Coiled-coil-helix-coiled-coil-helix domain containing 10
about
P688
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvementFunctional annotation of heart enriched mitochondrial genes GBAS and CHCHD10 through guilt by associationCHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis.Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseases
P921
Coiled-coil-helix-coiled-coil-helix domain containing 10
description
humanes Protein
@de
mammalian protein found in Homo sapiens
@en
menselijk eiwit
@nl
protein
@id
protein
@sv
proteinë
@sq
protèin
@ace
protéine humaine
@fr
بروتين بشري
@ar
name
Coiled-coil-helix-coiled-coil-helix domain containing 10
@en
Coiled-coil-helix-coiled-coil-helix domain containing 10
@nl
type
label
Coiled-coil-helix-coiled-coil-helix domain containing 10
@en
Coiled-coil-helix-coiled-coil-helix domain containing 10
@nl
altLabel
CHCHD10
@en
MIX17 homolog A
@en
Protein N27C7-4
@en
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial
@en
prefLabel
Coiled-coil-helix-coiled-coil-helix domain containing 10
@en
Coiled-coil-helix-coiled-coil-helix domain containing 10
@nl
P681
P682
P705
P352
P638
P31
P352
P527
P637
NP_001288268
P682
P702
P703
P705
ENSP00000384973
ENSP00000418428
ENSP00000429976
ENSP00000430042
ENSP00000480602
ENSP00000486207
ENSP00000486793
ENSP00000487006