AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Tunnus
Narrow chest
Reduced width of the chest from side to side, associated with a reduced distance from the sternal notch to the tip of the shoulder.
Kokkuvõte
- Teised nimetused
- Low chest circumference, Narrow shoulders, Narrow thorax, Reduced anterior-posterior chest diameter
- Kehasüsteem
- Abnormality of the musculoskeletal system
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/narrow-chest.json"
page <- fromJSON(url)
page$trait$nameNarrow chestHP:0000774
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Lugege välja geenid, mis on seotud Narrow chest-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test138 geeni on seotud tunnusega Narrow chest
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Narrow chest. 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 |
|---|---|---|
| BNIP1BCL2 interacting protein 1 | Alati | Esineb 1 haiguses |
| CEP120centrosomal protein 120 | Alati | Esineb 2 haiguses |
| CILK1ciliogenesis associated kinase 1 | Alati | Esineb 2 haiguses |
| CREB3L1cAMP responsive element binding protein 3 like 1 | Alati | Esineb 1 haiguses |
| CUL7cullin 7 | Alati | Esineb 1 haiguses |
| DONSONDNA replication fork stabilization factor DONSON | Alati | Esineb 2 haiguses |
| DSTdystonin | Alati | Esineb 1 haiguses |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Alati | Esineb 3 haiguses |
| FBN1fibrillin 1 | Alati | Esineb 2 haiguses |
| FGFR3fibroblast growth factor receptor 3 | Alati | Esineb 5 haiguses |
| FLNAfilamin A | Alati | Esineb 4 haiguses |
| HHAThedgehog acyltransferase | Alati | Esineb 2 haiguses |
| IFT122intraflagellar transport 122 | Alati | Esineb 2 haiguses |
| IFT140intraflagellar transport 140 | Alati | Esineb 3 haiguses |
| IFT43intraflagellar transport 43 | Alati | Esineb 2 haiguses |
| IFT52intraflagellar transport 52 | Alati | Esineb 2 haiguses |
| KAT6Alysine acetyltransferase 6A | Alati | Esineb 1 haiguses |
| KIAA0753KIAA0753 | Alati | Esineb 2 haiguses |
| MYOD1myogenic differentiation 1 | Alati | Esineb 1 haiguses |
| PAM16presequence translocase associated motor 16 | Alati | Esineb 1 haiguses |
| PAN2poly(A) specific ribonuclease subunit PAN2 | Alati | Esineb 1 haiguses |
| PLCB3phospholipase C beta 3 | Alati | Esineb 1 haiguses |
| PPIBpeptidylprolyl isomerase B | Alati | Esineb 1 haiguses |
| PTH1Rparathyroid hormone 1 receptor | Alati | Esineb 2 haiguses |
| SEC23ASEC23 homolog A, COPII component | Alati | Esineb 2 haiguses |
| SLC35D1solute carrier family 35 member D1 | Alati | Esineb 2 haiguses |
| SLC37A4solute carrier family 37 member 4 | Alati | Esineb 1 haiguses |
| TAF4TATA-box binding protein associated factor 4 | Alati | Esineb 1 haiguses |
| TBX5T-box transcription factor 5 | Alati | Esineb 1 haiguses |
| TOMM7translocase of outer mitochondrial membrane 7 | Alati | Esineb 1 haiguses |
| TRIP11thyroid hormone receptor interactor 11 | Alati | Esineb 4 haiguses |
| TTC21Btetratricopeptide repeat domain 21B | Alati | Esineb 2 haiguses |
| WDR19WD repeat domain 19 | Alati | Esineb 4 haiguses |
| WDR35WD repeat domain 35 | Alati | Esineb 4 haiguses |
| CASRcalcium sensing receptor | Väga sageli (80–99%) | Esineb 2 haiguses |
| CLCN7Cl-/H+ antiporter 7 | Väga sageli (80–99%) | Esineb 1 haiguses |
| COL11A1collagen type XI alpha 1 chain | Väga sageli (80–99%) | Esineb 2 haiguses |
| COL11A2collagen type XI alpha 2 chain | Väga sageli (80–99%) | Esineb 1 haiguses |
| COL2A1collagen type II alpha 1 chain | Väga sageli (80–99%) | Esineb 3 haiguses |
| DYNC2H1dynein cytoplasmic 2 heavy chain 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
Näita veel 98 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| DYNC2I1dynein 2 intermediate chain 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| DYNC2I2dynein 2 intermediate chain 2 | Väga sageli (80–99%) | Esineb 3 haiguses |
| EVCEvC ciliary complex subunit 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| EVC2EvC ciliary complex subunit 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| FLNBfilamin B | Väga sageli (80–99%) | Esineb 3 haiguses |
| GLI1GLI family zinc finger 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| IFT172intraflagellar transport 172 | Väga sageli (80–99%) | Esineb 1 haiguses |
| IFT80intraflagellar transport 80 | Väga sageli (80–99%) | Esineb 3 haiguses |
| INPPL1inositol polyphosphate phosphatase like 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| LBRlamin B receptor | Väga sageli (80–99%) | Esineb 2 haiguses |
| OSTM1osteoclastogenesis associated transmembrane protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Väga sageli (80–99%) | Esineb 1 haiguses |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Väga sageli (80–99%) | Esineb 2 haiguses |
| RUNX2RUNX family transcription factor 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SLC26A2solute carrier family 26 member 2 | Väga sageli (80–99%) | Esineb 3 haiguses |
| SNX10sorting nexin 10 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SOX9SRY-box transcription factor 9 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TMCO1transmembrane and coiled-coil domains 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TNFSF11TNF superfamily member 11 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TRPV6transient receptor potential cation channel subfamily V member 6 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ABCC9ATP binding cassette subfamily C member 9 | Sageli (30–79%) | Esineb 2 haiguses |
| ADAMTS3ADAM metallopeptidase with thrombospondin type 1 motif 3 | Sageli (30–79%) | Esineb 1 haiguses |
| ATP7AATPase copper transporting alpha | Sageli (30–79%) | Esineb 3 haiguses |
| CANT1calcium activated nucleotidase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CCBE1collagen and calcium binding EGF domains 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CCDC47coiled-coil domain containing 47 | Sageli (30–79%) | Esineb 1 haiguses |
| DCHS1dachsous cadherin-related 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DDR2discoidin domain receptor tyrosine kinase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| DLG3discs large MAGUK scaffold protein 3 | Sageli (30–79%) | Esineb 1 haiguses |
| DYNLT2Bdynein light chain Tctex-type 2B | Sageli (30–79%) | Esineb 1 haiguses |
| FAT4FAT atypical cadherin 4 | Sageli (30–79%) | Esineb 2 haiguses |
| FGF4fibroblast growth factor 4 | Sageli (30–79%) | Esineb 1 haiguses |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Sageli (30–79%) | Esineb 1 haiguses |
| GPX4glutathione peroxidase 4 | Sageli (30–79%) | Esineb 2 haiguses |
| HSPG2heparan sulfate proteoglycan 2 | Sageli (30–79%) | Esineb 1 haiguses |
| IHHIndian hedgehog signaling molecule | Sageli (30–79%) | Esineb 2 haiguses |
| KCNJ8potassium inwardly rectifying channel subfamily J member 8 | Sageli (30–79%) | Esineb 1 haiguses |
| KYNUkynureninase | Sageli (30–79%) | Esineb 1 haiguses |
| MESDmesoderm development LRP chaperone | Sageli (30–79%) | Esineb 1 haiguses |
| NEK9NIMA related kinase 9 | Sageli (30–79%) | Esineb 1 haiguses |
| POLR3ARNA polymerase III subunit A | Sageli (30–79%) | Esineb 1 haiguses |
| RMP64ribonuclease MRP subunit p64 | Sageli (30–79%) | Esineb 1 haiguses |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Sageli (30–79%) | Esineb 2 haiguses |
| TWIST1twist family bHLH transcription factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| WDR11WD repeat domain 11 | Sageli (30–79%) | Esineb 1 haiguses |
| ZBTB20zinc finger and BTB domain containing 20 | Sageli (30–79%) | Esineb 2 haiguses |
| ACTA1actin alpha 1, skeletal muscle | Mõnikord (5–29%) | Esineb 2 haiguses |
