Trait
Bleeding gums
Clinical name: Gingival bleeding
Hemorrhage affecting the gingiva.
Summary
- Also called
- Gingival haemorrhage, Gingival hemorrhage, Gingivorrhagia
Reference genomeGRCh38hg38
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Get my Genome Test61 genes linked to Bleeding gums
Changes in these genes cause rare conditions in which Bleeding gums 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 |
|---|---|---|
| ADAMTS2ADAM metallopeptidase with thrombospondin type 1 motif 2 | Always | In 1 condition |
| ELMO2engulfment and cell motility 2 | Always | In 1 condition |
| F13A1coagulation factor XIII A chain | Always | In 2 conditions |
| GALEUDP-galactose-4-epimerase | Always | In 1 condition |
| GGCXgamma-glutamyl carboxylase | Always | In 1 condition |
| HIVEP2HIVEP zinc finger 2 | Always | In 1 condition |
| HPS3HPS3 biogenesis of lysosomal organelles complex 2 subunit 1 | Always | In 1 condition |
| IL18BPinterleukin 18 binding protein | Always | In 1 condition |
| PLCG1phospholipase C gamma 1 | Always | In 1 condition |
| C1Rcomplement C1r | Very often (80–99%) | In 1 condition |
| C1Scomplement C1s | Very often (80–99%) | In 1 condition |
| FGAfibrinogen alpha chain | Very often (80–99%) | In 4 conditions |
| FGBfibrinogen beta chain | Very often (80–99%) | In 4 conditions |
| FGGfibrinogen gamma chain | Very often (80–99%) | In 4 conditions |
| JAK2Janus kinase 2 | Very often (80–99%) | In 1 condition |
| LYSTlysosomal trafficking regulator | Very often (80–99%) | In 2 conditions |
| BCORBCL6 corepressor | Often (30–79%) | In 1 condition |
| BLOC1S5biogenesis of lysosomal organelles complex 1 subunit 5 | Often (30–79%) | In 1 condition |
| F10coagulation factor X | Often (30–79%) | In 2 conditions |
| F7coagulation factor VII | Often (30–79%) | In 1 condition |
| F8coagulation factor VIII | Often (30–79%) | In 2 conditions |
| FIP1L1factor interacting with PAPOLA and CPSF1 | Often (30–79%) | In 1 condition |
| GBA1glucosylceramidase beta 1 | Often (30–79%) | In 1 condition |
| IRF2BP2interferon regulatory factor 2 binding protein 2 | Often (30–79%) | In 1 condition |
| ITGA2Bintegrin subunit alpha 2b | Often (30–79%) | In 2 conditions |
| ITGB3integrin subunit beta 3 | Often (30–79%) | In 1 condition |
| LMAN1lectin, mannose binding 1 | Often (30–79%) | In 1 condition |
| MCFD2multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Often (30–79%) | In 1 condition |
| MYD88MYD88 innate immune signal transduction adaptor | Often (30–79%) | In 1 condition |
| NABP1nucleic acid binding protein 1 | Often (30–79%) | In 1 condition |
| NPM1nucleophosmin 1 | Often (30–79%) | In 1 condition |
| NUMA1nuclear mitotic apparatus protein 1 | Often (30–79%) | In 1 condition |
| PMLPML nuclear body scaffold | Often (30–79%) | In 1 condition |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Often (30–79%) | In 1 condition |
| RARAretinoic acid receptor alpha | Often (30–79%) | In 1 condition |
| SCARB2scavenger receptor class B member 2 | Often (30–79%) | In 1 condition |
| STAT3signal transducer and activator of transcription 3 | Often (30–79%) | In 1 condition |
| STAT5Bsignal transducer and activator of transcription 5B | Often (30–79%) | In 1 condition |
| TBL1XR1TBL1X/Y related 1 | Often (30–79%) | In 1 condition |
| ZBTB16zinc finger and BTB domain containing 16 | Often (30–79%) | In 1 condition |
Show 21 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| ANO6anoctamin 6 | Sometimes (5–29%) | In 1 condition |
| CATcatalase | Sometimes (5–29%) | In 1 condition |
| F13Bcoagulation factor XIII B chain | Sometimes (5–29%) | In 1 condition |
| F5coagulation factor V | Sometimes (5–29%) | In 1 condition |
| FCGR2CFc gamma receptor IIc (gene/pseudogene) | Sometimes (5–29%) | In 1 condition |
| FYB1FYN binding protein 1 | Sometimes (5–29%) | In 1 condition |
| GP1BAglycoprotein Ib platelet subunit alpha | Sometimes (5–29%) | In 3 conditions |
| GP1BBglycoprotein Ib platelet subunit beta | Sometimes (5–29%) | In 2 conditions |
| GP9glycoprotein IX platelet | Sometimes (5–29%) | In 2 conditions |
| IFNGinterferon gamma | Sometimes (5–29%) | In 1 condition |
| KIF23kinesin family member 23 | Sometimes (5–29%) | In 1 condition |
| PRF1perforin 1 | Sometimes (5–29%) | In 1 condition |
| RACGAP1Rac GTPase activating protein 1 | Sometimes (5–29%) | In 1 condition |
| SBDSSBDS ribosome maturation factor | Sometimes (5–29%) | In 1 condition |
| SERPINF2serpin family F member 2 | Sometimes (5–29%) | In 1 condition |
| TERCtelomerase RNA component | Sometimes (5–29%) | In 1 condition |
| TERTtelomerase reverse transcriptase | Sometimes (5–29%) | In 1 condition |
| WASWASP actin nucleation promoting factor | Sometimes (5–29%) | In 2 conditions |
| BLOC1S3biogenesis of lysosomal organelles complex 1 subunit 3 | Not recorded | In 1 condition |
| F2coagulation factor II, thrombin | Not recorded | In 1 condition |
| HPS1HPS1 biogenesis of lysosomal organelles complex 3 subunit 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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