Chromosome 19 open reading frame 12

Preferred Label : Chromosome 19 open reading frame 12;

Symbol : C19ORF12;

CISMeF acronym : C19ORF12;

Type : Gene;

Ensembl ID : ENSG00000131943;

Prefixed ID : *614297;

Details

Origin ID

614297;

UMLS CUI

C1428487;

Automatic exact mappings (from CISMeF team)
- chromosome 19 open reading frame 12 [HGNC gene]
- chromosome 19 open reading frame 12 [ORDO Gene]
NCIt concept(s)
- C19orf12 Gene [NCIt concept]
- C19orf12 wt Allele [NCIt concept]
- Protein C19orf12 [NCIt concept]
ORDO concept(s)
- chromosome 19 open reading frame 12 [ORDO Gene]
Phenotypes related
- Neurodegeneration with brain iron accumulation 4 [OMIM Phenotype]
- Spastic paraplegia 43, autosomal recessive [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- C19orf12 Gene [NCIt concept]
- chromosome 19 open reading frame 12 [HGNC gene]

Keyword's position in hierarchy(ies) :

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