DUOX1 (dual oxidase 1) - Rat Genome Database

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Gene: DUOX1 (dual oxidase 1) Homo sapiens
Analyze
Symbol: DUOX1
Name: dual oxidase 1
RGD ID: 1345114
HGNC Page HGNC:3062
Description: Predicted to enable superoxide-generating NAD(P)H oxidase activity. Involved in several processes, including hydrogen peroxide biosynthetic process; positive regulation of wound healing; and response to cAMP. Located in several cellular components, including cell leading edge; cell surface; and endoplasmic reticulum.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: flavoprotein NADPH oxidase; large NOX 1; LNOX1; long NOX 1; MGC138840; MGC138841; NADPH thyroid oxidase 1; nicotinamide adenine dinucleotide phosphate oxidase; NOXEF1; THOX1; thyroid oxidase 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381545,129,994 - 45,165,574 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1545,129,933 - 45,165,576 (+)EnsemblGRCh38hg38GRCh38
GRCh371545,422,192 - 45,457,772 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361543,209,484 - 43,245,066 (+)NCBINCBI36Build 36hg18NCBI36
Build 341543,209,483 - 43,245,066NCBI
Celera1522,313,628 - 22,349,058 (+)NCBICelera
Cytogenetic Map15q21.1NCBI
HuRef1522,246,405 - 22,281,983 (+)NCBIHuRef
CHM1_11545,540,525 - 45,576,452 (+)NCBICHM1_1
T2T-CHM13v2.01542,938,016 - 42,973,584 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Plasma proteomic analysis of patients infected with H1N1 influenza virus. Choi S, etal., Proteomics. 2014 Aug;14(16):1933-42. doi: 10.1002/pmic.201400030. Epub 2014 Jul 9.
2. Cloning of two human thyroid cDNAs encoding new members of the NADPH oxidase family. De Deken X, etal., J Biol Chem 2000 Jul 28;275(30):23227-33.
3. Role and cellular source of nicotinamide adenine dinucleotide phosphate oxidase in hepatic fibrosis. De Minicis S, etal., Hepatology. 2010 Oct;52(4):1420-30. doi: 10.1002/hep.23804.
4. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
5. SMPDB Annotation Import Pipeline Pipeline to import SMPDB annotations from SMPDB into RGD
6. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
7. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8889548   PMID:10601291   PMID:11443211   PMID:11514595   PMID:11753072   PMID:11762710   PMID:11822874   PMID:12477932   PMID:12482831   PMID:12824283   PMID:14702039   PMID:15062544  
PMID:15210697   PMID:15489334   PMID:15561711   PMID:15640347   PMID:15677770   PMID:15972824   PMID:16111680   PMID:16478776   PMID:16608528   PMID:17135261   PMID:17337509   PMID:18177232  
PMID:18281478   PMID:18606821   PMID:19144650   PMID:19339556   PMID:19460756   PMID:19730683   PMID:19952225   PMID:20056178   PMID:20085766   PMID:20346360   PMID:20682913   PMID:20709024  
PMID:21389273   PMID:21411736   PMID:21873635   PMID:21915726   PMID:22523549   PMID:22814254   PMID:23225414   PMID:23281318   PMID:23349873   PMID:23362256   PMID:23691121   PMID:24128054  
PMID:24161126   PMID:24164541   PMID:24332816   PMID:24624333   PMID:25164816   PMID:25586178   PMID:25848056   PMID:26597162   PMID:27079415   PMID:27108801   PMID:27110716   PMID:27197753  
PMID:27262981   PMID:28633507   PMID:28982074   PMID:29405261   PMID:29849884   PMID:30021884   PMID:30375286   PMID:30575818   PMID:31706280   PMID:32393512   PMID:32513696   PMID:32764116  
PMID:33301419   PMID:33309621   PMID:33420071   PMID:33563887   PMID:33961781   PMID:34784249   PMID:36625485   PMID:36835420   PMID:37536262  


Genomics

Comparative Map Data
DUOX1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381545,129,994 - 45,165,574 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1545,129,933 - 45,165,576 (+)EnsemblGRCh38hg38GRCh38
GRCh371545,422,192 - 45,457,772 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361543,209,484 - 43,245,066 (+)NCBINCBI36Build 36hg18NCBI36
Build 341543,209,483 - 43,245,066NCBI
Celera1522,313,628 - 22,349,058 (+)NCBICelera
Cytogenetic Map15q21.1NCBI
HuRef1522,246,405 - 22,281,983 (+)NCBIHuRef
CHM1_11545,540,525 - 45,576,452 (+)NCBICHM1_1
T2T-CHM13v2.01542,938,016 - 42,973,584 (+)NCBIT2T-CHM13v2.0
Duox1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392122,143,525 - 122,178,454 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2122,146,153 - 122,178,453 (+)EnsemblGRCm39 Ensembl
GRCm382122,313,010 - 122,347,972 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2122,315,672 - 122,347,972 (+)EnsemblGRCm38mm10GRCm38
MGSCv372122,141,408 - 122,173,708 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv362122,005,116 - 122,039,413 (+)NCBIMGSCv36mm8
MGSCv362123,286,960 - 123,321,338 (+)NCBIMGSCv36mm8
Celera2123,465,585 - 123,497,811 (+)NCBICelera
Cytogenetic Map2E5NCBI
cM Map260.63NCBI
Duox1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83129,714,125 - 129,749,186 (+)NCBIGRCr8
mRatBN7.23109,260,526 - 109,295,588 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl3109,262,397 - 109,295,563 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx3112,936,198 - 112,969,389 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.03121,531,719 - 121,564,910 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.03119,192,095 - 119,225,286 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.03114,251,794 - 114,286,827 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl3114,253,637 - 114,286,802 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03120,791,108 - 120,826,222 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43109,095,250 - 109,128,415 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.13109,000,832 - 109,033,988 (+)NCBI
Celera3108,160,238 - 108,192,976 (+)NCBICelera
Cytogenetic Map3q35NCBI
Duox1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554098,229,199 - 8,255,003 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554098,228,754 - 8,256,575 (-)NCBIChiLan1.0ChiLan1.0
DUOX1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21634,370,156 - 34,405,770 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11538,548,314 - 38,585,332 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01524,077,557 - 24,113,206 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11542,432,792 - 42,466,446 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1542,431,595 - 42,467,943 (+)Ensemblpanpan1.1panPan2
DUOX1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13011,556,024 - 11,588,203 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl3011,556,024 - 11,588,202 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3011,612,190 - 11,644,063 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.03011,692,796 - 11,724,747 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl3011,692,815 - 11,724,746 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.13011,599,266 - 11,631,208 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.03011,721,544 - 11,753,719 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.03011,841,362 - 11,873,559 (+)NCBIUU_Cfam_GSD_1.0
Duox1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440864089,998,522 - 90,032,014 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364717,848,472 - 7,879,390 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364717,848,472 - 7,881,417 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
DUOX1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1126,572,492 - 126,603,082 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11126,572,533 - 126,603,084 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21141,171,519 - 141,206,750 (-)NCBISscrofa10.2Sscrofa10.2susScr3
DUOX1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12638,038,093 - 38,073,993 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2638,038,771 - 38,072,023 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666048102,986,753 - 103,021,591 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Duox1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473114,081,245 - 14,107,104 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473114,080,670 - 14,107,532 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in DUOX1
69 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_017434.4(DUOX1):c.2113A>G (p.Lys705Glu) single nucleotide variant Malignant melanoma [RCV000070800] Chr15:45144212 [GRCh38]
