-
Melanophilin is a
carrier protein which in
humans is
encoded by the MLPH gene.
Several alternatively spliced transcript variants of this gene have been...
- syndrome, flavism, isabellinism, xanthochromism, axanthism, amelanism, and
melanophilin mutations. Pale
patches of skin, feathers, or fur (often
referred to...
- Scott, C. Andre, M. Breen, T. Leeb:
Chromosomal ****ignment of the
canine melanophilin gene (MLPH): a
candidate gene for coat
color dilution in Pinschers. In:...
- produced.
Studies have
linked the
diluted trait to a
mutation in the
melanophilin (MLPH) gene. The
dilution factor was not
originally a
visible part of...
- be a
mutation caused by a
single base-pair
change in exon 1 of MLPH (
melanophilin) gene. In
genetic linkage studies, Lav
locus has been ****igned to a linkage...
- This type has a
grave prognosis if untreated. Type 3 has
mutations in
melanophilin and is
characterized by
partial albinism. This type does not pose a threat...
- on the X
chromosome in 2009. The
Dense pigment gene, D/d,
codes for
melanophilin (MLPH; A0SJ36), a
protein involved in the
transportation and deposition...
-
Torii S, Yi Z,
Igarashi M,
Okamoto K,
Takeuchi T,
Izumi T (Apr 2002). "
Melanophilin directly links Rab27a and
myosin Va
through its
distinct coiled-coil...
- (2002). "Synaptotagmin-like
protein (Slp)
homology domain 1 of Slac2-a/
melanophilin is a
critical determinant of GTP-dependent
specific binding to Rab27A"...
-
alleles cause specific shades or hues of brown. B is
dominant to b. The
melanophilin gene (MLPH) at the D
locus causes a
dilution mainly of eumelanin, while...
