- the
UQCRQ gene. This ubiqinone-binding
protein is a
subunit of
mitochondrial Complex III in the
electron transport chain. A
mutation in the
UQCRQ gene...
- "Mitochondrial
Complex III
Deficiency ****ociated with a
Homozygous Mutation in
UQCRQ". The
American Journal of
Human Genetics. 82 (5): 1211–1216. doi:10.1016/j...
-
Mitochondrial complex III deficiency,
nuclear type (MC3DN) BCS1L, TTC19,
UQCRQ, UQCRC2, CYC1, UQCC2, LYRM7, UQCC3, UQCRFS1 AR PS124000
Mitochondrial complex...
- / SU7
UQCRB Cytochrome b-c1
complex subunit 7 Pfam PF02271 8 QCR8 / SU8
UQCRQ Cytochrome b-c1
complex subunit 8 Pfam PF02939 9 QCR9 / SU9 UQCRFS1a (N-terminal...
-
Cytochrome C1, UQCRFS1 (this protein, a type of
Rieske protein), UQCRB,
UQCRQ ("11kDa protein"),
UQCRH (cyt c1
Hinge protein), UCRC ("cyt. c1 ****ociated...
- genes: UQCRC1, UQCRC2,
Cytochrome c1, UQCRFS1 (Rieske protein), UQCRB,
UQCRQ [1]("11kDa protein"),
UQCRH (cyt c1
Hinge protein),
Rieske Protein presequence...
-
reductase core
protein I (UQCRC1), mRNA UQCRC2 NM_003366
UQCRHL NM_001089591
UQCRQ NM_014402 Homo
sapiens low
molecular m**** ubiquinone-binding
protein (9...
- 17925
UQCRH HGNC:12590 P07919 17926
UQCRHL HGNC:51714 A0A096LP55 17927
UQCRQ HGNC:29594 O14949 17928 URAD HGNC:17785 A6NGE7 17929 URB1 HGNC:17344 O60287...
-
caused by AIMP1/p43 mutation.
Mitochondrial complex III
deficiency due to
UQCRQ mutation Congenital cataract (recessive) due to CRYBB1 mutation. Microphthalmia...
- UQCRC2) and six low-molecular
weight proteins (UQCRH/QCR6, UQCRB/QCR7,
UQCRQ/QCR8, UQCR10/QCR9, UQCR11/QCR10 and a
cleavage product of UQCRFS1). The...
