mutL homolog 1

Preferred Label : mutL homolog 1;

Approved symbol HGNC : MLH1;

Alias symbols HGNC : HNPCC; HNPCC2; FCC2; MLH-1;

Chromosome HGNC : 3p22.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000076242;

Details

Origin ID

HGNC:7127;

UMLS CUI

C0879389;

Automatic exact mappings (from CISMeF team)
- Dna mismatch repair protein mlh1 [OMIM gene]
- Lynch syndrome 2 [OMIM Phenotype]
- MutL Homolog 1 Measurement [NCIt concept]
- MutL Protein Homolog 1 [MeSH Descriptor]
- mutL homolog 1 [ORDO Gene]
NCIt concept
- MLH1 Gene [NCIt concept]
OMIM gene
- Dna mismatch repair protein mlh1 [OMIM gene]
Orphanet gene
- mutL homolog 1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Dna mismatch repair protein mlh1 [OMIM gene]
- MLH1 Gene [NCIt concept]
- MLH1 gene [LOINC component]

Keyword's position in hierarchy(ies) :

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