Egenskap
Increased plasma triglycerides
Klinisk navn: Hypertriglyceridemia
The concentration of triglyceride in the blood circulation is above the upper limit of normal.
Sammendrag
- Også kalt
- Increased serum triglycerides, Increased triglycerides, Elevated triglyceride concentration, Elevated triglyceride level, Elevated triglyceride level in blood, Increased circulating Tg levels, Increased plasma Tg levels, Increased triglyceride concentration, Increased triglyceride level, Increased triglyceride level in blood
- Kroppssystem
- Laboratory abnormality
ReferansegenomGRCh38hg38
Posisjoner på gen- og variantsidene følger dette valget i denne nettleseren.
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Få mitt Genome Test131 gener knyttet til Increased plasma triglycerides
Endringer i disse genene forårsaker sjeldne tilstander der Increased plasma triglycerides forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| ADRA2Aadrenoceptor alpha 2A | Alltid | I 1 tilstand |
| AK2adenylate kinase 2 | Alltid | I 1 tilstand |
| APOC2apolipoprotein C2 | Alltid | I 1 tilstand |
| CAV1caveolin 1 | Alltid | I 2 tilstander |
| CIDECcell death inducing DFFA like effector c | Alltid | I 2 tilstander |
| CREB3L3cAMP responsive element binding protein 3 like 3 | Alltid | I 1 tilstand |
| FARSAphenylalanyl-tRNA synthetase subunit alpha | Alltid | I 1 tilstand |
| GPD1glycerol-3-phosphate dehydrogenase 1 | Alltid | I 1 tilstand |
| GPIHBP1glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 | Alltid | I 1 tilstand |
| LDLRAP1low density lipoprotein receptor adaptor protein 1 | Alltid | I 1 tilstand |
| LIPClipase C, hepatic type | Alltid | I 2 tilstander |
| LMF1lipase maturation factor 1 | Alltid | I 1 tilstand |
| MCM10minichromosome maintenance 10 replication initiation factor | Alltid | I 1 tilstand |
| NSMCE2NSE2 SUMO ligase component of SMC5/6 complex | Alltid | I 2 tilstander |
| PCYT1Aphosphate cytidylyltransferase 1A, choline | Alltid | I 1 tilstand |
| PIK3CGphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | Alltid | I 1 tilstand |
| PLIN1perilipin 1 | Alltid | I 2 tilstander |
| PLVAPplasmalemma vesicle associated protein | Alltid | I 1 tilstand |
| PPARGperoxisome proliferator activated receptor gamma | Alltid | I 2 tilstander |
| RBSNrabenosyn, RAB effector | Alltid | I 2 tilstander |
| RC3H1ring finger and CCCH-type domains 1 | Alltid | I 1 tilstand |
| SLC19A1solute carrier family 19 member 1 | Alltid | I 1 tilstand |
| STX11syntaxin 11 | Alltid | I 2 tilstander |
| SUPT7LSPT7 like, STAGA complex subunit gamma | Alltid | I 1 tilstand |
| WRNWRN RecQ like helicase | Alltid | I 1 tilstand |
| YARS1tyrosyl-tRNA synthetase 1 | Alltid | I 1 tilstand |
| ABCA1ATP binding cassette subfamily A member 1 | Svært ofte (80–99 %) | I 2 tilstander |
| AGLamylo-alpha-1,6-glucosidase and 4-alpha-glucanotransferase | Svært ofte (80–99 %) | I 1 tilstand |
| AKT2AKT serine/threonine kinase 2 | Svært ofte (80–99 %) | I 1 tilstand |
| ALMS1ALMS1 centrosome and basal body associated protein | Svært ofte (80–99 %) | I 2 tilstander |
| APOEapolipoprotein E | Svært ofte (80–99 %) | I 2 tilstander |
| CYP7A1cytochrome P450 family 7 subfamily A member 1 | Svært ofte (80–99 %) | I 1 tilstand |
| LIPElipase E, hormone sensitive type | Svært ofte (80–99 %) | I 1 tilstand |
| LMNAlamin A/C | Svært ofte (80–99 %) | I 8 tilstander |
| PHKBphosphorylase kinase regulatory subunit beta | Svært ofte (80–99 %) | I 1 tilstand |
| SLC25A13solute carrier family 25 member 13 | Svært ofte (80–99 %) | I 4 tilstander |
| SLC37A4solute carrier family 37 member 4 | Svært ofte (80–99 %) | I 1 tilstand |
| SMPD1sphingomyelin phosphodiesterase 1 | Svært ofte (80–99 %) | I 3 tilstander |
| XIAPX-linked inhibitor of apoptosis | Svært ofte (80–99 %) | I 1 tilstand |
| XRCC4X-ray repair cross complementing 4 | Svært ofte (80–99 %) | I 1 tilstand |
Vis 91 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| ABHD5abhydrolase domain containing 5, lysophosphatidic acid acyltransferase | Ofte (30–79 %) | I 1 tilstand |
| ADCY3adenylate cyclase 3 | Ofte (30–79 %) | I 1 tilstand |
| ARL6ARF like GTPase 6 | Ofte (30–79 %) | I 1 tilstand |
| BBIP1BBSome interacting protein 1 | Ofte (30–79 %) | I 1 tilstand |
| BBS1Bardet-Biedl syndrome 1 | Ofte (30–79 %) | I 1 tilstand |
| BBS10Bardet-Biedl syndrome 10 | Ofte (30–79 %) | I 1 tilstand |
| BBS12Bardet-Biedl syndrome 12 | Ofte (30–79 %) | I 1 tilstand |
| BBS2Bardet-Biedl syndrome 2 | Ofte (30–79 %) | I 1 tilstand |
| BBS4Bardet-Biedl syndrome 4 | Ofte (30–79 %) | I 1 tilstand |
| BBS5Bardet-Biedl syndrome 5 | Ofte (30–79 %) | I 1 tilstand |
| BBS7Bardet-Biedl syndrome 7 | Ofte (30–79 %) | I 1 tilstand |
| BBS9Bardet-Biedl syndrome 9 | Ofte (30–79 %) | I 1 tilstand |
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Ofte (30–79 %) | I 3 tilstander |
| CAVIN1caveolae associated protein 1 | Ofte (30–79 %) | I 1 tilstand |
| CELA2Achymotrypsin like elastase 2A | Ofte (30–79 %) | I 1 tilstand |
| CEP19centrosomal protein 19 | Ofte (30–79 %) | I 2 tilstander |
| CEP290centrosomal protein 290 | Ofte (30–79 %) | I 1 tilstand |
| CFAP418cilia and flagella associated protein 418 | Ofte (30–79 %) | I 1 tilstand |
| DEF6DEF6 guanine nucleotide exchange factor | Ofte (30–79 %) | I 1 tilstand |
| EMDemerin | Ofte (30–79 %) | I 1 tilstand |
| EXTL3exostosin like glycosyltransferase 3 | Ofte (30–79 %) | I 1 tilstand |
| FHL1four and a half LIM domains 1 | Ofte (30–79 %) | I 1 tilstand |
| GUK1guanylate kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| IFT172intraflagellar transport 172 | Ofte (30–79 %) | I 1 tilstand |
| IFT27intraflagellar transport 27 | Ofte (30–79 %) | I 1 tilstand |
| IFT74intraflagellar transport 74 | Ofte (30–79 %) | I 1 tilstand |
| LEPleptin | Ofte (30–79 %) | I 1 tilstand |
| LEPRleptin receptor | Ofte (30–79 %) | I 1 tilstand |
| LIPAlipase A, lysosomal acid type | Ofte (30–79 %) | I 2 tilstander |
| LZTFL1leucine zipper transcription factor like 1 | Ofte (30–79 %) | I 1 tilstand |
| MKKSMKKS centrosomal shuttling protein | Ofte (30–79 %) | I 1 tilstand |
| MKS1MKS transition zone complex subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| NPHP1nephrocystin 1 | Ofte (30–79 %) | I 1 tilstand |
| PHKA2phosphorylase kinase regulatory subunit alpha 2 | Ofte (30–79 %) | I 2 tilstander |
| PHKG2phosphorylase kinase catalytic subunit gamma 2 | Ofte (30–79 %) | I 2 tilstander |
| PIGHphosphatidylinositol glycan anchor biosynthesis class H | Ofte (30–79 %) | I 1 tilstand |
| PLAAT3phospholipase A and acyltransferase 3 | Ofte (30–79 %) | I 1 tilstand |
| PNPLA2patatin like domain 2, triacylglycerol lipase | Ofte (30–79 %) | I 2 tilstander |
| POLD1DNA polymerase delta 1, catalytic subunit | Ofte (30–79 %) | I 1 tilstand |
| POLR3ARNA polymerase III subunit A | Ofte (30–79 %) | I 2 tilstander |
| PRF1perforin 1 | Ofte (30–79 %) | I 2 tilstander |
| RAI1retinoic acid induced 1 | Ofte (30–79 %) | I 2 tilstander |
| SCAPERS-phase cyclin A associated protein in the ER | Ofte (30–79 %) | I 1 tilstand |
