Trait
Normocytic anemia
A kind of anemia in which the volume of the red blood cells is normal.
Summary
- Also called
- Normocytic anaemia
Reference genomeGRCh38hg38
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Get my Genome Test19 genes linked to Normocytic anemia
Changes in these genes cause rare conditions in which Normocytic anemia 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 |
|---|---|---|
| ATP6AP1ATPase H+ transporting accessory protein 1 | Always | In 1 condition |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Always | In 1 condition |
| MTRR5-methyltetrahydrofolate-homocysteine methyltransferase reductase | Always | In 1 condition |
| TBXAS1thromboxane A synthase 1 | Always | In 1 condition |
| TOR1Atorsin family 1 member A | Always | In 1 condition |
| EFL1elongation factor like GTPase 1 | Very often (80–99%) | In 2 conditions |
| ASXL1ASXL transcriptional regulator 1 | Often (30–79%) | In 1 condition |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Often (30–79%) | In 1 condition |
| KITKIT proto-oncogene, receptor tyrosine kinase | Often (30–79%) | In 1 condition |
| MYD88MYD88 innate immune signal transduction adaptor | Often (30–79%) | In 1 condition |
| SBDSSBDS ribosome maturation factor | Often (30–79%) | In 1 condition |
| SF3B1splicing factor 3b subunit 1 | Often (30–79%) | In 1 condition |
| SRSF2serine and arginine rich splicing factor 2 | Often (30–79%) | In 1 condition |
| TET2tet methylcytosine dioxygenase 2 | Often (30–79%) | In 3 conditions |
| TREX1three prime repair exonuclease 1 | Often (30–79%) | In 1 condition |
| ALDOAaldolase, fructose-bisphosphate A | Not recorded | In 1 condition |
| HK1hexokinase 1 | Not recorded | In 1 condition |
| RPS29ribosomal protein S29 | Not recorded | In 1 condition |
| TPI1triosephosphate isomerase 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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