Træk
Lack of feeling, emotion, interest
Klinisk navn: Apathy
Apathy is a quantitative reduction of interest, motivation and the initiation and persistence of goal-directed behavior, where often the accompanying emotions, thoughts, and social interactions are also diminished. The individual is typically non-reactive to provocations, positive or negative, and appears to not care. Distinguished from lethargy which involves lack of physical or mental energy.
Resumé
- Også kaldet
- Lack of feeling, emotion, interest, motivation, initiation, State of indifference
- Kropssystem
- Abnormality of the nervous system
ReferencegenomGRCh38hg38
Positioner på gen- og variantsider følger dette valg i denne browser.
Read the genes linked to Lack of feeling, emotion, interest, and the rest of your genome, with one test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test94 gener knyttet til Lack of feeling, emotion, interest
Ændringer i disse gener forårsager sjældne tilstande, hvor Lack of feeling, emotion, interest ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| APOEapolipoprotein E | Altid | I 1 tilstand |
| GFAPglial fibrillary acidic protein | Altid | I 1 tilstand |
| LAMB1laminin subunit beta 1 | Altid | I 1 tilstand |
| PLP1proteolipid protein 1 | Altid | I 1 tilstand |
| PSEN2presenilin 2 | Altid | I 1 tilstand |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Altid | I 1 tilstand |
| SCO2synthesis of cytochrome C oxidase 2 | Altid | I 1 tilstand |
| VPS13Avacuolar protein sorting 13 homolog A | Altid | I 2 tilstande |
| DCTN1dynactin subunit 1 | Meget ofte (80–99 %) | I 2 tilstande |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Meget ofte (80–99 %) | I 1 tilstand |
| ACAT1acetyl-CoA acetyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Ofte (30–79 %) | I 2 tilstande |
| CDONcell adhesion associated, oncogene regulated | Ofte (30–79 %) | I 4 tilstande |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Ofte (30–79 %) | I 1 tilstand |
| COQ2coenzyme Q2, polyprenyltransferase | Ofte (30–79 %) | I 2 tilstande |
| CRIPTOcripto, EGF-CFC family member | Ofte (30–79 %) | I 4 tilstande |
| DISP1dispatched RND transporter family member 1 | Ofte (30–79 %) | I 4 tilstande |
| DLL1delta like canonical Notch ligand 1 | Ofte (30–79 %) | I 4 tilstande |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Ofte (30–79 %) | I 1 tilstand |
| FGF8fibroblast growth factor 8 | Ofte (30–79 %) | I 4 tilstande |
| FGFR1fibroblast growth factor receptor 1 | Ofte (30–79 %) | I 2 tilstande |
| FOXH1forkhead box H1 | Ofte (30–79 %) | I 4 tilstande |
| FUSFUS RNA binding protein | Ofte (30–79 %) | I 1 tilstand |
| GAS1growth arrest specific 1 | Ofte (30–79 %) | I 4 tilstande |
| GDAP2ganglioside induced differentiation associated protein 2 | Ofte (30–79 %) | I 1 tilstand |
| GLI2GLI family zinc finger 2 | Ofte (30–79 %) | I 4 tilstande |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Ofte (30–79 %) | I 2 tilstande |
| HTRA2HtrA serine peptidase 2 | Ofte (30–79 %) | I 1 tilstand |
| HTThuntingtin | Ofte (30–79 %) | I 1 tilstand |
| LRRK2leucine rich repeat kinase 2 | Ofte (30–79 %) | I 2 tilstande |
| MAPTmicrotubule associated protein tau | Ofte (30–79 %) | I 6 tilstande |
| MRPL39mitochondrial ribosomal protein L39 | Ofte (30–79 %) | I 1 tilstand |
| NODALnodal growth differentiation factor | Ofte (30–79 %) | I 4 tilstande |
| NOTCH3notch receptor 3 | Ofte (30–79 %) | I 1 tilstand |
| PARK7Parkinsonism associated deglycase | Ofte (30–79 %) | I 1 tilstand |
| PINK1PTEN induced kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| PLCH1phospholipase C eta 1 | Ofte (30–79 %) | I 1 tilstand |
| PODXLpodocalyxin like | Ofte (30–79 %) | I 1 tilstand |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | Ofte (30–79 %) | I 1 tilstand |
| PRKNparkin RBR E3 ubiquitin protein ligase | Ofte (30–79 %) | I 1 tilstand |
Vis 54 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| PRNPprion protein (Kanno blood group) | Ofte (30–79 %) | I 2 tilstande |
