80–99%) | In 1 condition |
| TRIP11thyroid hormone receptor interactor 11 | Very often (80–99%) | In 2 conditions |
| WDR35WD repeat domain 35 | Very often (80–99%) | In 1 condition |
| WNT5AWnt family member 5A | Very often (80–99%) | In 2 conditions |
| ADAMTS2ADAM metallopeptidase with thrombospondin type 1 motif 2 | Often (30–79%) | In 1 condition |
| ADAMTSL2ADAMTS like 2 | Often (30–79%) | In 3 conditions |
| ATP7AATPase copper transporting alpha | Often (30–79%) | In 1 condition |
| CAMTA1calmodulin binding transcription activator 1 | Often (30–79%) | In 1 condition |
| FGFR1fibroblast growth factor receptor 1 | Often (30–79%) | In 2 conditions |
| FGFR2fibroblast growth factor receptor 2 | Often (30–79%) | In 1 condition |
| FGFR3fibroblast growth factor receptor 3 | Often (30–79%) | In 1 condition |
| FLNAfilamin A | Often (30–79%) | In 2 conditions |
| HDAC4histone deacetylase 4 | Often (30–79%) | In 1 condition |
| HNRNPRheterogeneous nuclear ribonucleoprotein R | Often (30–79%) | In 1 condition |
| IGF1Rinsulin like growth factor 1 receptor | Often (30–79%) | In 1 condition |
| KRASKRas proto-oncogene, GTPase | Often (30–79%) | In 1 condition |
| MBD5methyl-CpG binding domain protein 5 | Often (30–79%) | In 2 conditions |
| MSL3MSL complex subunit 3 | Often (30–79%) | In 1 condition |
| PDGFRBplatelet derived growth factor receptor beta | Often (30–79%) | In 1 condition |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Often (30–79%) | In 1 condition |
| PTH1Rparathyroid hormone 1 receptor | Often (30–79%) | In 1 condition |
| RAI1retinoic acid induced 1 | Often (30–79%) | In 1 condition |
| RSPRY1ring finger and SPRY domain containing 1 | Often (30–79%) | In 1 condition |
| SH3PXD2BSH3 and PX domains 2B | Often (30–79%) | In 1 condition |
| SIL1SIL1 nucleotide exchange factor | Often (30–79%) | In 1 condition |
| SNIP1Smad nuclear interacting protein 1 | Often (30–79%) | In 1 condition |
| YY1AP1YY1 associated protein 1 | Often (30–79%) | In 1 condition |
| BCRBCR activator of RhoGEF and GTPase | Sometimes (5–29%) | In 1 condition |
| CHSY1chondroitin sulfate synthase 1 | Sometimes (5–29%) | In 1 condition |
| CRKLCRK like proto-oncogene, adaptor protein | Sometimes (5–29%) | In 1 condition |
| FBXO11F-box protein 11 | Sometimes (5–29%) | In 1 condition |
| GPC3glypican 3 | Sometimes (5–29%) | In 1 condition |
| KDM4Blysine demethylase 4B | Sometimes (5–29%) | In 1 condition |
| KDM5Clysine demethylase 5C | Sometimes (5–29%) | In 1 condition |
| LEF1lymphoid enhancer binding factor 1 | Sometimes (5–29%) | In 1 condition |
| MAPK1mitogen-activated protein kinase 1 | Sometimes (5–29%) | In 1 condition |
| MAPRE2microtubule associated protein RP/EB family member 2 | Sometimes (5–29%) | In 1 condition |
| NAV3neuron navigator 3 | Sometimes (5–29%) | In 1 condition |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sometimes (5–29%) | In 1 condition |
| PUF60poly(U) binding splicing factor 60 | Sometimes (5–29%) | In 1 condition |
| RBPJrecombination signal binding protein for immunoglobulin kappa J region | Sometimes (5–29%) | In 1 condition |
| TCF4transcription factor 4 | Sometimes (5–29%) | In 1 condition |
| TMEM53transmembrane protein 53 | Sometimes (5–29%) | In 1 condition |
| TONSLtonsoku like, DNA repair protein | Sometimes (5–29%) | In 1 condition |
| TRIOtrio Rho guanine nucleotide exchange factor | Sometimes (5–29%) | In 1 condition |
| WACWW domain containing adaptor with coiled-coil | Sometimes (5–29%) | In 1 condition |
| BGNbiglycan | Not recorded | In 1 condition |
| CCBE1collagen and calcium binding EGF domains 1 | Not recorded | In 1 condition |
| COL11A1collagen type XI alpha 1 chain | Not recorded | In 1 condition |
| COL11A2collagen type XI alpha 2 chain | Not recorded | In 1 condition |
| COL9A2collagen type IX alpha 2 chain | Not recorded | In 1 condition |
| CRLF1cytokine receptor like factor 1 | Not recorded | In 1 condition |
| DPM1dolichyl-phosphate mannosyltransferase subunit 1, catalytic | Not recorded | In 1 condition |
| EVCEvC ciliary complex subunit 1 | Not recorded | In 1 condition |
| EVC2EvC ciliary complex subunit 2 | Not recorded | In 1 condition |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Not recorded | In 1 condition |
| NEK1NIMA related kinase 1 | Not recorded | In 1 condition |
| ORC1origin recognition complex subunit 1 | Not recorded | In 1 condition |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Not recorded | In 1 condition |
| RECQL4RecQ like helicase 4 | Not recorded | In 1 condition |
| SIN3ASIN3 transcription regulator family member A | Not recorded | In 1 condition |
| TBCEtubulin folding cofactor E | Not recorded | In 2 conditions |
| TBL1XR1TBL1X/Y related 1 | Not recorded | In 1 condition |
| TRPS1transcriptional repressor GATA binding 1 | Not recorded | In 1 condition |
| WDR81WD repeat domain 81 | 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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