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Tctn1 protein, human MeSH Supplementary Concept Data 2025


MeSH Supplementary
Tctn1 protein, human
Unique ID
C561486
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C561486
Entry Term(s)
tectonic1 protein, human
Registry Numbers
0
Heading Mapped to
*Membrane Proteins
Frequency
17
Note
mutation leads to Joubert syndrome; RefSeq NM_001082538
Source
Nat Genet 2011 Aug;43(8):776-84
Date of Entry
2011/10/02
Revision Date
2011/10/02
Tctn1 protein, human Preferred
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