| Entrez gene ID | | 171133 |
| Official gene symbol | | Gcsh |
| Full name | | glycine cleavage system protein H (aminomethyl carrier) |
| Aliases | | MGC108603 |
| Gene summary | | component of the mitochondrial multienzyme glycine cleavage system (GCS); deficiency of the GCS in human causes nonketotic hyperglycinemia (NKH), an inborn error of glycine metabolism [RGD] |
| Location | | Chromosome: 19 Locus: 19q12 |
| Gene position | | 47091225 - 47101982 Map Viewer |
| Gene orientation | | minus |
| Gene size | | 10758 bp |
| Gene sequence |
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