| SCLT1sodium channel and clathrin linker 1 | Ofte (30–79 %) | I 1 tilstand |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | Ofte (30–79 %) | I 1 tilstand |
| SLC7A7solute carrier family 7 member 7 | Ofte (30–79 %) | I 1 tilstand |
| STXBP2syntaxin binding protein 2 | Ofte (30–79 %) | I 2 tilstander |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Ofte (30–79 %) | I 1 tilstand |
| SYNE2spectrin repeat containing nuclear envelope protein 2 | Ofte (30–79 %) | I 1 tilstand |
| TBCKTBC1 domain containing kinase | Ofte (30–79 %) | I 1 tilstand |
| TMEM43transmembrane protein 43 | Ofte (30–79 %) | I 1 tilstand |
| TNFRSF9TNF receptor superfamily member 9 | Ofte (30–79 %) | I 1 tilstand |
| TRIM32tripartite motif containing 32 | Ofte (30–79 %) | I 1 tilstand |
| TTC8tetratricopeptide repeat domain 8 | Ofte (30–79 %) | I 1 tilstand |
| UNC13Dunc-13 homolog D | Ofte (30–79 %) | I 2 tilstander |
| WDPCPWD repeat containing planar cell polarity effector | Ofte (30–79 %) | I 1 tilstand |
| AEBP1AE binding protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| AIPAHR interacting HSP90 co-chaperone | Noen ganger (5–29 %) | I 1 tilstand |
| ASLargininosuccinate lyase | Noen ganger (5–29 %) | I 1 tilstand |
| DYRK1Bdual specificity tyrosine phosphorylation regulated kinase 1B | Noen ganger (5–29 %) | I 1 tilstand |
| GPR101G protein-coupled receptor 101 | Noen ganger (5–29 %) | I 1 tilstand |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| LYSTlysosomal trafficking regulator | Noen ganger (5–29 %) | I 1 tilstand |
| MAGEL2MAGE family member L2 | Noen ganger (5–29 %) | I 1 tilstand |
| MC4Rmelanocortin 4 receptor | Noen ganger (5–29 %) | I 1 tilstand |
| MKRN3makorin ring finger protein 3 | Noen ganger (5–29 %) | I 1 tilstand |
| MTX2metaxin 2 | Noen ganger (5–29 %) | I 1 tilstand |
| NPAP1nuclear pore associated protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Noen ganger (5–29 %) | I 1 tilstand |
| PSMB8proteasome 20S subunit beta 8 | Noen ganger (5–29 %) | I 1 tilstand |
| PWAR1Prader Willi/Angelman region RNA 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC29A3solute carrier family 29 member 3 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC2A2solute carrier family 2 member 2 | Noen ganger (5–29 %) | I 1 tilstand |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Noen ganger (5–29 %) | I 1 tilstand |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Noen ganger (5–29 %) | I 1 tilstand |
| AGPAT21-acylglycerol-3-phosphate O-acyltransferase 2 | Ikke registrert | I 1 tilstand |
| APOA5apolipoprotein A5 | Ikke registrert | I 1 tilstand |
| FECHferrochelatase | Ikke registrert | I 1 tilstand |
| GKglycerol kinase | Ikke registrert | I 1 tilstand |
| HAVCR2hepatitis A virus cellular receptor 2 | Ikke registrert | I 1 tilstand |
| JAG1jagged canonical Notch ligand 1 | Ikke registrert | I 1 tilstand |
| LCATlecithin-cholesterol acyltransferase | Ikke registrert | I 2 tilstander |
| LRP6LDL receptor related protein 6 | Ikke registrert | I 1 tilstand |
| NOTCH3notch receptor 3 | Ikke registrert | I 1 tilstand |
| PSMB4proteasome 20S subunit beta 4 | Ikke registrert | I 1 tilstand |
| PYGLglycogen phosphorylase L | Ikke registrert | I 1 tilstand |
| RSPO1R-spondin 1 | Ikke registrert | I 1 tilstand |
| SAR1Bsecretion associated Ras related GTPase 1B | Ikke registrert | I 1 tilstand |
| SGPL1sphingosine-1-phosphate lyase 1 | Ikke registrert | I 1 tilstand |
| TTPAalpha tocopherol transfer protein | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
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