Tunnus
Malabsorption
Impaired ability to absorb one or more nutrients from the intestine.
Kokkuvõte
- Teised nimetused
- Intestinal malabsorption
- Kehasüsteem
- Abnormality of the digestive system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Malabsorption, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test190 geeni on seotud tunnusega Malabsorption
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Malabsorption. 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 |
|---|---|---|
| CD55CD55 molecule (Cromer blood group) | Alati | Esineb 1 haiguses |
| DSG1desmoglein 1 | Alati | Esineb 1 haiguses |
| HYOU1hypoxia up-regulated 1 | Alati | Esineb 1 haiguses |
| NEUROG3neurogenin 3 | Alati | Esineb 2 haiguses |
| SPINK5serine peptidase inhibitor Kazal type 5 | Alati | Esineb 2 haiguses |
| ADAMTS3ADAM metallopeptidase with thrombospondin type 1 motif 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ANTXR2ANTXR cell adhesion molecule 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ATMATM serine/threonine kinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| BMPR1Abone morphogenetic protein receptor type 1A | Väga sageli (80–99%) | Esineb 1 haiguses |
| BRCA2BRCA2 DNA repair associated | Väga sageli (80–99%) | Esineb 1 haiguses |
| CCBE1collagen and calcium binding EGF domains 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CD4CD4 molecule | Väga sageli (80–99%) | Esineb 1 haiguses |
| CEACAM3CEA cell adhesion molecule 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CEACAM6CEA cell adhesion molecule 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CFTRCF transmembrane conductance regulator | Väga sageli (80–99%) | Esineb 1 haiguses |
| CHEK2checkpoint kinase 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CLCA4chloride channel accessory 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CYBAcytochrome b-245 alpha chain | Väga sageli (80–99%) | Esineb 1 haiguses |
| CYBBcytochrome b-245 beta chain | Väga sageli (80–99%) | Esineb 1 haiguses |
| CYBC1cytochrome b-245 chaperone 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DCTN4dynactin subunit 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| EDNRAendothelin receptor type A | Väga sageli (80–99%) | Esineb 1 haiguses |
| EPCAMepithelial cell adhesion molecule | Väga sageli (80–99%) | Esineb 2 haiguses |
| FAT4FAT atypical cadherin 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FLNAfilamin A | Väga sageli (80–99%) | Esineb 1 haiguses |
| GCLCglutamate-cysteine ligase catalytic subunit | Väga sageli (80–99%) | Esineb 1 haiguses |
| GLAgalactosidase alpha | Väga sageli (80–99%) | Esineb 1 haiguses |
| GSTM3glutathione S-transferase mu 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| HFEhomeostatic iron regulator | Väga sageli (80–99%) | Esineb 1 haiguses |
| HMOX1heme oxygenase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| HSD3B7hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | Väga sageli (80–99%) | Esineb 1 haiguses |
| IRF4interferon regulatory factor 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KCNN4potassium calcium-activated channel subfamily N member 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KRASKRas proto-oncogene, GTPase | Väga sageli (80–99%) | Esineb 1 haiguses |
| MIFmacrophage migration inhibitory factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| MLH1mutL homolog 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MSH2mutS homolog 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MSH6mutS homolog 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MUTYHmutY DNA glycosylase | Väga sageli (80–99%) | Esineb 1 haiguses |
| NCF1neutrophil cytosolic factor 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
Näita veel 150 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| NCF2neutrophil cytosolic factor 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NCF4neutrophil cytosolic factor 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NPATnuclear protein, coactivator of histone transcription | Väga sageli (80–99%) | Esineb 1 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Väga sageli (80–99%) | Esineb 1 haiguses |
| PMS1PMS1 homolog 1, mismatch repair system component | Väga sageli (80–99%) | Esineb 1 haiguses |
| PMS2PMS1 homolog 2, mismatch repair system component | Väga sageli (80–99%) | Esineb 1 haiguses |
| POLD1DNA polymerase delta 1, catalytic subunit | Väga sageli (80–99%) | Esineb 1 haiguses |
| POLEDNA polymerase epsilon, catalytic subunit | Väga sageli (80–99%) | Esineb 1 haiguses |
| RPS20ribosomal protein S20 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SEMA4Asemaphorin 4A | Väga sageli (80–99%) | Esineb 1 haiguses |
| SERPINA1serpin family A member 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC11A1solute carrier family 11 member 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC26A9solute carrier family 26 member 9 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC39A4solute carrier family 39 member 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC6A14solute carrier family 6 member 14 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC9A3solute carrier family 9 member A3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| STX1Asyntaxin 1A | Väga sageli (80–99%) | Esineb 2 haiguses |
| TGFB1transforming growth factor beta 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TGFBR2transforming growth factor beta receptor 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ACDACD shelterin complex subunit and telomerase recruitment factor | Sageli (30–79%) | Esineb 1 haiguses |
| AK2adenylate kinase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| APCAPC regulator of Wnt signaling pathway | Sageli (30–79%) | Esineb 1 haiguses |
| ARXaristaless related homeobox | Sageli (30–79%) | Esineb 1 haiguses |
| ASXL1ASXL transcriptional regulator 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ATP7AATPase copper transporting alpha | Sageli (30–79%) | Esineb 1 haiguses |
| CAV1caveolin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CBLCbl proto-oncogene | Sageli (30–79%) | Esineb 1 haiguses |
| CCN2cellular communication network factor 2 | Sageli (30–79%) | Esineb 1 haiguses |
| CCR6C-C motif chemokine receptor 6 | Sageli (30–79%) | Esineb 1 haiguses |
| CDCA7cell division cycle associated 7 | Sageli (30–79%) | Esineb 1 haiguses |
| CLTRNcollectrin, amino acid transport regulator | Sageli (30–79%) | Esineb 1 haiguses |
| CTC1CST telomere replication complex component 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CTNNB1catenin beta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DKC1dyskerin pseudouridine synthase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DMP1dentin matrix acidic phosphoprotein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DNMT3BDNA methyltransferase 3 beta | Sageli (30–79%) | Esineb 2 haiguses |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| HELLShelicase, lymphoid specific | Sageli (30–79%) | Esineb 1 haiguses |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| IRF5interferon regulatory factor 5 | Sageli (30–79%) | Esineb 1 haiguses |
| NHP2NHP2 ribonucleoprotein | Sageli (30–79%) | Esineb 1 haiguses |
| NOP10NOP10 ribonucleoprotein | Sageli (30–79%) | Esineb 1 haiguses |
| NPM1nucleophosmin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PARNpoly(A)-specific ribonuclease | Sageli (30–79%) | Esineb 1 haiguses |
| PEX1peroxisomal biogenesis factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PEX10peroxisomal biogenesis factor 10 | Sageli (30–79%) | Esineb 1 haiguses |
| PEX11Bperoxisomal biogenesis factor 11 beta | Sageli (30–79%) | Esineb 1 haiguses |
| PEX12peroxisomal biogenesis factor 12 | Sageli (30–79%) | Esineb 1 haiguses |
| PEX13peroxisomal biogenesis factor 13 | Sageli (30–79%) | Esineb 1 haiguses |
| PEX14peroxisomal biogenesis factor 14 | Sageli (30–79%) | Esineb 1 haiguses |
| PEX16peroxisomal biogenesis factor 16 | Sageli (30–79%) | Esineb 1 haiguses |
| PEX19peroxisomal biogenesis factor 19 | Sageli (30–79%) | Esineb 1 haiguses |
| PEX2peroxisomal biogenesis factor 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PEX26peroxisomal biogenesis factor 26 | Sageli (30–79%) | Esineb 1 haiguses |
| PEX3peroxisomal biogenesis factor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| PEX5peroxisomal biogenesis factor 5 | Sageli (30–79%) | Esineb 1 haiguses |
| PEX6peroxisomal biogenesis factor 6 | Sageli (30–79%) | Esineb 1 haiguses |
| RECQL4RecQ like helicase 4 | Sageli (30–79%) | Esineb 1 haiguses |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Sageli (30–79%) | Esineb 2 haiguses |
| RTEL1regulator of telomere elongation helicase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| RUNX1RUNX family transcription factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SAA1serum amyloid A1 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC6A19solute carrier family 6 member 19 | Sageli (30–79%) | Esineb 1 haiguses |
| SRSF2serine and arginine rich splicing factor 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TERCtelomerase RNA component | Sageli (30–79%) | Esineb 1 haiguses |
| TERTtelomerase reverse transcriptase | Sageli (30–79%) | Esineb 1 haiguses |
| TET2tet methylcytosine dioxygenase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TINF2TERF1 interacting nuclear factor 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TRMT5tRNA methyltransferase 5 | Sageli (30–79%) | Esineb 1 haiguses |
| TYMSthymidylate synthetase | Sageli (30–79%) | Esineb 1 haiguses |
| UHRF1ubiquitin like with PHD and ring finger domains 1 | Sageli (30–79%) | Esineb 1 haiguses |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| WRAP53WD repeat containing antisense to TP53 | Sageli (30–79%) | Esineb 1 haiguses |
| ZBTB24zinc finger and BTB domain containing 24 | Sageli (30–79%) | Esineb 1 haiguses |
| AGAaspartylglucosaminidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| AIREautoimmune regulator | Mõnikord (5–29%) | Esineb 2 haiguses |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Mõnikord (5–29%) | Esineb 1 haiguses |
| BLNKB cell linker | Mõnikord (5–29%) | Esineb 1 haiguses |
| BTKBruton tyrosine kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| C4Acomplement C4A (Chido/Rodgers blood group) | Mõnikord (5–29%) | Esineb 1 haiguses |
| CALRcalreticulin | Mõnikord (5–29%) | Esineb 1 haiguses |
| CCR1C-C motif chemokine receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CD79ACD79a molecule | Mõnikord (5–29%) | Esineb 1 haiguses |
| CD79BCD79b molecule | Mõnikord (5–29%) | Esineb 1 haiguses |
| CISD2CDGSH iron sulfur domain 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CLIP2CAP-Gly domain containing linker protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Mõnikord (5–29%) | Esineb 1 haiguses |
| EIF4Heukaryotic translation initiation factor 4H | Mõnikord (5–29%) | Esineb 1 haiguses |
| ELNelastin | Mõnikord (5–29%) | Esineb 1 haiguses |
| ERAP1endoplasmic reticulum aminopeptidase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| F5coagulation factor V | Mõnikord (5–29%) | Esineb 1 haiguses |
| FASFas cell surface death receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Mõnikord (5–29%) | Esineb 1 haiguses |
| FOXN1forkhead box N1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FOXP3forkhead box P3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GTF2Igeneral transcription factor IIi | Mõnikord (5–29%) | Esineb 1 haiguses |
| GTF2IRD1GTF2I repeat domain containing 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GTF2IRD2GTF2I repeat domain containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HLA-Bmajor histocompatibility complex, class I, B | Mõnikord (5–29%) | Esineb 1 haiguses |
| HPGD15-hydroxyprostaglandin dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| IFNGR1interferon gamma receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IGHMimmunoglobulin heavy constant mu | Mõnikord (5–29%) | Esineb 1 haiguses |
| IGLL1immunoglobulin lambda like polypeptide 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 |
| JAK2Janus kinase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KLRC4killer cell lectin like receptor C4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LIG4DNA ligase 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LIMK1LIM domain kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LPIN2lipin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LRRC8Aleucine rich repeat containing 8 VRAC subunit A | Mõnikord (5–29%) | Esineb 1 haiguses |
| MADDMAP kinase activating death domain | Mõnikord (5–29%) | Esineb 1 haiguses |
| MEFVMEFV innate immunity regulator, pyrin | Mõnikord (5–29%) | Esineb 2 haiguses |
| METTL27methyltransferase like 27 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MYD88MYD88 innate immune signal transduction adaptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Mõnikord (5–29%) | Esineb 2 haiguses |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| RFC2replication factor C subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC29A3solute carrier family 29 member 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPI1Spi-1 proto-oncogene | Mõnikord (5–29%) | Esineb 1 haiguses |
| STAT4signal transducer and activator of transcription 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TBL2transducin beta like 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TCF3transcription factor 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TLR4toll like receptor 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TMEM270transmembrane protein 270 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TREHtrehalase | Mõnikord (5–29%) | Esineb 1 haiguses |
| UBAC2UBA domain containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| VPS37DVPS37D subunit of ESCRT-I | Mõnikord (5–29%) | Esineb 1 haiguses |
| WFS1wolframin ER transmembrane glycoprotein | Mõnikord (5–29%) | Esineb 1 haiguses |
| ABCB11ATP binding cassette subfamily B member 11 | Pole registreeritud | Esineb 1 haiguses |
| ABCB4ATP binding cassette subfamily B member 4 | Pole registreeritud | Esineb 1 haiguses |
| ATP8B1ATPase phospholipid transporting 8B1 | Pole registreeritud | Esineb 1 haiguses |
| CIITAclass II major histocompatibility complex transactivator | Pole registreeritud | Esineb 1 haiguses |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Pole registreeritud | Esineb 1 haiguses |
| KDM6Alysine demethylase 6A | Pole registreeritud | Esineb 1 haiguses |
| KMT2Dlysine methyltransferase 2D | Pole registreeritud | Esineb 1 haiguses |
| PCSK1proprotein convertase subtilisin/kexin type 1 | Pole registreeritud | Esineb 1 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Pole registreeritud | Esineb 2 haiguses |
| RFX6regulatory factor X6 | Pole registreeritud | Esineb 1 haiguses |
| SIsucrase-isomaltase | Pole registreeritud | Esineb 1 haiguses |
| SLC2A2solute carrier family 2 member 2 | Pole registreeritud | Esineb 1 haiguses |
| SLC46A1solute carrier family 46 member 1 | Pole registreeritud | Esineb 1 haiguses |
| SLC5A1solute carrier family 5 member 1 | Pole registreeritud | Esineb 1 haiguses |
| TYMPthymidine phosphorylase | 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.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast