NDUFA7

Chr 19p13.2

NADH:ubiquinone oxidoreductase subunit A7

Aliases:: B14.5a
MANE:: ENST00000301457.3

OMIM: 602139 ↗NCBI: 4701 ↗Ensembl ↗

Annotations refreshed 9 hours ago.

Predicted protein structure

AlphaFold predicted structure

NDUFA7 · O95182

v62025-08-01

Predicted Aligned Error matrix for NDUFA7 — diagonal shows residue index, colour shows pairwise prediction confidence (lower is better) — Predicted Aligned Error

Mean pLDDT

86.8/ 100

Confident

113 residues

Confidence breakdown

Very high(≥ 90)71%
Confident(70–90)13%
Low(50–70)10%
Very low(< 50)6%

Open interactive 3D viewer

AlphaFold (Jumper et al., 2021) · CC BY 4.0

Clinical relevance (Genomics England PanelApp)

Moderate Evidence (Amber)

Mitochondrial disorder with complex I deficiency
Unknown
Possible mitochondrial disorder - nuclear genes
Unknown
Likely inborn error of metabolism
Unknown
Mitochondrial disorders

Disease associations (Open Targets)

type 2 diabetes mellitus
0.61
diabetes mellitus
0.58
polycystic ovary syndrome
0.42
gestational diabetes
0.41
Insulin resistance
0.40
prediabetes syndrome
0.40
Parkinson disease
0.40
type 1 diabetes mellitus
0.39
metabolic syndrome
0.39
obesity disorder
0.39

Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.

Protein function (UniProt)

NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 7

Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone