Tunnus
Back pain
An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the back.
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Telli oma Genome Test68 geeni on seotud tunnusega Back pain
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Back pain. 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 |
|---|---|---|
| FHL1four and a half LIM domains 1 | Alati | Esineb 2 haiguses |
| RAB32RAB32, member RAS oncogene family | Alati | Esineb 1 haiguses |
| TRAPPC2trafficking protein particle complex subunit 2 | Alati | Esineb 2 haiguses |
| VCPvalosin containing protein | Alati | Esineb 2 haiguses |
| ATP7BATPase copper transporting beta | Väga sageli (80–99%) | Esineb 1 haiguses |
| BRCA1BRCA1 DNA repair associated | Väga sageli (80–99%) | Esineb 1 haiguses |
| BRCA2BRCA2 DNA repair associated | Väga sageli (80–99%) | Esineb 1 haiguses |
| CDKN2Acyclin dependent kinase inhibitor 2A | Väga sageli (80–99%) | Esineb 1 haiguses |
| KRASKRas proto-oncogene, GTPase | Väga sageli (80–99%) | Esineb 1 haiguses |
| PALB2partner and localizer of BRCA2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PALLDpalladin, cytoskeletal associated protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| RABL3RAB, member of RAS oncogene family like 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SMAD4SMAD family member 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TP53tumor protein p53 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CLCN7Cl-/H+ antiporter 7 | Sageli (30–79%) | Esineb 1 haiguses |
| DLL3delta like canonical Notch ligand 3 | Sageli (30–79%) | Esineb 1 haiguses |
| EMDemerin | Sageli (30–79%) | Esineb 1 haiguses |
| FLNCfilamin C | Sageli (30–79%) | Esineb 1 haiguses |
| HGDhomogentisate 1,2-dioxygenase | Sageli (30–79%) | Esineb 1 haiguses |
| HMBShydroxymethylbilane synthase | Sageli (30–79%) | Esineb 1 haiguses |
| HTRA1HtrA serine peptidase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| LMNAlamin A/C | Sageli (30–79%) | Esineb 2 haiguses |
| LMX1BLIM homeobox transcription factor 1 beta | Sageli (30–79%) | Esineb 2 haiguses |
| MESP2mesoderm posterior bHLH transcription factor 2 | Sageli (30–79%) | Esineb 1 haiguses |
| NKX3-2NK3 homeobox 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PLEKHM1pleckstrin homology and RUN domain containing M1 | Sageli (30–79%) | Esineb 1 haiguses |
| POLR3GLRNA polymerase III subunit GL | Sageli (30–79%) | Esineb 1 haiguses |
| PPOXprotoporphyrinogen oxidase | Sageli (30–79%) | Esineb 1 haiguses |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SYNE2spectrin repeat containing nuclear envelope protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Sageli (30–79%) | Esineb 1 haiguses |
| TMEM43transmembrane protein 43 | Sageli (30–79%) | Esineb 1 haiguses |
| TNXBtenascin XB | Sageli (30–79%) | Esineb 1 haiguses |
| ABCD1ATP binding cassette subfamily D member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CCND1cyclin D1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CD46CD46 molecule | Mõnikord (5–29%) | Esineb 1 haiguses |
| CFHcomplement factor H | Mõnikord (5–29%) | Esineb 1 haiguses |
| CFIcomplement factor I | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL2A1collagen type II alpha 1 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
Näita veel 28 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| CPOXcoproporphyrinogen oxidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| HELLPARHELLP associated long non-coding RNA | Mõnikord (5–29%) | Esineb 1 haiguses |
| LRP5LDL receptor related protein 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRKCSHPRKCSH beta subunit of glucosidase II | Mõnikord (5–29%) | Esineb 2 haiguses |
| RASA1RAS p21 protein activator 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SEC63SEC63 protein translocation regulator | Mõnikord (5–29%) | Esineb 1 haiguses |
| SFRP4secreted frizzled related protein 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC22A12solute carrier family 22 member 12 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC2A9solute carrier family 2 member 9 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TBX18T-box transcription factor 18 | Mõnikord (5–29%) | Esineb 1 haiguses |
| VHLvon Hippel-Lindau tumor suppressor | Mõnikord (5–29%) | Esineb 1 haiguses |
| AKT1AKT serine/threonine kinase 1 | Harva (1–4%) | Esineb 1 haiguses |
| BAP1BRCA1 associated deubiquitinase 1 | Harva (1–4%) | Esineb 1 haiguses |
| MATN3matrilin 3 | Harva (1–4%) | Esineb 1 haiguses |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Harva (1–4%) | Esineb 1 haiguses |
| PDGFBplatelet derived growth factor subunit B | Harva (1–4%) | Esineb 1 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Harva (1–4%) | Esineb 1 haiguses |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Harva (1–4%) | Esineb 1 haiguses |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Harva (1–4%) | Esineb 1 haiguses |
| SMOsmoothened, frizzled class receptor | Harva (1–4%) | Esineb 1 haiguses |
| SPTBN1spectrin beta, non-erythrocytic 1 | Harva (1–4%) | Esineb 1 haiguses |
| SUFUSUFU negative regulator of hedgehog signaling | Harva (1–4%) | Esineb 1 haiguses |
| TERTtelomerase reverse transcriptase | Harva (1–4%) | Esineb 1 haiguses |
| TRAF7TNF receptor associated factor 7 | Harva (1–4%) | Esineb 1 haiguses |
| CAPN3calpain 3 | Pole registreeritud | Esineb 1 haiguses |
| HLA-Bmajor histocompatibility complex, class I, B | Pole registreeritud | Esineb 1 haiguses |
| VANGL1VANGL planar cell polarity protein 1 | 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.
Kitsamad tunnused
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