Microtubule-associated protein 1b

Preferred Label : Microtubule-associated protein 1b;

Symbol : MAP1B;

CISMeF acronym : MAP1B;

Type : Gene;

Alternative titles and symbols : Futsch, drosophila, homolog of; FUTSCH;

Ensembl ID : ENSG00000131711;

Prefixed ID : *157129;

Details

Origin ID

157129;

UMLS CUI

C1417004;

Automatic exact mappings (from CISMeF team)
- microtubule associated protein 1B [HGNC gene]
- microtubule associated protein 1B [ORDO Gene]
- microtubule-associated protein 1B [MeSH Supplementary Concept]
- microtubule-associated protein 1B [MeSH concept]
HGNC gene
- microtubule associated protein 1B [HGNC gene]
NCIt concept(s)
- MAP1B Gene [NCIt concept]
- MAP1B wt Allele [NCIt concept]
- Microtubule-Associated Protein 1B [NCIt concept]
ORDO concept(s)
- microtubule associated protein 1B [ORDO Gene]
Phenotypes related
- Deafness, autosomal dominant 83 [OMIM Phenotype]
- Periventricular nodular heterotopia 9 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- microtubule associated protein 1B [HGNC gene]

Keyword's position in hierarchy(ies) :

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