Træk
Wide based walk
Klinisk navn: Broad-based gait
An abnormal gait pattern in which persons stand and walk with their feet spaced widely apart. This is often a component of cerebellar ataxia.
Resumé
- Også kaldet
- Broad based gait, Wide based gait, Wide-based gait
- Kropssystem
- Abnormality of the nervous system
ReferencegenomGRCh38hg38
Positioner på gen- og variantsider følger dette valg i denne browser.
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Bestil min Genome Test128 gener knyttet til Wide based walk
Ændringer i disse gener forårsager sjældne tilstande, hvor Wide based walk 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 |
|---|---|---|
| AHDC1AT-hook DNA binding motif containing 1 | Altid | I 1 tilstand |
| ASPNATaspartate N-acetyltransferase | Altid | I 1 tilstand |
| CADcarbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase | Altid | I 1 tilstand |
| CTSAcathepsin A | Altid | I 1 tilstand |
| CWF19L1CWF19 like cell cycle control factor 1 | Altid | I 1 tilstand |
| EBF3EBF transcription factor 3 | Altid | I 1 tilstand |
| EGR2early growth response 2 | Altid | I 1 tilstand |
| FEM1Bfem-1 homolog B | Altid | I 1 tilstand |
| GTPBP2GTP binding protein 2 | Altid | I 1 tilstand |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Altid | I 2 tilstande |
| MAP1Bmicrotubule associated protein 1B | Altid | I 1 tilstand |
| MPZmyelin protein zero | Altid | I 1 tilstand |
| NDUFAF2NADH:ubiquinone oxidoreductase complex assembly factor 2 | Altid | I 1 tilstand |
| NKX2-1NK2 homeobox 1 | Altid | I 1 tilstand |
| PLP1proteolipid protein 1 | Altid | I 1 tilstand |
| PMP22peripheral myelin protein 22 | Altid | I 1 tilstand |
| PRDM13PR/SET domain 13 | Altid | I 1 tilstand |
| PRXperiaxin | Altid | I 2 tilstande |
| RAB11BRAB11B, member RAS oncogene family | Altid | I 1 tilstand |
| RAB3ARAB3A, member RAS oncogene family | Altid | I 1 tilstand |
| RNF113Aring finger protein 113A | Altid | I 1 tilstand |
| RNU12RNA, U12 small nuclear | Altid | I 2 tilstande |
| RNU6ATACRNA, U6atac small nuclear | Altid | I 1 tilstand |
| SEL1LSEL1L adaptor subunit of SYVN1 ubiquitin ligase | Altid | I 1 tilstand |
| SPTAN1spectrin alpha, non-erythrocytic 1 | Altid | I 1 tilstand |
| SPTBN2spectrin beta, non-erythrocytic 2 | Altid | I 1 tilstand |
| TINF2TERF1 interacting nuclear factor 2 | Altid | I 1 tilstand |
| TM2D3TM2 domain containing 3 | Altid | I 1 tilstand |
| TOP3ADNA topoisomerase III alpha | Altid | I 1 tilstand |
| UROC1urocanate hydratase 1 | Altid | I 2 tilstande |
| UBE3Aubiquitin protein ligase E3A | Meget ofte (80–99 %) | I 5 tilstande |
| AP5Z1adaptor related protein complex 5 subunit zeta 1 | Ofte (30–79 %) | I 2 tilstande |
| ATCAYATCAY kinesin light chain interacting caytaxin | Ofte (30–79 %) | I 2 tilstande |
| BICD2BICD cargo adaptor 2 | Ofte (30–79 %) | I 1 tilstand |
| CAMTA1calmodulin binding transcription activator 1 | Ofte (30–79 %) | I 1 tilstand |
| CARS1cysteinyl-tRNA synthetase 1 | Ofte (30–79 %) | I 1 tilstand |
| CCDC88Ccoiled-coil and HOOK domain protein 88C | Ofte (30–79 %) | I 2 tilstande |
| CERT1ceramide transporter 1 | Ofte (30–79 %) | I 1 tilstand |
| COPB2coat protein complex I subunit beta 2 | Ofte (30–79 %) | I 1 tilstand |
| COQ2coenzyme Q2, polyprenyltransferase | Ofte (30–79 %) | I 1 tilstand |
Vis 88 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| CUL4Bcullin 4B | Ofte (30–79 %) | I 1 tilstand |
| DDX3XDEAD-box helicase 3 X-linked | Ofte (30–79 %) | I 2 tilstande |
| DEAF1DEAF1 transcription factor | Ofte (30–79 %) | I 1 tilstand |
| DLATdihydrolipoamide S-acetyltransferase | Ofte (30–79 %) | I 1 tilstand |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Ofte (30–79 %) | I 1 tilstand |
| EXT2exostosin glycosyltransferase 2 | Ofte (30–79 %) | I 1 tilstand |
| FNIP1folliculin interacting protein 1 | Ofte (30–79 %) | I 1 tilstand |
| GPT2glutamic--pyruvic transaminase 2 | Ofte (30–79 %) | I 1 tilstand |
| HTThuntingtin | Ofte (30–79 %) | I 1 tilstand |
| MAB21L1mab-21 like 1 | Ofte (30–79 %) | I 1 tilstand |
| MED12mediator complex subunit 12 | Ofte (30–79 %) | I 1 tilstand |
| NSUN2NOP2/Sun RNA methyltransferase 2 | Ofte (30–79 %) | I 1 tilstand |
| PPFIA3PPFI scaffold protein A3 | Ofte (30–79 %) | I 1 tilstand |
| PPM1Dprotein phosphatase, Mg2+/Mn2+ dependent 1D | Ofte (30–79 %) | I 1 tilstand |
| RNU2-2RNA, U2 small nuclear 2 | Ofte (30–79 %) | I 1 tilstand |
| SGCBsarcoglycan beta | Ofte (30–79 %) | I 1 tilstand |
| SGCGsarcoglycan gamma | Ofte (30–79 %) | I 1 tilstand |
| SHANK3SH3 and multiple ankyrin repeat domains 3 | Ofte (30–79 %) | I 1 tilstand |
| SLC6A8solute carrier family 6 member 8 | Ofte (30–79 %) | I 1 tilstand |
| SNX14sorting nexin 14 | Ofte (30–79 %) | I 1 tilstand |
| TMEM222transmembrane protein 222 | Ofte (30–79 %) | I 1 tilstand |
| TPP1tripeptidyl peptidase 1 | Ofte (30–79 %) | I 1 tilstand |
| TPRtranslocated promoter region, nuclear basket protein | Ofte (30–79 %) | I 1 tilstand |
| TRAPPC6Btrafficking protein particle complex subunit 6B | Ofte (30–79 %) | I 1 tilstand |
| WASF1WASP family member 1 | Ofte (30–79 %) | I 1 tilstand |
| WDR81WD repeat domain 81 | Ofte (30–79 %) | I 1 tilstand |
| ZEB2zinc finger E-box binding homeobox 2 | Ofte (30–79 %) | I 2 tilstande |
| ACTL6Bactin like 6B | Nogle gange (5–29 %) | I 1 tilstand |
| ATP10AATPase phospholipid transporting 10A (putative) | Nogle gange (5–29 %) | I 1 tilstand |
| BCL11ABCL11 transcription factor A | Nogle gange (5–29 %) | I 1 tilstand |
| BCORL1BCL6 corepressor like 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CDK10cyclin dependent kinase 10 | Nogle gange (5–29 %) | I 1 tilstand |
| CHD3chromodomain helicase DNA binding protein 3 | Nogle gange (5–29 %) | I 1 tilstand |
| CLTCclathrin heavy chain | Nogle gange (5–29 %) | I 1 tilstand |
| COL9A2collagen type IX alpha 2 chain | Nogle gange (5–29 %) | I 1 tilstand |
| FBXO22F-box protein 22 | Nogle gange (5–29 %) | I 1 tilstand |
| GBA2glucosylceramidase beta 2 | Nogle gange (5–29 %) | I 1 tilstand |
| GNB2G protein subunit beta 2 | Nogle gange (5–29 %) | I 1 tilstand |
| GTF2E2general transcription factor IIE subunit 2 | Nogle gange (5–29 %) | I 1 tilstand |
| KCND3potassium voltage-gated channel subfamily D member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| MAN1B1mannosidase alpha class 1B member 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MECP2methyl-CpG binding protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| MPV17mitochondrial inner membrane protein MPV17 | Nogle gange (5–29 %) | I 1 tilstand |
| MTTPmicrosomal triglyceride transfer protein | Nogle gange (5–29 %) | I 1 tilstand |
| NBEAneurobeachin | Nogle gange (5–29 %) | I 1 tilstand |
| NRXN1neurexin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| OCA2OCA2 melanosomal transmembrane protein | Nogle gange (5–29 %) | I 1 tilstand |
| PACS2phosphofurin acidic cluster sorting protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| PEX5peroxisomal biogenesis factor 5 | Nogle gange (5–29 %) | I 1 tilstand |
| PPP1R15Bprotein phosphatase 1 regulatory subunit 15B | Nogle gange (5–29 %) | I 1 tilstand |
| PURApurine rich element binding protein A | Nogle gange (5–29 %) | I 2 tilstande |
| RAI1retinoic acid induced 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RBM10RNA binding motif protein 10 | Nogle gange (5–29 %) | I 1 tilstand |
| RFX7regulatory factor X7 | Nogle gange (5–29 %) | I 1 tilstand |
| RNASEH1ribonuclease H1 | Nogle gange (5–29 %) | I 1 tilstand |
| SATB2SATB homeobox 2 | Nogle gange (5–29 %) | I 2 tilstande |
| SIM1SIM bHLH transcription factor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC9A7solute carrier family 9 member A7 | Nogle gange (5–29 %) | I 1 tilstand |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Nogle gange (5–29 %) | I 1 tilstand |
| SRCAPSnf2 related CREBBP activator protein | Nogle gange (5–29 %) | I 1 tilstand |
| TRMT10AtRNA methyltransferase 10A | Nogle gange (5–29 %) | I 1 tilstand |
| VCPvalosin containing protein | Nogle gange (5–29 %) | I 1 tilstand |
| WDR26WD repeat domain 26 | Nogle gange (5–29 %) | I 2 tilstande |
| GALCgalactosylceramidase | Sjældent (1–4%) | I 1 tilstand |
| RNU4-2RNA, U4 small nuclear 2 | Sjældent (1–4%) | I 1 tilstand |
| SPTBN1spectrin beta, non-erythrocytic 1 | Sjældent (1–4%) | I 1 tilstand |
| ADGRG1adhesion G protein-coupled receptor G1 | Ikke registreret | I 1 tilstand |
| DNAJC12DnaJ heat shock protein family (Hsp40) member C12 | Ikke registreret | I 1 tilstand |
| FLVCR1FLVCR choline and heme transporter 1 | Ikke registreret | I 1 tilstand |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Ikke registreret | I 1 tilstand |
| KMT2Alysine methyltransferase 2A | Ikke registreret | I 1 tilstand |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Ikke registreret | I 1 tilstand |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Ikke registreret | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Ikke registreret | I 1 tilstand |
| RLIMring finger protein, LIM domain interacting | Ikke registreret | I 1 tilstand |
| SMSspermine synthase | Ikke registreret | I 1 tilstand |
| TBC1D23TBC1 domain family member 23 | Ikke registreret | I 1 tilstand |
| TBPTATA-box binding protein | Ikke registreret | I 1 tilstand |
| THRAthyroid hormone receptor alpha | Ikke registreret | I 1 tilstand |
| TKFCtriokinase and FMN cyclase | Ikke registreret | I 1 tilstand |
| TMEM106Btransmembrane protein 106B | Ikke registreret | I 1 tilstand |
| TRIM2tripartite motif containing 2 | Ikke registreret | I 1 tilstand |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Ikke registreret | I 1 tilstand |
| TWNKtwinkle mtDNA helicase | Ikke registreret | I 1 tilstand |
| VLDLRvery low density lipoprotein receptor | Ikke registreret | I 1 tilstand |
| XRCC4X-ray repair cross complementing 4 | Ikke registreret | I 1 tilstand |
| YWHAGtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma | Ikke registreret | I 1 tilstand |
| ZSWIM6zinc finger SWIM-type containing 6 | 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