Trait
Delayed fine motor development
A type of motor delay characterized by a delay in acquiring the ability to control the fingers and hands.
Summary
- Body system
- Abnormality of the nervous system
Reference genomeGRCh38hg38
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Read the genes linked to Delayed fine motor development, and the rest of your genome, with one test.
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Get my Genome Test66 genes linked to Delayed fine motor development
Changes in these genes cause rare conditions in which Delayed fine motor development 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 |
|---|---|---|
| APC2APC regulator of Wnt signaling pathway 2 | Always | In 1 condition |
| ARID2AT-rich interaction domain 2 | Always | In 1 condition |
| AUTS2activator of transcription and developmental regulator AUTS2 | Always | In 1 condition |
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Always | In 1 condition |
| CARS1cysteinyl-tRNA synthetase 1 | Always | In 1 condition |
| CCNKcyclin K | Always | In 1 condition |
| CDC40cell division cycle 40 | Always | In 1 condition |
| CDH11cadherin 11 | Always | In 1 condition |
| CITcitron rho-interacting serine/threonine kinase | Always | In 1 condition |
| CLCN3Cl-/H+ antiporter 3 | Always | In 2 conditions |
| CLCN7Cl-/H+ antiporter 7 | Always | In 1 condition |
| CRELD1CRELD disulfide isomerase 1 | Always | In 1 condition |
| CTNNA2catenin alpha 2 | Always | In 1 condition |
| DAND5DAN domain BMP antagonist family member 5 | Always | In 1 condition |
| EIF4A2eukaryotic translation initiation factor 4A2 | Always | In 1 condition |
| FASTKD5FASTK mitochondrial RNA regulator 5 | Always | In 1 condition |
| FDXRferredoxin reductase | Always | In 2 conditions |
| FNIP1folliculin interacting protein 1 | Always | In 1 condition |
| GRIA1glutamate ionotropic receptor AMPA type subunit 1 | Always | In 2 conditions |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Always | In 2 conditions |
| KAT8lysine acetyltransferase 8 | Always | In 1 condition |
| KCNK4potassium two pore domain channel subfamily K member 4 | Always | In 1 condition |
| KDM2Blysine demethylase 2B | Always | In 1 condition |
| LNPKlunapark, ER junction formation factor | Always | In 1 condition |
| LRRC7leucine rich repeat containing 7 | Always | In 1 condition |
| MED16mediator complex subunit 16 | Always | In 1 condition |
| MINPP1multiple inositol-polyphosphate phosphatase 1 | Always | In 1 condition |
| NDST1N-deacetylase and N-sulfotransferase 1 | Always | In 1 condition |
| NFIAnuclear factor I A | Always | In 1 condition |
| PAX3paired box 3 | Always | In 1 condition |
| PI4KAphosphatidylinositol 4-kinase alpha | Always | In 1 condition |
| PLAAphospholipase A2 activating protein | Always | In 1 condition |
| POGZpogo transposable element derived with ZNF domain | Always | In 1 condition |
| SNX14sorting nexin 14 | Always | In 2 conditions |
| TMTC3transmembrane O-mannosyltransferase targeting cadherins 3 | Always | In 1 condition |
| TRAPPC6Btrafficking protein particle complex subunit 6B | Always | In 1 condition |
| TRRAPtransformation/transcription domain associated protein | Always | In 1 condition |
| TSEN15tRNA splicing endonuclease subunit 15 | Always | In 1 condition |
| WASHC4WASH complex subunit 4 | Always | In 1 condition |
| WSB2WD repeat and SOCS box containing 2 | Always | In 1 condition |
Show 26 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| YWHAZtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta | Always | In 1 condition |
| CLP1cleavage factor polyribonucleotide kinase subunit 1 | Very often (80–99%) | In 1 condition |
| FIG4FIG4 phosphoinositide 5-phosphatase | Very often (80–99%) | In 1 condition |
| HNRNPCheterogeneous nuclear ribonucleoprotein C | Very often (80–99%) | In 1 condition |
| MYT1Lmyelin transcription factor 1 like | Very often (80–99%) | In 1 condition |
| TET3tet methylcytosine dioxygenase 3 | Very often (80–99%) | In 1 condition |
| TNRC6Btrinucleotide repeat containing adaptor 6B | Very often (80–99%) | In 1 condition |
| ZFXzinc finger protein X-linked | Very often (80–99%) | In 1 condition |
| ASCC3activating signal cointegrator 1 complex subunit 3 | Often (30–79%) | In 1 condition |
| DPH2diphthamide biosynthesis 2 | Often (30–79%) | In 1 condition |
| EBF3EBF transcription factor 3 | Often (30–79%) | In 1 condition |
| FEM1Bfem-1 homolog B | Often (30–79%) | In 1 condition |
| KDM4Blysine demethylase 4B | Often (30–79%) | In 1 condition |
| SEC24DSEC24 homolog D, COPII component | Often (30–79%) | In 1 condition |
| SFXN4sideroflexin 4 | Often (30–79%) | In 1 condition |
| TUBB3tubulin beta 3 class III | Often (30–79%) | In 1 condition |
| WLSWnt ligand secretion mediator | Often (30–79%) | In 1 condition |
| CDH2cadherin 2 | Sometimes (5–29%) | In 1 condition |
| COL12A1collagen type XII alpha 1 chain | Sometimes (5–29%) | In 1 condition |
| CPLX1complexin 1 | Sometimes (5–29%) | In 1 condition |
| PORcytochrome p450 oxidoreductase | Sometimes (5–29%) | In 1 condition |
| SCN8Asodium voltage-gated channel alpha subunit 8 | Sometimes (5–29%) | In 1 condition |
| SIN3ASIN3 transcription regulator family member A | Sometimes (5–29%) | In 1 condition |
| TBC1D24TBC1 domain family member 24 | Sometimes (5–29%) | In 1 condition |
| SPTBN1spectrin beta, non-erythrocytic 1 | Rarely (1–4%) | In 1 condition |
| CNOT3CCR4-NOT transcription complex subunit 3 | 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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