| Type | Description |
|---|---|
| Definition | NADH:ubiquinone oxidoreductase subunit A1 |
| Date | Results | Publications |
|---|---|---|
| 2018-07-23 13:14:00 | Results from a study on gene expression variability markers in early-stage human embryos shows that NDUF1A is a putative expression variability marker for the 3-day, 8-cell embryo stage. | 26288249 |
| 2017-06-24 11:26:00 | The gene signature of OPA1, CTSA, NDUFA1, STK10 and PRDX1 was able to identify patients post-implant with a sensitivity of 91% and a specificity of 86% in discrimination between post-implant group and healthy controls. | 27177495 |
| 2014-03-15 12:25:00 | Fanconi anemia complementation group A mutants show defective respiration through Complex I, diminished ATP production and metabolic sufferance with an increased AMP/ATP ratio. | 23791750 |
| 2012-02-25 11:09:00 | Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency | 21596602 |
| 2010-05-31 11:16:00 | Mutations in the NDUFA1 gene is linked to a delayed mitochondrial network recovery in OXPHOS disorders. | 20153825 |
| Type | IDs |
|---|---|
| Synonymous | CI-MWFE, MC1DN12, MWFE, ZNF183 |
| Gene |
UniProtKB-ID:
NDUA1_HUMAN,
Q6IBB5_HUMAN
UniprotKB:
O15239,
Q6IBB5
UniParc:
UPI000013018C
EMBL:
BC000266,
U54993,
AB451304,
CR456889,
AB451435,
X81900,
CH471161
Ensembl:
ENSG00000125356
KO:
hsa:4694
|
| Nucleutide sequences |
EMBL-CDS:
AAD00084.1,
AAH00266.1,
CAA57489.1,
BAG70118.1,
EAW89840.1,
CAG33170.1,
BAG70249.1
Gene_ORFName:
hCG_23184
Ensembl_TRS:
ENST00000371437
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000360492
RefSeq:
NP_004532.1
|
| Others |
UniRef100:
UniRef100_O15239
UniRef90:
UniRef90_O15239
UniRef50:
UniRef50_O15239
UniGene:
Hs.534168
CCDS:
CCDS14590.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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