NDUFS8

GENERAL INFORMATION

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Gene name

NDUFS8

Gene description

NADH dehydrogenase (ubiquinone) Fe-S protein 8, 23kDa (NADH-coenzyme Q reductase)

Protein class

Disease related genes
Enzymes
Mitochondrial proteins
Potential drug targets
Predicted intracellular proteins
Predicted secreted proteins

Predicted localization

Intracellular,Secreted

Number of transcripts

6
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

The gastrointestinal tract, airway epithelia, renal tubuli and male genital tract showed moderate cytoplasmic staining. Strong positivity was observed in gastric parietal cells, cardiac and skeletal muscle. Lymphoid tissues, liver, squamous epithelia and most cells in the female genital tract were negative.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA018524
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

NDUFS8 (HGNC Symbol)

Synonyms

CI-23k, TYKY

Description

NADH dehydrogenase (ubiquinone) Fe-S protein 8, 23kDa (NADH-coenzyme Q reductase) (HGNC Symbol)

Entrez gene summary

This gene encodes a subunit of mitochondrial NADH:ubiquinone oxidoreductase, or Complex I, a multimeric enzyme of the respiratory chain responsible for NADH oxidation, ubiquinone reduction, and the ejection of protons from mitochondria. The encoded protein is involved in the binding of two of the six to eight iron-sulfur clusters of Complex I and, as such, is required in the electron transfer process. Mutations in this gene have been associated with Leigh syndrome. [provided by RefSeq, Mar 2010]

Chromosome

11

Cytoband

q13.2

Chromosome location (bp)

68030617 - 68036644

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000110717 (version 78.38)

Entrez gene

4728

UniProt

O00217 (UniProt - Evidence at protein level)

neXtProt

NX_O00217

Antibodypedia

NDUFS8 antibodies


PROTEIN BROWSER

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ENST00000313468
 
ENST00000453471
 
ENST00000525419
 
ENST00000525628
 
ENST00000526339
 
ENST00000528492
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

NDUFS8-001 ENSP00000315774
ENST00000313468
O00217
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Show » Show » 210 23.7 Yes 0
NDUFS8-004 ENSP00000432848
ENST00000528492
Q08E91
Show all »
Show » Show » 64 7.4 No 0
NDUFS8-011 ENSP00000403972
ENST00000453471
F8W9K7
Show all »
Show » Show » 124 13.9 Yes 0
NDUFS8-013 ENSP00000433521
ENST00000525419
E9PKH6
Show all »
Show » Show » 138 15.9 No 0
NDUFS8-014 ENSP00000432968
ENST00000525628
E9PN51
Show all »
Show » 110 12.4 Yes 0
NDUFS8-015 ENSP00000436287
ENST00000526339
E9PPW7
Show all »
Show » Show » 184 20.7 Yes 0