Trait
Hypopituitarism
Summary
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Hypopituitarism, and the rest of your genome, with one test.
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Get my Genome Test28 genes linked to Hypopituitarism
Changes in these genes cause rare conditions in which Hypopituitarism 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 |
|---|---|---|
| FAAP100FA core complex associated protein 100 | Always | In 1 condition |
| FARSAphenylalanyl-tRNA synthetase subunit alpha | Always | In 1 condition |
| FOXA2forkhead box A2 | Always | In 1 condition |
| GLI2GLI family zinc finger 2 | Always | In 2 conditions |
| GPR101G protein-coupled receptor 101 | Always | In 1 condition |
| HESX1HESX homeobox 1 | Always | In 2 conditions |
| LHX4LIM homeobox 4 | Always | In 2 conditions |
| OTX2orthodenticle homeobox 2 | Always | In 1 condition |
| POU1F1POU class 1 homeobox 1 | Always | In 3 conditions |
| PROP1PROP paired-like homeobox 1 | Always | In 3 conditions |
| PTBP1polypyrimidine tract binding protein 1 | Always | In 1 condition |
| SOX3SRY-box transcription factor 3 | Always | In 1 condition |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Very often (80–99%) | In 1 condition |
| CTNNB1catenin beta 1 | Very often (80–99%) | In 1 condition |
| TMEM67transmembrane protein 67 | Very often (80–99%) | In 1 condition |
| GLI3GLI family zinc finger 3 | Often (30–79%) | In 1 condition |
| LHX3LIM homeobox 3 | Often (30–79%) | In 1 condition |
| MANFmesencephalic astrocyte derived neurotrophic factor | Often (30–79%) | In 1 condition |
| PUS1pseudouridine synthase 1 | Often (30–79%) | In 1 condition |
| ZSWIM6zinc finger SWIM-type containing 6 | Often (30–79%) | In 2 conditions |
| ALX3ALX homeobox 3 | Sometimes (5–29%) | In 1 condition |
| HBBhemoglobin subunit beta | Sometimes (5–29%) | In 2 conditions |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Sometimes (5–29%) | In 1 condition |
| NFKBIANFKB inhibitor alpha | Sometimes (5–29%) | In 1 condition |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Rarely (1–4%) | In 1 condition |
| EFL1elongation factor like GTPase 1 | Rarely (1–4%) | In 1 condition |
| SBDSSBDS ribosome maturation factor | Rarely (1–4%) | In 1 condition |
| APOA5apolipoprotein A5 | 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.
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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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