connexin 32 - CISMeF

Preferred Label : connexin 32;

MeSH note : was SY to gap junction protein (NM); use connexins (NM) to search through 1993; defective GJB1 in human are a cause of X-linked CHARCOT MARIE TOOTH DISEASE (CMT-X); RefSeq NM_000166 (human); NM_017251 (rat); NM_008124 (mouse);

CISMeF synonym : GJB1 protein, human; Gjb1 protein, mouse; Gjb1 protein, rat;

MeSH synonym : connexin Cx32; beta1 connexin;

MeSH hyponym : connexin 32 protein, rat; Cx32 protein, rat; gap junction membrane channel protein beta 1, rat; connexin 32 protein, mouse; Cx32 protein, mouse; gap junction membrane channel protein beta 1, mouse; CX32 protein, human; Charcot-Marie-Tooth neuropathy, X-linked protein, human; gap-junction membrane channel protein beta 1, human; connexin 32 protein, human;

Is substance : O;

Details

Origin ID

C082918;

UMLS CUI

C0163743;

Automatic exact mappings (from CISMeF team)
- Gap junction protein, beta-1 [OMIM gene]
- gap junction protein beta 1 [ORDO Gene]
- gap junction protein beta 1 [HGNC gene]
Currated CISMeF NLP mapping
- Connexin 32 [FMA entity]
MeSH term(s) associated for indexing
- connexins [MeSH Descriptor]
Record concept(s)
- GJB1 protein, human [MeSH concept]
- Gjb1 protein, mouse [MeSH concept]
- Gjb1 protein, rat [MeSH concept]
- connexin 32 [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]
UMLS correspondences (same concept)
- Connexin 32 [FMA entity]

Keyword's position in hierarchy(ies) :

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