Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Axonal degeneration, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test23 genes linked to Axonal degeneration
Changes in these genes cause rare conditions in which Axonal degeneration 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 |
|---|---|---|
| LAMA2laminin subunit alpha 2 | Always | In 1 condition |
| REEP1receptor accessory protein 1 | Always | In 1 condition |
| SERPING1serpin family G member 1 | Always | In 1 condition |
| SLC25A21solute carrier family 25 member 21 | Always | In 1 condition |
| ABCD1ATP binding cassette subfamily D member 1 | Very often (80–99%) | In 1 condition |
| LMNAlamin A/C | Very often (80–99%) | In 1 condition |
| TXN2thioredoxin 2 | Very often (80–99%) | In 2 conditions |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Often (30–79%) | In 1 condition |
| FLVCR1FLVCR choline and heme transporter 1 | Often (30–79%) | In 1 condition |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Sometimes (5–29%) | In 1 condition |
| APTXaprataxin | Not recorded | In 1 condition |
| CTDP1CTD phosphatase 1 | Not recorded | In 1 condition |
| DNM2dynamin 2 | Not recorded | In 1 condition |
| GDAP1ganglioside induced differentiation associated protein 1 | Not recorded | In 1 condition |
| GJB1gap junction protein beta 1 | Not recorded | In 1 condition |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Not recorded | In 2 conditions |
| LRSAM1leucine rich repeat and sterile alpha motif containing 1 | Not recorded | In 1 condition |
| NAGAalpha-N-acetylgalactosaminidase | Not recorded | In 1 condition |
| SEPTIN9septin 9 | Not recorded | In 1 condition |
| SETXsenataxin | Not recorded | In 1 condition |
| SH3TC2SH3 domain and tetratricopeptide repeats 2 | Not recorded | In 1 condition |
| TFGtrafficking from ER to golgi regulator | Not recorded | In 1 condition |
| TRIM2tripartite motif containing 2 | 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.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks