Tunnus
Increased CSF protein concentration
Increased concentration of protein in the cerebrospinal fluid.
Kokkuvõte
- Teised nimetused
- Cerebrospinal fluid protein increased, Cerebrospinal fluid with increased protein, Elevated cerebrospinal fluid protein, Elevated csf protein, Hyperproteinorrhachia, Increased CSF protein, Increased protein in csf, Spinal fluid protein elevated
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Increased CSF protein concentration, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test64 geeni on seotud tunnusega Increased CSF protein concentration
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Increased CSF protein concentration. 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 |
|---|---|---|
| ARHGAP19Rho GTPase activating protein 19 | Alati | Esineb 1 haiguses |
| BCAT2branched chain amino acid transaminase 2 | Alati | Esineb 1 haiguses |
| MICU1mitochondrial calcium uptake 1 | Alati | Esineb 1 haiguses |
| MPV17mitochondrial inner membrane protein MPV17 | Alati | Esineb 1 haiguses |
| NOTCH2NLCnotch 2 N-terminal like C | Alati | Esineb 2 haiguses |
| PRF1perforin 1 | Alati | Esineb 1 haiguses |
| PSAPprosaposin | Alati | Esineb 6 haiguses |
| PSMB9proteasome 20S subunit beta 9 | Alati | Esineb 1 haiguses |
| SLC12A6solute carrier family 12 member 6 | Alati | Esineb 1 haiguses |
| TTRtransthyretin | Alati | Esineb 1 haiguses |
| GALCgalactosylceramidase | Väga sageli (80–99%) | Esineb 4 haiguses |
| OCLNoccludin | Väga sageli (80–99%) | Esineb 1 haiguses |
| RANBP2RAN binding protein 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TXN2thioredoxin 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ABHD5abhydrolase domain containing 5, lysophosphatidic acid acyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Sageli (30–79%) | Esineb 1 haiguses |
| ARSAarylsulfatase A | Sageli (30–79%) | Esineb 4 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 1 haiguses |
| DNM1Ldynamin 1L | Sageli (30–79%) | Esineb 1 haiguses |
| LIG3DNA ligase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| MPZmyelin protein zero | Sageli (30–79%) | Esineb 2 haiguses |
| MT-ATP8mitochondrially encoded ATP synthase membrane subunit 8 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Sageli (30–79%) | Esineb 1 haiguses |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Sageli (30–79%) | Esineb 1 haiguses |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Sageli (30–79%) | Esineb 1 haiguses |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Sageli (30–79%) | Esineb 1 haiguses |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Sageli (30–79%) | Esineb 2 haiguses |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Sageli (30–79%) | Esineb 1 haiguses |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Sageli (30–79%) | Esineb 1 haiguses |
| NDUFS4NADH:ubiquinone oxidoreductase subunit S4 | Sageli (30–79%) | Esineb 1 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Sageli (30–79%) | Esineb 3 haiguses |
| PRRT2proline rich transmembrane protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 24 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| RCC1regulator of chromosome condensation 1 | Sageli (30–79%) | Esineb 1 haiguses |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sageli (30–79%) | Esineb 2 haiguses |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TBK1TANK binding kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TICAM1TIR domain containing adaptor molecule 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TLR3toll like receptor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| TRAF3TNF receptor associated factor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| TYMPthymidine phosphorylase | Sageli (30–79%) | Esineb 1 haiguses |
| UNC93B1unc-93B1 regulator of TLR signaling | Sageli (30–79%) | Esineb 1 haiguses |
| BTNL2butyrophilin like 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GBE11,4-alpha-glucan branching enzyme 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRNPprion protein (Kanno blood group) | Mõnikord (5–29%) | Esineb 2 haiguses |
| FTLferritin light chain | Harva (1–4%) | Esineb 1 haiguses |
| LMNB1lamin B1 | Harva (1–4%) | Esineb 1 haiguses |
| CD59CD59 molecule (CD59 blood group) | Pole registreeritud | Esineb 1 haiguses |
| EGR2early growth response 2 | Pole registreeritud | Esineb 1 haiguses |
| GFAPglial fibrillary acidic protein | Pole registreeritud | Esineb 1 haiguses |
| PEX7peroxisomal biogenesis factor 7 | Pole registreeritud | Esineb 1 haiguses |
| PHYHphytanoyl-CoA 2-hydroxylase | Pole registreeritud | Esineb 1 haiguses |
| PMP22peripheral myelin protein 22 | Pole registreeritud | Esineb 1 haiguses |
| PRXperiaxin | Pole registreeritud | Esineb 1 haiguses |
| SUMF1sulfatase modifying factor 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.
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.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast