Advanced Search (OLGA)

Gene: NDUFS8 (NADH:ubiquinone oxidoreductase core subunit S8) Homo sapiens

Subscribe to Updates

Analyze

Symbol:

NDUFS8

Name:

NADH:ubiquinone oxidoreductase core subunit S8

RGD ID:

1319779

HGNC Page

HGNC:7715

Description:

Contributes to NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial electron transport, NADH to ubiquinone and mitochondrial respiratory chain complex I assembly. Located in mitochondrial inner membrane. Part of respiratory chain complex I. Implicated in nuclear type mitochondrial complex I deficiency 2.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

CI-23k; CI23KD; complex I 23kDa subunit; complex I-23kD; MC1DN2; NADH dehydrogenase (ubiquinone) Fe-S protein 8, 23kDa (NADH-coenzyme Q reductase); NADH dehydrogenase [ubiquinone] iron-sulfur protein 8, mitochondrial; NADH-ubiquinone oxidoreductase 23 kDa subunit; TYKY

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	68,030,681 - 68,036,644 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	68,030,617 - 68,036,644 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	67,798,148 - 67,804,111 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	67,554,685 - 67,560,690 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	11	67,554,684 - 67,560,690	NCBI
Celera	11	65,131,755 - 65,137,785 (+)	NCBI		Celera
Cytogenetic Map	11	q13.2	NCBI
HuRef	11	64,133,431 - 64,139,457 (+)	NCBI		HuRef
CHM1_1	11	67,681,851 - 67,687,870 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	11	68,034,333 - 68,040,285 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NDUFS8	Human	Aicardi-Goutieres Syndrome 3		IAGP	RGD:156438208	8554872	ClinVar Annotator: match by term: Aicardi-Goutieres syndrome 3	ClinVar	PMID:28492532
NDUFS8	Human	genetic disease		IAGP	RGD:243064005	8554872	ClinVar Annotator: match by term: Inborn genetic diseases	ClinVar	PMID:25741868
NDUFS8	Human	genetic disease		IAGP	RGD:156033070\|RGD:156149022\|RGD:156259646\|RGD:156333291\|RGD:329393711\|RGD:405806713\|RGD:597720937\|RGD:597720944	8554872	ClinVar Annotator: match by term: Inborn genetic diseases	ClinVar
NDUFS8	Human	genetic disease		IAGP	RGD:10411061	8554872	ClinVar Annotator: match by term: Inborn genetic diseases	ClinVar	PMID:20818383\|PMID:25741868\|PMID:26764160\|PMID:28492532\|PMID:30094188\|PMID:33233646\|PMID:35551192
NDUFS8	Human	genetic disease		IAGP	RGD:156279481	8554872	ClinVar Annotator: match by term: Inborn genetic diseases	ClinVar	PMID:23430795\|PMID:28492532\|PMID:32445240
NDUFS8	Human	immunodeficiency 90		IAGP	RGD:156438208	8554872	ClinVar Annotator: match by term: Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations	ClinVar	PMID:28492532
NDUFS8	Human	intellectual disability		IAGP	RGD:42723466	8554872	ClinVar Annotator: match by term: Intellectual disability	ClinVar
NDUFS8	Human	Leigh disease		IAGP	RGD:10409760\|RGD:11615129\|RGD:11619045\|RGD:126736261\|RGD:15150961	8554872	ClinVar Annotator: match by term: Leigh syndrome \| ClinVar Annotator: match by term: Subacute necrotizing more ...	ClinVar	PMID:25741868\|PMID:28492532
NDUFS8	Human	Leigh disease		IAGP	RGD:8692236	8554872	ClinVar Annotator: match by term: Leigh syndrome	ClinVar	PMID:24595071\|PMID:25741868
NDUFS8	Human	Leigh disease		IAGP	RGD:11665664\|RGD:13592700	8554872	ClinVar Annotator: match by term: Leigh syndrome	ClinVar	PMID:25741868
NDUFS8	Human	Leigh disease		IAGP	RGD:11600632\|RGD:11602725\|RGD:11604305\|RGD:11615100\|RGD:11618751\|RGD:11650213\|RGD:11653406\|RGD:11666456\|RGD:13508733\|RGD:28873178\|RGD:28899037\|RGD:28912006	8554872	ClinVar Annotator: match by term: Leigh syndrome	ClinVar
NDUFS8	Human	Leigh disease		IAGP	RGD:10411061	8554872	ClinVar Annotator: match by term: Subacute necrotizing encephalopathy	ClinVar	PMID:20818383\|PMID:25741868\|PMID:26764160\|PMID:28492532\|PMID:30094188\|PMID:33233646\|PMID:35551192
NDUFS8	Human	Leigh disease		IAGP	RGD:10405972	8554872	ClinVar Annotator: match by term: Leigh syndrome	ClinVar	PMID:25326637\|PMID:25741868\|PMID:28492532
NDUFS8	Human	Leigh disease		IAGP	RGD:8559967	8554872	ClinVar Annotator: match by term: Subacute necrotizing encephalopathy	ClinVar	PMID:25741868\|PMID:9837812
NDUFS8	Human	Leigh disease		IAGP	RGD:11598875\|RGD:11599491\|RGD:11604369\|RGD:11607354\|RGD:11609406\|RGD:11618512\|RGD:12841046	8554872	ClinVar Annotator: match by term: Leigh syndrome \| ClinVar Annotator: match by term: Leigh's disease more ...	ClinVar	PMID:28492532
NDUFS8	Human	mitochondrial complex I deficiency		IAGP	RGD:11598875\|RGD:12841046	8554872	ClinVar Annotator: match by term: MITOCHONDRIAL NADH DEHYDROGENASE COMPONENT OF COMPLEX I, DEFICIENCY OF	ClinVar	PMID:28492532
NDUFS8	Human	mitochondrial complex I deficiency		IAGP	RGD:10409760\|RGD:11615129	8554872	ClinVar Annotator: match by term: MITOCHONDRIAL NADH DEHYDROGENASE COMPONENT OF COMPLEX I, DEFICIENCY OF \| more ...	ClinVar	PMID:25741868\|PMID:28492532
NDUFS8	Human	mitochondrial complex I deficiency		IAGP	RGD:11665664	8554872	ClinVar Annotator: match by term: Mitochondrial complex I deficiency	ClinVar	PMID:25741868
NDUFS8	Human	mitochondrial complex I deficiency		IAGP	RGD:11600632\|RGD:11653406\|RGD:11666456	8554872	ClinVar Annotator: match by term: Mitochondrial complex I deficiency	ClinVar
NDUFS8	Human	mitochondrial complex I deficiency		IAGP	RGD:10411061	8554872	ClinVar Annotator: match by term: MITOCHONDRIAL NADH DEHYDROGENASE COMPONENT OF COMPLEX I, DEFICIENCY OF	ClinVar	PMID:20818383\|PMID:25741868\|PMID:26764160\|PMID:28492532\|PMID:30094188\|PMID:33233646\|PMID:35551192
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 1		IAGP	RGD:11615129\|RGD:11619045\|RGD:15150961	8554872	ClinVar Annotator: match by term: Mitochondrial complex I deficiency, nuclear type 1	ClinVar	PMID:25741868\|PMID:28492532
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 1		IAGP	RGD:11598875\|RGD:11599491\|RGD:11604369\|RGD:11607354\|RGD:11609406\|RGD:11618512\|RGD:12841046	8554872	ClinVar Annotator: match by term: Mitochondrial complex I deficiency, nuclear type 1	ClinVar	PMID:28492532
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 1		IAGP	RGD:8692236	8554872	ClinVar Annotator: match by term: Mitochondrial complex I deficiency, nuclear type 1	ClinVar	PMID:24595071\|PMID:25741868
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 1		IAGP	RGD:11602725\|RGD:11604305\|RGD:11615100\|RGD:11618751\|RGD:11650213\|RGD:11666456\|RGD:28873178\|RGD:28899037\|RGD:28912006	8554872	ClinVar Annotator: match by term: Mitochondrial complex I deficiency, nuclear type 1	ClinVar
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 1		IAGP	RGD:11665664	8554872	ClinVar Annotator: match by term: Mitochondrial complex I deficiency, nuclear type 1	ClinVar	PMID:25741868
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 1		IAGP	RGD:10411061	8554872	ClinVar Annotator: match by term: Mitochondrial complex I deficiency, nuclear type 1	ClinVar	PMID:20818383\|PMID:25741868\|PMID:26764160\|PMID:28492532\|PMID:30094188\|PMID:33233646\|PMID:35551192
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 2		IAGP	RGD:401797499	8554872	ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2	ClinVar	PMID:23430795\|PMID:32445240\|PMID:34052969
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 2		IAGP	RGD:11615129\|RGD:151773653\|RGD:156313227	8554872	ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2	ClinVar	PMID:25741868\|PMID:28492532
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 2		IAGP	RGD:8559967\|RGD:8559968	8554872	ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2	ClinVar	PMID:25741868\|PMID:9837812
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 2		IAGP	RGD:10411061	8554872	ClinVar Annotator: match by term: NDUFS8-related condition	ClinVar	PMID:20818383\|PMID:25741868\|PMID:26764160\|PMID:28492532\|PMID:30094188\|PMID:33233646\|PMID:35551192
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 2		IAGP	RGD:8570665\|RGD:8570666	8554872	ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2	ClinVar	PMID:22499348
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 2		IAGP	RGD:12905518\|RGD:155794815\|RGD:34890841\|RGD:405281141	8554872	ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2 \| ClinVar Annotator: more ...	ClinVar
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 2		IAGP	RGD:11598875\|RGD:12841046\|RGD:12847559	8554872	ClinVar Annotator: match by term: NDUFS8-related condition	ClinVar	PMID:28492532
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 2		IAGP	RGD:13462662\|RGD:150434093\|RGD:155643005\|RGD:155796950\|RGD:243064005\|RGD:404998843\|RGD:407429211	8554872	ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2	ClinVar	PMID:25741868
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 2		IAGP	RGD:8559970	8554872	ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2	ClinVar	PMID:15159508\|PMID:28492532
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 2		IAGP	RGD:598125965\|RGD:598125967	8554872	ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2	ClinVar	PMID:25741868\|PMID:38703036
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 2		IAGP	RGD:8570664	8554872	ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2	ClinVar	PMID:22499348\|PMID:25741868
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 2		IAGP	RGD:8559969	8554872	ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2	ClinVar	PMID:15159508
NDUFS8	Human	osteopetrosis		IAGP	RGD:11666456	8554872	ClinVar Annotator: match by term: Osteopetrosis	ClinVar
NDUFS8	Human	osteopetrosis		IAGP	RGD:11665664	8554872	ClinVar Annotator: match by term: Osteopetrosis	ClinVar	PMID:25741868
NDUFS8	Human	Subacute Necrotizing Encephalopathy of Leigh, Infantile		IAGP	RGD:11615129	8554872	ClinVar Annotator: match by term: Leigh's necrotizing encephalopathy	ClinVar	PMID:25741868\|PMID:28492532
NDUFS8	Human	Subacute Necrotizing Encephalopathy of Leigh, Infantile		IAGP	RGD:11598875\|RGD:12841046	8554872	ClinVar Annotator: match by term: Leigh's necrotizing encephalopathy	ClinVar	PMID:28492532
NDUFS8	Human	Subacute Necrotizing Encephalopathy of Leigh, Infantile		IAGP	RGD:10411061	8554872	ClinVar Annotator: match by term: Leigh's necrotizing encephalopathy	ClinVar	PMID:20818383\|PMID:25741868\|PMID:26764160\|PMID:28492532\|PMID:30094188\|PMID:33233646\|PMID:35551192
NDUFS8	Human	Subacute Necrotizing Encephalopathy of Leigh, Infantile		IAGP	RGD:8559967	8554872	ClinVar Annotator: match by term: Leigh's necrotizing encephalopathy	ClinVar	PMID:25741868\|PMID:9837812

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NDUFS8	Human	osteoarthritis		EXP		11554173	CTD Direct Evidence: marker/mechanism	CTD	PMID:18784066

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NDUFS8	Human	nuclear type mitochondrial complex I deficiency 2		IAGP		7240710		OMIM

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NDUFS8	Human	(-)-epigallocatechin 3-gallate	decreases expression	ISO	RGD:1319780	6480464	epigallocatechin gallate results in decreased expression of NDUFS8 mRNA	CTD	PMID:29175576
NDUFS8	Human	1,2-dichloroethane	decreases expression	ISO	RGD:1319780	6480464	ethylene dichloride results in decreased expression of NDUFS8 mRNA	CTD	PMID:28960355
NDUFS8	Human	1,2-dimethylhydrazine	multiple interactions	ISO	RGD:1319780	6480464	[1,2-Dimethylhydrazine co-treated with Folic Acid] results in decreased expression of NDUFS8 mRNA	CTD	PMID:22206623
NDUFS8	Human	17alpha-ethynylestradiol	increases expression	ISO	RGD:1319780	6480464	Ethinyl Estradiol results in increased expression of NDUFS8 mRNA	CTD	PMID:17942748
NDUFS8	Human	17alpha-ethynylestradiol	multiple interactions	ISO	RGD:1319780	6480464	[Tetrachlorodibenzodioxin co-treated with Ethinyl Estradiol] results in increased expression of NDUFS8 mRNA	CTD	PMID:17942748
NDUFS8	Human	17beta-estradiol	decreases expression	ISO	RGD:1319780	6480464	Estradiol results in decreased expression of NDUFS8 mRNA	CTD	PMID:39298647
NDUFS8	Human	2,3,7,8-tetrachlorodibenzodioxine	multiple interactions	ISO	RGD:1319780	6480464	[Tetrachlorodibenzodioxin co-treated with Ethinyl Estradiol] results in increased expression of NDUFS8 mRNA	CTD	PMID:17942748
NDUFS8	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	RGD:1309436	6480464	Tetrachlorodibenzodioxin results in increased expression of NDUFS8 mRNA	CTD	PMID:33387578
NDUFS8	Human	2,3,7,8-tetrachlorodibenzodioxine	affects expression	ISO	RGD:1319780	6480464	Tetrachlorodibenzodioxin affects the expression of NDUFS8 mRNA	CTD	PMID:21570461
NDUFS8	Human	2,3,7,8-tetrachlorodibenzodioxine	decreases expression	ISO	RGD:1319780	6480464	Tetrachlorodibenzodioxin results in decreased expression of NDUFS8 mRNA	CTD	PMID:21354282
NDUFS8	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	RGD:1319780	6480464	Tetrachlorodibenzodioxin results in increased expression of NDUFS8 mRNA	CTD	PMID:17942748\|PMID:20399798
NDUFS8	Human	2,4-dinitrotoluene	affects expression	ISO	RGD:1309436	6480464	2,4-dinitrotoluene affects the expression of NDUFS8 mRNA	CTD	PMID:21346803
NDUFS8	Human	2-bromohexadecanoic acid	multiple interactions	EXP		6480464	2-bromopalmitate inhibits the reaction [[Cadmium Chloride results in increased abundance of Cadmium] which results in more ...	CTD	PMID:38195004
NDUFS8	Human	5-aza-2'-deoxycytidine	increases expression	EXP		6480464	Decitabine results in increased expression of NDUFS8 mRNA	CTD	PMID:20231622
NDUFS8	Human	6-propyl-2-thiouracil	increases expression	ISO	RGD:1309436	6480464	Propylthiouracil results in increased expression of NDUFS8 mRNA	CTD	PMID:30047161
NDUFS8	Human	acrylamide	increases expression	ISO	RGD:1309436	6480464	Acrylamide results in increased expression of NDUFS8 mRNA	CTD	PMID:28959563
NDUFS8	Human	all-trans-retinoic acid	decreases expression	EXP		6480464	Tretinoin results in decreased expression of NDUFS8 mRNA	CTD	PMID:17218384
NDUFS8	Human	alpha-Zearalanol	multiple interactions	ISO	RGD:1309436	6480464	[Zeranol co-treated with perfluorooctanoic acid] results in decreased expression of NDUFS8 mRNA	CTD	PMID:35163327
NDUFS8	Human	amitrole	increases expression	ISO	RGD:1309436	6480464	Amitrole results in increased expression of NDUFS8 mRNA	CTD	PMID:30047161
NDUFS8	Human	arsenous acid	increases expression	ISO	RGD:1319780	6480464	Arsenic Trioxide results in increased expression of NDUFS8 mRNA	CTD	PMID:24831965
NDUFS8	Human	bis(2-ethylhexyl) phthalate	increases expression	ISO	RGD:1319780	6480464	Diethylhexyl Phthalate results in increased expression of NDUFS8 mRNA	CTD	PMID:33754040
NDUFS8	Human	bisphenol A	decreases expression	ISO	RGD:1309436	6480464	bisphenol A results in decreased expression of NDUFS8 mRNA	CTD	PMID:30816183\|PMID:32528016
NDUFS8	Human	bisphenol A	decreases expression	ISO	RGD:1319780	6480464	bisphenol A results in decreased expression of NDUFS8 mRNA	CTD	PMID:35598803
NDUFS8	Human	bisphenol A	increases expression	ISO	RGD:1319780	6480464	bisphenol A results in increased expression of NDUFS8 protein	CTD	PMID:38021376
NDUFS8	Human	bisphenol A	decreases expression	EXP		6480464	bisphenol A results in decreased expression of NDUFS8 protein	CTD	PMID:34186270
NDUFS8	Human	bisphenol A	increases expression	EXP		6480464	bisphenol A results in increased expression of NDUFS8 protein	CTD	PMID:37567409
NDUFS8	Human	bisphenol AF	increases expression	EXP		6480464	bisphenol AF results in increased expression of NDUFS8 protein	CTD	PMID:34186270
NDUFS8	Human	bisphenol F	decreases expression	ISO	RGD:1319780	6480464	bisphenol F results in decreased expression of NDUFS8 mRNA	CTD	PMID:38685157
NDUFS8	Human	cadmium atom	multiple interactions	EXP		6480464	2-bromopalmitate inhibits the reaction [[Cadmium Chloride results in increased abundance of Cadmium] which results in more ...	CTD	PMID:38195004
NDUFS8	Human	cadmium dichloride	increases expression	ISO	RGD:1319780	6480464	Cadmium Chloride results in increased expression of NDUFS8 mRNA	CTD	PMID:24982889
NDUFS8	Human	cadmium dichloride	multiple interactions	EXP		6480464	2-bromopalmitate inhibits the reaction [[Cadmium Chloride results in increased abundance of Cadmium] which results in more ...	CTD	PMID:38195004
NDUFS8	Human	chloropicrin	decreases expression	EXP		6480464	chloropicrin results in decreased expression of NDUFS8 mRNA	CTD	PMID:26352163
NDUFS8	Human	cisplatin	affects response to substance	EXP		6480464	NDUFS8 protein affects the susceptibility to Cisplatin	CTD	PMID:16217747
NDUFS8	Human	clofibrate	increases expression	ISO	RGD:1309436	6480464	Clofibrate results in increased expression of NDUFS8 protein	CTD	PMID:16470657
NDUFS8	Human	clofibric acid	multiple interactions	ISO	RGD:1309436	6480464	[Diethylnitrosamine co-treated with Clofibric Acid] affects the expression of NDUFS8 mRNA	CTD	PMID:17602206
NDUFS8	Human	cobalt dichloride	decreases expression	EXP		6480464	cobaltous chloride results in decreased expression of NDUFS8 mRNA	CTD	PMID:19376846
NDUFS8	Human	copper atom	decreases expression	ISO	RGD:1309436	6480464	Copper results in decreased expression of NDUFS8 mRNA	CTD	PMID:22465980
NDUFS8	Human	copper(0)	decreases expression	ISO	RGD:1309436	6480464	Copper results in decreased expression of NDUFS8 mRNA	CTD	PMID:22465980
NDUFS8	Human	coumestrol	decreases expression	EXP		6480464	Coumestrol results in decreased expression of NDUFS8 mRNA	CTD	PMID:19167446
NDUFS8	Human	CU-O LINKAGE	increases expression	ISO	RGD:1319780	6480464	cupric oxide analog results in increased expression of NDUFS8 protein	CTD	PMID:23882024
NDUFS8	Human	cyclosporin A	decreases methylation	EXP		6480464	Cyclosporine results in decreased methylation of NDUFS8 promoter	CTD	PMID:27989131
NDUFS8	Human	diarsenic trioxide	increases expression	ISO	RGD:1319780	6480464	Arsenic Trioxide results in increased expression of NDUFS8 mRNA	CTD	PMID:24831965
NDUFS8	Human	Dibutyl phosphate	affects expression	EXP		6480464	di-n-butylphosphoric acid affects the expression of NDUFS8 mRNA	CTD	PMID:37042841
NDUFS8	Human	dibutyl phthalate	decreases expression	ISO	RGD:1319780	6480464	Dibutyl Phthalate results in decreased expression of NDUFS8 mRNA	CTD	PMID:17361019\|PMID:21266533
NDUFS8	Human	doxorubicin	decreases expression	ISO	RGD:1309436	6480464	Doxorubicin results in decreased expression of NDUFS8 mRNA	CTD	PMID:19915844
NDUFS8	Human	doxorubicin	decreases expression	ISO	RGD:1319780	6480464	Doxorubicin results in decreased expression of NDUFS8 mRNA	CTD	PMID:25896364\|PMID:26873546
NDUFS8	Human	flutamide	increases expression	ISO	RGD:1309436	6480464	Flutamide results in increased expression of NDUFS8 mRNA	CTD	PMID:24136188
NDUFS8	Human	flutamide	increases expression	ISO	RGD:1319780	6480464	Flutamide results in increased expression of NDUFS8 mRNA	CTD	PMID:19442681
NDUFS8	Human	folic acid	multiple interactions	ISO	RGD:1319780	6480464	[1,2-Dimethylhydrazine co-treated with Folic Acid] results in decreased expression of NDUFS8 mRNA	CTD	PMID:22206623
NDUFS8	Human	formaldehyde	increases expression	EXP		6480464	Formaldehyde results in increased expression of NDUFS8 mRNA	CTD	PMID:23649840
NDUFS8	Human	isoniazide	affects expression	ISO	RGD:1319780	6480464	Isoniazid affects the expression of NDUFS8 mRNA	CTD	PMID:24848797
NDUFS8	Human	isoprenaline	multiple interactions	ISO	RGD:1309436	6480464	[Isoproterenol co-treated with POSTN protein] results in decreased expression of NDUFS8 mRNA	CTD	PMID:30303030
NDUFS8	Human	isotretinoin	decreases expression	EXP		6480464	Isotretinoin results in decreased expression of NDUFS8 mRNA	CTD	PMID:20436886
NDUFS8	Human	ivermectin	decreases expression	EXP		6480464	Ivermectin results in decreased expression of NDUFS8 protein	CTD	PMID:32959892
NDUFS8	Human	lipopolysaccharide	multiple interactions	EXP		6480464	[Acetaminophen co-treated with Lipopolysaccharides] results in decreased expression of NDUFS8 mRNA	CTD	PMID:31059760
NDUFS8	Human	metformin	multiple interactions	ISO	RGD:1319780	6480464	Metformin inhibits the reaction [[Streptozocin co-treated with Dietary Fats] results in decreased expression of NDUFS8 more ...	CTD	PMID:37337224
NDUFS8	Human	methamphetamine	affects expression	ISO	RGD:1309436	6480464	Methamphetamine affects the expression of NDUFS8 protein	CTD	PMID:17904249
NDUFS8	Human	methimazole	increases expression	ISO	RGD:1309436	6480464	Methimazole results in increased expression of NDUFS8 mRNA	CTD	PMID:30047161
NDUFS8	Human	methotrexate	affects response to substance	EXP		6480464	NDUFS8 protein affects the susceptibility to Methotrexate	CTD	PMID:16217747
NDUFS8	Human	N,N-diethyl-m-toluamide	multiple interactions	ISO	RGD:1309436	6480464	[Pyridostigmine Bromide co-treated with DEET co-treated with Permethrin] results in increased expression of NDUFS8 mRNA	CTD	PMID:28659758
NDUFS8	Human	N-methyl-4-phenylpyridinium	decreases expression	EXP		6480464	1-Methyl-4-phenylpyridinium results in decreased expression of NDUFS8 mRNA	CTD	PMID:24810058
NDUFS8	Human	N-nitrosodiethylamine	multiple interactions	ISO	RGD:1309436	6480464	[Diethylnitrosamine co-treated with Clofibric Acid] affects the expression of NDUFS8 mRNA	CTD	PMID:17602206
NDUFS8	Human	niclosamide	decreases expression	EXP		6480464	Niclosamide results in decreased expression of NDUFS8 mRNA	CTD	PMID:22576131
NDUFS8	Human	nitrates	multiple interactions	ISO	RGD:1319780	6480464	[Particulate Matter results in increased abundance of Nitrates] which results in increased expression of NDUFS8 more ...	CTD	PMID:35964746
NDUFS8	Human	ochratoxin A	decreases expression	ISO	RGD:1309436	6480464	ochratoxin A results in decreased expression of NDUFS8 mRNA	CTD	PMID:23358140
NDUFS8	Human	ozone	multiple interactions	EXP		6480464	[Air Pollutants results in increased abundance of Ozone] which affects the expression of NDUFS8 mRNA	CTD	PMID:35430440
NDUFS8	Human	paclitaxel	affects response to substance	EXP		6480464	NDUFS8 protein affects the susceptibility to Paclitaxel	CTD	PMID:16217747
NDUFS8	Human	paracetamol	affects expression	ISO	RGD:1319780	6480464	Acetaminophen affects the expression of NDUFS8 mRNA	CTD	PMID:17562736
NDUFS8	Human	paracetamol	decreases expression	ISO	RGD:1309436	6480464	Acetaminophen results in decreased expression of NDUFS8 mRNA	CTD	PMID:33387578
NDUFS8	Human	paracetamol	multiple interactions	EXP		6480464	[Acetaminophen co-treated with Lipopolysaccharides] results in decreased expression of NDUFS8 mRNA	CTD	PMID:31059760
NDUFS8	Human	paracetamol	decreases expression	EXP		6480464	Acetaminophen results in decreased expression of NDUFS8 mRNA	CTD	PMID:25704631\|PMID:31059760
NDUFS8	Human	perfluorooctanoic acid	increases expression	ISO	RGD:1309436	6480464	perfluorooctanoic acid results in increased expression of NDUFS8 mRNA	CTD	PMID:19616056
NDUFS8	Human	perfluorooctanoic acid	multiple interactions	ISO	RGD:1309436	6480464	[Zeranol co-treated with perfluorooctanoic acid] results in decreased expression of NDUFS8 mRNA	CTD	PMID:35163327
NDUFS8	Human	permethrin	multiple interactions	ISO	RGD:1309436	6480464	[Pyridostigmine Bromide co-treated with DEET co-treated with Permethrin] results in increased expression of NDUFS8 mRNA	CTD	PMID:28659758
NDUFS8	Human	phlorizin	increases expression	ISO	RGD:1319780	6480464	Phlorhizin results in increased expression of NDUFS8 mRNA	CTD	PMID:22538082
NDUFS8	Human	Pyridostigmine bromide	multiple interactions	ISO	RGD:1309436	6480464	[Pyridostigmine Bromide co-treated with DEET co-treated with Permethrin] results in increased expression of NDUFS8 mRNA	CTD	PMID:28659758
NDUFS8	Human	resveratrol	multiple interactions	ISO	RGD:1319780	6480464	SIRT1 protein affects the reaction [Resveratrol results in increased expression of NDUFS8 mRNA]; STK11 protein more ...	CTD	PMID:34216621
NDUFS8	Human	resveratrol	increases expression	ISO	RGD:1319780	6480464	Resveratrol results in increased expression of NDUFS8 mRNA	CTD	PMID:34216621
NDUFS8	Human	rimonabant	multiple interactions	ISO	RGD:1319780	6480464	Rimonabant inhibits the reaction [Dietary Fats results in decreased expression of NDUFS8 mRNA]	CTD	PMID:19030233
NDUFS8	Human	rotenone	increases expression	EXP		6480464	Rotenone results in increased expression of NDUFS8 mRNA	CTD	PMID:18191903
NDUFS8	Human	sodium arsenite	decreases expression	EXP		6480464	sodium arsenite results in decreased expression of NDUFS8 mRNA	CTD	PMID:38568856
NDUFS8	Human	sodium fluoride	increases expression	ISO	RGD:1319780	6480464	Sodium Fluoride results in increased expression of NDUFS8 protein	CTD	PMID:28918527
NDUFS8	Human	streptozocin	multiple interactions	ISO	RGD:1319780	6480464	[Streptozocin co-treated with Dietary Fats] results in decreased expression of NDUFS8 mRNA; Metformin inhibits the more ...	CTD	PMID:37337224
NDUFS8	Human	sulfadimethoxine	increases expression	ISO	RGD:1309436	6480464	Sulfadimethoxine results in increased expression of NDUFS8 mRNA	CTD	PMID:30047161
NDUFS8	Human	T-2 toxin	increases expression	ISO	RGD:1309436	6480464	T-2 Toxin results in increased expression of NDUFS8 mRNA	CTD	PMID:29870751
NDUFS8	Human	temozolomide	decreases expression	EXP		6480464	Temozolomide results in decreased expression of NDUFS8 mRNA	CTD	PMID:31758290
NDUFS8	Human	thapsigargin	decreases expression	ISO	RGD:1319780	6480464	Thapsigargin results in decreased expression of NDUFS8 protein	CTD	PMID:24648495
NDUFS8	Human	thioacetamide	decreases expression	ISO	RGD:1309436	6480464	Thioacetamide results in decreased expression of NDUFS8 mRNA	CTD	PMID:34492290
NDUFS8	Human	thiram	decreases expression	EXP		6480464	Thiram results in decreased expression of NDUFS8 mRNA	CTD	PMID:38568856
NDUFS8	Human	toluene	affects expression	ISO	RGD:1309436	6480464	Toluene affects the expression of NDUFS8 mRNA	CTD	PMID:21827849
NDUFS8	Human	trichloroethene	affects expression	ISO	RGD:1319780	6480464	Trichloroethylene affects the expression of NDUFS8 mRNA	CTD	PMID:21135412
NDUFS8	Human	Triptolide	decreases expression	ISO	RGD:1319780	6480464	triptolide results in decreased expression of NDUFS8 mRNA	CTD	PMID:29723566
NDUFS8	Human	tungsten	increases expression	ISO	RGD:1319780	6480464	Tungsten results in increased expression of NDUFS8 mRNA	CTD	PMID:30912803
NDUFS8	Human	valproic acid	increases methylation	EXP		6480464	Valproic Acid results in increased methylation of NDUFS8 gene	CTD	PMID:29154799
NDUFS8	Human	valproic acid	increases expression	EXP		6480464	Valproic Acid results in increased expression of NDUFS8 mRNA	CTD	PMID:23179753\|PMID:27188386
NDUFS8	Human	vinclozolin	decreases expression	ISO	RGD:1309436	6480464	vinclozolin results in decreased expression of NDUFS8 mRNA	CTD	PMID:23034163
NDUFS8	Human	vorinostat	increases expression	EXP		6480464	vorinostat results in increased expression of NDUFS8 protein	CTD	PMID:17593366

Biological Process

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NDUFS8	Human	aerobic respiration	involved_in	NAS		150520179	PMID:30030361	ComplexPortal	PMID:30030361
NDUFS8	Human	mitochondrial electron transport, NADH to ubiquinone	involved_in	IMP		150520179	PMID:22499348	UniProt	PMID:22499348
NDUFS8	Human	mitochondrial electron transport, NADH to ubiquinone	involved_in	IBA	PANTHER:PTN000091257\|UniProtKB:O00217\|WB:WBGene00020636	150520179		GO_Central	GO_REF:0000033
NDUFS8	Human	mitochondrial electron transport, NADH to ubiquinone	involved_in	NAS		150520179	PMID:9666055, PMID:9878551	UniProt	PMID:9666055\|PMID:9878551
NDUFS8	Human	mitochondrial respiratory chain complex I assembly	involved_in	IMP		150520179	PMID:11112787, PMID:15159508, PMID:22499348	UniProt	PMID:11112787\|PMID:15159508\|PMID:22499348
NDUFS8	Human	mitochondrial respiratory chain complex I assembly	involved_in	IBA	PANTHER:PTN000091257\|UniProtKB:O00217	150520179		GO_Central	GO_REF:0000033
NDUFS8	Human	proton motive force-driven mitochondrial ATP synthesis	involved_in	NAS		150520179	PMID:30030361	ComplexPortal	PMID:30030361
NDUFS8	Human	proton transmembrane transport	involved_in	IEA	GO:0008137	150520179		GOC	GO_REF:0000108

Cellular Component

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NDUFS8	Human	membrane	located_in	IEA	InterPro:IPR010226	150520179		InterPro	GO_REF:0000002
NDUFS8	Human	membrane	located_in	IEA	UniProtKB-KW:KW-0472	150520179		UniProt	GO_REF:0000043
NDUFS8	Human	mitochondrial inner membrane	located_in	IEA	UniProtKB-SubCell:SL-0168	150520179		UniProt	GO_REF:0000044
NDUFS8	Human	mitochondrial inner membrane	is_active_in	IEA	UniProtKB:Q8K3J1\|ensembl:ENSMUSP00000158541	150520179		Ensembl	GO_REF:0000107
NDUFS8	Human	mitochondrial inner membrane	located_in	IDA		150520179	PMID:28844695	ComplexPortal	PMID:28844695
NDUFS8	Human	mitochondrial inner membrane	located_in	IEA	UniProtKB-KW:KW-0999	150520179		UniProt	GO_REF:0000043
NDUFS8	Human	mitochondrial matrix	located_in	TAS		150520179		Reactome	Reactome:R-HSA-163217\|Reactome:R-HSA-6788523\|Reactome:R-HSA-6799178\|Reactome:R-HSA-6799179\|Reactome:R-HSA-6799191\|Reactome:R-HSA-6799196\|Reactome:R-HSA-6799197\|Reactome:R-HSA-6799202\|Reactome:R-HSA-6799203\|Reactome:R-HSA-6800868
NDUFS8	Human	mitochondrion	located_in	HTP		150520179	PMID:34800366	FlyBase	PMID:34800366
NDUFS8	Human	mitochondrion	located_in	IEA	UniProtKB-KW:KW-0496	150520179		UniProt	GO_REF:0000043
NDUFS8	Human	mitochondrion	located_in	IDA		150520179	PMID:9666055	UniProt	PMID:9666055
NDUFS8	Human	respiratory chain complex I	part_of	NAS		150520179	PMID:9878551	UniProt	PMID:9878551
NDUFS8	Human	respiratory chain complex I	part_of	IBA	FB:FBgn0017567\|MGI:2385079\|PANTHER:PTN000091257\|TAIR:locus:2207285\|UniProtKB:O00217\|UniProtKB:P42028	150520179		GO_Central	GO_REF:0000033
NDUFS8	Human	respiratory chain complex I	part_of	IEA	UniProtKB:Q8K3J1\|ensembl:ENSMUSP00000158541	150520179		Ensembl	GO_REF:0000107
NDUFS8	Human	respiratory chain complex I	part_of	IDA		150520179	PMID:12611891, PMID:31536960	UniProt	PMID:12611891\|PMID:31536960
NDUFS8	Human	respiratory chain complex I	part_of	IMP		150520179	PMID:11112787	UniProt	PMID:11112787

Molecular Function

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NDUFS8	Human	4 iron, 4 sulfur cluster binding	enables	IEA	InterPro:IPR010226	150520179		InterPro	GO_REF:0000002
NDUFS8	Human	4 iron, 4 sulfur cluster binding	enables	IEA	UniProtKB-KW:KW-0004	150520179		UniProt	GO_REF:0000043
NDUFS8	Human	iron-sulfur cluster binding	enables	IEA	UniProtKB-KW:KW-0411	150520179		UniProt	GO_REF:0000043
NDUFS8	Human	metal ion binding	enables	IEA	UniProtKB-KW:KW-0479	150520179		UniProt	GO_REF:0000043
NDUFS8	Human	NADH dehydrogenase (ubiquinone) activity	enables	NAS		150520179	PMID:9878551	UniProt	PMID:9878551
NDUFS8	Human	NADH dehydrogenase (ubiquinone) activity	enables	IEA	RHEA:29091	150520179		RHEA	GO_REF:0000116
NDUFS8	Human	NADH dehydrogenase (ubiquinone) activity	enables	IMP		150520179	PMID:22499348	UniProt	PMID:22499348
NDUFS8	Human	NADH dehydrogenase (ubiquinone) activity	contributes_to	IMP		150520179	PMID:9837812	UniProt	PMID:9837812
NDUFS8	Human	NADH dehydrogenase (ubiquinone) activity	enables	IEA	EC:7.1.1.2	150520179		UniProt	GO_REF:0000003
NDUFS8	Human	NADH dehydrogenase activity	contributes_to	IMP		150520179	PMID:14749350, PMID:15159508	UniProt	PMID:14749350\|PMID:15159508
NDUFS8	Human	NADH dehydrogenase activity	contributes_to	IBA	PANTHER:PTN000091255\|UniProtKB:O00217\|UniProtKB:P0AFD6	150520179		GO_Central	GO_REF:0000033
NDUFS8	Human	oxidoreductase activity	enables	IEA	UniProtKB-KW:KW-0560	150520179		UniProt	GO_REF:0000043
NDUFS8	Human	oxidoreductase activity, acting on NAD(P)H	enables	IEA	InterPro:IPR010226	150520179		InterPro	GO_REF:0000002
NDUFS8	Human	protein binding	enables	IPI	UniProtKB:Q9BUV8	150520179	PMID:31536960	UniProt	PMID:31536960

Imported Annotations - KEGG (archival)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NDUFS8	Human	Alzheimer's disease pathway		IEA		6907045		KEGG	hsa:05010
NDUFS8	Human	Huntington's disease pathway		IEA		6907045		KEGG	hsa:05016
NDUFS8	Human	oxidative phosphorylation pathway		IEA		6907045		KEGG	hsa:00190
NDUFS8	Human	Parkinson's disease pathway		IEA		6907045		KEGG	hsa:05012

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NDUFS8	Human	Abnormal mitochondria in muscle tissue		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Ankle clonus		IAGP		8699517		HPO	MIM:618222\|PMID:9837812
NDUFS8	Human	Apnea		IAGP		8699517		HPO	MIM:618222
NDUFS8	Human	Apneic episodes in infancy		IAGP		8699517		HPO	MIM:618222\|PMID:9837812
NDUFS8	Human	Ataxia		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Autosomal recessive inheritance		IAGP		8699517		HPO	MIM:618222\|PMID:9837812
NDUFS8	Human	Blindness		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Brisk reflexes		IAGP		8699517		HPO	MIM:618222\|PMID:9837812
NDUFS8	Human	Decreased activity of mitochondrial complex I		IAGP		8699517		HPO	MIM:618222\|PMID:15159508\|ORPHA:2609
NDUFS8	Human	Diabetes mellitus		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Drowsiness		IAGP		8699517		HPO	MIM:618222\|PMID:9837812
NDUFS8	Human	Dysarthria		IAGP		8699517		HPO	MIM:618222\|PMID:15159508
NDUFS8	Human	Dyskinesia		IAGP		8699517		HPO	MIM:618222
NDUFS8	Human	Dystonia		IAGP		8699517		HPO	MIM:618222\|PMID:15159508
NDUFS8	Human	Encephalopathy		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Failure to thrive		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Falls		IAGP		8699517		HPO	MIM:618222\|PMID:15159508
NDUFS8	Human	Feeding difficulties		IAGP		8699517		HPO	MIM:618222\|PMID:9837812\|ORPHA:2609
NDUFS8	Human	Fetal distress		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Focal T2 hyperintense brainstem lesion		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Gait disturbance		IAGP		8699517		HPO	MIM:618222
NDUFS8	Human	Gliosis		IAGP		8699517		HPO	MIM:618222\|PMID:9837812
NDUFS8	Human	Global developmental delay		IAGP		8699517		HPO	MIM:618222\|ORPHA:2609
NDUFS8	Human	Hepatomegaly		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Hypercapnia		IAGP		8699517		HPO	MIM:618222\|PMID:9837812
NDUFS8	Human	Hyperreflexia		IAGP		8699517		HPO	MIM:618222
NDUFS8	Human	Hypertrophic cardiomyopathy		IAGP		8699517		HPO	MIM:618222\|ORPHA:2609
NDUFS8	Human	Hypoglycemia		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Hypotonia		IAGP		8699517		HPO	MIM:618222\|PMID:9837812\|ORPHA:2609
NDUFS8	Human	Increased circulating lactate concentration		IAGP		8699517		HPO	MIM:618222\|PMID:9837812
NDUFS8	Human	Increased circulating pyruvate concentration		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Increased CSF lactate		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Intrauterine growth retardation		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Juvenile onset		IAGP		8699517		HPO	MIM:618222\|PMID:15159508
NDUFS8	Human	Lactic acidosis		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Lethargy		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Leukodystrophy		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Leukoencephalopathy		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Microcephaly		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Mitochondrial myopathy		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Muscle weakness		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Neonatal onset		IAGP		8699517		HPO	MIM:618222\|PMID:9837812
NDUFS8	Human	Nystagmus		IAGP		8699517		HPO	MIM:618222\|ORPHA:2609
NDUFS8	Human	Optic disc pallor		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Optic neuropathy		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Paroxysmal involuntary eye movements		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Poor head control		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Poor suck		IAGP		8699517		HPO	MIM:618222\|PMID:9837812
NDUFS8	Human	Primitive reflex		IAGP		8699517		HPO	MIM:618222\|PMID:9837812
NDUFS8	Human	Proximal tubulopathy		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Ptosis		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Reduced eye contact		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Respiratory insufficiency		IAGP		8699517		HPO	MIM:618222\|ORPHA:2609
NDUFS8	Human	Seizure		IAGP		8699517		HPO	MIM:618222
NDUFS8	Human	Sensorineural hearing impairment		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Strabismus		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Ventriculomegaly		IAGP		8699517		HPO	MIM:618222\|PMID:9837812
NDUFS8	Human	Vertical nystagmus		IAGP		8699517		HPO	MIM:618222\|PMID:15159508
NDUFS8	Human	Vomiting		IAGP		8699517		HPO	ORPHA:2609
NDUFS8	Human	Weak cry		IAGP		8699517		HPO	MIM:618222\|PMID:9837812

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
NDUFS8	Human	Intellectual disability		IAGP	RGD:42723466	8554872	ClinVar Annotator: match by term: Intellectual disability	ClinVar
NDUFS8	Human	Osteopetrosis		IAGP	RGD:11665664	8554872	ClinVar Annotator: match by term: Osteopetrosis	ClinVar	PMID:25741868
NDUFS8	Human	Osteopetrosis		IAGP	RGD:11666456	8554872	ClinVar Annotator: match by term: Osteopetrosis	ClinVar

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	KEGG: Kyoto Encyclopedia of Genes and Genomes	KEGG
3.	OMIM Disease Annotation Pipeline	OMIM Disease Annotation Pipeline
4.	KEGG Annotation Import Pipeline	Pipeline to import KEGG annotations from KEGG into RGD
5.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
6.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
7.	RGD HPO Phenotype Annotation Pipeline	RGD automated import pipeline for human HPO-to-gene-to-disease annotations

PMID:8125298	PMID:9116042	PMID:9345899	PMID:9666055	PMID:9837812	PMID:9878551	PMID:11112787	PMID:11955626	PMID:12477932	PMID:12611891	PMID:12857734	PMID:14702039
PMID:14749350	PMID:15159508	PMID:15250827	PMID:15489334	PMID:17601350	PMID:18029348	PMID:18624398	PMID:18977241	PMID:19343046	PMID:20186120	PMID:20379614	PMID:20877624
PMID:21873635	PMID:22190034	PMID:22499348	PMID:22939629	PMID:24344204	PMID:26186194	PMID:26344197	PMID:26425749	PMID:26496610	PMID:26638075	PMID:26972000	PMID:27432908
PMID:27499296	PMID:27516145	PMID:27609421	PMID:28190767	PMID:28380382	PMID:28514442	PMID:28515276	PMID:28844695	PMID:29229926	PMID:29331416	PMID:29395067	PMID:29507755
PMID:29509190	PMID:29509794	PMID:29568061	PMID:29934401	PMID:30022168	PMID:30030361	PMID:30572598	PMID:30804502	PMID:30833792	PMID:30948266	PMID:31056398	PMID:31056421
PMID:31073040	PMID:31091453	PMID:31527615	PMID:31536960	PMID:31617661	PMID:31871319	PMID:32628020	PMID:32807901	PMID:32877691	PMID:33545068	PMID:33845483	PMID:33957083
PMID:33961781	PMID:34079125	PMID:34709727	PMID:34800366	PMID:35241646	PMID:35545034	PMID:35563538	PMID:35944360	PMID:36180527	PMID:36282215	PMID:36373674	PMID:36490346
PMID:36538041	PMID:36634849	PMID:37071682	PMID:37314216	PMID:37609425	PMID:38113892	PMID:38496616	PMID:38594244	PMID:38697112

NDUFS8
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	68,030,681 - 68,036,644 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	68,030,617 - 68,036,644 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	67,798,148 - 67,804,111 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	67,554,685 - 67,560,690 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	11	67,554,684 - 67,560,690	NCBI
Celera	11	65,131,755 - 65,137,785 (+)	NCBI		Celera
Cytogenetic Map	11	q13.2	NCBI
HuRef	11	64,133,431 - 64,139,457 (+)	NCBI		HuRef
CHM1_1	11	67,681,851 - 67,687,870 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	11	68,034,333 - 68,040,285 (+)	NCBI		T2T-CHM13v2.0

Ndufs8
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	19	3,958,863 - 3,962,774 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	19	3,958,863 - 3,962,774 (-)	Ensembl		GRCm39 Ensembl
GRCm38	19	3,908,863 - 3,912,774 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	19	3,908,863 - 3,912,774 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	19	3,908,870 - 3,912,717 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	19	3,908,871 - 3,912,760 (-)	NCBI		MGSCv36	mm8
Celera	19	3,789,245 - 3,793,092 (-)	NCBI		Celera
Cytogenetic Map	19	A	NCBI
cM Map	19	3.63	NCBI

Ndufs8
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	210,569,823 - 210,573,707 (-)	NCBI		GRCr8
mRatBN7.2	1	201,140,585 - 201,144,573 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	201,140,585 - 201,144,511 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	1	209,513,776 - 209,517,650 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	1	216,602,574 - 216,606,449 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	1	209,276,776 - 209,280,651 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	1	219,141,289 - 219,144,610 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	1	219,141,292 - 219,144,610 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	1	226,013,894 - 226,017,284 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	1	206,433,596 - 206,437,478 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	1	206,587,046 - 206,589,998 (-)	NCBI
Celera	1	198,693,138 - 198,697,932 (-)	NCBI		Celera
Cytogenetic Map	1	q43	NCBI

Ndufs8
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955422	17,781,204 - 17,784,404 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955422	17,781,374 - 17,785,395 (-)	NCBI	ChiLan1.0	ChiLan1.0

NDUFS8
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	9	68,981,112 - 68,987,279 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	11	70,024,356 - 70,030,542 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	11	63,112,536 - 63,118,600 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	11	66,421,076 - 66,427,101 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	11	66,421,378 - 66,427,101 (+)	Ensembl	panpan1.1		panPan2

NDUFS8
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	18	49,796,558 - 49,800,805 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	18	49,796,560 - 49,799,979 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	18	48,405,896 - 48,410,143 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	18	50,717,789 - 50,722,042 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	18	50,716,518 - 50,721,799 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	18	49,931,355 - 49,935,599 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	18	49,506,173 - 49,510,431 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	18	50,299,726 - 50,303,986 (-)	NCBI		UU_Cfam_GSD_1.0

Ndufs8
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024404947	5,639,144 - 5,643,676 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936599	2,081,079 - 2,084,730 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936599	2,081,493 - 2,085,635 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

NDUFS8
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	2	4,862,589 - 4,867,393 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	2	4,863,295 - 4,867,392 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	2	3,491,223 - 3,495,317 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

NDUFS8
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	1	6,499,371 - 6,505,685 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	1	6,499,249 - 6,505,699 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666038	103,777,597 - 103,783,589 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Ndufs8
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624767	18,822,526 - 18,827,057 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624767	18,822,763 - 18,826,907 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in NDUFS8
140 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_002496.4(NDUFS8):c.229C>T (p.Arg77Trp)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV000033054]\|not provided [RCV000523226]	Chr11:68033140 [GRCh38] Chr11:67800607 [GRCh37] Chr11:11q13.2	pathogenic\|uncertain significance
NM_002496.4(NDUFS8):c.476C>A (p.Ala159Asp)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV000033055]	Chr11:68036356 [GRCh38] Chr11:67803823 [GRCh37] Chr11:11q13.2	pathogenic
NM_002496.4(NDUFS8):c.187G>C (p.Glu63Gln)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV000033056]	Chr11:68033000 [GRCh38] Chr11:67800467 [GRCh37] Chr11:11q13.2	pathogenic
NM_002496.4(NDUFS8):c.236C>T (p.Pro79Leu)	single nucleotide variant	Leigh syndrome [RCV000762861]\|Mitochondrial complex 1 deficiency, nuclear type 2 [RCV000007941]\|not provided [RCV000442702]	Chr11:68033147 [GRCh38] Chr11:67800614 [GRCh37] Chr11:11q13.2	pathogenic\|likely pathogenic
NM_002496.4(NDUFS8):c.305G>A (p.Arg102His)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV000007942]\|not provided [RCV000426335]	Chr11:68033216 [GRCh38] Chr11:67800683 [GRCh37] Chr11:11q13.2	pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance
NM_002496.4(NDUFS8):c.254C>T (p.Pro85Leu)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV000007943]	Chr11:68033165 [GRCh38] Chr11:67800632 [GRCh37] Chr11:11q13.2	pathogenic
NM_002496.4(NDUFS8):c.413G>A (p.Arg138His)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV000007944]\|not provided [RCV002512884]	Chr11:68036293 [GRCh38] Chr11:67803760 [GRCh37] Chr11:11q13.2	pathogenic\|uncertain significance
GRCh38/hg38 11q13.2(chr11:67446153-68679073)x1	copy number loss	See cases [RCV000052683]	Chr11:67446153..68679073 [GRCh38] Chr11:67213624..68446541 [GRCh37] Chr11:66970200..68203117 [NCBI36] Chr11:11q13.2	pathogenic
NM_002496.3(NDUFS8):c.79C>T (p.Leu27Phe)	single nucleotide variant	Malignant melanoma [RCV000069640]	Chr11:68032306 [GRCh38] Chr11:67799773 [GRCh37] Chr11:67556349 [NCBI36] Chr11:11q13.2	not provided
NM_002496.3(NDUFS8):c.492C>T (p.Ala164=)	single nucleotide variant	Malignant melanoma [RCV000062334]	Chr11:68036372 [GRCh38] Chr11:67803839 [GRCh37] Chr11:67560415 [NCBI36] Chr11:11q13.2	not provided
NM_002496.4(NDUFS8):c.-45A>C	single nucleotide variant	Leigh syndrome [RCV001108402]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV001108401]\|not provided [RCV004704982]\|not specified [RCV000127164]	Chr11:68030689 [GRCh38] Chr11:67798156 [GRCh37] Chr11:11q13.2	benign\|likely benign
Single allele	deletion	Intellectual disability [RCV001293382]	Chr11:118359328..118372573 [GRCh37] Chr11:11p15.3-q23.3	pathogenic
GRCh38/hg38 11q13.2-13.3(chr11:67217264-69448598)x1	copy number loss	See cases [RCV000135609]	Chr11:67217264..69448598 [GRCh38] Chr11:66984735..69263366 [GRCh37] Chr11:66741311..68972547 [NCBI36] Chr11:11q13.2-13.3	likely pathogenic
NM_002496.4(NDUFS8):c.460G>A (p.Gly154Ser)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV001027993]\|not provided [RCV000514571]	Chr11:68036340 [GRCh38] Chr11:67803807 [GRCh37] Chr11:11q13.2	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance
GRCh38/hg38 11q13.2-13.4(chr11:68031693-71593495)x1	copy number loss	See cases [RCV000142138]	Chr11:68031693..71593495 [GRCh38] Chr11:67799160..71304541 [GRCh37] Chr11:67555736..70982189 [NCBI36] Chr11:11q13.2-13.4	likely pathogenic
NM_002496.4(NDUFS8):c.343A>G (p.Lys115Glu)	single nucleotide variant	Leigh syndrome [RCV000200148]\|not provided [RCV001853220]	Chr11:68033254 [GRCh38] Chr11:67800721 [GRCh37] Chr11:11q13.2	pathogenic\|likely pathogenic\|uncertain significance
NM_002496.4(NDUFS8):c.64C>T (p.Pro22Ser)	single nucleotide variant	Leigh syndrome [RCV000389629]\|Mitochondrial complex I deficiency [RCV000276295]\|not provided [RCV001731428]	Chr11:68032291 [GRCh38] Chr11:67799758 [GRCh37] Chr11:11q13.2	likely benign\|uncertain significance
NM_002496.4(NDUFS8):c.428A>T (p.Tyr143Phe)	single nucleotide variant	not provided [RCV000197784]	Chr11:68036308 [GRCh38] Chr11:67803775 [GRCh37] Chr11:11q13.2	likely pathogenic
NM_002496.4(NDUFS8):c.611A>T (p.Gln204Leu)	single nucleotide variant	not provided [RCV000197878]	Chr11:68036571 [GRCh38] Chr11:67804038 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.313C>T (p.Pro105Ser)	single nucleotide variant	not provided [RCV000195877]	Chr11:68033224 [GRCh38] Chr11:67800691 [GRCh37] Chr11:11q13.2	likely pathogenic\|uncertain significance
NM_002496.4(NDUFS8):c.4C>T (p.Arg2Cys)	single nucleotide variant	Inborn genetic diseases [RCV002517245]\|Leigh syndrome [RCV000765008]\|Mitochondrial complex 1 deficiency, nuclear type 2 [RCV003458354]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV001108403]\|NDUFS8-related disorder [RCV003907737]\|not provided [RCV000726015]	Chr11:68032155 [GRCh38] Chr11:67799622 [GRCh37] Chr11:11q13.2	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance
NM_002496.3(NDUFS8):c.481C>A (p.Pro161Thr)	single nucleotide variant	not provided [RCV000196020]	Chr11:68036361 [GRCh38] Chr11:67803828 [GRCh37] Chr11:11q13.2	likely pathogenic
NM_002496.4(NDUFS8):c.373-5C>T	single nucleotide variant	NDUFS8-related disorder [RCV003902735]\|not provided [RCV000487603]	Chr11:68036248 [GRCh38] Chr11:67803715 [GRCh37] Chr11:11q13.2	likely benign\|uncertain significance
NM_002496.4(NDUFS8):c.199+5G>A	single nucleotide variant	Leigh syndrome [RCV000282341]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV000337029]	Chr11:68033017 [GRCh38] Chr11:67800484 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.199+15T>G	single nucleotide variant	Leigh syndrome [RCV000283040]\|Mitochondrial complex 1 deficiency, nuclear type 2 [RCV001778899]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV000377576]\|not provided [RCV001515841]	Chr11:68033027 [GRCh38] Chr11:67800494 [GRCh37] Chr11:11q13.2	benign
NM_002496.4(NDUFS8):c.299C>T (p.Ala100Val)	single nucleotide variant	Leigh syndrome [RCV000307867]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV000344135]\|not provided [RCV000490220]	Chr11:68033210 [GRCh38] Chr11:67800677 [GRCh37] Chr11:11q13.2	likely pathogenic\|uncertain significance
NM_002496.4(NDUFS8):c.459C>T (p.Cys153=)	single nucleotide variant	Leigh syndrome [RCV000308579]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV000390917]\|not provided [RCV000907728]	Chr11:68036339 [GRCh38] Chr11:67803806 [GRCh37] Chr11:11q13.2	benign\|likely benign\|uncertain significance
NM_002496.3(NDUFS8):c.-76C>T	single nucleotide variant	Leigh syndrome [RCV000275260]\|Mitochondrial complex I deficiency [RCV000330456]	Chr11:68030658 [GRCh38] Chr11:67798125 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.502-10C>T	single nucleotide variant	Leigh syndrome [RCV000315895]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV000260796]\|NDUFS8-related disorder [RCV003950032]\|not provided [RCV000898642]\|not specified [RCV000602666]	Chr11:68036452 [GRCh38] Chr11:67803919 [GRCh37] Chr11:11q13.2	likely benign\|uncertain significance
NM_002496.4(NDUFS8):c.*44C>T	single nucleotide variant	Leigh syndrome [RCV000352578]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV000293152]	Chr11:68036637 [GRCh38] Chr11:67804104 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.597C>T (p.Ile199=)	single nucleotide variant	Leigh syndrome [RCV000356692]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV000265926]\|not provided [RCV001718621]	Chr11:68036557 [GRCh38] Chr11:67804024 [GRCh37] Chr11:11q13.2	benign\|likely benign\|uncertain significance
NM_002496.4(NDUFS8):c.200-14C>T	single nucleotide variant	Leigh syndrome [RCV000342747]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV000401109]\|not provided [RCV002520746]	Chr11:68033097 [GRCh38] Chr11:67800564 [GRCh37] Chr11:11q13.2	likely benign\|uncertain significance
NM_002496.4(NDUFS8):c.501+12C>G	single nucleotide variant	Leigh syndrome [RCV000367973]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV000390827]\|not provided [RCV002056233]	Chr11:68036393 [GRCh38] Chr11:67803860 [GRCh37] Chr11:11q13.2	likely benign\|uncertain significance
NM_002496.4(NDUFS8):c.598G>A (p.Ala200Thr)	single nucleotide variant	Leigh syndrome [RCV000380344]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV000321000]\|not provided [RCV002520747]	Chr11:68036558 [GRCh38] Chr11:67804025 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.502-13C>T	single nucleotide variant	Leigh syndrome [RCV000369510]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV000314847]\|not provided [RCV002056234]\|not specified [RCV000427186]	Chr11:68036449 [GRCh38] Chr11:67803916 [GRCh37] Chr11:11q13.2	benign\|likely benign\|uncertain significance
NM_002496.4(NDUFS8):c.133G>A (p.Glu45Lys)	single nucleotide variant	Leigh syndrome [RCV000372098]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV000317408]	Chr11:68032946 [GRCh38] Chr11:67800413 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.*26T>G	single nucleotide variant	Leigh syndrome [RCV000291771]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV000381321]	Chr11:68036619 [GRCh38] Chr11:67804086 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.*40A>G	single nucleotide variant	Leigh syndrome [RCV000346629]\|Mitochondrial complex I deficiency [RCV000399461]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV001109242]\|Osteopetrosis [RCV000370635]\|not provided [RCV001660604]	Chr11:68036633 [GRCh38] Chr11:67804100 [GRCh37] Chr11:11q13.2	benign\|likely benign\|uncertain significance
NM_002496.3(NDUFS8):c.-98G>A	single nucleotide variant	Leigh syndrome [RCV000310649]\|Mitochondrial complex I deficiency [RCV000365206]	Chr11:68030636 [GRCh38] Chr11:67798103 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.*14C>T	single nucleotide variant	Leigh syndrome [RCV000285968]\|Mitochondrial complex I deficiency [RCV000326666]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV001114885]\|Osteopetrosis [RCV000313524]\|not provided [RCV001653506]	Chr11:68036607 [GRCh38] Chr11:67804074 [GRCh37] Chr11:11q13.2	benign\|likely benign
NM_002496.4(NDUFS8):c.170G>A (p.Arg57His)	single nucleotide variant	not provided [RCV002524834]\|not specified [RCV000437809]	Chr11:68032983 [GRCh38] Chr11:67800450 [GRCh37] Chr11:11q13.2	likely benign\|uncertain significance
NM_002496.4(NDUFS8):c.573C>T (p.Asn191=)	single nucleotide variant	not provided [RCV000964211]	Chr11:68036533 [GRCh38] Chr11:67804000 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.576G>T (p.Gly192=)	single nucleotide variant	not specified [RCV000431345]	Chr11:68036536 [GRCh38] Chr11:67804003 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.255G>A (p.Pro85=)	single nucleotide variant	Leigh syndrome [RCV001111480]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV001111479]\|NDUFS8-related disorder [RCV003912624]\|not provided [RCV000676967]\|not specified [RCV000431887]	Chr11:68033166 [GRCh38] Chr11:67800633 [GRCh37] Chr11:11q13.2	benign\|likely benign\|uncertain significance
NM_002496.4(NDUFS8):c.199+15T>A	single nucleotide variant	not provided [RCV002062376]\|not specified [RCV000442240]	Chr11:68033027 [GRCh38] Chr11:67800494 [GRCh37] Chr11:11q13.2	benign\|likely benign
NM_002496.4(NDUFS8):c.200-8G>T	single nucleotide variant	not provided [RCV002059726]\|not specified [RCV000435423]	Chr11:68033103 [GRCh38] Chr11:67800570 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.110-11C>T	single nucleotide variant	not provided [RCV002519553]\|not specified [RCV000419159]	Chr11:68032912 [GRCh38] Chr11:67800379 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.300G>A (p.Ala100=)	single nucleotide variant	NDUFS8-related disorder [RCV004757230]\|not provided [RCV000910288]	Chr11:68033211 [GRCh38] Chr11:67800678 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.372+11G>T	single nucleotide variant	not specified [RCV000426890]	Chr11:68033294 [GRCh38] Chr11:67800761 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.*19C>T	single nucleotide variant	not provided [RCV001703471]	Chr11:68036612 [GRCh38] Chr11:67804079 [GRCh37] Chr11:11q13.2	likely benign
GRCh37/hg19 11q13.2(chr11:67764080-67811086)x3	copy number gain	See cases [RCV000448016]	Chr11:67764080..67811086 [GRCh37] Chr11:11q13.2	benign
GRCh37/hg19 11q13.2-13.4(chr11:67799160-70701268)x1	copy number loss	See cases [RCV000510219]	Chr11:67799160..70701268 [GRCh37] Chr11:11q13.2-13.4	likely pathogenic
NM_002496.4(NDUFS8):c.436G>A (p.Asp146Asn)	single nucleotide variant	not provided [RCV000493719]	Chr11:68036316 [GRCh38] Chr11:67803783 [GRCh37] Chr11:11q13.2	likely pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)	copy number gain	See cases [RCV000511729]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
NM_002496.4(NDUFS8):c.292G>A (p.Glu98Lys)	single nucleotide variant	not provided [RCV000492994]	Chr11:68033203 [GRCh38] Chr11:67800670 [GRCh37] Chr11:11q13.2	likely pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3	copy number gain	See cases [RCV000510881]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
NM_002496.4(NDUFS8):c.484G>A (p.Val162Met)	single nucleotide variant	Leigh syndrome [RCV000625885]	Chr11:68036364 [GRCh38] Chr11:67803831 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.-16GCG[2]	microsatellite	not specified [RCV000602140]	Chr11:68030718..68030720 [GRCh38] Chr11:67798185..67798187 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.441G>C (p.Met147Ile)	single nucleotide variant	Leigh syndrome [RCV000578254]\|not provided [RCV001815416]	Chr11:68036321 [GRCh38] Chr11:67803788 [GRCh37] Chr11:11q13.2	likely pathogenic
NM_002496.4(NDUFS8):c.237G>A (p.Pro79=)	single nucleotide variant	not provided [RCV005056276]\|not specified [RCV000600231]	Chr11:68033148 [GRCh38] Chr11:67800615 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.373-211dup	duplication	not provided [RCV001665261]	Chr11:68036017..68036018 [GRCh38] Chr11:67803484..67803485 [GRCh37] Chr11:11q13.2	benign
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3	copy number gain	not provided [RCV000737348]	Chr11:198510..134934063 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3	copy number gain	not provided [RCV000749874]	Chr11:70864..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
NM_002496.4(NDUFS8):c.1-35C>T	single nucleotide variant	not provided [RCV001586558]	Chr11:68032117 [GRCh38] Chr11:67799584 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.109+123T>C	single nucleotide variant	not provided [RCV001707337]	Chr11:68032459 [GRCh38] Chr11:67799926 [GRCh37] Chr11:11q13.2	benign
NM_002496.4(NDUFS8):c.19C>A (p.Pro7Thr)	single nucleotide variant	Leigh syndrome [RCV001103232]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV001103233]\|not provided [RCV000923575]	Chr11:68032170 [GRCh38] Chr11:67799637 [GRCh37] Chr11:11q13.2	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance
NM_002496.4(NDUFS8):c.59-10C>G	single nucleotide variant	not provided [RCV000942556]	Chr11:68032276 [GRCh38] Chr11:67799743 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.373-267T>G	single nucleotide variant	not provided [RCV000831000]	Chr11:68035986 [GRCh38] Chr11:67803453 [GRCh37] Chr11:11q13.2	benign
NM_002496.4(NDUFS8):c.384C>G (p.Ile128Met)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV001174541]	Chr11:68036264 [GRCh38] Chr11:67803731 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.269C>T (p.Pro90Leu)	single nucleotide variant	Leigh syndrome [RCV001111481]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV001111482]	Chr11:68033180 [GRCh38] Chr11:67800647 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.5G>A (p.Arg2His)	single nucleotide variant	Leigh syndrome [RCV001103231]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV001103230]	Chr11:68032156 [GRCh38] Chr11:67799623 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.-1+38G>C	single nucleotide variant	not provided [RCV001576712]	Chr11:68030771 [GRCh38] Chr11:67798238 [GRCh37] Chr11:11q13.2	likely benign
NC_000011.9:g.(?_64973914)_(70052579_?)dup	duplication	Aicardi-Goutieres syndrome 3 [RCV003113322]\|FADD-related immunodeficiency [RCV003107753]	Chr11:64973914..70052579 [GRCh37] Chr11:11q13.1-13.3	uncertain significance
NC_000011.9:g.(?_67759017)_(68216538_?)dup	duplication	not provided [RCV003107647]	Chr11:67759017..68216538 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.1-139G>C	single nucleotide variant	not provided [RCV001681105]	Chr11:68032013 [GRCh38] Chr11:67799480 [GRCh37] Chr11:11q13.2	benign
NM_002496.4(NDUFS8):c.110-284C>T	single nucleotide variant	not provided [RCV001552647]	Chr11:68032639 [GRCh38] Chr11:67800106 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.574G>A (p.Gly192Arg)	single nucleotide variant	Leigh syndrome [RCV001114883]\|Mitochondrial complex I deficiency, nuclear type 1 [RCV001114884]	Chr11:68036534 [GRCh38] Chr11:67804001 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.325G>A (p.Glu109Lys)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV002470355]	Chr11:68033236 [GRCh38] Chr11:67800703 [GRCh37] Chr11:11q13.2	uncertain significance
GRCh37/hg19 11q13.2(chr11:66820585-67979510)x3	copy number gain	not provided [RCV001006414]	Chr11:66820585..67979510 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.373-221_373-211del	deletion	not provided [RCV001617029]	Chr11:68036018..68036028 [GRCh38] Chr11:67803485..67803495 [GRCh37] Chr11:11q13.2	benign
NM_002496.4(NDUFS8):c.*1C>T	single nucleotide variant	not provided [RCV001698852]	Chr11:68036594 [GRCh38] Chr11:67804061 [GRCh37] Chr11:11q13.2	likely benign
NC_000011.10:g.68036689C>T	single nucleotide variant	not provided [RCV001681629]	Chr11:68036689 [GRCh38] Chr11:67804156 [GRCh37] Chr11:11q13.2	benign
NM_002496.4(NDUFS8):c.53G>T (p.Arg18Leu)	single nucleotide variant	Leigh syndrome [RCV001335040]\|not provided [RCV002547333]	Chr11:68032204 [GRCh38] Chr11:67799671 [GRCh37] Chr11:11q13.2	uncertain significance
NC_000011.9:g.(?_59596957)_(68707199_?)dup	duplication	Familial temporal lobe epilepsy 8 [RCV001372442]	Chr11:59596957..68707199 [GRCh37] Chr11:11q12.1-13.3	uncertain significance
NM_002496.4(NDUFS8):c.59-22C>G	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV001779274]\|not provided [RCV001643648]	Chr11:68032264 [GRCh38] Chr11:67799731 [GRCh37] Chr11:11q13.2	benign
NM_002496.4(NDUFS8):c.347T>C (p.Leu116Pro)	single nucleotide variant	not provided [RCV001762765]	Chr11:68033258 [GRCh38] Chr11:67800725 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.454T>C (p.Tyr152His)	single nucleotide variant	See cases [RCV002252520]	Chr11:68036334 [GRCh38] Chr11:67803801 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.328C>T (p.Arg110Cys)	single nucleotide variant	not provided [RCV001771136]	Chr11:68033239 [GRCh38] Chr11:67800706 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.592G>A (p.Glu198Lys)	single nucleotide variant	not provided [RCV001768863]	Chr11:68036552 [GRCh38] Chr11:67804019 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.585G>A (p.Trp195Ter)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV003107938]\|not provided [RCV002025602]	Chr11:68036545 [GRCh38] Chr11:67804012 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.457T>C (p.Cys153Arg)	single nucleotide variant	not provided [RCV001984552]	Chr11:68036337 [GRCh38] Chr11:67803804 [GRCh37] Chr11:11q13.2	uncertain significance
NC_000011.9:g.(?_67759017)_(67800770_?)dup	duplication	Herpes simplex encephalitis, susceptibility to, 1 [RCV001943213]	Chr11:67759017..67800770 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.85A>G (p.Ser29Gly)	single nucleotide variant	not provided [RCV001942945]	Chr11:68032312 [GRCh38] Chr11:67799779 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.605A>C (p.Asn202Thr)	single nucleotide variant	not provided [RCV002030935]	Chr11:68036565 [GRCh38] Chr11:67804032 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.380C>T (p.Thr127Ile)	single nucleotide variant	not provided [RCV001998349]	Chr11:68036260 [GRCh38] Chr11:67803727 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.243C>A (p.Thr81=)	single nucleotide variant	not provided [RCV002147858]	Chr11:68033154 [GRCh38] Chr11:67800621 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.110-10C>T	single nucleotide variant	not provided [RCV002188508]	Chr11:68032913 [GRCh38] Chr11:67800380 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.318C>T (p.Ser106=)	single nucleotide variant	not provided [RCV002174156]	Chr11:68033229 [GRCh38] Chr11:67800696 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.591C>T (p.Ala197=)	single nucleotide variant	not provided [RCV002131305]	Chr11:68036551 [GRCh38] Chr11:67804018 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.273G>A (p.Leu91=)	single nucleotide variant	not provided [RCV002154455]	Chr11:68033184 [GRCh38] Chr11:67800651 [GRCh37] Chr11:11q13.2	likely benign
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3	copy number gain	MISSED ABORTION [RCV002282973]	Chr11:32799481..134938470 [GRCh37] Chr11:11p13-q25	pathogenic
NM_002496.4(NDUFS8):c.499G>A (p.Glu167Lys)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV002289103]	Chr11:68036379 [GRCh38] Chr11:67803846 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.170G>C (p.Arg57Pro)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV002468753]	Chr11:68032983 [GRCh38] Chr11:67800450 [GRCh37] Chr11:11q13.2	likely pathogenic
NM_002496.4(NDUFS8):c.159C>A (p.Asp53Glu)	single nucleotide variant	not provided [RCV002572003]	Chr11:68032972 [GRCh38] Chr11:67800439 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.372+17A>G	single nucleotide variant	not provided [RCV002639203]	Chr11:68033300 [GRCh38] Chr11:67800767 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.551A>T (p.Asn184Ile)	single nucleotide variant	not provided [RCV002658899]	Chr11:68036511 [GRCh38] Chr11:67803978 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.53G>A (p.Arg18His)	single nucleotide variant	not provided [RCV002781361]	Chr11:68032204 [GRCh38] Chr11:67799671 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.415C>T (p.Arg139Trp)	single nucleotide variant	Inborn genetic diseases [RCV002758211]	Chr11:68036295 [GRCh38] Chr11:67803762 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.223C>T (p.Leu75=)	single nucleotide variant	not provided [RCV002620043]	Chr11:68033134 [GRCh38] Chr11:67800601 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.169C>T (p.Arg57Cys)	single nucleotide variant	not provided [RCV002591503]	Chr11:68032982 [GRCh38] Chr11:67800449 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.132C>T (p.Pro44=)	single nucleotide variant	not provided [RCV002625496]	Chr11:68032945 [GRCh38] Chr11:67800412 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.297T>C (p.His99=)	single nucleotide variant	not provided [RCV002741148]	Chr11:68033208 [GRCh38] Chr11:67800675 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.200-13G>A	single nucleotide variant	not provided [RCV002800624]	Chr11:68033098 [GRCh38] Chr11:67800565 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.628C>T (p.Arg210Trp)	single nucleotide variant	Inborn genetic diseases [RCV002764002]	Chr11:68036588 [GRCh38] Chr11:67804055 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.600C>T (p.Ala200=)	single nucleotide variant	not provided [RCV002626685]	Chr11:68036560 [GRCh38] Chr11:67804027 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.371A>G (p.Gln124Arg)	single nucleotide variant	not provided [RCV003042017]	Chr11:68033282 [GRCh38] Chr11:67800749 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.216G>A (p.Leu72=)	single nucleotide variant	not provided [RCV002890394]	Chr11:68033127 [GRCh38] Chr11:67800594 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.605del (p.Asn202fs)	deletion	not provided [RCV003031785]	Chr11:68036564 [GRCh38] Chr11:67804031 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.32G>A (p.Arg11Gln)	single nucleotide variant	Inborn genetic diseases [RCV002964432]	Chr11:68032183 [GRCh38] Chr11:67799650 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.307C>T (p.Arg103Trp)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV003108141]\|not provided [RCV003011235]	Chr11:68033218 [GRCh38] Chr11:67800685 [GRCh37] Chr11:11q13.2	likely pathogenic\|uncertain significance
NM_002496.4(NDUFS8):c.161G>A (p.Arg54Gln)	single nucleotide variant	Inborn genetic diseases [RCV003289525]\|not provided [RCV002577432]	Chr11:68032974 [GRCh38] Chr11:67800441 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.185C>G (p.Thr62Ser)	single nucleotide variant	not provided [RCV002963015]	Chr11:68032998 [GRCh38] Chr11:67800465 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.495C>T (p.Ile165=)	single nucleotide variant	not provided [RCV002580483]	Chr11:68036375 [GRCh38] Chr11:67803842 [GRCh37] Chr11:11q13.2	likely benign\|uncertain significance
NM_002496.4(NDUFS8):c.392A>G (p.Glu131Gly)	single nucleotide variant	Inborn genetic diseases [RCV002702945]	Chr11:68036272 [GRCh38] Chr11:67803739 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.412C>T (p.Arg138Cys)	single nucleotide variant	not provided [RCV002725619]	Chr11:68036292 [GRCh38] Chr11:67803759 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.501+16G>A	single nucleotide variant	not provided [RCV002608499]	Chr11:68036397 [GRCh38] Chr11:67803864 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.416G>A (p.Arg139Gln)	single nucleotide variant	not provided [RCV002583678]	Chr11:68036296 [GRCh38] Chr11:67803763 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.18G>A (p.Thr6=)	single nucleotide variant	not provided [RCV002613175]	Chr11:68032169 [GRCh38] Chr11:67799636 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.59-17C>T	single nucleotide variant	not provided [RCV002588898]	Chr11:68032269 [GRCh38] Chr11:67799736 [GRCh37] Chr11:11q13.2	benign
NM_002496.4(NDUFS8):c.84C>T (p.His28=)	single nucleotide variant	not provided [RCV002589182]	Chr11:68032311 [GRCh38] Chr11:67799778 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.367G>T (p.Ala123Ser)	single nucleotide variant	Inborn genetic diseases [RCV003269547]\|Mitochondrial complex 1 deficiency, nuclear type 2 [RCV003142644]	Chr11:68033278 [GRCh38] Chr11:67800745 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.308G>A (p.Arg103Gln)	single nucleotide variant	Inborn genetic diseases [RCV003193309]	Chr11:68033219 [GRCh38] Chr11:67800686 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.160C>T (p.Arg54Trp)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV003324450]	Chr11:68032973 [GRCh38] Chr11:67800440 [GRCh37] Chr11:11q13.2	pathogenic
NM_002496.4(NDUFS8):c.502-3C>T	single nucleotide variant	not provided [RCV003332783]	Chr11:68036459 [GRCh38] Chr11:67803926 [GRCh37] Chr11:11q13.2	uncertain significance
GRCh37/hg19 11q13.2(chr11:67799161-68393180)x1	copy number loss	not provided [RCV003483126]	Chr11:67799161..68393180 [GRCh37] Chr11:11q13.2	pathogenic
GRCh37/hg19 11q12.2-13.5(chr11:59923608-76272324)x3	copy number gain	not provided [RCV003484842]	Chr11:59923608..76272324 [GRCh37] Chr11:11q12.2-13.5	pathogenic
NM_002496.4(NDUFS8):c.201C>T (p.Gly67=)	single nucleotide variant	not provided [RCV003693009]	Chr11:68033112 [GRCh38] Chr11:67800579 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.1A>G (p.Met1Val)	single nucleotide variant	not provided [RCV003849202]	Chr11:68032152 [GRCh38] Chr11:67799619 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.110-20C>G	single nucleotide variant	not provided [RCV003546182]	Chr11:68032903 [GRCh38] Chr11:67800370 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.329G>A (p.Arg110His)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV003493105]	Chr11:68033240 [GRCh38] Chr11:67800707 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.319G>A (p.Gly107Arg)	single nucleotide variant	not provided [RCV003828599]	Chr11:68033230 [GRCh38] Chr11:67800697 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.405T>C (p.Asp135=)	single nucleotide variant	not provided [RCV003664141]	Chr11:68036285 [GRCh38] Chr11:67803752 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.502-11T>G	single nucleotide variant	not provided [RCV003696794]	Chr11:68036451 [GRCh38] Chr11:67803918 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.426C>G (p.Arg142=)	single nucleotide variant	not provided [RCV003702562]	Chr11:68036306 [GRCh38] Chr11:67803773 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.78C>T (p.Ser26=)	single nucleotide variant	not provided [RCV003541842]	Chr11:68032305 [GRCh38] Chr11:67799772 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.373-4G>A	single nucleotide variant	not provided [RCV003722852]	Chr11:68036249 [GRCh38] Chr11:67803716 [GRCh37] Chr11:11q13.2	likely benign
GRCh37/hg19 11q12.1-13.3(chr11:56895955-69295402)x3	copy number gain	not specified [RCV003986944]	Chr11:56895955..69295402 [GRCh37] Chr11:11q12.1-13.3	likely pathogenic
NM_002496.4(NDUFS8):c.372+1G>A	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV003988300]	Chr11:68033284 [GRCh38] Chr11:67800751 [GRCh37] Chr11:11q13.2	likely pathogenic
NM_002496.4(NDUFS8):c.*10G>A	single nucleotide variant	NDUFS8-related disorder [RCV003894454]	Chr11:68036603 [GRCh38] Chr11:67804070 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.121A>C (p.Met41Leu)	single nucleotide variant	not provided [RCV004592345]	Chr11:68032934 [GRCh38] Chr11:67800401 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.5G>T (p.Arg2Leu)	single nucleotide variant	Inborn genetic diseases [RCV004480345]	Chr11:68032156 [GRCh38] Chr11:67799623 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.417G>C (p.Arg139=)	single nucleotide variant	not provided [RCV004585278]	Chr11:68036297 [GRCh38] Chr11:67803764 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.220_372+130del	deletion	not provided [RCV004576098]	Chr11:68033125..68033407 [GRCh38] Chr11:67800592..67800874 [GRCh37] Chr11:11q13.2	likely pathogenic
NM_002496.4(NDUFS8):c.376A>G (p.Ile126Val)	single nucleotide variant	not provided [RCV004575108]	Chr11:68036256 [GRCh38] Chr11:67803723 [GRCh37] Chr11:11q13.2	likely pathogenic
NM_002496.4(NDUFS8):c.423C>G (p.Thr141=)	single nucleotide variant	not provided [RCV004585279]	Chr11:68036303 [GRCh38] Chr11:67803770 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.429T>C (p.Tyr143=)	single nucleotide variant	not provided [RCV004585280]	Chr11:68036309 [GRCh38] Chr11:67803776 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.456C>T (p.Tyr152=)	single nucleotide variant	not provided [RCV004585281]	Chr11:68036336 [GRCh38] Chr11:67803803 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.501+5G>A	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV004595007]	Chr11:68036386 [GRCh38] Chr11:67803853 [GRCh37] Chr11:11q13.2	likely pathogenic
NM_002496.4(NDUFS8):c.424C>T (p.Arg142Cys)	single nucleotide variant	not provided [RCV004771373]	Chr11:68036304 [GRCh38] Chr11:67803771 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.329G>T (p.Arg110Leu)	single nucleotide variant	not provided [RCV004781119]	Chr11:68033240 [GRCh38] Chr11:67800707 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.197G>C (p.Arg66Pro)	single nucleotide variant	not provided [RCV004776158]	Chr11:68033010 [GRCh38] Chr11:67800477 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.367G>A (p.Ala123Thr)	single nucleotide variant	Inborn genetic diseases [RCV004961500]	Chr11:68033278 [GRCh38] Chr11:67800745 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.230G>A (p.Arg77Gln)	single nucleotide variant	Inborn genetic diseases [RCV004961501]	Chr11:68033141 [GRCh38] Chr11:67800608 [GRCh37] Chr11:11q13.2	uncertain significance
NM_002496.4(NDUFS8):c.304C>T (p.Arg102Cys)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV005233251]	Chr11:68033215 [GRCh38] Chr11:67800682 [GRCh37] Chr11:11q13.2	likely pathogenic
NM_002496.4(NDUFS8):c.342C>A (p.Cys114Ter)	single nucleotide variant	Mitochondrial complex 1 deficiency, nuclear type 2 [RCV005233252]	Chr11:68033253 [GRCh38] Chr11:67800720 [GRCh37] Chr11:11q13.2	likely pathogenic
NM_002496.4(NDUFS8):c.378C>T (p.Ile126=)	single nucleotide variant	not provided [RCV005132175]	Chr11:68036258 [GRCh38] Chr11:67803725 [GRCh37] Chr11:11q13.2	likely benign
NM_002496.4(NDUFS8):c.548A>G (p.Tyr183Cys)	single nucleotide variant	not provided [RCV005151981]	Chr11:68036508 [GRCh38] Chr11:67803975 [GRCh37] Chr11:11q13.2	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	5181
Count of miRNA genes:	987
Interacting mature miRNAs:	1226
Transcripts:	ENST00000313468, ENST00000432321, ENST00000453471, ENST00000524810, ENST00000525419, ENST00000525628, ENST00000526339, ENST00000526446, ENST00000526542, ENST00000528492, ENST00000529645, ENST00000531228, ENST00000531282, ENST00000531796, ENST00000532399
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
1357380	BW64_H	Body weight QTL 64 (human)	2.2		Body weight	percent fat after exercise training	11	60978937	86978937	Human

RH69713

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	67,796,568 - 67,796,732	UniSTS	GRCh37
Build 36	11	67,553,144 - 67,553,308	RGD	NCBI36
Celera	11	65,130,240 - 65,130,404	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	64,131,915 - 64,132,079	UniSTS
GeneMap99-GB4 RH Map	11	259.82	UniSTS

STS-R17000

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	67,803,788 - 67,804,098	UniSTS	GRCh37
Build 36	11	67,560,364 - 67,560,674	RGD	NCBI36
Celera	11	65,137,459 - 65,137,769	RGD
Cytogenetic Map	11	q13	UniSTS
HuRef	11	64,139,131 - 64,139,441	UniSTS
GeneMap99-GB4 RH Map	11	263.07	UniSTS

D10S16

No map positions available.

D15S1477

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	4	q32-q35	UniSTS
Cytogenetic Map	5	q11	UniSTS
Cytogenetic Map	10	p12.1	UniSTS
Cytogenetic Map	10	p12.1-p11.2	UniSTS
Cytogenetic Map	15	q13	UniSTS
Cytogenetic Map	21	q21.3	UniSTS
Cytogenetic Map	12	p13.3	UniSTS
Cytogenetic Map	1	q25	UniSTS
Cytogenetic Map	20	q13.3	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	11	p15.4	UniSTS
Cytogenetic Map	12	q12	UniSTS
Cytogenetic Map	3	p24.3	UniSTS
Cytogenetic Map	5	q14	UniSTS
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	7	p21.3	UniSTS
Cytogenetic Map	1	q22	UniSTS
Cytogenetic Map	14	q32.33	UniSTS
Cytogenetic Map	14	q23.3	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	14	q31-q32	UniSTS
Cytogenetic Map	10	q25.2	UniSTS
Cytogenetic Map	16	p13.13-p13.12	UniSTS
Cytogenetic Map	3	q12.3	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	10	p15.3	UniSTS
Cytogenetic Map	2	p22.1	UniSTS
Cytogenetic Map	13	q13.1	UniSTS
Cytogenetic Map	5	q23.3	UniSTS
Cytogenetic Map	15	q21.1	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	3	p21.3	UniSTS
Cytogenetic Map	12	q24.13	UniSTS
Cytogenetic Map	4	q21.1	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	2	q37.3	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	19	p13	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	1	p31.3	UniSTS
Cytogenetic Map	20	q13.31	UniSTS
Cytogenetic Map	10	q22	UniSTS
Cytogenetic Map	1	q41	UniSTS
Cytogenetic Map	9	q34.3	UniSTS
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	2	p13.1	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	10	q24.2	UniSTS
Cytogenetic Map	1	q42.11	UniSTS
Cytogenetic Map	1	q32.1	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	2	p13.3	UniSTS
Cytogenetic Map	7	p22.1	UniSTS
Cytogenetic Map	11	q24	UniSTS
Cytogenetic Map	6	q16.2	UniSTS
Cytogenetic Map	2	q14	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	16	q24	UniSTS
Cytogenetic Map	X	q26.3	UniSTS
Cytogenetic Map	10	q23.1	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	4	q12	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	7	q21.2	UniSTS
Cytogenetic Map	17	q22.2	UniSTS
Cytogenetic Map	8	q22.3	UniSTS
Cytogenetic Map	4	q25	UniSTS
Cytogenetic Map	11	q14.2	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	5	q23	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	13	q12.1	UniSTS
Cytogenetic Map	6	p21.32	UniSTS
Cytogenetic Map	2	q31	UniSTS
Cytogenetic Map	10	p14	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	3	p21.2	UniSTS
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	14	q12	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	4	q28.2	UniSTS
Cytogenetic Map	1	p13.2	UniSTS
Cytogenetic Map	22	q12.3	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	16	p12.3	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	1	p34.3	UniSTS
Cytogenetic Map	1	p36.31	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	11	p13	UniSTS
Cytogenetic Map	12	q13.3	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	1	p35.3	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	4	p14	UniSTS
Cytogenetic Map	15	q11-q13	UniSTS
Cytogenetic Map	19	p	UniSTS
Cytogenetic Map	7	q22	UniSTS
Cytogenetic Map	9	q22.3	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	8	q11.21	UniSTS
Cytogenetic Map	15	q15	UniSTS
Cytogenetic Map	15	q15.1	UniSTS
Cytogenetic Map	2	q22.3	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	5	q13.2	UniSTS
Cytogenetic Map	10	q23.2	UniSTS
Cytogenetic Map	7	p22.3	UniSTS
Cytogenetic Map	9	q34.13	UniSTS
Cytogenetic Map	1	q32	UniSTS
Cytogenetic Map	1	q31.3	UniSTS
Cytogenetic Map	4	q35	UniSTS
Cytogenetic Map	9	p13	UniSTS
Cytogenetic Map	3	p24.2	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	6	q25.2-q25.3	UniSTS
Cytogenetic Map	15	q21	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	1	q42.3	UniSTS
Cytogenetic Map	7	q22.3	UniSTS
Cytogenetic Map	9	q34.2	UniSTS
Cytogenetic Map	17	q24	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	19	q13.3-q13.4	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	3	q21	UniSTS
Cytogenetic Map	20	q13	UniSTS
Cytogenetic Map	22	q12.2	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	14	q22.1	UniSTS
Cytogenetic Map	11	q23.1	UniSTS
Cytogenetic Map	17	q22-q23	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.3	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	7	p15.2	UniSTS
Cytogenetic Map	1	q21	UniSTS
Cytogenetic Map	12	q23.1	UniSTS
Cytogenetic Map	16	q12.2	UniSTS
Cytogenetic Map	13	q11	UniSTS
Cytogenetic Map	X	p22.3	UniSTS
Cytogenetic Map	3	p25-p24	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	X	q22.1	UniSTS
Cytogenetic Map	X	p11.3	UniSTS
Cytogenetic Map	3	p12	UniSTS
Cytogenetic Map	1	q25.1	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	X	p11.2	UniSTS
Cytogenetic Map	11	q13.1-q13.2	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	17	p13	UniSTS
Cytogenetic Map	5	p13.2	UniSTS
Cytogenetic Map	7	q21-q22	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	3	q26.2	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	8	p22	UniSTS
Cytogenetic Map	4	q35.1	UniSTS
Cytogenetic Map	10	q23.31	UniSTS
Cytogenetic Map	6	p21.1-p12.2	UniSTS
Cytogenetic Map	12	q14.1	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	1	p35	UniSTS
Cytogenetic Map	12	q	UniSTS
Cytogenetic Map	1	q21.2	UniSTS
Cytogenetic Map	8	q23.1	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	14	q11.1	UniSTS
Cytogenetic Map	21	q22.11	UniSTS
Cytogenetic Map	3	p14.1	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	19	p13.3-p13.2	UniSTS
Cytogenetic Map	1	p36.11-p34.2	UniSTS
Cytogenetic Map	9	p22	UniSTS
Cytogenetic Map	1	q42.12	UniSTS
Cytogenetic Map	2	q35	UniSTS
Cytogenetic Map	9	p22.1	UniSTS
Cytogenetic Map	11	q24.2	UniSTS
Cytogenetic Map	12	q15	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	8	q22.1	UniSTS
Cytogenetic Map	9	q21.13	UniSTS
Cytogenetic Map	11	p15.1	UniSTS
Cytogenetic Map	1	p32.3	UniSTS
Cytogenetic Map	12	q21.1	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	3	p21	UniSTS
Cytogenetic Map	20	p11.23	UniSTS
Cytogenetic Map	15	q15.2	UniSTS
Cytogenetic Map	8	p21.1	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	18	q12.1	UniSTS
Cytogenetic Map	8	q12.1	UniSTS
Cytogenetic Map	14	q21.2	UniSTS
Cytogenetic Map	3	q27.1	UniSTS
Cytogenetic Map	3	p14.3	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	6	p22.1	UniSTS
Cytogenetic Map	12	p13.2	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	15	q21.3	UniSTS
Cytogenetic Map	X	p11.22	UniSTS
Cytogenetic Map	12	p12	UniSTS
Cytogenetic Map	15	q15.3	UniSTS
Cytogenetic Map	18	q12.3	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	12	q11-q12	UniSTS
Cytogenetic Map	3	q13.33	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	2	p24	UniSTS
Cytogenetic Map	8	q24.21	UniSTS
Cytogenetic Map	12	q22-q23.1	UniSTS
Cytogenetic Map	3	q26.33	UniSTS
Cytogenetic Map	5	q32	UniSTS
Cytogenetic Map	15	q21-q22	UniSTS
Cytogenetic Map	8	p21.2	UniSTS
Cytogenetic Map	10	q23	UniSTS
Cytogenetic Map	1	p22	UniSTS
Cytogenetic Map	16	p13.13	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	10	q24	UniSTS
Cytogenetic Map	8	q11.2	UniSTS
Cytogenetic Map	7	p14-p13	UniSTS
Cytogenetic Map	11	q22-q23	UniSTS
Cytogenetic Map	6	q22-q23	UniSTS
Cytogenetic Map	2	p16.1	UniSTS
Cytogenetic Map	15	q26.3	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	4	q21.22	UniSTS
Cytogenetic Map	1	q21.1	UniSTS
Cytogenetic Map	17	q21.33	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	16	p12.1	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	11	q24.3	UniSTS
Cytogenetic Map	11	q13.1-q13.3	UniSTS
Cytogenetic Map	14	q24.2	UniSTS
Cytogenetic Map	17	q23.3	UniSTS
Cytogenetic Map	2	q24	UniSTS
Cytogenetic Map	1	q23.3	UniSTS
Cytogenetic Map	10	q25	UniSTS
Cytogenetic Map	9	q32	UniSTS
Cytogenetic Map	3	q25.33	UniSTS
Cytogenetic Map	2	p14	UniSTS
Cytogenetic Map	15	q21-q23	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	3	p22.1	UniSTS
Cytogenetic Map	19	q13.11	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	10	q26.3	UniSTS
Cytogenetic Map	6	p21	UniSTS
Cytogenetic Map	2	p25.2	UniSTS
Cytogenetic Map	14	q23.1	UniSTS
Cytogenetic Map	1	p31.1	UniSTS
Cytogenetic Map	15	q14-q15	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	1	p34	UniSTS
Cytogenetic Map	X	q22.3	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	6	p25.2	UniSTS
Cytogenetic Map	6	q25.1	UniSTS
Cytogenetic Map	12	p12.1	UniSTS
Cytogenetic Map	X	q25	UniSTS
Cytogenetic Map	14	q23.2	UniSTS
Cytogenetic Map	11	q12	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	5	q35	UniSTS
Cytogenetic Map	16	q21	UniSTS
Cytogenetic Map	6	p23	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	4	p16.1	UniSTS
Cytogenetic Map	3	q25.31	UniSTS
Cytogenetic Map	2	q33.1	UniSTS
Cytogenetic Map	17	q21.2	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	10	q24.31	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	1	p22.1	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	6	q13	UniSTS
Cytogenetic Map	10	q21.3	UniSTS
Cytogenetic Map	17	p12	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	4	q31.1	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	18	q21.3	UniSTS
Cytogenetic Map	11	q21	UniSTS
Cytogenetic Map	5	q13	UniSTS
Cytogenetic Map	11	q23.2	UniSTS
Cytogenetic Map	8	q12	UniSTS
Cytogenetic Map	4	q28-q32	UniSTS
Cytogenetic Map	19	q13.33	UniSTS
Cytogenetic Map	15	q21.2	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	12	q24.11	UniSTS
Cytogenetic Map	9	q21.12	UniSTS
Cytogenetic Map	9	q33.3	UniSTS
Cytogenetic Map	11	q22.3	UniSTS
Cytogenetic Map	20	p11.22-p11.1	UniSTS
Cytogenetic Map	10	q24.32	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	16	q23.1	UniSTS
Cytogenetic Map	13	q14.2	UniSTS
Cytogenetic Map	2	q24.3	UniSTS
Cytogenetic Map	8	p12	UniSTS
Cytogenetic Map	7	p13	UniSTS
Cytogenetic Map	9	q31-q33	UniSTS
Cytogenetic Map	6	p24.1	UniSTS
Cytogenetic Map	10	p11.23	UniSTS
Cytogenetic Map	6	q15	UniSTS
Cytogenetic Map	5	q35.2	UniSTS
Cytogenetic Map	14	q32	UniSTS
Cytogenetic Map	3	q26.1-q26.2	UniSTS
Cytogenetic Map	5	q11.2-q13.2	UniSTS
Cytogenetic Map	1	p36.11	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	X	p11.4	UniSTS
Cytogenetic Map	X	q13.3	UniSTS
Cytogenetic Map	8	q22.2	UniSTS
Cytogenetic Map	7	q11.21	UniSTS
Cytogenetic Map	5	q35.1	UniSTS
Cytogenetic Map	5	q33.1	UniSTS
Cytogenetic Map	4	q21.21	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	18	p11.21	UniSTS
Cytogenetic Map	X	q13.1	UniSTS
Cytogenetic Map	X	q21.1	UniSTS
Cytogenetic Map	10	p11.21	UniSTS
Cytogenetic Map	12	q14.3	UniSTS
Cytogenetic Map	5	q34	UniSTS
Cytogenetic Map	2	q36.1	UniSTS
Cytogenetic Map	12	p11.21	UniSTS
Cytogenetic Map	5	q33.3	UniSTS
Cytogenetic Map	16	q23.2	UniSTS
Cytogenetic Map	9	q31.3	UniSTS
Cytogenetic Map	15	q24	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	12	q21	UniSTS
Cytogenetic Map	8	p11.2	UniSTS
Cytogenetic Map	7	q22-q31	UniSTS
Cytogenetic Map	22	q12	UniSTS
Cytogenetic Map	4	q22	UniSTS
Cytogenetic Map	17	q21.32	UniSTS
Cytogenetic Map	12	q14	UniSTS
Cytogenetic Map	11	q23.1-q23.2	UniSTS
Cytogenetic Map	13	q14	UniSTS
Cytogenetic Map	13	q32.2	UniSTS
Cytogenetic Map	17	q	UniSTS
Cytogenetic Map	2	q33	UniSTS
Cytogenetic Map	7	q	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	20	q13.12	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	13	q22.1	UniSTS
Cytogenetic Map	3	p25.2	UniSTS
Cytogenetic Map	5	q21.3	UniSTS
Cytogenetic Map	9	q22.2	UniSTS
Cytogenetic Map	3	p22.2	UniSTS
Cytogenetic Map	6	p24.2	UniSTS

D8S2279

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	21	q22.12	UniSTS
Cytogenetic Map	15	q13	UniSTS
Cytogenetic Map	9	q32	UniSTS
Cytogenetic Map	15	q22.3	UniSTS
Cytogenetic Map	17	p12	UniSTS
Cytogenetic Map	21	q21.3	UniSTS
Cytogenetic Map	3	p22-p21.3	UniSTS
Cytogenetic Map	1	q21.1	UniSTS
Cytogenetic Map	2	q24.2	UniSTS
Cytogenetic Map	17	q24.2	UniSTS
Cytogenetic Map	1	q32	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	20	q13.3	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	1	q21	UniSTS
Cytogenetic Map	3	p14.1	UniSTS
Cytogenetic Map	2	q37.3	UniSTS
Cytogenetic Map	7	p14.1	UniSTS
Cytogenetic Map	2	q22.3	UniSTS
Cytogenetic Map	15	q13.2	UniSTS
Cytogenetic Map	12	q24.1	UniSTS
Cytogenetic Map	7	p15.2	UniSTS
Cytogenetic Map	5	q31.2	UniSTS
Cytogenetic Map	2	p25.2	UniSTS
Cytogenetic Map	3	p24.3	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	5	q14	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	1	p36.32	UniSTS
Cytogenetic Map	1	q42.12	UniSTS
Cytogenetic Map	7	q21.11	UniSTS
Cytogenetic Map	9	q34.2	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	8	q22.3	UniSTS
Cytogenetic Map	6	p21.1-p12	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	7	p21.3	UniSTS
Cytogenetic Map	4	q12	UniSTS
Cytogenetic Map	22	q11.22	UniSTS
Cytogenetic Map	11	p13	UniSTS
Cytogenetic Map	1	q12	UniSTS
Cytogenetic Map	8	p23	UniSTS
Cytogenetic Map	11	q13.2-q13.3	UniSTS
Cytogenetic Map	13	q14.1-q14.3	UniSTS
Cytogenetic Map	3	q22-q24	UniSTS
Cytogenetic Map	3	q13.1-q13.2	UniSTS
Cytogenetic Map	16	q24	UniSTS
Cytogenetic Map	5	q23.3-q31.1	UniSTS
Cytogenetic Map	8	p21.3	UniSTS
Cytogenetic Map	14	q32.3	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	7	q32	UniSTS
Cytogenetic Map	14	q32.33	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	9	q34.3	UniSTS
Cytogenetic Map	1	p32.3	UniSTS
Cytogenetic Map	17	q11	UniSTS
Cytogenetic Map	17	p13.1-p12	UniSTS
Cytogenetic Map	18	q21.33	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	5	q14.1	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	1	q21-q23	UniSTS
Cytogenetic Map	X	p11.23	UniSTS
Cytogenetic Map	4	q21.1	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	14	q23.3	UniSTS
Cytogenetic Map	17	p12-p11.2	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	1	q24	UniSTS
Cytogenetic Map	1	q43	UniSTS
Cytogenetic Map	9	q34.13	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	2	q32	UniSTS
Cytogenetic Map	X	p22.2	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	2	q33	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	3	q27	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	4	p16.1	UniSTS
Cytogenetic Map	14	q22.3	UniSTS
Cytogenetic Map	10	q23-q24	UniSTS
Cytogenetic Map	2	q37.1	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	14	q31-q32	UniSTS
Cytogenetic Map	5	p15.33	UniSTS
Cytogenetic Map	1	q23.2	UniSTS
Cytogenetic Map	16	q24.3	UniSTS
Cytogenetic Map	4	p14	UniSTS
Cytogenetic Map	2	q32.3	UniSTS
Cytogenetic Map	15	q21.1	UniSTS
Cytogenetic Map	4	q32.2	UniSTS
Cytogenetic Map	10	q23	UniSTS
Cytogenetic Map	5	q14.2	UniSTS
Cytogenetic Map	4	q32.1	UniSTS
Cytogenetic Map	1	q25.1	UniSTS
Cytogenetic Map	11	q14.1	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	11	q23.1	UniSTS
Cytogenetic Map	3	p21.1	UniSTS
Cytogenetic Map	16	q22.2	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	16	q11.2	UniSTS
Cytogenetic Map	6	q22	UniSTS
Cytogenetic Map	10	p15.3	UniSTS
Cytogenetic Map	11	q23	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	12	q12	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	19	q13.11	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	15	q15	UniSTS
Cytogenetic Map	2	q33.1	UniSTS
Cytogenetic Map	22	q12.3	UniSTS
Cytogenetic Map	20	q11	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	3	p22.1	UniSTS
Cytogenetic Map	8	q22.1	UniSTS
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	18	p11.31	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	2	p22.1	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	1	p35.2	UniSTS
Cytogenetic Map	Y	p11.2	UniSTS
Cytogenetic Map	13	q13.1	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	18	q12	UniSTS
Cytogenetic Map	17	q21.33	UniSTS
Cytogenetic Map	15	q15.1	UniSTS
Cytogenetic Map	3	q27.2	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	5	p15.2	UniSTS
Cytogenetic Map	20	q13.12	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	1	q42	UniSTS
Cytogenetic Map	14	q32.11	UniSTS
Cytogenetic Map	17	q21.2-q21.3	UniSTS
Cytogenetic Map	5	q32-q34	UniSTS
Cytogenetic Map	15	q14	UniSTS
Cytogenetic Map	16	q13	UniSTS
Cytogenetic Map	3	q21.2	UniSTS
Cytogenetic Map	3	p21.3	UniSTS
Cytogenetic Map	14	q24.2	UniSTS
Cytogenetic Map	12	q24.13	UniSTS
Cytogenetic Map	13	q14.11	UniSTS
Cytogenetic Map	3	q27.3	UniSTS
Cytogenetic Map	1	q32.3	UniSTS
Cytogenetic Map	6	p22.1	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	6	q21	UniSTS
Cytogenetic Map	6	q25.3	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	13	q14.3	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	10	p12	UniSTS
Cytogenetic Map	2	q33.3	UniSTS
Cytogenetic Map	14	q21.3	UniSTS
Cytogenetic Map	8	p22-p21	UniSTS
Cytogenetic Map	18	q11.2	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	17	q22	UniSTS
Cytogenetic Map	12	q21.33	UniSTS
Cytogenetic Map	20	q13.32	UniSTS
Cytogenetic Map	1	p34.1	UniSTS
Cytogenetic Map	10	q26	UniSTS
Cytogenetic Map	8	p23.1	UniSTS
Cytogenetic Map	19	p13	UniSTS
Cytogenetic Map	7	q21.13	UniSTS
Cytogenetic Map	7	q31.1	UniSTS
Cytogenetic Map	1	p33	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	22	q12.2	UniSTS
Cytogenetic Map	9	q22.3	UniSTS
Cytogenetic Map	8	q13.1	UniSTS
Cytogenetic Map	3	q25	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	1	p31.3	UniSTS
Cytogenetic Map	14	q31.1	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	12	q13.2	UniSTS
Cytogenetic Map	22	q13.31-q13.33	UniSTS
Cytogenetic Map	20	q13.31	UniSTS
Cytogenetic Map	11	p11.2	UniSTS
Cytogenetic Map	1	q41	UniSTS
Cytogenetic Map	1	p36.11	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	17	q23.2	UniSTS
Cytogenetic Map	7	q32.2	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	1	q32.1	UniSTS
Cytogenetic Map	6	q25.1	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	2	p13.1	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	7	p13	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	14	q31-q32.1	UniSTS
Cytogenetic Map	1	q42.11	UniSTS
Cytogenetic Map	4	q35.1	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	2	p13.3	UniSTS
Cytogenetic Map	X	p11.3	UniSTS
Cytogenetic Map	2	q11.2-q12.1	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	1	p22	UniSTS
Cytogenetic Map	6	q16.2	UniSTS
Cytogenetic Map	18	q23	UniSTS
Cytogenetic Map	2	q14	UniSTS
Cytogenetic Map	20	p11.23-p11.21	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	8	p11.23	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	8	p11.21	UniSTS
Cytogenetic Map	12	q14.3	UniSTS
Cytogenetic Map	X	q26.3	UniSTS
Cytogenetic Map	8	q24.11	UniSTS
Cytogenetic Map	10	q23.1	UniSTS
Cytogenetic Map	1	q44	UniSTS
Cytogenetic Map	9	q22.33	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	9	q21.32	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	9	q33.3	UniSTS
Cytogenetic Map	1	p36.1	UniSTS
Cytogenetic Map	20	q12	UniSTS
Cytogenetic Map	4	q21.23	UniSTS
Cytogenetic Map	5	q13.2	UniSTS
Cytogenetic Map	22	q12.1	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	2	q21.3	UniSTS
Cytogenetic Map	7	q21.2	UniSTS
Cytogenetic Map	17	q22.2	UniSTS
Cytogenetic Map	17	p13	UniSTS
Cytogenetic Map	12	q24.11	UniSTS
Cytogenetic Map	18	q21	UniSTS
Cytogenetic Map	10	q11.1	UniSTS
Cytogenetic Map	22	q11.2	UniSTS
Cytogenetic Map	19	q12	UniSTS
Cytogenetic Map	7	q34-q35	UniSTS
Cytogenetic Map	15	q24.1	UniSTS
Cytogenetic Map	18	p11.21	UniSTS
Cytogenetic Map	1	q23.1	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	6	p25.1-p23	UniSTS
Cytogenetic Map	11	p15.4	UniSTS
Cytogenetic Map	10	q22	UniSTS
Cytogenetic Map	5	q35.3	UniSTS
Cytogenetic Map	18	q12.1-q21.1	UniSTS
Cytogenetic Map	12	p13.1	UniSTS
Cytogenetic Map	13	q12.1	UniSTS
Cytogenetic Map	12	q15	UniSTS
Cytogenetic Map	6	p21.32	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	10	p14	UniSTS
Cytogenetic Map	12	p13.1-p12.3	UniSTS
Cytogenetic Map	3	p25.2	UniSTS
Cytogenetic Map	6	p21.33	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	3	p21.2	UniSTS
Cytogenetic Map	10	q26.3	UniSTS
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	X	p21.2	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	14	q12	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	9	q21.12	UniSTS
Cytogenetic Map	15	q23	UniSTS
Cytogenetic Map	7	p22.2	UniSTS
Cytogenetic Map	8	p21.2	UniSTS
Cytogenetic Map	7	q33	UniSTS
Cytogenetic Map	15	q15.3	UniSTS
Cytogenetic Map	4	q21.22	UniSTS
Cytogenetic Map	12	q13.12	UniSTS
Cytogenetic Map	10	q24.31	UniSTS
Cytogenetic Map	12	p13.31	UniSTS
Cytogenetic Map	14	q32.12	UniSTS
Cytogenetic Map	10	q24.32	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	16	p12.3	UniSTS
Cytogenetic Map	1	p34.3	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	2	q24.3	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	1	p31.1	UniSTS
Cytogenetic Map	19	q13.33	UniSTS
Cytogenetic Map	1	p36.31	UniSTS
Cytogenetic Map	3	q13.31	UniSTS
Cytogenetic Map	15	q22.2	UniSTS
Cytogenetic Map	5	q32	UniSTS
Cytogenetic Map	6	q13	UniSTS
Cytogenetic Map	X	q24	UniSTS
Cytogenetic Map	6	q25	UniSTS
Cytogenetic Map	6	p21	UniSTS
Cytogenetic Map	2	q35	UniSTS
Cytogenetic Map	12	p13-p12	UniSTS
Cytogenetic Map	9	p13.2	UniSTS
Cytogenetic Map	6	p22	UniSTS
Cytogenetic Map	2	q12.1	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	9	q22.2	UniSTS
Cytogenetic Map	1	q22	UniSTS
Cytogenetic Map	1	p22.1	UniSTS
Cytogenetic Map	1	p36	UniSTS
Cytogenetic Map	9	q13-q21	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	X	p11.2	UniSTS
Cytogenetic Map	19	p	UniSTS
Cytogenetic Map	19	p13.1-p12	UniSTS
Cytogenetic Map	7	q22	UniSTS
Cytogenetic Map	12	q24.33	UniSTS
Cytogenetic Map	3	q21	UniSTS
Cytogenetic Map	8	q24	UniSTS
Cytogenetic Map	18	p11.31-p11.21	UniSTS
Cytogenetic Map	11	p15.3-p15.1	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	8	q22	UniSTS
Cytogenetic Map	4	p15.1	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	2	p16.3	UniSTS
Cytogenetic Map	16	p13.12	UniSTS
Cytogenetic Map	7	p21.2	UniSTS
Cytogenetic Map	12	q21.1	UniSTS
Cytogenetic Map	2	p14	UniSTS
Cytogenetic Map	6	q24.3	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	5	q23.1	UniSTS
Cytogenetic Map	10	q23.2	UniSTS
Cytogenetic Map	7	p22.3	UniSTS
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	6	q22.1	UniSTS
Cytogenetic Map	1	q42.1	UniSTS
Cytogenetic Map	1	q25	UniSTS
Cytogenetic Map	6	p22.3	UniSTS
Cytogenetic Map	1	q21.2	UniSTS
Cytogenetic Map	15	q22.1	UniSTS
Cytogenetic Map	12	p13.2	UniSTS
Cytogenetic Map	12	q22	UniSTS
Cytogenetic Map	3	p21-p12	UniSTS
Cytogenetic Map	4	q35	UniSTS
Cytogenetic Map	1	p34-p33	UniSTS
Cytogenetic Map	21	q22.11	UniSTS
Cytogenetic Map	3	p22-p21.33	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	3	q22.1	UniSTS
Cytogenetic Map	8	q21.11	UniSTS
Cytogenetic Map	X	q22.3	UniSTS
Cytogenetic Map	7	p14	UniSTS
Cytogenetic Map	17	q21.1	UniSTS
Cytogenetic Map	15	q21	UniSTS
Cytogenetic Map	1	q42.3	UniSTS
Cytogenetic Map	9	q22	UniSTS
Cytogenetic Map	2	q12.3	UniSTS
Cytogenetic Map	20	q11.2-q13.2	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	17	q24	UniSTS
Cytogenetic Map	3	q25.31	UniSTS
Cytogenetic Map	6	p24.3	UniSTS
Cytogenetic Map	2	q31.3	UniSTS
Cytogenetic Map	1	q31	UniSTS
Cytogenetic Map	7	q32-q33	UniSTS
Cytogenetic Map	7	q21.1	UniSTS
Cytogenetic Map	14	q23-q24.2	UniSTS
Cytogenetic Map	19	q13.3-q13.4	UniSTS
Cytogenetic Map	2	p24-p21	UniSTS
Cytogenetic Map	15	q11.2	UniSTS
Cytogenetic Map	15	q26.3	UniSTS
Cytogenetic Map	7	p22	UniSTS
Cytogenetic Map	12	p11	UniSTS
Cytogenetic Map	1	p35.3	UniSTS
Cytogenetic Map	1	p12	UniSTS
Cytogenetic Map	13	q32.3	UniSTS
Cytogenetic Map	5	q23.3	UniSTS
Cytogenetic Map	20	q13	UniSTS
Cytogenetic Map	17	q25.2	UniSTS
Cytogenetic Map	7	q36.1	UniSTS
Cytogenetic Map	10	p12.33	UniSTS
Cytogenetic Map	17	q21.32	UniSTS
Cytogenetic Map	X	p11.22	UniSTS
Cytogenetic Map	12	p13.3	UniSTS
Cytogenetic Map	X	q25-q26	UniSTS
Cytogenetic Map	2	q36.1	UniSTS
Cytogenetic Map	5	p13	UniSTS
Cytogenetic Map	15	q25	UniSTS
Cytogenetic Map	5	q12.1	UniSTS
Cytogenetic Map	5	p12	UniSTS
Cytogenetic Map	1	p36.22	UniSTS
Cytogenetic Map	3	q26.31	UniSTS
Cytogenetic Map	17	q22-q23	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.3	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	X	q13.2	UniSTS
Cytogenetic Map	12	q23.1	UniSTS
Cytogenetic Map	16	q12.2	UniSTS
Cytogenetic Map	3	q26.32	UniSTS
Cytogenetic Map	6	q22.31	UniSTS
Cytogenetic Map	3	q26.2-q27	UniSTS
Cytogenetic Map	1	q25.1-q25.2	UniSTS
Cytogenetic Map	14	q24	UniSTS
Cytogenetic Map	9	q21.13	UniSTS
Cytogenetic Map	10	q11.22	UniSTS
Cytogenetic Map	22	q13.31	UniSTS
Cytogenetic Map	3	p25.1	UniSTS
Cytogenetic Map	5	q21.3	UniSTS
Cytogenetic Map	5	p13.3	UniSTS
Cytogenetic Map	10	q22.1	UniSTS
Cytogenetic Map	14	q12-q13	UniSTS
Cytogenetic Map	X	p22	UniSTS
Cytogenetic Map	X	q23	UniSTS
Cytogenetic Map	20	p12.3-p11.21	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	17	q11.2-q12	UniSTS
Cytogenetic Map	4	q32-q34	UniSTS
Cytogenetic Map	X	q25-q26.1	UniSTS
Cytogenetic Map	2	p25-p24	UniSTS
Cytogenetic Map	2	p25	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	X	p22.2-p22.1	UniSTS
Cytogenetic Map	X	q22.1	UniSTS
Cytogenetic Map	4	q25	UniSTS
Cytogenetic Map	3	p24.2	UniSTS
Cytogenetic Map	22	q13	UniSTS
Cytogenetic Map	20	q11.22-q12	UniSTS
Cytogenetic Map	4	q34.2	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	22	q13.1-q13.2	UniSTS
Cytogenetic Map	X	q28	UniSTS
Cytogenetic Map	12	q13-q14	UniSTS
Cytogenetic Map	6	q14.1	UniSTS
Cytogenetic Map	12	q13.3	UniSTS
Cytogenetic Map	9	q31.2	UniSTS
Cytogenetic Map	11	q13.1-q13.2	UniSTS
Cytogenetic Map	12	q13	UniSTS
Cytogenetic Map	1	p32-p31	UniSTS
Cytogenetic Map	21	q21.2	UniSTS
Cytogenetic Map	10	q24.3	UniSTS
Cytogenetic Map	16	q21	UniSTS
Cytogenetic Map	8	q21.1	UniSTS
Cytogenetic Map	5	p13.2	UniSTS
Cytogenetic Map	1	p34	UniSTS
Cytogenetic Map	1	q32.2	UniSTS
Cytogenetic Map	4	q21.3	UniSTS
Cytogenetic Map	7	q21-q22	UniSTS
Cytogenetic Map	3	q26.2	UniSTS
Cytogenetic Map	2	q36.3	UniSTS
Cytogenetic Map	8	p22	UniSTS
Cytogenetic Map	11	q22.1	UniSTS
Cytogenetic Map	3	q25.33	UniSTS
Cytogenetic Map	10	q23.31	UniSTS
Cytogenetic Map	4	p15.32	UniSTS
Cytogenetic Map	18	q12.2	UniSTS
Cytogenetic Map	15	q15.2	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	14	q24.1	UniSTS
Cytogenetic Map	12	q14.1	UniSTS
Cytogenetic Map	6	p22.3-p22.1	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	6	q15	UniSTS
Cytogenetic Map	6	q23.3	UniSTS
Cytogenetic Map	13	q14	UniSTS
Cytogenetic Map	5	q35.2	UniSTS
Cytogenetic Map	10	q22.3	UniSTS
Cytogenetic Map	1	p35	UniSTS
Cytogenetic Map	3	q12.3	UniSTS
Cytogenetic Map	19	q13.31	UniSTS
Cytogenetic Map	8	q23.1	UniSTS
Cytogenetic Map	6	q27	UniSTS
Cytogenetic Map	2	q14.3	UniSTS
Cytogenetic Map	X	p11	UniSTS
Cytogenetic Map	11	p15.3	UniSTS
Cytogenetic Map	20	p12	UniSTS
Cytogenetic Map	15	q13.1	UniSTS
Cytogenetic Map	X	p22.3	UniSTS
Cytogenetic Map	11	q13.5	UniSTS
Cytogenetic Map	19	p13.3-p13.2	UniSTS
Cytogenetic Map	1	p36.11-p34.2	UniSTS
Cytogenetic Map	4	q22.1-q23	UniSTS
Cytogenetic Map	7	q22.3	UniSTS
Cytogenetic Map	9	p22	UniSTS
Cytogenetic Map	17	q23.3	UniSTS
Cytogenetic Map	16	q23.2	UniSTS
Cytogenetic Map	2	p16.1	UniSTS
Cytogenetic Map	3	q27.1	UniSTS
Cytogenetic Map	2	p22.3	UniSTS
Cytogenetic Map	X	q26.1	UniSTS
Cytogenetic Map	4	q21.21	UniSTS
Cytogenetic Map	22	q13.3	UniSTS
Cytogenetic Map	2	q32.1	UniSTS
Cytogenetic Map	Y	p11.32	UniSTS
Cytogenetic Map	11	p14	UniSTS
Cytogenetic Map	1	p32.1	UniSTS
Cytogenetic Map	2	p25.3	UniSTS
Cytogenetic Map	4	q34.3	UniSTS
Cytogenetic Map	9	p12	UniSTS
Cytogenetic Map	3	q13.13	UniSTS
Cytogenetic Map	13	q34	UniSTS
Cytogenetic Map	3	p21	UniSTS
Cytogenetic Map	11	q23.2	UniSTS
Cytogenetic Map	20	p11.23	UniSTS
Cytogenetic Map	3	p13	UniSTS
Cytogenetic Map	4	p13	UniSTS
Cytogenetic Map	16	q23.1	UniSTS
Cytogenetic Map	10	p11.23	UniSTS
Cytogenetic Map	8	p21.1	UniSTS
Cytogenetic Map	15	q22-q24	UniSTS
Cytogenetic Map	8	q23	UniSTS
Cytogenetic Map	16	q12.1	UniSTS
Cytogenetic Map	14	q13.2	UniSTS
Cytogenetic Map	18	q12.1	UniSTS
Cytogenetic Map	5	q31.3	UniSTS
Cytogenetic Map	11	q14	UniSTS
Cytogenetic Map	13	q33.1	UniSTS
Cytogenetic Map	14	q21.2	UniSTS
Cytogenetic Map	4	q31.3	UniSTS
Cytogenetic Map	15	q21-q22	UniSTS
Cytogenetic Map	3	p14.3	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	13	q12.11	UniSTS
Cytogenetic Map	6	p21.2	UniSTS
Cytogenetic Map	15	q21.3	UniSTS
Cytogenetic Map	3	q21.1	UniSTS
Cytogenetic Map	6	p21.31	UniSTS
Cytogenetic Map	10	p15.1	UniSTS
Cytogenetic Map	1	q24.2	UniSTS
Cytogenetic Map	12	p12	UniSTS
Cytogenetic Map	7	p22.1	UniSTS
Cytogenetic Map	11	q24	UniSTS
Cytogenetic Map	21	q22.13	UniSTS
Cytogenetic Map	15	q22.1-q22.31	UniSTS
Cytogenetic Map	15	q22	UniSTS
Cytogenetic Map	X	q13	UniSTS
Cytogenetic Map	1	q31-q41	UniSTS
Cytogenetic Map	6	p25	UniSTS
Cytogenetic Map	14	q32.1	UniSTS
Cytogenetic Map	16	q12-q13	UniSTS
Cytogenetic Map	X	q12-q13	UniSTS
Cytogenetic Map	14	q23	UniSTS
Cytogenetic Map	12	q11-q12	UniSTS
Cytogenetic Map	1	q42.1-q43	UniSTS
Cytogenetic Map	3	q13.33	UniSTS
Cytogenetic Map	7	q31	UniSTS
Cytogenetic Map	12	q24	UniSTS
Cytogenetic Map	X	p22.11	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	2	p25.1-p24.1	UniSTS
Cytogenetic Map	8	q24.21	UniSTS
Cytogenetic Map	12	q13.1	UniSTS
Cytogenetic Map	12	q22-q23.1	UniSTS
Cytogenetic Map	11	q12.2	UniSTS
Cytogenetic Map	1	p13.2	UniSTS
Cytogenetic Map	5	q31.2-q34	UniSTS
Cytogenetic Map	11	p15.1	UniSTS
Cytogenetic Map	6	q24.2	UniSTS
Cytogenetic Map	22	q	UniSTS
Cytogenetic Map	12	q13.11-q14.3	UniSTS
Cytogenetic Map	7	p11	UniSTS
Cytogenetic Map	X	p22.12-p22.11	UniSTS
Cytogenetic Map	7	q11.21	UniSTS
Cytogenetic Map	20	q11.22-q11.23	UniSTS
Cytogenetic Map	8	q24.22	UniSTS
Cytogenetic Map	8	p22-p21.3	UniSTS
Cytogenetic Map	10	q24	UniSTS
Cytogenetic Map	1	q21.2-q21.3	UniSTS
Cytogenetic Map	1	p36.12	UniSTS
Cytogenetic Map	9	p24.1	UniSTS
Cytogenetic Map	6	q25.2-q27	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	5	p13.1	UniSTS
Cytogenetic Map	8	q11.2	UniSTS
Cytogenetic Map	3	q28-q29	UniSTS
Cytogenetic Map	7	p14-p13	UniSTS
Cytogenetic Map	12	q24.2	UniSTS
Cytogenetic Map	6	p22.2	UniSTS
Cytogenetic Map	7	q22-qter	UniSTS
Cytogenetic Map	12	q24.2-q24.31	UniSTS
Cytogenetic Map	X	q13.1	UniSTS
Cytogenetic Map	6	p25.2	UniSTS
Cytogenetic Map	1	p21	UniSTS
Cytogenetic Map	1	q32.2-q41	UniSTS
Cytogenetic Map	11	q22-q23	UniSTS
Cytogenetic Map	3	q26.33	UniSTS
Cytogenetic Map	12	q23-q24.1	UniSTS
Cytogenetic Map	5	p15.1-p14.3	UniSTS
Cytogenetic Map	16	p13.11	UniSTS
Cytogenetic Map	6	q22-q23	UniSTS
Cytogenetic Map	9	p21	UniSTS
Cytogenetic Map	6	p12.3	UniSTS
Cytogenetic Map	3	p12.1	UniSTS
Cytogenetic Map	9	q21.11	UniSTS
Cytogenetic Map	17	q24.1	UniSTS
Cytogenetic Map	10	q11.21	UniSTS
Cytogenetic Map	14	q21	UniSTS
Cytogenetic Map	11	p15	UniSTS
Cytogenetic Map	16	q22	UniSTS
Cytogenetic Map	15	q11-q13	UniSTS
Cytogenetic Map	13	q12-q14	UniSTS
Cytogenetic Map	18	q21.1	UniSTS
Cytogenetic Map	2	q24	UniSTS
Cytogenetic Map	12	p13	UniSTS
Cytogenetic Map	3	q28	UniSTS
Cytogenetic Map	7	q32.1	UniSTS
Cytogenetic Map	X	q22.2	UniSTS
Cytogenetic Map	7	p12.3	UniSTS
Cytogenetic Map	7	p15.1	UniSTS
Cytogenetic Map	2	q37.2	UniSTS
Cytogenetic Map	18	q22.3	UniSTS
Cytogenetic Map	14	q32.13	UniSTS
Cytogenetic Map	14	q22.1	UniSTS
Cytogenetic Map	16	p13.1	UniSTS
Cytogenetic Map	7	q31.3	UniSTS
Cytogenetic Map	20	q13.2-q13.3	UniSTS
Cytogenetic Map	1	p21.2	UniSTS
Cytogenetic Map	9	q21.33	UniSTS
Cytogenetic Map	14	q32.2	UniSTS
Cytogenetic Map	13	q13.3	UniSTS
Cytogenetic Map	10	p12.31	UniSTS
Cytogenetic Map	22	q11.1	UniSTS
Cytogenetic Map	5	q33.2	UniSTS
Cytogenetic Map	13	q32.2	UniSTS
Cytogenetic Map	14	q23.1	UniSTS
Cytogenetic Map	8	q21.2	UniSTS
Cytogenetic Map	2	q24.1	UniSTS
Cytogenetic Map	10	q26.13	UniSTS
Cytogenetic Map	2	q23.3	UniSTS
Cytogenetic Map	19	p13.1	UniSTS
Cytogenetic Map	15	q14-q15	UniSTS
Cytogenetic Map	1	q42.13	UniSTS
Cytogenetic Map	14	q31	UniSTS
Cytogenetic Map	7	p21.1	UniSTS
Cytogenetic Map	8	p12-p11	UniSTS
Cytogenetic Map	18	p11.2	UniSTS
Cytogenetic Map	7	p11.1	UniSTS
Cytogenetic Map	1	q31-q32	UniSTS
Cytogenetic Map	2	q12	UniSTS
Cytogenetic Map	3	p21.32	UniSTS
Cytogenetic Map	2	p24.2	UniSTS
Cytogenetic Map	2	q33-q34	UniSTS
Cytogenetic Map	6	q24.1	UniSTS
Cytogenetic Map	4	q22.1	UniSTS
Cytogenetic Map	15	q13.3	UniSTS
Cytogenetic Map	10	q26.11	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	10	q23.33	UniSTS
Cytogenetic Map	12	p12.1	UniSTS
Cytogenetic Map	7	p13-p12	UniSTS
Cytogenetic Map	X	q25	UniSTS
Cytogenetic Map	17	q11-q21	UniSTS
Cytogenetic Map	12	q23	UniSTS
Cytogenetic Map	6	p24-p22.3	UniSTS
Cytogenetic Map	14	q23.2	UniSTS
Cytogenetic Map	7	q31.1-q31.2	UniSTS
Cytogenetic Map	8	q22.2	UniSTS
Cytogenetic Map	15	q21.2	UniSTS
Cytogenetic Map	3	p26.1-p25.1	UniSTS
Cytogenetic Map	5	q35	UniSTS
Cytogenetic Map	3	q13.2	UniSTS
Cytogenetic Map	4	p15.2	UniSTS
Cytogenetic Map	6	q16.3	UniSTS
Cytogenetic Map	17	q24-q25	UniSTS
Cytogenetic Map	X	q12	UniSTS
Cytogenetic Map	X	q27.1	UniSTS
Cytogenetic Map	8	q12.3	UniSTS
Cytogenetic Map	5	q21.2	UniSTS
Cytogenetic Map	5	q15	UniSTS
Cytogenetic Map	5	q35.1	UniSTS
Cytogenetic Map	4	q13.3	UniSTS
Cytogenetic Map	4	q35.2	UniSTS
Cytogenetic Map	3	p26.1	UniSTS
Cytogenetic Map	3	p11.1	UniSTS
Cytogenetic Map	17	q21.2	UniSTS
Cytogenetic Map	2	q21.2	UniSTS
Cytogenetic Map	19	p13.13	UniSTS
Cytogenetic Map	18	q12.3	UniSTS
Cytogenetic Map	18	p11.3	UniSTS
Cytogenetic Map	17	q11.1	UniSTS
Cytogenetic Map	15	q25.1	UniSTS
Cytogenetic Map	13	q12.3	UniSTS
Cytogenetic Map	12	q23.2	UniSTS
Cytogenetic Map	12	q12-q13	UniSTS
Cytogenetic Map	12	q14	UniSTS
Cytogenetic Map	5	q33.1	UniSTS
Cytogenetic Map	2	q32-q34	UniSTS
Cytogenetic Map	16	q22.3	UniSTS
Cytogenetic Map	2	p15-p13	UniSTS
Cytogenetic Map	X	p11.4	UniSTS
Cytogenetic Map	19	q13.33-q13.41	UniSTS
Cytogenetic Map	20	p11	UniSTS
Cytogenetic Map	6	q23-q24	UniSTS
Cytogenetic Map	2	p12	UniSTS
Cytogenetic Map	2	p13	UniSTS
Cytogenetic Map	13	q11-q12	UniSTS
Cytogenetic Map	6	p12.3-p11.2	UniSTS
Cytogenetic Map	6	q16.1-q16.3	UniSTS
Cytogenetic Map	22	q11	UniSTS
Cytogenetic Map	7	q31.2	UniSTS
Cytogenetic Map	10	q21.3	UniSTS
Cytogenetic Map	3	q25.2	UniSTS
Cytogenetic Map	3	p21.1-p14.3	UniSTS
Cytogenetic Map	6	p12.1	UniSTS
Cytogenetic Map	3	q23-q24	UniSTS
Cytogenetic Map	3	q12	UniSTS
Cytogenetic Map	7	q11.1	UniSTS
Cytogenetic Map	3	q22.3	UniSTS
Cytogenetic Map	7	q21.3	UniSTS
Cytogenetic Map	4	q31.1	UniSTS
Cytogenetic Map	22	q12-q13	UniSTS
Cytogenetic Map	4	q23	UniSTS
Cytogenetic Map	X	p22.12	UniSTS
Cytogenetic Map	6	q16.1	UniSTS
Cytogenetic Map	13	q14.13	UniSTS
Cytogenetic Map	18	q21.3	UniSTS
Cytogenetic Map	9	q33.2	UniSTS
Cytogenetic Map	11	q21	UniSTS
Cytogenetic Map	8	q12	UniSTS
Cytogenetic Map	4	q28-q32	UniSTS
Cytogenetic Map	17	q24.3	UniSTS
Cytogenetic Map	6	p23	UniSTS
Cytogenetic Map	8	p11	UniSTS
Cytogenetic Map	5	q34	UniSTS
Cytogenetic Map	1	q24.3	UniSTS
Cytogenetic Map	9	q33.1	UniSTS
Cytogenetic Map	1	q23.3	UniSTS
Cytogenetic Map	2	p16.2	UniSTS
Cytogenetic Map	9	q22.31	UniSTS
Cytogenetic Map	9	p24.3	UniSTS
Cytogenetic Map	7	q35	UniSTS
Cytogenetic Map	1	p36.2	UniSTS
Cytogenetic Map	11	q22.3	UniSTS
Cytogenetic Map	16	p12	UniSTS
Cytogenetic Map	1	q22-q23	UniSTS
Cytogenetic Map	13	q22.1	UniSTS
Cytogenetic Map	2	q12.2	UniSTS
Cytogenetic Map	8	p12	UniSTS
Cytogenetic Map	4	q21	UniSTS
Cytogenetic Map	13	q12.2	UniSTS
Cytogenetic Map	9	q31-q33	UniSTS
Cytogenetic Map	6	p24.1	UniSTS
Cytogenetic Map	1	q23	UniSTS
Cytogenetic Map	11	q12-q13	UniSTS
Cytogenetic Map	11	q13.3	UniSTS
Cytogenetic Map	11	q24.2	UniSTS
Cytogenetic Map	11	q12.1	UniSTS
Cytogenetic Map	3	p26	UniSTS
Cytogenetic Map	5	q13	UniSTS
Cytogenetic Map	8	p21	UniSTS
Cytogenetic Map	19	q13.1-q13.2	UniSTS
Cytogenetic Map	1	p33-p32	UniSTS
Cytogenetic Map	7	q36.2	UniSTS
Cytogenetic Map	4	q32.3	UniSTS
Cytogenetic Map	16	p13.2	UniSTS
Cytogenetic Map	14	q32	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	10	q26.1	UniSTS
Cytogenetic Map	9	q32-q33.3	UniSTS
Cytogenetic Map	9	q22.1-q22.2	UniSTS
Cytogenetic Map	3	q26.1-q26.2	UniSTS
Cytogenetic Map	5	q31-q34	UniSTS
Cytogenetic Map	9	q33-q34	UniSTS
Cytogenetic Map	5	q11.2-q13.2	UniSTS
Cytogenetic Map	13	q32	UniSTS
Cytogenetic Map	9	q22.32	UniSTS
Cytogenetic Map	1	p36.3	UniSTS
Cytogenetic Map	1	p36.3-p36.2	UniSTS
Cytogenetic Map	4	q28.1	UniSTS
Cytogenetic Map	5	q22	UniSTS
Cytogenetic Map	12	p11.21	UniSTS
Cytogenetic Map	X	q13.3	UniSTS
Cytogenetic Map	9	q31.3	UniSTS
Cytogenetic Map	3	p26.3	UniSTS
Cytogenetic Map	2	q11.1	UniSTS
Cytogenetic Map	21	q11.2	UniSTS
Cytogenetic Map	18	q21.32	UniSTS
Cytogenetic Map	15	q26.2	UniSTS
Cytogenetic Map	12	q24.23	UniSTS
Cytogenetic Map	10	q25.3	UniSTS
Cytogenetic Map	20	q11.23	UniSTS
Cytogenetic Map	20	p12.1	UniSTS
Cytogenetic Map	2	q31.1-q31.2	UniSTS
Cytogenetic Map	X	p22.31	UniSTS
Cytogenetic Map	X	p21.3	UniSTS
Cytogenetic Map	5	q33.3	UniSTS
Cytogenetic Map	4	q28.2	UniSTS
Cytogenetic Map	3	p14.2	UniSTS
Cytogenetic Map	3	q24	UniSTS
Cytogenetic Map	2	q13	UniSTS
Cytogenetic Map	20	q13.2	UniSTS
Cytogenetic Map	14	q11.2-q12	UniSTS
Cytogenetic Map	3	p24	UniSTS
Cytogenetic Map	12	q23.3	UniSTS
Cytogenetic Map	11	q24.3	UniSTS
Cytogenetic Map	11	q14.3	UniSTS
Cytogenetic Map	10	q25.2	UniSTS
Cytogenetic Map	3	q25.1	UniSTS
Cytogenetic Map	8	q13	UniSTS
Cytogenetic Map	1	p22.2	UniSTS
Cytogenetic Map	3	p22.3	UniSTS
Cytogenetic Map	18	q11.1	UniSTS
Cytogenetic Map	8	q23.3	UniSTS
Cytogenetic Map	15	q24	UniSTS
Cytogenetic Map	11	cen-q12	UniSTS
Cytogenetic Map	11	q25	UniSTS
Cytogenetic Map	3	p22.2	UniSTS
Cytogenetic Map	X	p21.1	UniSTS
Cytogenetic Map	7	q36	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	12	q21	UniSTS
Cytogenetic Map	7	p15	UniSTS
Cytogenetic Map	7	q22-q31	UniSTS
Cytogenetic Map	11	q22	UniSTS
Cytogenetic Map	5	p15.3	UniSTS
Cytogenetic Map	20	q13.3-qter	UniSTS
Cytogenetic Map	1	p35-p34	UniSTS
Cytogenetic Map	4	p13-p12	UniSTS
Cytogenetic Map	10	q21-q22	UniSTS
Cytogenetic Map	4	q22	UniSTS
Cytogenetic Map	7	p13-p11.1	UniSTS
Cytogenetic Map	9	q31-q34	UniSTS
Cytogenetic Map	7	q21.1-q22	UniSTS
Cytogenetic Map	15	q26.1	UniSTS
Cytogenetic Map	3	q13.13-q13.2	UniSTS
Cytogenetic Map	X	p22.13	UniSTS
Cytogenetic Map	13	q12.12	UniSTS
Cytogenetic Map	13	q14.2	UniSTS
Cytogenetic Map	12	q	UniSTS
Cytogenetic Map	1	p	UniSTS
Cytogenetic Map	16	p	UniSTS
Cytogenetic Map	15	q	UniSTS
Cytogenetic Map	7	q	UniSTS
Cytogenetic Map	2	q	UniSTS
Cytogenetic Map	5	q13.1	UniSTS
Cytogenetic Map	11	p14.1	UniSTS
Cytogenetic Map	4	q32	UniSTS
Cytogenetic Map	2	p22	UniSTS
Cytogenetic Map	5	q14.3	UniSTS
Cytogenetic Map	10	p12.1	UniSTS
Cytogenetic Map	5	q23.2	UniSTS
Cytogenetic Map	2	p24.1	UniSTS
Cytogenetic Map	8	q24.13	UniSTS
Cytogenetic Map	12	p13.32	UniSTS
Cytogenetic Map	9	p21.1	UniSTS
Cytogenetic Map	9	q34.2-q34.3	UniSTS

D10S16

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	3	p24.2	UniSTS
Cytogenetic Map	21	q21.3	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	11	q24.2	UniSTS
Cytogenetic Map	5	q23.3-q31.1	UniSTS
Cytogenetic Map	7	q32	UniSTS
Cytogenetic Map	1	q21-q23	UniSTS
Cytogenetic Map	X	p11.23	UniSTS
Cytogenetic Map	2	q11.2-q12	UniSTS
Cytogenetic Map	7	p13	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	3	p22	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	2	p12	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	9	p13.3-p12	UniSTS
Cytogenetic Map	3	p21.1	UniSTS
Cytogenetic Map	5	p13.1	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	2	p25.2	UniSTS
Cytogenetic Map	5	q21-q22	UniSTS
Cytogenetic Map	2	p22.1	UniSTS
Cytogenetic Map	1	q32.3	UniSTS
Cytogenetic Map	1	p36.11	UniSTS
Cytogenetic Map	18	q12	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	3	q27.3	UniSTS
Cytogenetic Map	2	q37.3	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	20	q13.32	UniSTS
Cytogenetic Map	10	q26	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	7	q21.13	UniSTS
Cytogenetic Map	1	p33	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	9	q22.3	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	12	q13.2	UniSTS
Cytogenetic Map	22	q13.31-q13.33	UniSTS
Cytogenetic Map	1	q24.1	UniSTS
Cytogenetic Map	7	q32.2	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	1	q42.11	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	19	p13.1	UniSTS
Cytogenetic Map	11	q13.5	UniSTS
Cytogenetic Map	11	q24	UniSTS
Cytogenetic Map	2	q11.2-q12.1	UniSTS
Cytogenetic Map	3	q21.2	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	19	p13	UniSTS
Cytogenetic Map	8	p11.21	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	20	q12	UniSTS
Cytogenetic Map	2	q13	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	17	q22.2	UniSTS
Cytogenetic Map	18	q21	UniSTS
Cytogenetic Map	11	q14.2	UniSTS
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	4	q34	UniSTS
Cytogenetic Map	2	p22-p21	UniSTS
Cytogenetic Map	10	q26.3	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	2	q37.1	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	1	p36.23	UniSTS
Cytogenetic Map	7	p22.2	UniSTS
Cytogenetic Map	12	q24.13	UniSTS
Cytogenetic Map	8	p21.2	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	14	q32.12	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	1	p36.31	UniSTS
Cytogenetic Map	1	p32.3	UniSTS
Cytogenetic Map	X	q26.3	UniSTS
Cytogenetic Map	8	p23.1	UniSTS
Cytogenetic Map	6	q13	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	9	p13.2	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	9	q22.2	UniSTS
Cytogenetic Map	14	q32.33	UniSTS
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	13	q12.11	UniSTS
Cytogenetic Map	16	p13.13	UniSTS
Cytogenetic Map	11	p15.4	UniSTS
Cytogenetic Map	7	q22	UniSTS
Cytogenetic Map	3	q21	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	22	q13	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	11	p15.3-p15.1	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	7	p22.3	UniSTS
Cytogenetic Map	3	p21	UniSTS
Cytogenetic Map	X	p22.3	UniSTS
Cytogenetic Map	1	q42.3	UniSTS
Cytogenetic Map	18	q11.2	UniSTS
Cytogenetic Map	6	p24.3	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	1	q25	UniSTS
Cytogenetic Map	15	q11.2	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	3	q26	UniSTS
Cytogenetic Map	12	p12.1-p11.2	UniSTS
Cytogenetic Map	11	q23.1	UniSTS
Cytogenetic Map	13	q14.11	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	7	p15.2	UniSTS
Cytogenetic Map	1	q21	UniSTS
Cytogenetic Map	10	q11.22	UniSTS
Cytogenetic Map	5	p12	UniSTS
Cytogenetic Map	6	q21	UniSTS
Cytogenetic Map	9	q21.13	UniSTS
Cytogenetic Map	5	q13.2	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	X	q23	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	22	q11.1	UniSTS
Cytogenetic Map	16	q13	UniSTS
Cytogenetic Map	16	p	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	X	p11.3	UniSTS
Cytogenetic Map	1	q25.1	UniSTS
Cytogenetic Map	10	q23-q24	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	7	q31	UniSTS
Cytogenetic Map	6	q23.3	UniSTS
Cytogenetic Map	X	p22.2	UniSTS
Cytogenetic Map	9	q32	UniSTS
Cytogenetic Map	1	q32.1	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	4	q35.1	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	6	q25.1	UniSTS
Cytogenetic Map	14	q24.1	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	14	q23.2	UniSTS
Cytogenetic Map	15	q24.1	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	8	q23.1	UniSTS
Cytogenetic Map	2	q14.3	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	21	q22.11	UniSTS
Cytogenetic Map	5	p15.1	UniSTS
Cytogenetic Map	15	q13.1	UniSTS
Cytogenetic Map	15	q26.1	UniSTS
Cytogenetic Map	7	q32.1	UniSTS
Cytogenetic Map	8	p21.3	UniSTS
Cytogenetic Map	1	p31.1	UniSTS
Cytogenetic Map	17	qter	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	12	q22	UniSTS
Cytogenetic Map	16	q22.2	UniSTS
Cytogenetic Map	14	q32	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.32	UniSTS
Cytogenetic Map	14	q24.2	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	13	q34	UniSTS
Cytogenetic Map	10	p11.23	UniSTS
Cytogenetic Map	15	q15.2	UniSTS
Cytogenetic Map	8	p21.1	UniSTS
Cytogenetic Map	22	q12.2	UniSTS
Cytogenetic Map	15	q22.2	UniSTS
Cytogenetic Map	15	q21	UniSTS
Cytogenetic Map	6	p21.31	UniSTS
Cytogenetic Map	10	q23.1	UniSTS
Cytogenetic Map	1	p36.2	UniSTS
Cytogenetic Map	2	p16.1	UniSTS
Cytogenetic Map	22	q11.2	UniSTS
Cytogenetic Map	17	q23.3	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	20	q12-q13.12	UniSTS
Cytogenetic Map	3	q26.33	UniSTS
Cytogenetic Map	5	q31.2-q34	UniSTS
Cytogenetic Map	5	q31.2	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	5	q35.3	UniSTS
Cytogenetic Map	X	q13-q21	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	1	pter-q31.3	UniSTS
Cytogenetic Map	15	q21.1	UniSTS
Cytogenetic Map	3	q13.33	UniSTS
Cytogenetic Map	X	q13.1	UniSTS
Cytogenetic Map	3	p23-p21	UniSTS
Cytogenetic Map	11	q22-q23	UniSTS
Cytogenetic Map	1	p34.1	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	7	p22.1	UniSTS
Cytogenetic Map	17	q21.33	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	10	q11.21	UniSTS
Cytogenetic Map	16	q22	UniSTS
Cytogenetic Map	2	q24	UniSTS
Cytogenetic Map	1	q23.3	UniSTS
Cytogenetic Map	3	q13.13	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	16	p13.1	UniSTS
Cytogenetic Map	19	q13.11	UniSTS
Cytogenetic Map	X	p22.12	UniSTS
Cytogenetic Map	9	q21.33	UniSTS
Cytogenetic Map	5	q32	UniSTS
Cytogenetic Map	16	q11.2	UniSTS
Cytogenetic Map	10	p12.31	UniSTS
Cytogenetic Map	3	q25.33	UniSTS
Cytogenetic Map	8	q21.2	UniSTS
Cytogenetic Map	10	q26.13	UniSTS
Cytogenetic Map	10	q25.3	UniSTS
Cytogenetic Map	15	q14-q15	UniSTS
Cytogenetic Map	8	p11.2	UniSTS
Cytogenetic Map	1	p34.3	UniSTS
Cytogenetic Map	4	p15.2	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	7	p21.1	UniSTS
Cytogenetic Map	1	p36.32	UniSTS
Cytogenetic Map	1	p36.1-p34	UniSTS
Cytogenetic Map	4	p13	UniSTS
Cytogenetic Map	7	q31.1-q31.2	UniSTS
Cytogenetic Map	8	q22.2	UniSTS
Cytogenetic Map	15	q21.1-q21.2	UniSTS
Cytogenetic Map	16	q21	UniSTS
Cytogenetic Map	X	q12	UniSTS
Cytogenetic Map	7	q36.1	UniSTS
Cytogenetic Map	7	p14.1	UniSTS
Cytogenetic Map	6	p23	UniSTS
Cytogenetic Map	3	p11.1	UniSTS
Cytogenetic Map	15	q21.3	UniSTS
Cytogenetic Map	13	q12	UniSTS
Cytogenetic Map	12	q23.2	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	16	q22.3	UniSTS
Cytogenetic Map	X	q21	UniSTS
Cytogenetic Map	15	q15	UniSTS
Cytogenetic Map	4	q25	UniSTS
Cytogenetic Map	3	q22.1	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	11	q14.3	UniSTS
Cytogenetic Map	10	q21.3	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	15	q24.2	UniSTS
Cytogenetic Map	2	p14	UniSTS
Cytogenetic Map	7	q11.1	UniSTS
Cytogenetic Map	6	p21	UniSTS
Cytogenetic Map	2	p25.1-p24.1	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	4	q13.3	UniSTS
Cytogenetic Map	12	p11.21	UniSTS
Cytogenetic Map	18	q21.3	UniSTS
Cytogenetic Map	17	p13	UniSTS
Cytogenetic Map	8	q12	UniSTS
Cytogenetic Map	2	q35	UniSTS
Cytogenetic Map	21	q22.13	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	17	q24.3	UniSTS
Cytogenetic Map	1	p21	UniSTS
Cytogenetic Map	X	q24	UniSTS
Cytogenetic Map	2	q34	UniSTS
Cytogenetic Map	8	p11.23	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	9	q34.3	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	9	q33.3	UniSTS
Cytogenetic Map	16	p12	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	20	q11.23	UniSTS
Cytogenetic Map	12	q15	UniSTS
Cytogenetic Map	2	q12.2	UniSTS
Cytogenetic Map	8	p12	UniSTS
Cytogenetic Map	7	q22.3	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	4	q35	UniSTS
Cytogenetic Map	19	q13.1-q13.2	UniSTS
Cytogenetic Map	16	p13.12	UniSTS
Cytogenetic Map	9	q34.1	UniSTS
Cytogenetic Map	7	q36.2	UniSTS
Cytogenetic Map	3	p23	UniSTS
Cytogenetic Map	6	p25	UniSTS
Cytogenetic Map	9	q22.1-q22.2	UniSTS
Cytogenetic Map	3	q26.1-q26.2	UniSTS
Cytogenetic Map	5	q31-q34	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	12	p13	UniSTS
Cytogenetic Map	4	q26	UniSTS
Cytogenetic Map	4	p15.3	UniSTS
Cytogenetic Map	2	q33.1	UniSTS
Cytogenetic Map	15	q15.1	UniSTS
Cytogenetic Map	1	p32-p31	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	4	q22.1	UniSTS
Cytogenetic Map	3	q13.2	UniSTS
Cytogenetic Map	2	q33.3	UniSTS
Cytogenetic Map	8	p22	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	18	q21.32	UniSTS
Cytogenetic Map	15	q26.3	UniSTS
Cytogenetic Map	12	q14.2	UniSTS
Cytogenetic Map	2	q31.1-q31.2	UniSTS
Cytogenetic Map	12	q13.11	UniSTS
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	6	p12.3	UniSTS
Cytogenetic Map	6	q22.32	UniSTS
Cytogenetic Map	5	q15	UniSTS
Cytogenetic Map	3	p14.2	UniSTS
Cytogenetic Map	3	p25.1	UniSTS
Cytogenetic Map	3	q27.1	UniSTS
Cytogenetic Map	2	q36.1	UniSTS
Cytogenetic Map	2	q37	UniSTS
Cytogenetic Map	19	q13.31	UniSTS
Cytogenetic Map	4	q23	UniSTS
Cytogenetic Map	16	q24.3	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	10	q22.1	UniSTS
Cytogenetic Map	18	q11.1	UniSTS
Cytogenetic Map	16	q23.2	UniSTS
Cytogenetic Map	12	q13	UniSTS
Cytogenetic Map	18	q21.1	UniSTS
Cytogenetic Map	12	q12-q13	UniSTS
Cytogenetic Map	9	p22.3	UniSTS
Cytogenetic Map	6	p21.2	UniSTS
Cytogenetic Map	6	p22.1	UniSTS
Cytogenetic Map	11	p15.1	UniSTS
Cytogenetic Map	19	qter	UniSTS
Cytogenetic Map	20	q13.3-qter	UniSTS
Cytogenetic Map	12	q14.1	UniSTS
Cytogenetic Map	7	p11	UniSTS
Cytogenetic Map	7	p15	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	16	p12.3	UniSTS
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	3	p21.3	UniSTS
Cytogenetic Map	13	q14	UniSTS
Cytogenetic Map	17	p	UniSTS
Cytogenetic Map	11	p14.1	UniSTS
Cytogenetic Map	2	p13.2	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	20	q13.12	UniSTS
Cytogenetic Map	13	q22.1	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	14	q23.3	UniSTS
Cytogenetic Map	3	q26.2	UniSTS

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2439	2788	2253	4974	1726	2351	6	624	1951	465	2270	7306	6472	53	3734	1	852	1744	1617	175	1


RefSeq Transcripts	NG_017040	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_002496	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AF038406	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK002110	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK223114	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK302449	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK314546	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AP002807	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC119753	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC119754	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471076	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068267	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB498707	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	U65579	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	Y16005	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000313468 ⟹ ENSP00000315774

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,030,681 - 68,036,644 (+)	Ensembl

Ensembl Acc Id:

ENST00000432321

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,030,617 - 68,033,730 (+)	Ensembl

Ensembl Acc Id:

ENST00000453471 ⟹ ENSP00000403972

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,030,665 - 68,033,284 (+)	Ensembl

Ensembl Acc Id:

ENST00000524810 ⟹ ENSP00000434283

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,033,141 - 68,036,644 (+)	Ensembl

Ensembl Acc Id:

ENST00000525419 ⟹ ENSP00000433521

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,030,760 - 68,036,348 (+)	Ensembl

Ensembl Acc Id:

ENST00000525628 ⟹ ENSP00000432968

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,030,966 - 68,033,241 (+)	Ensembl

Ensembl Acc Id:

ENST00000526339 ⟹ ENSP00000436287

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,030,743 - 68,036,514 (+)	Ensembl

Ensembl Acc Id:

ENST00000526446 ⟹ ENSP00000433645

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,030,684 - 68,036,537 (+)	Ensembl

Ensembl Acc Id:

ENST00000526542

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,033,852 - 68,036,301 (+)	Ensembl

Ensembl Acc Id:

ENST00000528492 ⟹ ENSP00000432848

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,030,688 - 68,036,639 (+)	Ensembl

Ensembl Acc Id:

ENST00000529645 ⟹ ENSP00000431293

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,032,161 - 68,035,683 (+)	Ensembl

Ensembl Acc Id:

ENST00000531228 ⟹ ENSP00000433054

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,030,743 - 68,033,223 (+)	Ensembl

Ensembl Acc Id:

ENST00000531282

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,036,029 - 68,036,644 (+)	Ensembl

Ensembl Acc Id:

ENST00000531796

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,030,653 - 68,032,685 (+)	Ensembl

Ensembl Acc Id:

ENST00000532399

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	68,030,713 - 68,035,278 (+)	Ensembl

RefSeq Acc Id:

NM_002496 ⟹ NP_002487

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	68,030,681 - 68,036,644 (+)	NCBI
GRCh37	11	67,798,084 - 67,804,114 (+)	ENTREZGENE
Build 36	11	67,554,685 - 67,560,690 (+)	NCBI Archive
HuRef	11	64,133,431 - 64,139,457 (+)	ENTREZGENE
CHM1_1	11	67,681,851 - 67,687,870 (+)	NCBI
T2T-CHM13v2.0	11	68,034,333 - 68,040,285 (+)	NCBI

Sequence:

show sequence

GCCTCCCGATTGACTGGCCTGCTTGGCAAGGCAAGTAGCGGCGGCGCTTCAAGATGCGCTGCCTGACCACGCCTATGCTGCTGCGGGCCCTGGCCCAGGCTGCACGTGCAGGACCTCCTGGTGGCCGG
AGCCTCCACAGCAGTGCAGTGGCAGCCACCTACAAGTATGTGAACATGCAGGATCCCGAGATGGACATGAAGTCAGTGACTGACCGGGCAGCCCGCACCCTGCTGTGGACTGAGCTCTTCCGAGGCCT
GGGCATGACCCTGAGCTACCTGTTCCGGGAACCGGCCACCATCAACTACCCGTTCGAGAAGGGCCCGCTGAGCCCTCGCTTCCGTGGGGAGCATGCGCTGCGCCGGTACCCATCCGGGGAGGAGCGTT
GCATTGCCTGCAAGCTCTGCGAGGCCATCTGCCCCGCCCAGGCCATCACCATCGAGGCTGAGCCAAGAGCTGATGGCAGCCGCCGGACCACCCGCTATGACATCGACATGACCAAGTGCATCTACTGC
GGCTTCTGCCAGGAGGCCTGTCCCGTGGATGCCATCGTCGAGGGCCCCAACTTTGAGTTCTCCACGGAGACCCATGAGGAGCTGCTGTACAACAAGGAGAAGTTGCTCAACAACGGGGACAAGTGGGA
GGCCGAGATCGCCGCCAACATCCAGGCTGACTACTTGTATCGGTGACGCCCCACCGGCCCGCAGCCCCTGCTGCCCAATAAAACCACTCCGACCCCA

hide sequence


Protein RefSeqs	NP_002487	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAB51776	(Get FASTA)	NCBI Sequence Viewer
	AAC34273	(Get FASTA)	NCBI Sequence Viewer
	AAI19754	(Get FASTA)	NCBI Sequence Viewer
	AAI19755	(Get FASTA)	NCBI Sequence Viewer
	BAD96834	(Get FASTA)	NCBI Sequence Viewer
	BAG37133	(Get FASTA)	NCBI Sequence Viewer
	BAG63745	(Get FASTA)	NCBI Sequence Viewer
	EAW74685	(Get FASTA)	NCBI Sequence Viewer
	EAW74686	(Get FASTA)	NCBI Sequence Viewer
	EAW74687	(Get FASTA)	NCBI Sequence Viewer
	EAW74688	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000315774
	ENSP00000315774.5
GenBank Protein	O00217	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_002487 ⟸ NM_002496
- Peptide Label:	precursor
- UniProtKB:	B2RB86 (UniProtKB/Swiss-Prot), Q0VDA8 (UniProtKB/Swiss-Prot), O00217 (UniProtKB/Swiss-Prot), Q53G17 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRCLTTPMLLRALAQAARAGPPGGRSLHSSAVAATYKYVNMQDPEMDMKSVTDRAARTLLWTELFRGLGMTLSYLFREPATINYPFEKGPLSPRFRGEHALRRYPSGEERCIACKLCEAICPAQAITI EAEPRADGSRRTTRYDIDMTKCIYCGFCQEACPVDAIVEGPNFEFSTETHEELLYNKEKLLNNGDKWEAEIAANIQADYLYR hide sequence

Ensembl Acc Id:

ENSP00000433054 ⟸ ENST00000531228

Ensembl Acc Id:

ENSP00000403972 ⟸ ENST00000453471

Ensembl Acc Id:

ENSP00000315774 ⟸ ENST00000313468

Ensembl Acc Id:

ENSP00000434283 ⟸ ENST00000524810

Protein Domains

4Fe-4S ferredoxin-type

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-O00217-F1-model_v2	AlphaFold	O00217	1-210	view protein structure

RGD ID:

6789155

Promoter ID:

HG_KWN:13504

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4

Transcripts:

NM_002496, UC009YSB.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	67,553,666 - 67,554,897 (+)	MPROMDB

RGD ID:

6851894

Promoter ID:

EP73753

Type:

initiation region

Name:

HS_NDUFS8

Description:

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

SO ACC ID:

SO:0000170

Source:

EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

NEDO full length human cDNA sequencing project.; Oligo-capping

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	67,554,735 - 67,554,795	EPD

RGD ID:

6789157

Promoter ID:

HG_KWN:13505

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid

Transcripts:

UC009YSC.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	67,556,011 - 67,556,511 (+)	MPROMDB

RGD ID:

7221309

Promoter ID:

EPDNEW_H16400

Type:

initiation region

Name:

NDUFS8_1

Description:

NADH:ubiquinone oxidoreductase core subunit S8

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H16401

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	68,030,692 - 68,030,752	EPDNEW

RGD ID:

7221311

Promoter ID:

EPDNEW_H16401

Type:

multiple initiation site

Name:

NDUFS8_2

Description:

NADH:ubiquinone oxidoreductase core subunit S8

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H16400

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	68,032,139 - 68,032,199	EPDNEW

Database	Acc Id	Source(s)
COSMIC	NDUFS8	COSMIC
Ensembl Genes	ENSG00000110717	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000313468	ENTREZGENE
	ENST00000313468.10	UniProtKB/Swiss-Prot
Gene3D-CATH	3.30.70.3270	UniProtKB/Swiss-Prot
GTEx	ENSG00000110717	GTEx
HGNC ID	HGNC:7715	ENTREZGENE
Human Proteome Map	NDUFS8	Human Proteome Map
InterPro	4Fe4S_Fe-S-bd	UniProtKB/Swiss-Prot
	4Fe4S_Fe_S_CS	UniProtKB/Swiss-Prot
	NADH_quinone_OxRdtase_chainI	UniProtKB/Swiss-Prot
KEGG Report	hsa:4728	UniProtKB/Swiss-Prot
NCBI Gene	4728	ENTREZGENE
OMIM	602141	OMIM
PANTHER	NADH DEHYDROGENASE [UBIQUINONE] IRON-SULFUR PROTEIN 8, MITOCHONDRIAL	UniProtKB/Swiss-Prot
	PTHR10849	UniProtKB/Swiss-Prot
Pfam	Fer4_7	UniProtKB/Swiss-Prot
PharmGKB	PA31525	PharmGKB
PROSITE	4FE4S_FER_1	UniProtKB/Swiss-Prot
	4FE4S_FER_2	UniProtKB/Swiss-Prot
Superfamily-SCOP	4Fe-4S ferredoxins	UniProtKB/Swiss-Prot
UniProt	B2RB86	ENTREZGENE
	E9PJY7_HUMAN	UniProtKB/TrEMBL
	E9PKH6_HUMAN	UniProtKB/TrEMBL
	E9PN51_HUMAN	UniProtKB/TrEMBL
	E9PPW7_HUMAN	UniProtKB/TrEMBL
	F8W9K7_HUMAN	UniProtKB/TrEMBL
	H0YCB2_HUMAN	UniProtKB/TrEMBL
	H0YDT4_HUMAN	UniProtKB/TrEMBL
	NDUS8_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
	Q08E91_HUMAN	UniProtKB/TrEMBL
	Q0VDA8	ENTREZGENE
	Q53G17	ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary	B2RB86	UniProtKB/Swiss-Prot
	Q0VDA8	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-11-24	NDUFS8	NADH:ubiquinone oxidoreductase core subunit S8		NADH dehydrogenase (ubiquinone) Fe-S protein 8, 23kDa (NADH-coenzyme Q reductase)	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailable


InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailable


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
		Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

Imported Disease Annotations - OMIM

Imported Annotations - KEGG (archival)

Imported Human Phenotype Annotations - HPO

Imported Human Phenotype Annotations - ClinVar

Send us a Message

Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

Imported Disease Annotations - OMIM

Imported Annotations - KEGG (archival)

Imported Human Phenotype Annotations - HPO

Imported Human Phenotype Annotations - ClinVar