MeSH Browser

MeSH Supplementary: TMEM67 protein, human
Unique ID: C468846
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C468846
Entry Term(s): MKS3 protein, human; Meckel syndrome, type 3 protein, human; transmembrane protein 67, human
Registry Numbers: 0
Previous Indexing: *PROTEINS (2002-2006)
Heading Mapped to: *Membrane Proteins
Frequency: 51
Note: mutated in nephronophthisis 11 (NPHP11); RefSeq NM_153704
Source: Hum Genet 2002 Oct;111(4-5):456-61
Date of Entry: 2002/12/06
Revision Date: 2011/02/03

Concept UI: M0443130
Registry Numbers: 0
Terms: TMEM67 protein, human Preferred Term
Term UI T677372
Date07/06/2006
LexicalTag NON
ThesaurusID NLM (2006); Meckel syndrome, type 3 protein, human
Term UI T656286
Date10/19/2005
LexicalTag NON
ThesaurusID NLM (2005); MKS3 protein, human
Term UI T527742
Date12/06/2002
LexicalTag NON
ThesaurusID NLM (2002); transmembrane protein 67, human
Term UI T677373
Date07/06/2006
LexicalTag NON
ThesaurusID NLM (2006)

TMEM67 protein, human MeSH Supplementary Concept Data 2025