Trait
Abnormal uterus bleeding
Clinical name: Metrorrhagia
Bleeding at irregular intervals.
Summary
- Also called
- Intermenstrual bleeding, Menstrual spotting
- Body system
- Abnormality of the genitourinary system
Reference genomeGRCh38hg38
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Get my Genome Test26 genes linked to Abnormal uterus bleeding
Changes in these genes cause rare conditions in which Abnormal uterus bleeding 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 |
|---|---|---|
| HPS5HPS5 biogenesis of lysosomal organelles complex 2 subunit 2 | Often (30–79%) | In 1 condition |
| ACTN1actinin alpha 1 | Sometimes (5–29%) | In 1 condition |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Sometimes (5–29%) | In 1 condition |
| GFI1Bgrowth factor independent 1B transcriptional repressor | Sometimes (5–29%) | In 1 condition |
| GP1BAglycoprotein Ib platelet subunit alpha | Sometimes (5–29%) | In 1 condition |
| GP1BBglycoprotein Ib platelet subunit beta | Sometimes (5–29%) | In 1 condition |
| ITGA2Bintegrin subunit alpha 2b | Sometimes (5–29%) | In 1 condition |
| ITGB3integrin subunit beta 3 | Sometimes (5–29%) | In 1 condition |
| TPM4tropomyosin 4 | Sometimes (5–29%) | In 1 condition |
| TRPM7transient receptor potential cation channel subfamily M member 7 | Sometimes (5–29%) | In 1 condition |
| TUBA8tubulin alpha 8 | Sometimes (5–29%) | In 1 condition |
| TUBB1tubulin beta 1 class VI | Sometimes (5–29%) | In 1 condition |
| BCORBCL6 corepressor | Rarely (1–4%) | In 1 condition |
| F5coagulation factor V | Rarely (1–4%) | In 1 condition |
| FIP1L1factor interacting with PAPOLA and CPSF1 | Rarely (1–4%) | In 1 condition |
| IRF2BP2interferon regulatory factor 2 binding protein 2 | Rarely (1–4%) | In 1 condition |
| NABP1nucleic acid binding protein 1 | Rarely (1–4%) | In 1 condition |
| NPM1nucleophosmin 1 | Rarely (1–4%) | In 1 condition |
| NUMA1nuclear mitotic apparatus protein 1 | Rarely (1–4%) | In 1 condition |
| PMLPML nuclear body scaffold | Rarely (1–4%) | In 1 condition |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Rarely (1–4%) | In 1 condition |
| RARAretinoic acid receptor alpha | Rarely (1–4%) | In 1 condition |
| STAT3signal transducer and activator of transcription 3 | Rarely (1–4%) | In 1 condition |
| STAT5Bsignal transducer and activator of transcription 5B | Rarely (1–4%) | In 1 condition |
| TBL1XR1TBL1X/Y related 1 | Rarely (1–4%) | In 1 condition |
| ZBTB16zinc finger and BTB domain containing 16 | Rarely (1–4%) | 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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