Tunnus
Delayed fine motor development
A type of motor delay characterized by a delay in acquiring the ability to control the fingers and hands.
Kokkuvõte
- Kehasüsteem
- Abnormality of the nervous system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Delayed fine motor development, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test66 geeni on seotud tunnusega Delayed fine motor development
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Delayed fine motor development. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| APC2APC regulator of Wnt signaling pathway 2 | Alati | Esineb 1 haiguses |
| ARID2AT-rich interaction domain 2 | Alati | Esineb 1 haiguses |
| AUTS2activator of transcription and developmental regulator AUTS2 | Alati | Esineb 1 haiguses |
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Alati | Esineb 1 haiguses |
| CARS1cysteinyl-tRNA synthetase 1 | Alati | Esineb 1 haiguses |
| CCNKcyclin K | Alati | Esineb 1 haiguses |
| CDC40cell division cycle 40 | Alati | Esineb 1 haiguses |
| CDH11cadherin 11 | Alati | Esineb 1 haiguses |
| CITcitron rho-interacting serine/threonine kinase | Alati | Esineb 1 haiguses |
| CLCN3Cl-/H+ antiporter 3 | Alati | Esineb 2 haiguses |
| CLCN7Cl-/H+ antiporter 7 | Alati | Esineb 1 haiguses |
| CRELD1CRELD disulfide isomerase 1 | Alati | Esineb 1 haiguses |
| CTNNA2catenin alpha 2 | Alati | Esineb 1 haiguses |
| DAND5DAN domain BMP antagonist family member 5 | Alati | Esineb 1 haiguses |
| EIF4A2eukaryotic translation initiation factor 4A2 | Alati | Esineb 1 haiguses |
| FASTKD5FASTK mitochondrial RNA regulator 5 | Alati | Esineb 1 haiguses |
| FDXRferredoxin reductase | Alati | Esineb 2 haiguses |
| FNIP1folliculin interacting protein 1 | Alati | Esineb 1 haiguses |
| GRIA1glutamate ionotropic receptor AMPA type subunit 1 | Alati | Esineb 2 haiguses |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Alati | Esineb 2 haiguses |
| KAT8lysine acetyltransferase 8 | Alati | Esineb 1 haiguses |
| KCNK4potassium two pore domain channel subfamily K member 4 | Alati | Esineb 1 haiguses |
| KDM2Blysine demethylase 2B | Alati | Esineb 1 haiguses |
| LNPKlunapark, ER junction formation factor | Alati | Esineb 1 haiguses |
| LRRC7leucine rich repeat containing 7 | Alati | Esineb 1 haiguses |
| MED16mediator complex subunit 16 | Alati | Esineb 1 haiguses |
| MINPP1multiple inositol-polyphosphate phosphatase 1 | Alati | Esineb 1 haiguses |
| NDST1N-deacetylase and N-sulfotransferase 1 | Alati | Esineb 1 haiguses |
| NFIAnuclear factor I A | Alati | Esineb 1 haiguses |
| PAX3paired box 3 | Alati | Esineb 1 haiguses |
| PI4KAphosphatidylinositol 4-kinase alpha | Alati | Esineb 1 haiguses |
| PLAAphospholipase A2 activating protein | Alati | Esineb 1 haiguses |
| POGZpogo transposable element derived with ZNF domain | Alati | Esineb 1 haiguses |
| SNX14sorting nexin 14 | Alati | Esineb 2 haiguses |
| TMTC3transmembrane O-mannosyltransferase targeting cadherins 3 | Alati | Esineb 1 haiguses |
| TRAPPC6Btrafficking protein particle complex subunit 6B | Alati | Esineb 1 haiguses |
| TRRAPtransformation/transcription domain associated protein | Alati | Esineb 1 haiguses |
| TSEN15tRNA splicing endonuclease subunit 15 | Alati | Esineb 1 haiguses |
| WASHC4WASH complex subunit 4 | Alati | Esineb 1 haiguses |
| WSB2WD repeat and SOCS box containing 2 | Alati | Esineb 1 haiguses |
Näita veel 26 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| YWHAZtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta | Alati | Esineb 1 haiguses |
| CLP1cleavage factor polyribonucleotide kinase subunit 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FIG4FIG4 phosphoinositide 5-phosphatase | Väga sageli (80–99%) | Esineb 1 haiguses |
| HNRNPCheterogeneous nuclear ribonucleoprotein C | Väga sageli (80–99%) | Esineb 1 haiguses |
| MYT1Lmyelin transcription factor 1 like | Väga sageli (80–99%) | Esineb 1 haiguses |
| TET3tet methylcytosine dioxygenase 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TNRC6Btrinucleotide repeat containing adaptor 6B | Väga sageli (80–99%) | Esineb 1 haiguses |
| ZFXzinc finger protein X-linked | Väga sageli (80–99%) | Esineb 1 haiguses |
| ASCC3activating signal cointegrator 1 complex subunit 3 | Sageli (30–79%) | Esineb 1 haiguses |
| DPH2diphthamide biosynthesis 2 | Sageli (30–79%) | Esineb 1 haiguses |
| EBF3EBF transcription factor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| FEM1Bfem-1 homolog B | Sageli (30–79%) | Esineb 1 haiguses |
| KDM4Blysine demethylase 4B | Sageli (30–79%) | Esineb 1 haiguses |
| SEC24DSEC24 homolog D, COPII component | Sageli (30–79%) | Esineb 1 haiguses |
| SFXN4sideroflexin 4 | Sageli (30–79%) | Esineb 1 haiguses |
| TUBB3tubulin beta 3 class III | Sageli (30–79%) | Esineb 1 haiguses |
| WLSWnt ligand secretion mediator | Sageli (30–79%) | Esineb 1 haiguses |
| CDH2cadherin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL12A1collagen type XII alpha 1 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| CPLX1complexin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PORcytochrome p450 oxidoreductase | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCN8Asodium voltage-gated channel alpha subunit 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SIN3ASIN3 transcription regulator family member A | Mõnikord (5–29%) | Esineb 1 haiguses |
| TBC1D24TBC1 domain family member 24 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPTBN1spectrin beta, non-erythrocytic 1 | Harva (1–4%) | Esineb 1 haiguses |
| CNOT3CCR4-NOT transcription complex subunit 3 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.16-c6eea6bf.
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Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast