Trait
EMG abnormality
Abnormal results of investigations using electromyography (EMG).
Summary
- Also called
- Abnormal electromyography finding, Abnormal EMG, Electromyogram abnormal, EMG abnormalities
- Body system
- Abnormality of the musculoskeletal system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to EMG abnormality, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test119 genes linked to EMG abnormality
Changes in these genes cause rare conditions in which EMG abnormality is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ADCY6adenylate cyclase 6 | Very often (80–99%) | In 1 condition |
| B3GALNT2beta-1,3-N-acetylgalactosaminyltransferase 2 | Very often (80–99%) | In 1 condition |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Very often (80–99%) | In 2 conditions |
| CASRcalcium sensing receptor | Very often (80–99%) | In 1 condition |
| CEP126centrosomal protein 126 | Very often (80–99%) | In 1 condition |
| CLCN1chloride voltage-gated channel 1 | Very often (80–99%) | In 1 condition |
| CNTNAP1contactin associated protein 1 | Very often (80–99%) | In 1 condition |
| CPLANE1ciliogenesis and planar polarity effector complex subunit 1 | Very often (80–99%) | In 1 condition |
| CRPPACDP-L-ribitol pyrophosphorylase A | Very often (80–99%) | In 1 condition |
| ELP1elongator acetyltransferase complex subunit 1 | Very often (80–99%) | In 1 condition |
| FKRPfukutin related protein | Very often (80–99%) | In 1 condition |
| FKTNfukutin | Very often (80–99%) | In 3 conditions |
| GABRA3gamma-aminobutyric acid type A receptor subunit alpha3 | Very often (80–99%) | In 1 condition |
| GDAP1ganglioside induced differentiation associated protein 1 | Very often (80–99%) | In 1 condition |
| GMPPBGDP-mannose pyrophosphorylase B | Very often (80–99%) | In 1 condition |
| GNA11G protein subunit alpha 11 | Very often (80–99%) | In 1 condition |
| HSPG2heparan sulfate proteoglycan 2 | Very often (80–99%) | In 1 condition |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Very often (80–99%) | In 1 condition |
| KCNE3potassium voltage-gated channel subfamily E regulatory subunit 3 | Very often (80–99%) | In 1 condition |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Very often (80–99%) | In 1 condition |
| LARGE1LARGE xylosyl- and glucuronyltransferase 1 | Very often (80–99%) | In 1 condition |
| LGI4leucine rich repeat LGI family member 4 | Very often (80–99%) | In 1 condition |
| MAFBMAF bZIP transcription factor B | Very often (80–99%) | In 1 condition |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Very often (80–99%) | In 1 condition |
| MT-RNR1mitochondrially encoded 12S rRNA | Very often (80–99%) | In 1 condition |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Very often (80–99%) | In 1 condition |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Very often (80–99%) | In 1 condition |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Very often (80–99%) | In 2 conditions |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Very often (80–99%) | In 3 conditions |
| MT-TPmitochondrially encoded tRNA-Pro (CCN) | Very often (80–99%) | In 1 condition |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Very often (80–99%) | In 1 condition |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Very often (80–99%) | In 2 conditions |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Very often (80–99%) | In 1 condition |
| NOTCH2NLCnotch 2 N-terminal like C | Very often (80–99%) | In 1 condition |
| POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Very often (80–99%) | In 1 condition |
| POMT1protein O-mannosyltransferase 1 | Very often (80–99%) | In 1 condition |
| POMT2protein O-mannosyltransferase 2 | Very often (80–99%) | In 1 condition |
| PUS1pseudouridine synthase 1 | Very often (80–99%) | In 1 condition |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Very often (80–99%) | In 4 conditions |
| SEPTIN9septin 9 | Very often (80–99%) | In 1 condition |
Show 79 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| TRIM32tripartite motif containing 32 | Very often (80–99%) | In 1 condition |
| YARS2tyrosyl-tRNA synthetase 2 | Very often (80–99%) | In 1 condition |
| ANO10anoctamin 10 | Often (30–79%) | In 1 condition |
| ATXN3ataxin 3 | Often (30–79%) | In 1 condition |
| CPT1Ccarnitine palmitoyltransferase 1C | Often (30–79%) | In 1 condition |
| LAMA2laminin subunit alpha 2 | Often (30–79%) | In 1 condition |
| LMNAlamin A/C | Often (30–79%) | In 2 conditions |
| MATR3matrin 3 | Often (30–79%) | In 1 condition |
| MT-ATP8mitochondrially encoded ATP synthase membrane subunit 8 | Often (30–79%) | In 1 condition |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Often (30–79%) | In 1 condition |
| MT-TNmitochondrially encoded tRNA-Asn (AAU/C) | Often (30–79%) | In 1 condition |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Often (30–79%) | In 1 condition |
| SMAD4SMAD family member 4 | Often (30–79%) | In 1 condition |
| ABCC9ATP binding cassette subfamily C member 9 | Sometimes (5–29%) | In 1 condition |
| ACTC1actin alpha cardiac muscle 1 | Sometimes (5–29%) | In 1 condition |
| ACTN2actinin alpha 2 | Sometimes (5–29%) | In 1 condition |
| ANKRD1ankyrin repeat domain 1 | Sometimes (5–29%) | In 1 condition |
| BAG3BAG cochaperone 3 | Sometimes (5–29%) | In 1 condition |
| BAG5BAG cochaperone 5 | Sometimes (5–29%) | In 1 condition |
| CAP2cyclase associated actin cytoskeleton regulatory protein 2 | Sometimes (5–29%) | In 1 condition |
| COQ8Acoenzyme Q8A | Sometimes (5–29%) | In 1 condition |
| CRYABcrystallin alpha B | Sometimes (5–29%) | In 1 condition |
| CSRP3cysteine and glycine rich protein 3 | Sometimes (5–29%) | In 1 condition |
| DESdesmin | Sometimes (5–29%) | In 1 condition |
| DMDdystrophin | Sometimes (5–29%) | In 1 condition |
| DOLKdolichol kinase | Sometimes (5–29%) | In 1 condition |
| DSG2desmoglein 2 | Sometimes (5–29%) | In 1 condition |
| DSPdesmoplakin | Sometimes (5–29%) | In 1 condition |
| FHL2four and a half LIM domains 2 | Sometimes (5–29%) | In 1 condition |
| FLNCfilamin C | Sometimes (5–29%) | In 1 condition |
| GATAD1GATA zinc finger domain containing 1 | Sometimes (5–29%) | In 1 condition |
| GBE11,4-alpha-glucan branching enzyme 1 | Sometimes (5–29%) | In 1 condition |
| GET3guided entry of tail-anchored proteins factor 3, ATPase | Sometimes (5–29%) | In 1 condition |
| HAND2heart and neural crest derivatives expressed 2 | Sometimes (5–29%) | In 1 condition |
| JPH2junctophilin 2 | Sometimes (5–29%) | In 1 condition |
| LAMA4laminin subunit alpha 4 | Sometimes (5–29%) | In 1 condition |
| LDB3LIM domain binding 3 | Sometimes (5–29%) | In 1 condition |
| LMOD2leiomodin 2 | Sometimes (5–29%) | In 1 condition |
| MYBPC3myosin binding protein C3 | Sometimes (5–29%) | In 1 condition |
| MYH6myosin heavy chain 6 | Sometimes (5–29%) | In 1 condition |
| MYH7myosin heavy chain 7 | Sometimes (5–29%) | In 1 condition |
| MYPNmyopalladin | Sometimes (5–29%) | In 1 condition |
| NEXNnexilin F-actin binding protein | Sometimes (5–29%) | In 1 condition |
| NRAPnebulin related anchoring protein | Sometimes (5–29%) | In 1 condition |
| PLNphospholamban | Sometimes (5–29%) | In 1 condition |
| PPCSphosphopantothenoylcysteine synthetase | Sometimes (5–29%) | In 1 condition |
| PRDM16PR/SET domain 16 | Sometimes (5–29%) | In 1 condition |
| PSEN1presenilin 1 | Sometimes (5–29%) | In 1 condition |
| PSEN2presenilin 2 | Sometimes (5–29%) | In 1 condition |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Sometimes (5–29%) | In 1 condition |
| RBM20RNA binding motif protein 20 | Sometimes (5–29%) | In 1 condition |
| RPL3Lribosomal protein L3 like | Sometimes (5–29%) | In 1 condition |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Sometimes (5–29%) | In 1 condition |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Sometimes (5–29%) | In 1 condition |
| SGCDsarcoglycan delta | Sometimes (5–29%) | In 1 condition |
| TAF1ATATA-box binding protein associated factor, RNA polymerase I subunit A | Sometimes (5–29%) | In 1 condition |
| TAFAZZINtafazzin, phospholipid-lysophospholipid transacylase | Sometimes (5–29%) | In 1 condition |
| TCAPtitin-cap | Sometimes (5–29%) | In 1 condition |
| TMPOthymopoietin | Sometimes (5–29%) | In 1 condition |
| TNNC1troponin C1, slow skeletal and cardiac type | Sometimes (5–29%) | In 1 condition |
| TNNI3troponin I3, cardiac type | Sometimes (5–29%) | In 1 condition |
| TNNT2troponin T2, cardiac type | Sometimes (5–29%) | In 1 condition |
| TPM1tropomyosin 1 | Sometimes (5–29%) | In 1 condition |
| TTNtitin | Sometimes (5–29%) | In 1 condition |
| TXNRD2thioredoxin reductase 2 | Sometimes (5–29%) | In 1 condition |
| VCLvinculin | Sometimes (5–29%) | In 1 condition |
| VEZF1vascular endothelial zinc finger 1 | Sometimes (5–29%) | In 1 condition |
| CAV3caveolin 3 | Not recorded | In 1 condition |
| KPNA3karyopherin subunit alpha 3 | Not recorded | In 1 condition |
| LAMB1laminin subunit beta 1 | Not recorded | In 1 condition |
| OATornithine aminotransferase | Not recorded | In 1 condition |
| PGAM2phosphoglycerate mutase 2 | Not recorded | In 1 condition |
| RTN2reticulon 2 | Not recorded | In 1 condition |
| SLC33A1solute carrier family 33 member 1 | Not recorded | In 1 condition |
| SMN1survival of motor neuron 1, telomeric | Not recorded | In 1 condition |
| TMTC3transmembrane O-mannosyltransferase targeting cadherins 3 | Not recorded | In 1 condition |
| UBAP1ubiquitin associated protein 1 | Not recorded | In 1 condition |
| WASHC5WASH complex subunit 5 | Not recorded | In 1 condition |
| ZFRzinc finger RNA binding protein | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Narrower traits
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks