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Tunnus
Pins and needles feeling
Kliiniline nimetus: Paresthesia
Abnormal sensations such as tingling, pricking, or numbness of the skin with no apparent physical cause.
Kokkuvõte
- Teised nimetused
- Tingling, Paresthesias
- Kehasüsteem
- Abnormality of the nervous system
Pins and needles feelingHP:0003401
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Logi sisseKüsiAlustaalates 449 $
Read the genes linked to Pins and needles feeling, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test127 geeni on seotud tunnusega Pins and needles feeling
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Pins and needles feeling. 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 |
|---|---|---|
| LAMB1laminin subunit beta 1 | Alati | Esineb 1 haiguses |
| RAB32RAB32, member RAS oncogene family | Alati | Esineb 1 haiguses |
| APPamyloid beta precursor protein | Väga sageli (80–99%) | Esineb 2 haiguses |
| CALRcalreticulin | Väga sageli (80–99%) | Esineb 1 haiguses |
| CASRcalcium sensing receptor | Väga sageli (80–99%) | Esineb 2 haiguses |
| CTDP1CTD phosphatase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GNA11G protein subunit alpha 11 | Väga sageli (80–99%) | Esineb 2 haiguses |
| JAK2Janus kinase 2 | Väga sageli (80–99%) | Esineb 3 haiguses |
| LIFRLIF receptor subunit alpha | Väga sageli (80–99%) | Esineb 1 haiguses |
| MPLMPL proto-oncogene, thrombopoietin receptor | Väga sageli (80–99%) | Esineb 2 haiguses |
| SERPING1serpin family G member 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SH2B3SH2B adaptor protein 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC19A2solute carrier family 19 member 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TET2tet methylcytosine dioxygenase 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TP53tumor protein p53 | Väga sageli (80–99%) | Esineb 1 haiguses |
| AIPAHR interacting HSP90 co-chaperone | Sageli (30–79%) | Esineb 1 haiguses |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Sageli (30–79%) | Esineb 1 haiguses |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Sageli (30–79%) | Esineb 2 haiguses |
| CCM2CCM2 scaffold protein | Sageli (30–79%) | Esineb 1 haiguses |
| GBE11,4-alpha-glucan branching enzyme 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GPR101G protein-coupled receptor 101 | Sageli (30–79%) | Esineb 1 haiguses |
| KRIT1KRIT1 ankyrin repeat containing | Sageli (30–79%) | Esineb 1 haiguses |
| KRT14keratin 14 | Sageli (30–79%) | Esineb 1 haiguses |
| KRT5keratin 5 | Sageli (30–79%) | Esineb 1 haiguses |
| LIG3DNA ligase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| LITAFlipopolysaccharide induced TNF factor | Sageli (30–79%) | Esineb 1 haiguses |
| MFN2mitofusin 2 | Sageli (30–79%) | Esineb 2 haiguses |
| OPA3outer mitochondrial membrane lipid metabolism regulator OPA3 | Sageli (30–79%) | Esineb 1 haiguses |
| PDCD10programmed cell death 10 | Sageli (30–79%) | Esineb 1 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Sageli (30–79%) | Esineb 2 haiguses |
| PMP22peripheral myelin protein 22 | Sageli (30–79%) | Esineb 2 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Sageli (30–79%) | Esineb 2 haiguses |
| PRNPprion protein (Kanno blood group) | Sageli (30–79%) | Esineb 1 haiguses |
| PRRT2proline rich transmembrane protein 2 | Sageli (30–79%) | Esineb 2 haiguses |
| RRM1ribonucleotide reductase catalytic subunit M1 | Sageli (30–79%) | Esineb 1 haiguses |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sageli (30–79%) | Esineb 1 haiguses |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SCYL1SCY1 like pseudokinase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| SEPTIN9septin 9 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC2A1solute carrier family 2 member 1 | Sageli (30–79%) | Esineb 3 haiguses |
Näita veel 87 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| THPOthrombopoietin | Sageli (30–79%) | Esineb 1 haiguses |
| TK2thymidine kinase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TOP3ADNA topoisomerase III alpha | Sageli (30–79%) | Esineb 1 haiguses |
| TRIM32tripartite motif containing 32 | Sageli (30–79%) | Esineb 1 haiguses |
| TYMPthymidine phosphorylase | Sageli (30–79%) | Esineb 1 haiguses |
| ATMATM serine/threonine kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATXN1ataxin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BMPR1Abone morphogenetic protein receptor type 1A | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRCA2BRCA2 DNA repair associated | Mõnikord (5–29%) | Esineb 1 haiguses |
| C4Acomplement C4A (Chido/Rodgers blood group) | Mõnikord (5–29%) | Esineb 1 haiguses |
| CBLIFcobalamin binding intrinsic factor | Mõnikord (5–29%) | Esineb 2 haiguses |
| CCND1cyclin D1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CCR1C-C motif chemokine receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CHEK2checkpoint kinase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| COQ6coenzyme Q6, monooxygenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| DEPDC5DEP domain containing 5, GATOR1 subcomplex subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| EPCAMepithelial cell adhesion molecule | Mõnikord (5–29%) | Esineb 1 haiguses |
