Trait
Short finger
Abnormally short finger associated with developmental hypoplasia.
Summary
- Also called
- Stubby finger, Hypoplastic digits, Hypoplastic fingers, Hypoplastic/small fingers, Stubby fingers
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test75 genes linked to Short finger
Changes in these genes cause rare conditions in which Short finger 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 |
|---|---|---|
| ACANaggrecan | Always | In 1 condition |
| DDR2discoidin domain receptor tyrosine kinase 2 | Always | In 1 condition |
| FBN1fibrillin 1 | Always | In 1 condition |
| FLNAfilamin A | Always | In 1 condition |
| FLNBfilamin B | Always | In 1 condition |
| GPC3glypican 3 | Always | In 1 condition |
| IFT140intraflagellar transport 140 | Always | In 1 condition |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Always | In 1 condition |
| PPOXprotoporphyrinogen oxidase | Always | In 1 condition |
| PRKG2protein kinase cGMP-dependent 2 | Always | In 1 condition |
| TBL1XR1TBL1X/Y related 1 | Always | In 2 conditions |
| FIG4FIG4 phosphoinositide 5-phosphatase | Very often (80–99%) | In 2 conditions |
| SLC26A2solute carrier family 26 member 2 | Very often (80–99%) | In 3 conditions |
| ASPHaspartate beta-hydroxylase | Often (30–79%) | In 1 condition |
| CTSKcathepsin K | Often (30–79%) | In 1 condition |
| LBRlamin B receptor | Often (30–79%) | In 1 condition |
| LMNB2lamin B2 | Often (30–79%) | In 1 condition |
| MCTP2multiple C2 and transmembrane domain containing 2 | Often (30–79%) | In 1 condition |
| OFD1OFD1 centriole and centriolar satellite protein | Often (30–79%) | In 1 condition |
| RYR3ryanodine receptor 3 | Often (30–79%) | In 1 condition |
| TNXBtenascin XB | Often (30–79%) | In 1 condition |
| VAC14VAC14 component of PIKFYVE complex | Often (30–79%) | In 1 condition |
| ALMS1ALMS1 centrosome and basal body associated protein | Sometimes (5–29%) | In 1 condition |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Sometimes (5–29%) | In 1 condition |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Sometimes (5–29%) | In 1 condition |
| AP1G1adaptor related protein complex 1 subunit gamma 1 | Sometimes (5–29%) | In 1 condition |
| CDC42BPBCDC42 binding protein kinase beta | Sometimes (5–29%) | In 1 condition |
| HESX1HESX homeobox 1 | Sometimes (5–29%) | In 2 conditions |
| IGF1Rinsulin like growth factor 1 receptor | Sometimes (5–29%) | In 1 condition |
| LHX3LIM homeobox 3 | Sometimes (5–29%) | In 1 condition |
| LHX4LIM homeobox 4 | Sometimes (5–29%) | In 1 condition |
| POU1F1POU class 1 homeobox 1 | Sometimes (5–29%) | In 1 condition |
| PROP1PROP paired-like homeobox 1 | Sometimes (5–29%) | In 1 condition |
| RPL10ribosomal protein L10 | Sometimes (5–29%) | In 2 conditions |
| ZMYM2zinc finger MYM-type containing 2 | Sometimes (5–29%) | In 1 condition |
| ARXaristaless related homeobox | Rarely (1–4%) | In 1 condition |
| ASAH1N-acylsphingosine amidohydrolase 1 | Rarely (1–4%) | In 1 condition |
| CACNA1Ecalcium voltage-gated channel subunit alpha1 E | Rarely (1–4%) | In 1 condition |
| CASKcalcium/calmodulin dependent serine protein kinase | Rarely (1–4%) | In 1 condition |
| CDKL5cyclin dependent kinase like 5 | Rarely (1–4%) | In 1 condition |
Show 35 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| DMXL2Dmx like 2 | Rarely (1–4%) | In 1 condition |
| GNAO1G protein subunit alpha o1 | Rarely (1–4%) | In 1 condition |
| GRIN1glutamate ionotropic receptor NMDA type subunit 1 | Rarely (1–4%) | In 1 condition |
| GRM7glutamate metabotropic receptor 7 | Rarely (1–4%) | In 1 condition |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Rarely (1–4%) | In 1 condition |
| LGI1leucine rich glioma inactivated 1 | Rarely (1–4%) | In 1 condition |
| NEUROD2neuronal differentiation 2 | Rarely (1–4%) | In 1 condition |
| PIGPphosphatidylinositol glycan anchor biosynthesis class P | Rarely (1–4%) | In 1 condition |
| PIGQphosphatidylinositol glycan anchor biosynthesis class Q | Rarely (1–4%) | In 1 condition |
| PNKPpolynucleotide kinase 3'-phosphatase | Rarely (1–4%) | In 1 condition |
| RHOBTB2Rho related BTB domain containing 2 | Rarely (1–4%) | In 1 condition |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Rarely (1–4%) | In 1 condition |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Rarely (1–4%) | In 1 condition |
| SIK1salt inducible kinase 1 | Rarely (1–4%) | In 1 condition |
| SLC25A22solute carrier family 25 member 22 | Rarely (1–4%) | In 1 condition |
| SLC32A1solute carrier family 32 member 1 | Rarely (1–4%) | In 1 condition |
| TRIM8tripartite motif containing 8 | Rarely (1–4%) | In 1 condition |
| ABCA12ATP binding cassette subfamily A member 12 | Not recorded | In 1 condition |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Not recorded | In 1 condition |
| BMPR1Bbone morphogenetic protein receptor type 1B | Not recorded | In 1 condition |
| CHRNA1cholinergic receptor nicotinic alpha 1 subunit | Not recorded | In 1 condition |
| CHRNDcholinergic receptor nicotinic delta subunit | Not recorded | In 1 condition |
| CHRNGcholinergic receptor nicotinic gamma subunit | Not recorded | In 1 condition |
| GNASGNAS complex locus | Not recorded | In 1 condition |
| GPX4glutathione peroxidase 4 | Not recorded | In 1 condition |
| LRP4LDL receptor related protein 4 | Not recorded | In 1 condition |
| NOGnoggin | Not recorded | In 1 condition |
| PCYT1Aphosphate cytidylyltransferase 1A, choline | Not recorded | In 1 condition |
| PORCNporcupine O-acyltransferase | Not recorded | In 1 condition |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Not recorded | In 1 condition |
| SMAD4SMAD family member 4 | Not recorded | In 1 condition |
| TCTN3tectonic family member 3 | Not recorded | In 1 condition |
| TRPS1transcriptional repressor GATA binding 1 | Not recorded | In 1 condition |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Not recorded | In 1 condition |
| ZMIZ1zinc finger MIZ-type containing 1 | 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.
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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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