Chr15:45436410 [GRCh37]
Chr15:43223702 [NCBI36]
Chr15:15q21.1
not provided
NM_017434.4(DUOX1):c.943G>A (p.Asp315Asn) single nucleotide variant Malignant melanoma [RCV000062871] Chr15:45136546 [GRCh38]
Chr15:45428744 [GRCh37]
Chr15:43216036 [NCBI36]
Chr15:15q21.1
not provided
NM_017434.4(DUOX1):c.1769G>A (p.Gly590Asp) single nucleotide variant Malignant melanoma [RCV000062872] Chr15:45142059 [GRCh38]
Chr15:45434257 [GRCh37]
Chr15:43221549 [NCBI36]
Chr15:15q21.1
not provided
GRCh38/hg38 15q21.1(chr15:44765914-45476854)x3 copy number gain See cases [RCV000139024] Chr15:44765914..45476854 [GRCh38]
Chr15:45058112..45769052 [GRCh37]
Chr15:42845404..43556344 [NCBI36]
Chr15:15q21.1
uncertain significance
GRCh38/hg38 15q21.1(chr15:45026980-45579878)x3 copy number gain See cases [RCV000143255] Chr15:45026980..45579878 [GRCh38]
Chr15:45319178..45872076 [GRCh37]
Chr15:43106470..43659368 [NCBI36]
Chr15:15q21.1
uncertain significance
GRCh38/hg38 15q21.1(chr15:45032714-45592481)x3 copy number gain See cases [RCV000143502] Chr15:45032714..45592481 [GRCh38]
Chr15:45324912..45884679 [GRCh37]
Chr15:43112204..43671971 [NCBI36]
Chr15:15q21.1
uncertain significance
GRCh37/hg19 15q21.1(chr15:45059827-45725363)x3 copy number gain See cases [RCV000239920] Chr15:45059827..45725363 [GRCh37]
Chr15:15q21.1
uncertain significance
GRCh37/hg19 15q15.3-21.1(chr15:44484701-47475522)x1 copy number loss See cases [RCV000240380] Chr15:44484701..47475522 [GRCh37]
Chr15:15q15.3-21.1
uncertain significance
GRCh37/hg19 15q15.1-26.3(chr15:41745084-102354798)x4 copy number gain See cases [RCV000447123] Chr15:41745084..102354798 [GRCh37]
Chr15:15q15.1-26.3
pathogenic
GRCh37/hg19 15q15.2-21.2(chr15:42850434-49592633)x1 copy number loss See cases [RCV000447035] Chr15:42850434..49592633 [GRCh37]
Chr15:15q15.2-21.2
pathogenic
GRCh37/hg19 15q21.1(chr15:45056077-45772114)x3 copy number gain See cases [RCV000447851] Chr15:45056077..45772114 [GRCh37]
Chr15:15q21.1
uncertain significance
GRCh37/hg19 15q11.2-26.3(chr15:20733395-102511616)x4 copy number gain See cases [RCV000447765] Chr15:20733395..102511616 [GRCh37]
Chr15:15q11.2-26.3
pathogenic
GRCh37/hg19 15q15.1-21.2(chr15:41689327-52446981)x1 copy number loss See cases [RCV000448968] Chr15:41689327..52446981 [GRCh37]
Chr15:15q15.1-21.2
pathogenic
NM_175940.3(DUOX1):c.3524+15_3524+16del deletion not specified [RCV000455079] Chr15:45153494..45153495 [GRCh38]
Chr15:45445692..45445693 [GRCh37]
Chr15:15q21.1
benign
GRCh37/hg19 15q21.1(chr15:45056077-45772114)x3 copy number gain See cases [RCV000510282] Chr15:45056077..45772114 [GRCh37]
Chr15:15q21.1
uncertain significance
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)x3 copy number gain See cases [RCV000510717] Chr15:22770422..102429112 [GRCh37]
Chr15:15q11.2-26.3
pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112) copy number gain See cases [RCV000512019] Chr15:22770422..102429112 [GRCh37]
Chr15:15q11.2-26.3
pathogenic
NM_175940.3(DUOX1):c.3949G>A (p.Glu1317Lys) single nucleotide variant Inborn genetic diseases [RCV003252079] Chr15:45161830 [GRCh38]
Chr15:45454028 [GRCh37]
Chr15:15q21.1
uncertain significance
Single allele duplication not provided [RCV000677926] Chr15:31115047..102354857 [GRCh37]
Chr15:15q13.2-26.3
pathogenic
GRCh37/hg19 15q21.1(chr15:45360338-45437443)x2 copy number loss not provided [RCV000659227] Chr15:45360338..45437443 [GRCh37]
Chr15:15q21.1
likely pathogenic
GRCh37/hg19 15q15.3-21.3(chr15:43759773-53252240)x1 copy number loss not provided [RCV000683686] Chr15:43759773..53252240 [GRCh37]
Chr15:15q15.3-21.3
pathogenic
NC_000015.9:g.(?_45152372)_(45670671_?)dup duplication Arginine:glycine amidinotransferase deficiency [RCV000708477] Chr15:44860174..45378473 [GRCh38]
Chr15:45152372..45670671 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3087G>C (p.Gln1029His) single nucleotide variant not provided [RCV001572691] Chr15:45151946 [GRCh38]
Chr15:45444144 [GRCh37]
Chr15:15q21.1
uncertain significance
GRCh37/hg19 15q21.1(chr15:45142419-45889706)x3 copy number gain not provided [RCV000751298] Chr15:45142419..45889706 [GRCh37]
Chr15:15q21.1
benign
GRCh37/hg19 15q11.1-26.3(chr15:20016811-102493540)x3 copy number gain not provided [RCV000751155] Chr15:20016811..102493540 [GRCh37]
Chr15:15q11.1-26.3
pathogenic
GRCh37/hg19 15q11.1-26.3(chr15:20071673-102461162)x3 copy number gain not provided [RCV000751156] Chr15:20071673..102461162 [GRCh37]
Chr15:15q11.1-26.3
pathogenic
NM_175940.3(DUOX1):c.4242T>C (p.Cys1414=) single nucleotide variant not provided [RCV000891753] Chr15:45162371 [GRCh38]
Chr15:45454569 [GRCh37]
Chr15:15q21.1
benign
NM_175940.3(DUOX1):c.851T>C (p.Ile284Thr) single nucleotide variant Inborn genetic diseases [RCV003267447] Chr15:45135935 [GRCh38]
Chr15:45428133 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.2383C>T (p.Arg795Trp) single nucleotide variant not provided [RCV000950795] Chr15:45147493 [GRCh38]
Chr15:45439691 [GRCh37]
Chr15:15q21.1
benign
NM_175940.3(DUOX1):c.1134T>C (p.Ala378=) single nucleotide variant not provided [RCV000969658] Chr15:45139086 [GRCh38]
Chr15:45431284 [GRCh37]
Chr15:15q21.1
benign
NM_175940.3(DUOX1):c.1389+8G>A single nucleotide variant not provided [RCV000883409] Chr15:45139607 [GRCh38]
Chr15:45431805 [GRCh37]
Chr15:15q21.1
benign
NM_175940.3(DUOX1):c.1821G>A (p.Leu607=) single nucleotide variant not provided [RCV000883411] Chr15:45142111 [GRCh38]
Chr15:45434309 [GRCh37]
Chr15:15q21.1
benign
NM_175940.3(DUOX1):c.1081C>T (p.Leu361Phe) single nucleotide variant Inborn genetic diseases [RCV003271175] Chr15:45137982 [GRCh38]
Chr15:45430180 [GRCh37]
Chr15:15q21.1
uncertain significance
GRCh37/hg19 15q21.1(chr15:45063803-45772378)x3 copy number gain not provided [RCV000846392] Chr15:45063803..45772378 [GRCh37]
Chr15:15q21.1
uncertain significance
NC_000015.9:g.(?_45152372)_(45670651_?)dup duplication Arginine:glycine amidinotransferase deficiency [RCV003107422] Chr15:45152372..45670651 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1859G>A (p.Arg620Gln) single nucleotide variant Inborn genetic diseases [RCV003241733] Chr15:45143226 [GRCh38]
Chr15:45435424 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1797C>T (p.Ile599=) single nucleotide variant not provided [RCV000883410] Chr15:45142087 [GRCh38]
Chr15:45434285 [GRCh37]
Chr15:15q21.1
benign
NM_175940.3(DUOX1):c.3567C>T (p.Thr1189=) single nucleotide variant not provided [RCV000935632] Chr15:45153993 [GRCh38]
Chr15:45446191 [GRCh37]
Chr15:15q21.1
benign
NM_175940.3(DUOX1):c.3522T>C (p.Asp1174=) single nucleotide variant not provided [RCV000913263] Chr15:45153477 [GRCh38]
Chr15:45445675 [GRCh37]
Chr15:15q21.1
likely benign
NM_175940.3(DUOX1):c.4534-9C>T single nucleotide variant not provided [RCV000913264] Chr15:45164770 [GRCh38]
Chr15:45456968 [GRCh37]
Chr15:15q21.1
likely benign
NM_175940.3(DUOX1):c.3282T>C (p.Ser1094=) single nucleotide variant not provided [RCV000957274] Chr15:45152374 [GRCh38]
Chr15:45444572 [GRCh37]
Chr15:15q21.1
benign
NM_175940.3(DUOX1):c.1389+9G>T single nucleotide variant not provided [RCV001695287] Chr15:45139608 [GRCh38]
Chr15:45431806 [GRCh37]
Chr15:15q21.1
benign
GRCh37/hg19 15q21.1(chr15:45056077-45772378)x3 copy number gain not provided [RCV001259210] Chr15:45056077..45772378 [GRCh37]
Chr15:15q21.1
uncertain significance
NC_000015.9:g.(?_44855319)_(45898712_?)dup duplication Arginine:glycine amidinotransferase deficiency [RCV001304383] Chr15:44855319..45898712 [GRCh37]
Chr15:15q21.1
uncertain significance
NC_000015.9:g.(?_32964879)_(91358519_?)dup duplication Bloom syndrome [RCV001343104]|Familial colorectal cancer [RCV001325176] Chr15:32964879..91358519 [GRCh37]
Chr15:15q13.3-26.1
uncertain significance
NM_175940.3(DUOX1):c.2468T>C (p.Met823Thr) single nucleotide variant not provided [RCV001726953] Chr15:45147578 [GRCh38]
Chr15:45439776 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3532C>T (p.Leu1178Phe) single nucleotide variant not provided [RCV001733439] Chr15:45153958 [GRCh38]
Chr15:45446156 [GRCh37]
Chr15:15q21.1
benign
GRCh37/hg19 15q21.1(chr15:45056077-45772114) copy number gain not specified [RCV002052469] Chr15:45056077..45772114 [GRCh37]
Chr15:15q21.1
uncertain significance
GRCh37/hg19 15q15.2-21.2(chr15:42850434-49592633) copy number loss not specified [RCV002052466] Chr15:42850434..49592633 [GRCh37]
Chr15:15q15.2-21.2
pathogenic
NC_000015.9:g.(?_45152372)_(45457099_?)dup duplication not provided [RCV001967757] Chr15:45152372..45457099 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.2513G>A (p.Arg838Gln) single nucleotide variant Inborn genetic diseases [RCV003254892] Chr15:45147623 [GRCh38]
Chr15:45439821 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1283G>A (p.Arg428Gln) single nucleotide variant Inborn genetic diseases [RCV002777041] Chr15:45139493 [GRCh38]
Chr15:45431691 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1733C>T (p.Ala578Val) single nucleotide variant Inborn genetic diseases [RCV002906570] Chr15:45142023 [GRCh38]
Chr15:45434221 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3107G>A (p.Arg1036His) single nucleotide variant Inborn genetic diseases [RCV002973541] Chr15:45151966 [GRCh38]
Chr15:45444164 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.4463G>A (p.Arg1488His) single nucleotide variant Inborn genetic diseases [RCV002969819] Chr15:45163848 [GRCh38]
Chr15:45456046 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.2059C>G (p.Gln687Glu) single nucleotide variant Inborn genetic diseases [RCV002728270] Chr15:45144158 [GRCh38]
Chr15:45436356 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3376G>C (p.Ala1126Pro) single nucleotide variant Inborn genetic diseases [RCV002860203] Chr15:45152468 [GRCh38]
Chr15:45444666 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.610G>A (p.Ala204Thr) single nucleotide variant Inborn genetic diseases [RCV002859152] Chr15:45135588 [GRCh38]
Chr15:45427786 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.2096G>A (p.Arg699His) single nucleotide variant Inborn genetic diseases [RCV002686887] Chr15:45144195 [GRCh38]
Chr15:45436393 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.2839A>G (p.Ile947Val) single nucleotide variant Inborn genetic diseases [RCV002945593] Chr15:45150652 [GRCh38]
Chr15:45442850 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.2788G>A (p.Glu930Lys) single nucleotide variant Inborn genetic diseases [RCV002682296] Chr15:45148417 [GRCh38]
Chr15:45440615 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.337G>A (p.Val113Met) single nucleotide variant Inborn genetic diseases [RCV002968958] Chr15:45135133 [GRCh38]
Chr15:45427331 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.4133A>G (p.His1378Arg) single nucleotide variant Inborn genetic diseases [RCV002778190] Chr15:45162262 [GRCh38]
Chr15:45454460 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.448C>T (p.Arg150Cys) single nucleotide variant Inborn genetic diseases [RCV002818606] Chr15:45135244 [GRCh38]
Chr15:45427442 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3646C>T (p.Arg1216Cys) single nucleotide variant Inborn genetic diseases [RCV002821228] Chr15:45155873 [GRCh38]
Chr15:45448071 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3448G>A (p.Val1150Met) single nucleotide variant Inborn genetic diseases [RCV002758060] Chr15:45153403 [GRCh38]
Chr15:45445601 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1111G>A (p.Glu371Lys) single nucleotide variant Inborn genetic diseases [RCV002849192] Chr15:45138012 [GRCh38]
Chr15:45430210 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.2188C>T (p.Arg730Trp) single nucleotide variant Inborn genetic diseases [RCV002924632] Chr15:45144946 [GRCh38]
Chr15:45437144 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.4581G>C (p.Lys1527Asn) single nucleotide variant Inborn genetic diseases [RCV002737032] Chr15:45164826 [GRCh38]
Chr15:45457024 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.890C>G (p.Pro297Arg) single nucleotide variant Inborn genetic diseases [RCV002768337] Chr15:45136375 [GRCh38]
Chr15:45428573 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3361G>C (p.Val1121Leu) single nucleotide variant Inborn genetic diseases [RCV002713521] Chr15:45152453 [GRCh38]
