| Type | Description |
|---|---|
| Definition | acyl-CoA dehydrogenase family member 9 |
| Date | Results | Publications |
|---|---|---|
| 2018-11-24 12:06:00 | Mutations in the ND6, NDUFV1 or ACAD9 genes are responsible for the mitochondrial complex I deficiency. | 29348607 |
| 2017-09-02 11:48:00 | Study identified new mutations in ACAD9 responsible for a wide spectrum of heart diseases in the presence of elevated serum lactate levels. | 27233227 |
| 2017-07-29 11:35:00 | ACAD9 mutation is the most frequent cause of cardiac hypertrophy and isolated complex I deficiency. | 26669660 |
| 2016-06-11 11:56:00 | Case Report: neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules. | 26826406 |
| 2016-02-20 11:06:00 | In cells where it is strongly expressed, ACAD9 plays a physiological role in fatty acid oxidation. | 25721401 |
| Type | IDs |
|---|---|
| Synonymous | MC1DN20, NPD002 |
| Gene |
UniProtKB-ID:
ACAD9_HUMAN
UniprotKB:
Q9H845
UniParc:
UPI00000498C3
EMBL:
BC007970,
AK024012,
AF327351,
BC013354,
CH471052
Ensembl:
ENSG00000177646
KO:
hsa:28976
|
| Nucleutide sequences |
EMBL-CDS:
AAH13354.1,
BAB14775.1,
AAL56011.1,
AAH07970.1,
EAW79296.1,
EAW79295.1
Ensembl_TRS:
ENST00000308982
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000312618
RefSeq:
NP_054768.2,
XP_024309252.1,
XP_024309253.1
|
| Others |
UniRef100:
UniRef100_Q9H845
UniRef90:
UniRef90_Q9H845
UniRef50:
UniRef50_Q9H845
UniGene:
Hs.567482
CCDS:
CCDS3053.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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