| ACTG2actin gamma 2, smooth muscle | Mõnikord (5–29%) | Esineb 1 haiguses |
| CFAP410cilia and flagella associated protein 410 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CFL2cofilin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DDX3XDEAD-box helicase 3 X-linked | Mõnikord (5–29%) | Esineb 1 haiguses |
| DLK1delta like non-canonical Notch ligand 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GAD1glutamate decarboxylase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KBTBD13kelch repeat and BTB domain containing 13 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KLHL41kelch like family member 41 | Mõnikord (5–29%) | Esineb 3 haiguses |
| LMNAlamin A/C | Mõnikord (5–29%) | Esineb 1 haiguses |
| LMOD3leiomodin 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MED12mediator complex subunit 12 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MEG3maternally expressed 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MYPNmyopalladin | Mõnikord (5–29%) | Esineb 1 haiguses |
| NEBnebulin | Mõnikord (5–29%) | Esineb 2 haiguses |
| PCNTpericentrin | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Mõnikord (5–29%) | Esineb 2 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| PORcytochrome p450 oxidoreductase | Mõnikord (5–29%) | Esineb 2 haiguses |
| PUF60poly(U) binding splicing factor 60 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RTL1retrotransposon Gag like 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SKISKI proto-oncogene | Mõnikord (5–29%) | Esineb 1 haiguses |
| TCTN2tectonic family member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TPM2tropomyosin 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| TPM3tropomyosin 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| UPF3BUPF3B regulator of nonsense mediated mRNA decay | Mõnikord (5–29%) | Esineb 1 haiguses |
| XYLT1xylosyltransferase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTSKcathepsin K | Harva (1–4%) | Esineb 1 haiguses |
| AGRNagrin | Pole registreeritud | Esineb 1 haiguses |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Pole registreeritud | Esineb 1 haiguses |
| B4GALT7beta-1,4-galactosyltransferase 7 | Pole registreeritud | Esineb 1 haiguses |
| BCORBCL6 corepressor | Pole registreeritud | Esineb 1 haiguses |
| CHST3carbohydrate sulfotransferase 3 | Pole registreeritud | Esineb 1 haiguses |
| CRTAPcartilage associated protein | Pole registreeritud | Esineb 1 haiguses |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Pole registreeritud | Esineb 1 haiguses |
| FGFR2fibroblast growth factor receptor 2 | Pole registreeritud | Esineb 1 haiguses |
| IFT81intraflagellar transport 81 | Pole registreeritud | Esineb 1 haiguses |
| INTUinturned planar cell polarity protein | Pole registreeritud | Esineb 1 haiguses |
| ITGA3integrin subunit alpha 3 | Pole registreeritud | Esineb 1 haiguses |
| KIAA0586KIAA0586 | Pole registreeritud | Esineb 1 haiguses |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Pole registreeritud | Esineb 1 haiguses |
| NEK1NIMA related kinase 1 | Pole registreeritud | Esineb 1 haiguses |
| ORC6origin recognition complex subunit 6 | Pole registreeritud | Esineb 1 haiguses |
| PCGF2polycomb group ring finger 2 | Pole registreeritud | Esineb 1 haiguses |
| RPS19ribosomal protein S19 | Pole registreeritud | Esineb 1 haiguses |
| SBDSSBDS ribosome maturation factor | Pole registreeritud | Esineb 1 haiguses |
| SERPINH1serpin family H member 1 | Pole registreeritud | Esineb 1 haiguses |
| SLC9A6solute carrier family 9 member A6 | Pole registreeritud | Esineb 1 haiguses |
| SRP54signal recognition particle 54 | Pole registreeritud | Esineb 1 haiguses |
| ZC4H2zinc finger C4H2-type containing | Pole registreeritud | Esineb 2 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.
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast