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EPS8L2 protein, human MeSH Supplementary Concept Data 2025


MeSH Supplementary
EPS8L2 protein, human
Unique ID
C000606951
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C000606951
Entry Term(s)
epidermal growth factor receptor kinase substrate 8-like protein 2, human
Registry Numbers
0
Previous Indexing
*Membrane Proteins (2016-2020)
Heading Mapped to
*Microfilament Proteins
Frequency
2
Note
EPS8L2 is causal gene for childhood onset autosomal recessive progressive hearing loss; RefSeq NM_022772.3
Source
Orphanet J Rare Dis. 2015;10() (dup#6); 96
Date of Entry
2016/04/22
Revision Date
2019/12/11
EPS8L2 protein, human Preferred
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