histidine degradation
Pathways in the histidine degradation SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | histidine degradation | PubChem | |
| 2 | Histidine catabolism | Reactome | |
| 3 | L-histidine degradation III | PubChem | |
| 4 | histamine biosynthesis | PubChem | |
| 5 | formate assimilation into 5,10-methylenetetrahydrofolate | PubChem | |
| 6 | L-histidine degradation VI | PubChem |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
| # | Symbol | Description | Category | # Related Pathways |
|---|---|---|---|---|
| 1 | HAL | Histidine Ammonia-Lyase | Protein Coding | 4 |
| 2 | MTHFD1 | Methylenetetrahydrofolate Dehydrogenase, Cyclohydrolase And Formyltetrahydrofolate Synthetase 1 | Protein Coding | 3 |
| 3 | UROC1 | Urocanate Hydratase 1 | Protein Coding | 2 |
| 4 | AMDHD1 | Amidohydrolase Domain Containing 1 | Protein Coding | 2 |
| 5 | FTCD | Formimidoyltransferase Cyclodeaminase | Protein Coding | 2 |
| 6 | HDC | Histidine Decarboxylase | Protein Coding | 2 |
| 7 | CARNMT1 | Carnosine N-Methyltransferase 1 | Protein Coding | 1 |
| 8 | HNMT | Histamine N-Methyltransferase | Protein Coding | 1 |
| 9 | CARNS1 | Carnosine Synthase 1 | Protein Coding | 1 |
Disorders associated with histidine degradation SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Histidinemia | Enrichment | HAL | 4.13 |
| 2 | Gilles de la tourette syndrome | Enrichment | HDC | 3.83 |
| 3 | Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia | Enrichment | MTHFD1 | 3.83 |
| 4 | Neural tube defects, folate-sensitive | Enrichment | MTHFD1 | 3.53 |
| 5 | Urocanase deficiency | Enrichment | UROC1 | 3.43 |
| 6 | Intellectual developmental disorder, autosomal recessive 51 | Enrichment | HNMT | 3.23 |
| 7 | Glutamate formiminotransferase deficiency | Enrichment | FTCD | 3.13 |
| 8 | Severe combined immunodeficiency | Enrichment | MTHFD1 | 2.61 |
| 9 | Asthma | Enrichment | HNMT | 2.19 |
| 10 | Autosomal recessive non-syndromic intellectual disability | Enrichment | HNMT | 1.47 |