- motif-containing protein,
mitochondrial is a
protein that in
humans is
encoded by the
LRPPRC gene.
Transcripts ranging in size from 4.8 to 7.0 kb
which result from alternative...
- COX ****embly factors: SURF1, SCO1, SCO2, COX10, COX15, COX20, COA5 and
LRPPRC.
Mutations in
these proteins can
result in
altered functionality of sub-complex...
- HGNC:16936 Q86VZ4 8873 LRP12 HGNC:31708 Q9Y561 8874 LRPAP1 HGNC:6701 P30533 8875
LRPPRC HGNC:15714 P42704 8876 LRR1 HGNC:19742 Q96L50 8877 LRRC1 HGNC:14307 Q9BTT6...
- Saguenay–Lac-Saint-Jean
region of
Quebec is
caused by a
mutation in the
LRPPRC gene,
located on the
small ('p') arm of
chromosome 2. Both
compound heterozygosity...
-
encoding proteins containing this
repeat include: DENND4A, DENND4B, DENND4C
LRPPRC PTCD1, PTCD2, PTCD3 MRPS27
Mingler MK,
Hingst AM,
Clement SL, Yu LE, Reifur...
-
cytochrome c
oxidase deficiency; COX deficiency) SURF1, SCO2, COX10, SCO1,
LRPPRC, COX15, COX6B1, TACO1, COX14, COX20, PET100, COA6, COA3, COX8A, COX4I1,...
- eIF4E
directly binds to the
leucine rich
pentatricopeptide repeat protein (
LRPPRC)
which directly binds the
dorsal surface of eIF4E and
simultaneously to...
- difficulties. This
disorder is
caused by an
autosomal recessive mutation in the
LRPPRC gene in
chromosome 2p16. To be more specific, it is
caused by a base pair...
- PMC 139241. PMID 12477932. Liu L,
McKeehan WL (2002). "Sequence
analysis of
LRPPRC and its SEC1
domain interaction partners suggests roles in cytoskeletal...
-
Library of Medicine. Liu L,
McKeehan WL (Feb 2002). "Sequence
analysis of
LRPPRC and its SEC1
domain interaction partners suggests roles in cytoskeletal...