| ERAP1endoplasmic reticulum aminopeptidase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ERLIN2ER lipid raft associated 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FASFas cell surface death receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GNA14G protein subunit alpha 14 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GNASGNAS complex locus | Mõnikord (5–29%) | Esineb 4 haiguses |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | Mõnikord (5–29%) | Esineb 1 haiguses |
| HINT1histidine triad nucleotide binding protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HLA-Bmajor histocompatibility complex, class I, B | Mõnikord (5–29%) | Esineb 2 haiguses |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| HPDL4-hydroxyphenylpyruvate dioxygenase like | Mõnikord (5–29%) | Esineb 1 haiguses |
| IFNGR1interferon gamma receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL10interleukin 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL12Ainterleukin 12A | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL12A-AS1IL12A antisense RNA 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL23Rinterleukin 23 receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| KIF5Akinesin family member 5A | Mõnikord (5–29%) | Esineb 1 haiguses |
| KLRC4killer cell lectin like receptor C4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KRASKRas proto-oncogene, GTPase | Mõnikord (5–29%) | Esineb 1 haiguses |
| LZTR1leucine zipper like post translational regulator 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MEFVMEFV innate immunity regulator, pyrin | Mõnikord (5–29%) | Esineb 1 haiguses |
| MEN1menin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MLH1mutL homolog 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MSH2mutS homolog 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MSH6mutS homolog 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MUTYHmutY DNA glycosylase | Mõnikord (5–29%) | Esineb 1 haiguses |
| NAGAalpha-N-acetylgalactosaminidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| NEFLneurofilament light chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Mõnikord (5–29%) | Esineb 1 haiguses |
| NPATnuclear protein, coactivator of histone transcription | Mõnikord (5–29%) | Esineb 1 haiguses |
| NPRL2NPR2 like, GATOR1 complex subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| NPRL3NPR3 like, GATOR1 complex subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PMS1PMS1 homolog 1, mismatch repair system component | Mõnikord (5–29%) | Esineb 1 haiguses |
| PMS2PMS1 homolog 2, mismatch repair system component | Mõnikord (5–29%) | Esineb 1 haiguses |
| POLD1DNA polymerase delta 1, catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| POLEDNA polymerase epsilon, catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RPS20ribosomal protein S20 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SBF2SET binding factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCN3Asodium voltage-gated channel alpha subunit 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SEMA4Asemaphorin 4A | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SRPX2sushi repeat containing protein X-linked 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| STAT4signal transducer and activator of transcription 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| STX16syntaxin 16 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TGFBR2transforming growth factor beta receptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TLR4toll like receptor 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TNFRSF1ATNF receptor superfamily member 1A | Mõnikord (5–29%) | Esineb 1 haiguses |
| UBAC2UBA domain containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| VCPvalosin containing protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| VWA1von Willebrand factor A domain containing 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| YY1YY1 transcription factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| CLCNKBchloride voltage-gated channel Kb | Harva (1–4%) | Esineb 1 haiguses |
| GATA1GATA binding protein 1 | Harva (1–4%) | Esineb 1 haiguses |
| SLC12A3solute carrier family 12 member 3 | Harva (1–4%) | Esineb 2 haiguses |
| TRAPPC2trafficking protein particle complex subunit 2 | Harva (1–4%) | Esineb 1 haiguses |
| URODuroporphyrinogen decarboxylase | Harva (1–4%) | Esineb 1 haiguses |
| UROSuroporphyrinogen III synthase | Harva (1–4%) | Esineb 1 haiguses |
| ALADaminolevulinate dehydratase | Pole registreeritud | Esineb 1 haiguses |
| ATL1atlastin GTPase 1 | Pole registreeritud | Esineb 1 haiguses |
| CUBNcubilin | Pole registreeritud | Esineb 1 haiguses |
| GLAgalactosidase alpha | Pole registreeritud | Esineb 1 haiguses |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Pole registreeritud | Esineb 1 haiguses |
| HMBShydroxymethylbilane synthase | Pole registreeritud | Esineb 1 haiguses |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Pole registreeritud | Esineb 1 haiguses |
| MTHFRmethylenetetrahydrofolate reductase | Pole registreeritud | Esineb 1 haiguses |
| NAGLUN-acetyl-alpha-glucosaminidase | Pole registreeritud | Esineb 1 haiguses |
| SLC12A1solute carrier family 12 member 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.
Kellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiAlustaalates 449 $
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast