Trait
Elevated urine calcium levels
Clinical name: Hypercalciuria
Summary
- Also called
- Hypercalcinuria
Reference genomeGRCh38hg38
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Read the genes linked to Elevated urine calcium levels, and the rest of your genome, with one test.
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Get my Genome Test66 genes linked to Elevated urine calcium levels
Changes in these genes cause rare conditions in which Elevated urine calcium levels 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 |
|---|---|---|
| ADCY10adenylate cyclase 10 | Always | In 2 conditions |
| CLDN19claudin 19 | Always | In 1 condition |
| CYP24A1cytochrome P450 family 24 subfamily A member 1 | Always | In 1 condition |
| FGF23fibroblast growth factor 23 | Always | In 1 condition |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Always | In 1 condition |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Always | In 2 conditions |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Always | In 1 condition |
| SLC12A1solute carrier family 12 member 1 | Always | In 1 condition |
| SLC34A1solute carrier family 34 member 1 | Always | In 5 conditions |
| SLC34A3solute carrier family 34 member 3 | Always | In 2 conditions |
| TNFRSF11BTNF receptor superfamily member 11b | Always | In 1 condition |
| CASRcalcium sensing receptor | Very often (80–99%) | In 4 conditions |
| CDC73cell division cycle 73 | Very often (80–99%) | In 3 conditions |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Very often (80–99%) | In 1 condition |
| CLDN16claudin 16 | Very often (80–99%) | In 1 condition |
| GCM2GCM transcription factor 2 | Very often (80–99%) | In 2 conditions |
| GNA11G protein subunit alpha 11 | Very often (80–99%) | In 1 condition |
| MEN1menin 1 | Very often (80–99%) | In 2 conditions |
| RRAGDRas related GTP binding D | Very often (80–99%) | In 1 condition |
| ATP6V0A4ATPase H+ transporting V0 subunit a4 | Often (30–79%) | In 1 condition |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Often (30–79%) | In 1 condition |
| BSNDbarttin CLCNK type accessory subunit beta | Often (30–79%) | In 1 condition |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Often (30–79%) | In 1 condition |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Often (30–79%) | In 1 condition |
| CDKN2Bcyclin dependent kinase inhibitor 2B | Often (30–79%) | In 1 condition |
| CLCN5Cl-/H+ antiporter 5 | Often (30–79%) | In 4 conditions |
| CLCNKAchloride voltage-gated channel Ka | Often (30–79%) | In 1 condition |
| CLCNKBchloride voltage-gated channel Kb | Often (30–79%) | In 1 condition |
| CLIP2CAP-Gly domain containing linker protein 2 | Often (30–79%) | In 1 condition |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Often (30–79%) | In 1 condition |
| EIF4Heukaryotic translation initiation factor 4H | Often (30–79%) | In 1 condition |
| ELNelastin | Often (30–79%) | In 2 conditions |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Often (30–79%) | In 1 condition |
| GTF2Igeneral transcription factor IIi | Often (30–79%) | In 1 condition |
| GTF2IRD1GTF2I repeat domain containing 1 | Often (30–79%) | In 1 condition |
| GTF2IRD2GTF2I repeat domain containing 2 | Often (30–79%) | In 1 condition |
| HNF1BHNF1 homeobox B | Often (30–79%) | In 1 condition |
| LIMK1LIM domain kinase 1 | Often (30–79%) | In 1 condition |
| METTL27methyltransferase like 27 | Often (30–79%) | In 1 condition |
| MLXIPLMLX interacting protein like | Often (30–79%) | In 1 condition |
Show 26 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| NCF1neutrophil cytosolic factor 1 | Often (30–79%) | In 1 condition |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Often (30–79%) | In 2 conditions |
| PTH1Rparathyroid hormone 1 receptor | Often (30–79%) | In 2 conditions |
| RFC2replication factor C subunit 2 | Often (30–79%) | In 1 condition |
| SLC2A2solute carrier family 2 member 2 | Often (30–79%) | In 2 conditions |
| STX1Asyntaxin 1A | Often (30–79%) | In 1 condition |
| TBL2transducin beta like 2 | Often (30–79%) | In 1 condition |
| TMEM270transmembrane protein 270 | Often (30–79%) | In 1 condition |
| VPS37DVPS37D subunit of ESCRT-I | Often (30–79%) | In 1 condition |
| BTNL2butyrophilin like 2 | Sometimes (5–29%) | In 1 condition |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Sometimes (5–29%) | In 1 condition |
| GATMglycine amidinotransferase | Sometimes (5–29%) | In 1 condition |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Sometimes (5–29%) | In 2 conditions |
| INSRinsulin receptor | Sometimes (5–29%) | In 1 condition |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Sometimes (5–29%) | In 2 conditions |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Sometimes (5–29%) | In 1 condition |
| SLC22A12solute carrier family 22 member 12 | Sometimes (5–29%) | In 1 condition |
| SLC2A9solute carrier family 2 member 9 | Sometimes (5–29%) | In 1 condition |
| ALPLalkaline phosphatase, biomineralization associated | Not recorded | In 1 condition |
| AMMECR1AMMECR nuclear protein 1 | Not recorded | In 1 condition |
| ATP7BATPase copper transporting beta | Not recorded | In 1 condition |
| CFTRCF transmembrane conductance regulator | Not recorded | In 1 condition |
| FCGR2AFc gamma receptor IIa | Not recorded | In 1 condition |
| MAGED2MAGE family member D2 | Not recorded | In 1 condition |
| PIK3C2Aphosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | Not recorded | In 1 condition |
| TGFB1transforming growth factor beta 1 | 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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