about
P688
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) miceTMHS is an integral component of the mechanotransduction machinery of cochlear hair cellsTargeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutationThe murine catecholamine methyltransferase mTOMT is essential for mechanotransduction by cochlear hair cells.
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
proteinë
@sq
proteïne in Lipoma HMGIC fusion partner-like 5
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protèin
@ace
بروتين في فأر المنازل
@ar
name
Lipoma HMGIC fusion partner-like 5
@en
Lipoma HMGIC fusion partner-like 5
@nl
type
label
Lipoma HMGIC fusion partner-like 5
@en
Lipoma HMGIC fusion partner-like 5
@nl
altLabel
LHFPL tetraspan subfamily member 5 protein
@en
Lhfpl5
@en
lipoma HMGIC fusion partner-like 5 protein
@en
tetraspan membrane protein of hair cell stereocilia
@en
tetraspan transmembrane protein, hair cell stereocilia
@en
prefLabel
Lipoma HMGIC fusion partner-like 5
@en
Lipoma HMGIC fusion partner-like 5
@nl
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XP_006524496
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ENSMUSP00000079598