Tunnus
Increased appetite
Kliiniline nimetus: Polyphagia
A neurological anomaly with gross overeating associated with an abnormally strong desire or need to eat.
Kokkuvõte
- Teised nimetused
- Voracious appetite, Hyperphagia
- Kehasüsteem
- Abnormality of the nervous system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Increased appetite, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test81 geeni on seotud tunnusega Increased appetite
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Increased appetite. 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 |
|---|---|---|
| ADCY3adenylate cyclase 3 | Alati | Esineb 1 haiguses |
| ATP5F1BATP synthase F1 subunit beta | Alati | Esineb 1 haiguses |
| BBS9Bardet-Biedl syndrome 9 | Alati | Esineb 1 haiguses |
| FAM177A1family with sequence similarity 177 member A1 | Alati | Esineb 1 haiguses |
| FASTKD5FASTK mitochondrial RNA regulator 5 | Alati | Esineb 1 haiguses |
| IFT74intraflagellar transport 74 | Alati | Esineb 1 haiguses |
| LEPleptin | Alati | Esineb 2 haiguses |
| LRRC7leucine rich repeat containing 7 | Alati | Esineb 1 haiguses |
| MN1MN1 proto-oncogene, transcriptional regulator | Alati | Esineb 1 haiguses |
| NTRK2neurotrophic receptor tyrosine kinase 2 | Alati | Esineb 1 haiguses |
| OFD1OFD1 centriole and centriolar satellite protein | Alati | Esineb 1 haiguses |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Alati | Esineb 1 haiguses |
| LEPRleptin receptor | Väga sageli (80–99%) | Esineb 2 haiguses |
| MAGEL2MAGE family member L2 | Väga sageli (80–99%) | Esineb 7 haiguses |
| MC4Rmelanocortin 4 receptor | Väga sageli (80–99%) | Esineb 2 haiguses |
| NDNnecdin, MAGE family member | Väga sageli (80–99%) | Esineb 4 haiguses |
| OCA2OCA2 melanosomal transmembrane protein | Väga sageli (80–99%) | Esineb 3 haiguses |
| PCSK1proprotein convertase subtilisin/kexin type 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| POMCproopiomelanocortin | Väga sageli (80–99%) | Esineb 2 haiguses |
| PREPLprolyl endopeptidase like | Väga sageli (80–99%) | Esineb 1 haiguses |
| SH2B1SH2B adaptor protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SIM1SIM bHLH transcription factor 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| SLC3A1solute carrier family 3 member 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Väga sageli (80–99%) | Esineb 5 haiguses |
| ADNPactivity dependent neuroprotector homeobox | Sageli (30–79%) | Esineb 2 haiguses |
| ALMS1ALMS1 centrosome and basal body associated protein | Sageli (30–79%) | Esineb 1 haiguses |
| ATP10AATPase phospholipid transporting 10A (putative) | Sageli (30–79%) | Esineb 1 haiguses |
| CHD8chromodomain helicase DNA binding protein 8 | Sageli (30–79%) | Esineb 1 haiguses |
| EZH2enhancer of zeste 2 polycomb repressive complex 2 subunit | Sageli (30–79%) | Esineb 1 haiguses |
| GNASGNAS complex locus | Sageli (30–79%) | Esineb 2 haiguses |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MBD5methyl-CpG binding domain protein 5 | Sageli (30–79%) | Esineb 2 haiguses |
| MEN1menin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MKRN3makorin ring finger protein 3 | Sageli (30–79%) | Esineb 1 haiguses |
| MYT1Lmyelin transcription factor 1 like | Sageli (30–79%) | Esineb 2 haiguses |
| NPAP1nuclear pore associated protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PWAR1Prader Willi/Angelman region RNA 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Sageli (30–79%) | Esineb 1 haiguses |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 41 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| SUPT16HSPT16 homolog, facilitates chromatin remodeling subunit | Sageli (30–79%) | Esineb 1 haiguses |
| TRANK1tetratricopeptide repeat and ankyrin repeat containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| UBE3Aubiquitin protein ligase E3A | Sageli (30–79%) | Esineb 1 haiguses |
| YY1YY1 transcription factor | Sageli (30–79%) | Esineb 1 haiguses |
| ABCC8ATP binding cassette subfamily C member 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CASZ1castor zinc finger 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTNNB1catenin beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Mõnikord (5–29%) | Esineb 1 haiguses |
| HNF1AHNF1 homeobox A | Mõnikord (5–29%) | Esineb 2 haiguses |
| HSPG2heparan sulfate proteoglycan 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HTThuntingtin | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNAB2potassium voltage-gated channel subfamily A regulatory beta subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LUZP1leucine zipper protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAN1B1mannosidase alpha class 1B member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MMP23Bmatrix metallopeptidase 23B | Mõnikord (5–29%) | Esineb 1 haiguses |
| PDPNpodoplanin | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRDM16PR/SET domain 16 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRKCZprotein kinase C zeta | Mõnikord (5–29%) | Esineb 1 haiguses |
| REREarginine-glutamic acid dipeptide repeats | Mõnikord (5–29%) | Esineb 1 haiguses |
| RFX7regulatory factor X7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SATB2SATB homeobox 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SKISKI proto-oncogene | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC2A3solute carrier family 2 member 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPENspen family transcriptional repressor | Mõnikord (5–29%) | Esineb 1 haiguses |
| SRRM2serine/arginine repetitive matrix 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| UBE4Bubiquitination factor E4B | Mõnikord (5–29%) | Esineb 1 haiguses |
| UCP2uncoupling protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZFXzinc finger protein X-linked | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZSCAN10zinc finger and SCAN domain containing 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ACBD6acyl-CoA binding domain containing 6 | Harva (1–4%) | Esineb 1 haiguses |
| AGPAT21-acylglycerol-3-phosphate O-acyltransferase 2 | Pole registreeritud | Esineb 1 haiguses |
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Pole registreeritud | Esineb 1 haiguses |
| GPR101G protein-coupled receptor 101 | Pole registreeritud | Esineb 1 haiguses |
| GRNgranulin precursor | Pole registreeritud | Esineb 1 haiguses |
| IL6interleukin 6 | Pole registreeritud | Esineb 1 haiguses |
| MAPTmicrotubule associated protein tau | Pole registreeritud | Esineb 2 haiguses |
| PSEN1presenilin 1 | Pole registreeritud | Esineb 2 haiguses |
| SETD2SET domain containing 2, histone lysine methyltransferase | Pole registreeritud | Esineb 1 haiguses |
| SLC5A2solute carrier family 5 member 2 | 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.
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Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast