Trait
Mildly elevated creatine kinase
Summary
- Also called
- Mildly elevated CPK, Mildly elevated creatine phosphokinase, Mildly elevated serum CK, Mildly elevated serum CPK, Mildly elevated serum phospho-CK, Mildly increased creatine kinase, Mildly increased serum creatine kinase, Moderately elevated serum CK, Moderately elevated serum CPK, Moderately increased serum creatine kinase
- Body system
- Laboratory abnormality
Reference genomeGRCh38hg38
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Get my Genome Test70 genes linked to Mildly elevated creatine kinase
Changes in these genes cause rare conditions in which Mildly elevated creatine kinase 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 |
|---|---|---|
| ADSS1adenylosuccinate synthase 1 | Always | In 1 condition |
| ARHGAP19Rho GTPase activating protein 19 | Always | In 1 condition |
| COX18cytochrome c oxidase assembly factor COX18 | Always | In 1 condition |
| DNM2dynamin 2 | Always | In 2 conditions |
| FILIP1filamin A interacting protein 1 | Always | In 1 condition |
| HSPB8heat shock protein family B (small) member 8 | Always | In 1 condition |
| MEGF10multiple EGF like domains 10 | Always | In 1 condition |
| MTMR14myotubularin related protein 14 | Always | In 2 conditions |
| PLEKHG5pleckstrin homology and RhoGEF domain containing G5 | Always | In 1 condition |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Always | In 2 conditions |
| TBCKTBC1 domain containing kinase | Always | In 1 condition |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Very often (80–99%) | In 2 conditions |
| FLNCfilamin C | Very often (80–99%) | In 2 conditions |
| GABRA3gamma-aminobutyric acid type A receptor subunit alpha3 | Very often (80–99%) | In 1 condition |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | 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 |
| ALG2ALG2 alpha-1,3/1,6-mannosyltransferase | Often (30–79%) | In 1 condition |
| BIN1bridging integrator 1 | Often (30–79%) | In 1 condition |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Often (30–79%) | In 1 condition |
| COL25A1collagen type XXV alpha 1 chain | Often (30–79%) | In 1 condition |
| COL6A1collagen type VI alpha 1 chain | Often (30–79%) | In 2 conditions |
| CRPPACDP-L-ribitol pyrophosphorylase A | Often (30–79%) | In 1 condition |
| ERGIC1endoplasmic reticulum-golgi intermediate compartment 1 | Often (30–79%) | In 1 condition |
| FKRPfukutin related protein | Often (30–79%) | In 1 condition |
| FKTNfukutin | Often (30–79%) | In 1 condition |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Often (30–79%) | In 2 conditions |
| MATR3matrin 3 | Often (30–79%) | In 1 condition |
| MSTO1misato mitochondrial distribution and morphology regulator 1 | Often (30–79%) | In 1 condition |
| MT-TEmitochondrially encoded tRNA-Glu (GAA/G) | Often (30–79%) | In 1 condition |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | 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 |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Often (30–79%) | In 1 condition |
| MYF6myogenic factor 6 | Often (30–79%) | In 1 condition |
| MYH14myosin heavy chain 14 | Often (30–79%) | In 2 conditions |
| MYH7myosin heavy chain 7 | Often (30–79%) | In 3 conditions |
| PEX6peroxisomal biogenesis factor 6 | Often (30–79%) | In 1 condition |
| POMT1protein O-mannosyltransferase 1 | Often (30–79%) | In 1 condition |
| QRICH1glutamine rich 1 | Often (30–79%) | In 1 condition |
Show 30 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| RYR1ryanodine receptor 1 | Often (30–79%) | In 1 condition |
| SCYL2SCY1 like pseudokinase 2 | Often (30–79%) | In 1 condition |
| SQSTM1sequestosome 1 | Often (30–79%) | In 1 condition |
| TIA1TIA1 cytotoxic granule associated RNA binding protein | Often (30–79%) | In 2 conditions |
| TRMUtRNA mitochondrial 2-thiouridylase | Often (30–79%) | In 1 condition |
| TTNtitin | Often (30–79%) | In 1 condition |
| VCPvalosin containing protein | Often (30–79%) | In 1 condition |
| ACTA1actin alpha 1, skeletal muscle | Sometimes (5–29%) | In 3 conditions |
| COL12A1collagen type XII alpha 1 chain | Sometimes (5–29%) | In 1 condition |
| HADHhydroxyacyl-CoA dehydrogenase | Sometimes (5–29%) | In 1 condition |
| KBTBD13kelch repeat and BTB domain containing 13 | Sometimes (5–29%) | In 1 condition |
| KLHL41kelch like family member 41 | Sometimes (5–29%) | In 1 condition |
| MICU1mitochondrial calcium uptake 1 | Sometimes (5–29%) | In 1 condition |
| MYPNmyopalladin | Sometimes (5–29%) | In 1 condition |
| NEBnebulin | Sometimes (5–29%) | In 2 conditions |
| POLGDNA polymerase gamma, catalytic subunit | Sometimes (5–29%) | In 2 conditions |
| POLRMTRNA polymerase mitochondrial | Sometimes (5–29%) | In 1 condition |
| SNUPNsnurportin 1 | Sometimes (5–29%) | In 1 condition |
| TPM2tropomyosin 2 | Sometimes (5–29%) | In 1 condition |
| TPM3tropomyosin 3 | Sometimes (5–29%) | In 1 condition |
| TRIP4thyroid hormone receptor interactor 4 | Sometimes (5–29%) | In 1 condition |
| TWNKtwinkle mtDNA helicase | Sometimes (5–29%) | In 1 condition |
| UBA1ubiquitin like modifier activating enzyme 1 | Sometimes (5–29%) | In 1 condition |
| YME1L1YME1 like 1 ATPase | Sometimes (5–29%) | In 1 condition |
| COL9A3collagen type IX alpha 3 chain | Not recorded | In 1 condition |
| DOK7docking protein 7 | Not recorded | In 1 condition |
| GFPT1glutamine--fructose-6-phosphate transaminase 1 | Not recorded | In 1 condition |
| LMNAlamin A/C | Not recorded | In 1 condition |
| MPV17mitochondrial inner membrane protein MPV17 | Not recorded | In 1 condition |
| TFGtrafficking from ER to golgi regulator | 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.
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.
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