Ndufs2 MGI Mouse Gene Detail - MGI:2385112 - NADH:ubiquinone oxidoreductase core subunit S2

Symbol

Ndufs2
Name

NADH:ubiquinone oxidoreductase core subunit S2
Synonyms

MGC:27667

Feature Type

protein coding gene
IDs

MGI:2385112
NCBI Gene: 226646
Alliance

genome feature page
Transcription Start Sites

1 TSS
Candidate for QTL

1 QTL

Sequence Map

Chr1:171062426-171078956 bp, - strand
From NCBI annotation of GRCm39
View this region in JBrowse
Genome Browsers

Ensembl | UCSC | NCBI

Genetic Map

Chromosome 1, 79.25 cM
Mapping Data

3 experiments

SNPs within 2kb

508 from dbSNP Build 142
Strain Annotations

19

For selected strains:

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_2385112	protein coding gene	Chr1:171062422-171078957 (-)
129S1/SvImJ	ENSMUSG00200046157	protein coding gene	Chr1:168546400-168563730 (-)
A/J	ENSMUSG00195047981	protein coding gene	Chr1:167901744-167918938 (-)
AKR/J	ENSMUSG00220026192	protein coding gene	Chr1:167646043-167663168 (-)
BALB/cJ	ENSMUSG00180043903	protein coding gene	Chr1:168186656-168203984 (-)
C3H/HeJ	ENSMUSG00175040008	protein coding gene	Chr1:168197755-168215082 (-)
C57BL/6NJ	ENSMUSG00215044003	protein coding gene	Chr1:168018907-168036031 (-)
CAROLI/EiJ	MGP_CAROLIEiJ_G0014859	protein coding gene	Chr1:161496366-161513021 (-)
CAST/EiJ	ENSTCUG00005043003	protein coding gene	Chr1:166533110-166550226 (-)
CBA/J	ENSMUSG00210033686	protein coding gene	Chr1:168076646-168093991 (-)
DBA/2J	ENSMUSG00185027148	protein coding gene	Chr1:172390586-172407938 (-)
FVB/NJ	ENSMUSG00205033061	protein coding gene	Chr1:167085750-167102931 (-)
JF1/MsJ	ENSUMUG00000005834	protein coding gene	Chr1:171515661-171532775 (-)
LP/J	ENSMUSG00230024771	protein coding gene	Chr1:171963516-171980845 (-)
NOD/ShiLtJ	ENSMUSG00190030981	protein coding gene	Chr1:167863865-167881202 (-)
NZO/HlLtJ	ENSMUSG00225003651	protein coding gene	Chr1:175585309-175602497 (-)
PWK/PhJ	ENSLUMG00010029107	protein coding gene	Chr1:166868528-166885719 (-)
SPRET/EiJ	ENSMSPG00010047406	protein coding gene	Chr1:170398474-170415492 (-)
WSB/EiJ	ENSIUOG00005036941	protein coding gene	Chr1:167285902-167302923 (-)

Human Ortholog

NDUFS2, NADH:ubiquinone oxidoreductase core subunit S2

Vertebrate Orthologs

2

Vertebrate Orthology Source

Alliance of Genome Resources

Human Ortholog

NDUFS2, NADH:ubiquinone oxidoreductase core subunit S2
Synonyms

CI-49, LHONAR2, MC1DN6
Links

HGNC:7708

NCBI Gene ID: 4720

UniProt: O75306
Chr Location

1q23.3; chr1:161197104-161214723 (+) GRCh38

MGI Vertebrate Homology

Ndufs2 stringent orthology
1 human;1 mouse;1 rat
HCOP

vertebrate homology predictions: NDUFS2
Gene Tree

Ndufs2

Diseases

5 with human NDUFS2 associations

				Human Disease	Mouse Models
				hypertrophic cardiomyopathy IDs hypertrophic cardiomyopathy DOID:11984 DOID:11986 ICD9CM:425.1 ICD9CM:425.11 KEGG:05410 MESH:D002312 NCI:C34449 ORDO:217569 UMLS_CUI:C0007194
				inherited metabolic disorder IDs inherited metabolic disorder DOID:655 MESH:D008661 NCI:C34816 UMLS_CUI:C0025521
				Leigh disease IDs Leigh disease DOID:3652 ICD10CM:G31.82 MESH:D007888 NCI:C84814 OMIM:256000 ORDO:506 UMLS_CUI:C0023264
				multiple sclerosis IDs multiple sclerosis DOID:2377 ICD10CM:G35 ICD9CM:340 MESH:D009103 NCI:C3243 OMIM:612594 OMIM:612595 OMIM:612596 UMLS_CUI:C0026769
				nuclear type mitochondrial complex I deficiency 6 IDs nuclear type mitochondrial complex I deficiency 6 DOID:0112066 OMIM:618228

Click on a disease name to see all genes associated with that disease.

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Phenotype Summary

4 phenotypes from 1 allele in 1 genetic background
24 phenotype references

Phenotype Overview

Blue squares indicate phenotypes directly attributed to mutations/alleles of this gene.

adipose tissue	behavior/neurological	cardiovascular system	cellular	craniofacial	digestive/alimentary system	embryo	endocrine/exocrine glands	growth/size/body	hearing/vestibular/ear	hematopoietic system	homeostasis/metabolism	integument	immune system	limbs/digits/tail	liver/biliary system	mortality/aging	muscle	nervous system	pigmentation	renal/urinary system	reproductive system	respiratory system	skeleton	taste/olfaction	neoplasm	vision/eye

Click cells to view annotations.

All Mutations and Alleles

10
Chemically induced (other)

2
Endonuclease-mediated

6
Gene trapped

1
Targeted

1
Genomic Mutations

2 involving Ndufs2
Incidental Mutations

Mutagenetix , APF
Find Mice (IMSR)

33 strains or lines available

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All GO Annotations

66
GO References

20

Molecular Function

carbohydrate derivative binding	cytoskeletal protein binding	DNA binding	enzyme regulator	hydrolase	ligase	lipid binding	oxidoreductase	RNA binding	signaling receptor activity	signaling receptor binding	transcription	transferase	transporter

Biological Process

carbohydrate derivative metabolism	cell differentiation	cell population proliferation	cellular component organization	DNA-templated transcription	establishment of localization	homeostatic process	immune system process	lipid metabolic process	programmed cell death	protein metabolic process	response to stimulus	signaling	system development

Cellular Component

cell projection	cytoplasmic vesicle	cytoskeleton	cytosol	endoplasmic reticulum	endosome	extracellular region	Golgi apparatus	mitochondrion	membraneless organelle	nucleus	organelle envelope	organelle lumen	plasma membrane	protein-containing complex	synapse	vacuole

Click cells to view annotations.

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Expression Overview

GXD's primary emphasis is on endogenous gene expression during development. Click on grid cells to view annotations.

Blue cells = expressed in wild-type.
Gray triangles = other expression annotations only
(e.g. absence of expression or data from mutants).

early conceptus	embryo ectoderm	embryo endoderm	embryo mesoderm	embryo mesenchyme	extraembryonic component	alimentary system	auditory system	branchial arches	cardiovascular system	connective tissue	endocrine system	exocrine system	hemolymphoid system	integumental system	limbs	liver and biliary system	musculoskeletal system	nervous system	olfactory system	reproductive system	respiratory system	urinary system	visual system

Click cells to view annotations.

Assay Results

703
Tissues

101
cDNA Data

315
Literature Summary

7

Images

Tissue x Stage Matrix

Other Mouse Links

Allen Institute

GEO

Expression Atlas
Other Vertebrate Links

Xenbase ndufs2

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All Sequences

80
RefSeq

6
UniProt

4
CCDS

CCDS15484.1

Ensembl

ENSMUSG00000013593 (Evidence)
NCBI Gene

226646

			Length	Strain/Species	Flank
genomic	226646	NCBI Gene Model \| MGI Sequence Detail	16531	C57BL/6J	± kb
transcript	NM_153064	RefSeq \| MGI Sequence Detail	1603	C57BL/6
polypeptide	Q91WD5	UniProt \| EBI \| MGI Sequence Detail	463	Not Applicable

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UniProt

4 Sequences
Protein Ontology

PR:000011097 NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrial

(term hierarchy)
PDB

6G2J, 6G72, 6ZR2, 6ZTQ, 7AK5, 7AK6, 7B93, 7PSA, 8C2S, 8CA3, 8CA5, 8IAO, 8IAP, 8IAQ, 8IB4, 8IB5, 8IB6, 8IB9, 8IBA, 8IBB, 8IBD, 8IBE, 8IBF, 8IC2, 8IC3, 8IC4, 8OLT, 8OM1, 8PW5, 8PW6, 8PW7, 8RGP, 8RGQ, 8RGR, 8RGT, 8UCA, 8XNL, 8XNM, 8XNN, 8XNO, 8XNP, 8XNQ, 8XNR, 8XNS, 8XNT, 8XNU, 8XNV, 8XNW, 8XNX, 8XNY, 8XNZ, 8XO0
EC

7.1.1.2
InterPro Domains

IPR001135 NADH-quinone oxidoreductase, subunit D

IPR014029 NADH:ubiquinone oxidoreductase, 49kDa subunit, conserved site

IPR022885 NAD(P)H-quinone oxidoreductase subunit D/H

IPR029014 [NiFe]-hydrogenase, large subunit
GlyGen

Q91WD5 1 site, 1 O-linked glycan (1 site)

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All nucleic 320

cDNA 315

Primer pair 5

Antibodies 1

Microarray probesets 3

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MGI:2138402

Summaries

All 72

Developmental Gene Expression 7

Gene Ontology 20

Phenotypes 24
Earliest

J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573
Latest

J:382314 Hepler C, et al., Adipocyte NADH dehydrogenase reverses circadian and diet-induced metabolic syndrome. Nat Metab. 2026 Feb 18;

TSS for Ndufs2:

(View these features in JBrowse)

Transcription Start Site	Location	Distance from Gene 5'-end
Tssr15024	Chr1:171079233-171079244 (-)	-283 bp

Ndufs2 is Candidate Gene for:

QTL	Genetic Location*	Genome Location (GRCm39)	Reference	QTL Note
Thcir5	Chr1, syntenic		J:314541	Top positional candidate genes include: Ndufs2 (MGI:2385112) for Thcir5; Scp2 (MGI:98254) for Thcir6; Rps6kb1 (MGI:1270849) for Thcir2; Pde4d (MGI:99555) for Thcir4; and Pten (MGI:109583) for Thcir3. These genes are likely to play a role in modulating initial response to THC based on location within modulatory QTL, putative functional sequence variants between B and D haplotypes that segregate among BXD progeny, evidence of genetic control of expression in brain tissue, and previously reported involvement in endocannabinoid/cannabinoid receptor signaling pathways.

*cM position of peak correlated region/marker

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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