Trait
Streak ovary
A developmental disorder characterized by the progressive loss of primordial germ cells in the developing ovaries of an embryo, leading to hypoplastic ovaries composed of wavy connective tissue with occasional clumps of granulosa cells, and frequently mesonephric or hilar cells.
Summary
- Body system
- Abnormality of the genitourinary system
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Get my Genome Test41 genes linked to Streak ovary
Changes in these genes cause rare conditions in which Streak ovary 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 |
|---|---|---|
| BMP15bone morphogenetic protein 15 | Always | In 2 conditions |
| DAP3death associated protein 3 | Always | In 1 condition |
| DHHdesert hedgehog signaling molecule | Always | In 2 conditions |
| ERAL1Era like 12S mitochondrial rRNA chaperone 1 | Always | In 1 condition |
| HARS2histidyl-tRNA synthetase 2, mitochondrial | Always | In 1 condition |
| STAG3STAG3 cohesin complex component | Always | In 1 condition |
| DCAF17DDB1 and CUL4 associated factor 17 | Very often (80–99%) | In 1 condition |
| DHX37DEAH-box helicase 37 | Very often (80–99%) | In 1 condition |
| GATA4GATA binding protein 4 | Very often (80–99%) | In 1 condition |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Very often (80–99%) | In 1 condition |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Very often (80–99%) | In 1 condition |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Very often (80–99%) | In 2 conditions |
| SOX9SRY-box transcription factor 9 | Very often (80–99%) | In 1 condition |
| SRYsex determining region Y | Very often (80–99%) | In 2 conditions |
| VAMP7vesicle associated membrane protein 7 | Very often (80–99%) | In 1 condition |
| WT1WT1 transcription factor | Very often (80–99%) | In 3 conditions |
| WWOXWW domain containing oxidoreductase | Very often (80–99%) | In 1 condition |
| ZFPM2zinc finger protein, FOG family member 2 | Very often (80–99%) | In 1 condition |
| BNC1basonuclin zinc finger protein 1 | Often (30–79%) | In 1 condition |
| FIGLAfolliculogenesis specific bHLH transcription factor | Often (30–79%) | In 2 conditions |
| FSHRfollicle stimulating hormone receptor | Often (30–79%) | In 1 condition |
| MRPS22mitochondrial ribosomal protein S22 | Often (30–79%) | In 1 condition |
| MSH4mutS homolog 4 | Often (30–79%) | In 1 condition |
| NUP107nucleoporin 107 | Often (30–79%) | In 1 condition |
| PAX6paired box 6 | Often (30–79%) | In 1 condition |
| POLR3HRNA polymerase III subunit H | Often (30–79%) | In 1 condition |
| PSMC3IPPSMC3 interacting protein | Often (30–79%) | In 1 condition |
| SPIDRscaffold protein involved in DNA repair | Often (30–79%) | In 1 condition |
| TP63tumor protein p63 | Often (30–79%) | In 1 condition |
| ZSWIM7zinc finger SWIM-type containing 7 | Often (30–79%) | In 2 conditions |
| CLPPcaseinolytic mitochondrial matrix peptidase proteolytic subunit | Sometimes (5–29%) | In 1 condition |
| CPLX1complexin 1 | Sometimes (5–29%) | In 1 condition |
| CTBP1C-terminal binding protein 1 | Sometimes (5–29%) | In 1 condition |
| FOXL2forkhead box L2 | Sometimes (5–29%) | In 1 condition |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Sometimes (5–29%) | In 1 condition |
| NELFAnegative elongation factor complex member A | Sometimes (5–29%) | In 1 condition |
| NOBOXNOBOX oogenesis homeobox | Sometimes (5–29%) | In 1 condition |
| NSD2nuclear receptor binding SET domain protein 2 | Sometimes (5–29%) | In 1 condition |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Sometimes (5–29%) | In 1 condition |
| PPP1R12Aprotein phosphatase 1 regulatory subunit 12A | Sometimes (5–29%) | In 1 condition |
Show 1 more gene
| Gene | How often it is seen | Conditions |
|---|---|---|
| SETBP1SET binding protein 1 | Sometimes (5–29%) | 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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