| PTCH1patched 1 | Ofte (30–79 %) | I 4 tilstande |
| SHHsonic hedgehog signaling molecule | Ofte (30–79 %) | I 4 tilstande |
| SIX3SIX homeobox 3 | Ofte (30–79 %) | I 4 tilstande |
| SLC2A3solute carrier family 2 member 3 | Ofte (30–79 %) | I 1 tilstand |
| SMC1Astructural maintenance of chromosomes 1A | Ofte (30–79 %) | I 1 tilstand |
| SNCAsynuclein alpha | Ofte (30–79 %) | I 2 tilstande |
| SQSTM1sequestosome 1 | Ofte (30–79 %) | I 3 tilstande |
| STAG2STAG2 cohesin complex component | Ofte (30–79 %) | I 2 tilstande |
| STILSTIL centriolar assembly protein | Ofte (30–79 %) | I 4 tilstande |
| SYNJ1synaptojanin 1 | Ofte (30–79 %) | I 1 tilstand |
| TARDBPTAR DNA binding protein | Ofte (30–79 %) | I 2 tilstande |
| TBK1TANK binding kinase 1 | Ofte (30–79 %) | I 2 tilstande |
| TGIF1TGFB induced factor homeobox 1 | Ofte (30–79 %) | I 4 tilstande |
| TRANK1tetratricopeptide repeat and ankyrin repeat containing 1 | Ofte (30–79 %) | I 1 tilstand |
| TSFMTs translation elongation factor, mitochondrial | Ofte (30–79 %) | I 1 tilstand |
| UCHL1ubiquitin C-terminal hydrolase L1 | Ofte (30–79 %) | I 1 tilstand |
| VCPvalosin containing protein | Ofte (30–79 %) | I 2 tilstande |
| VPS13Cvacuolar protein sorting 13 homolog C | Ofte (30–79 %) | I 2 tilstande |
| ZIC2Zic family zinc finger 2 | Ofte (30–79 %) | I 4 tilstande |
| ALADaminolevulinate dehydratase | Nogle gange (5–29 %) | I 1 tilstand |
| ATP13A2ATPase cation transporting 13A2 | Nogle gange (5–29 %) | I 1 tilstand |
| ATXN10ataxin 10 | Nogle gange (5–29 %) | I 1 tilstand |
| CHD2chromodomain helicase DNA binding protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| CHMP2Bcharged multivesicular body protein 2B | Nogle gange (5–29 %) | I 2 tilstande |
| CPceruloplasmin | Nogle gange (5–29 %) | I 1 tilstand |
| CUX2cut like homeobox 2 | Nogle gange (5–29 %) | I 1 tilstand |
| DNAJC13DnaJ heat shock protein family (Hsp40) member C13 | Nogle gange (5–29 %) | I 1 tilstand |
| DNM1dynamin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| EHMT1euchromatic histone lysine methyltransferase 1 | Nogle gange (5–29 %) | I 2 tilstande |
| EIF4G1eukaryotic translation initiation factor 4 gamma 1 | Nogle gange (5–29 %) | I 1 tilstand |
| GABRB3gamma-aminobutyric acid type A receptor subunit beta3 | Nogle gange (5–29 %) | I 1 tilstand |
| GBA1glucosylceramidase beta 1 | Nogle gange (5–29 %) | I 2 tilstande |
| GIGYF2GRB10 interacting GYF protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| GRNgranulin precursor | Nogle gange (5–29 %) | I 2 tilstande |
| HTRA1HtrA serine peptidase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MAPK10mitogen-activated protein kinase 10 | Nogle gange (5–29 %) | I 1 tilstand |
| PSEN1presenilin 1 | Nogle gange (5–29 %) | I 3 tilstande |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TMEM106Btransmembrane protein 106B | Nogle gange (5–29 %) | I 1 tilstand |
| TREM2triggering receptor expressed on myeloid cells 2 | Nogle gange (5–29 %) | I 1 tilstand |
| TREX1three prime repair exonuclease 1 | Nogle gange (5–29 %) | I 1 tilstand |
| VPS35VPS35 retromer complex component | Nogle gange (5–29 %) | I 1 tilstand |
| BMP6bone morphogenetic protein 6 | Sjældent (1–4%) | I 1 tilstand |
| HFEhomeostatic iron regulator | Sjældent (1–4%) | I 1 tilstand |
| PDGFBplatelet derived growth factor subunit B | Sjældent (1–4%) | I 1 tilstand |
| C9orf72C9orf72-SMCR8 complex subunit | Ikke registreret | I 1 tilstand |
| DNMT1DNA methyltransferase 1 | Ikke registreret | I 1 tilstand |
| GM2Aganglioside GM2 activator | Ikke registreret | I 1 tilstand |
| HEXAhexosaminidase subunit alpha | Ikke registreret | I 1 tilstand |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Ikke registreret | I 1 tilstand |
| JPH3junctophilin 3 | Ikke registreret | I 1 tilstand |
| SPASTspastin | Ikke registreret | I 1 tilstand |
| TMEM240transmembrane protein 240 | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.16-c6eea6bf.
Én test. Svar for hele livet.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger