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TMEM138 protein, human
MeSH Supplementary Concept Data 2025
Details
Concepts
MeSH Supplementary
TMEM138 protein, human
Unique ID
C570597
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C570597
Registry Numbers
0
Heading Mapped to
*Membrane Proteins
Frequency
7
Note
mutation leads to ciliopathy; RefSeq NM_016464
Source
Science. 2012 Feb 24;335(6071):966-9.
Date of Entry
2012/03/11
Revision Date
1955/01/01
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TMEM138 protein, human
Preferred
Concept UI
M0571727
Registry Numbers
0
Terms
TMEM138 protein, human
Preferred Term
Term UI
T819278
Date
03/11/2012
LexicalTag
NON
ThesaurusID
NLM (2012)
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