SHMT1 wt Allele

Preferred Label : SHMT1 wt Allele;

NCIt synonyms : SHMT; CSHMT; MGC15229; Serine Hydroxymethyltransferase 1 (Soluble) wt Allele; MGC24556;

NCIt definition : Human SHMT1 wild-type allele is located in the vicinity of 17p11.2 and is approximately 36 kb in length. This allele, which encodes serine hydroxymethyltransferase, cytosolic protein, plays a role in the metabolism of both amino acids and folate.;

GenBank Accession Number : NM_004169;

Details

Origin ID

C104969;

UMLS CUI

C3538792;

OMIM relation
- Serine hydroxymethyltransferase, cytosolic [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 17p11.2 [NCIt concept]
gene_is_element_in_pathway
- Cyanoamino Acid Metabolism Pathway [NCIt concept]
- Glycine, Serine and Threonine Metabolism Pathway [NCIt concept]
- Glyoxylate and Dicarboxylate Metabolism Pathway [NCIt concept]
- One Carbon Pool by Folate Pathway [NCIt concept]
gene_plays_role_in_process
- Amino Acid Biosynthesis [NCIt concept]
- Folic Acid Metabolic Process [NCIt concept]
- Methylation [NCIt concept]
- Nucleotide Biosynthesis Process [NCIt concept]

Keyword's position in hierarchy(ies) :

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