Chr15:45444651 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.2698G>C (p.Val900Leu) single nucleotide variant Inborn genetic diseases [RCV002708489] Chr15:45148327 [GRCh38]
Chr15:45440525 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1975G>A (p.Val659Met) single nucleotide variant Inborn genetic diseases [RCV002804365] Chr15:45144074 [GRCh38]
Chr15:45436272 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.569G>C (p.Arg190Pro) single nucleotide variant Inborn genetic diseases [RCV002744908] Chr15:45135547 [GRCh38]
Chr15:45427745 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1519C>T (p.Arg507Trp) single nucleotide variant Inborn genetic diseases [RCV002984590] Chr15:45141024 [GRCh38]
Chr15:45433222 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1058G>A (p.Arg353Gln) single nucleotide variant Inborn genetic diseases [RCV002763417] Chr15:45137959 [GRCh38]
Chr15:45430157 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.2713C>T (p.Arg905Trp) single nucleotide variant Inborn genetic diseases [RCV002665386] Chr15:45148342 [GRCh38]
Chr15:45440540 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.4162G>A (p.Gly1388Arg) single nucleotide variant Inborn genetic diseases [RCV002916370] Chr15:45162291 [GRCh38]
Chr15:45454489 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.2794C>T (p.Arg932Cys) single nucleotide variant Inborn genetic diseases [RCV002743739] Chr15:45148423 [GRCh38]
Chr15:45440621 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.4418G>A (p.Arg1473Gln) single nucleotide variant Inborn genetic diseases [RCV002961503] Chr15:45163803 [GRCh38]
Chr15:45456001 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1140T>A (p.Asp380Glu) single nucleotide variant Inborn genetic diseases [RCV002668290] Chr15:45139092 [GRCh38]
Chr15:45431290 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3104A>T (p.Lys1035Met) single nucleotide variant Inborn genetic diseases [RCV002855772] Chr15:45151963 [GRCh38]
Chr15:45444161 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1703C>T (p.Pro568Leu) single nucleotide variant Inborn genetic diseases [RCV002649063] Chr15:45141993 [GRCh38]
Chr15:45434191 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3728T>C (p.Leu1243Pro) single nucleotide variant Inborn genetic diseases [RCV002959348] Chr15:45160862 [GRCh38]
Chr15:45453060 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3640C>T (p.Arg1214Cys) single nucleotide variant Inborn genetic diseases [RCV002809867] Chr15:45155867 [GRCh38]
Chr15:45448065 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3860T>C (p.Val1287Ala) single nucleotide variant Inborn genetic diseases [RCV002792764] Chr15:45161741 [GRCh38]
Chr15:45453939 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.872C>T (p.Ala291Val) single nucleotide variant Inborn genetic diseases [RCV002672313] Chr15:45136357 [GRCh38]
Chr15:45428555 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1375C>T (p.Arg459Trp) single nucleotide variant Inborn genetic diseases [RCV002668374] Chr15:45139585 [GRCh38]
Chr15:45431783 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1921G>A (p.Val641Met) single nucleotide variant Inborn genetic diseases [RCV002677516] Chr15:45143288 [GRCh38]
Chr15:45435486 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1148C>T (p.Ala383Val) single nucleotide variant Inborn genetic diseases [RCV003218680] Chr15:45139100 [GRCh38]
Chr15:45431298 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1774G>A (p.Gly592Arg) single nucleotide variant Inborn genetic diseases [RCV003211521] Chr15:45142064 [GRCh38]
Chr15:45434262 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.4147T>C (p.Ser1383Pro) single nucleotide variant Inborn genetic diseases [RCV003189266] Chr15:45162276 [GRCh38]
Chr15:45454474 [GRCh37]
Chr15:15q21.1
uncertain significance
GRCh38/hg38 15q21.1(chr15:45092835-45433283) copy number gain Anomalous pulmonary venous return [RCV003223576] Chr15:45092835..45433283 [GRCh38]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3394C>G (p.Leu1132Val) single nucleotide variant Inborn genetic diseases [RCV003265465] Chr15:45152486 [GRCh38]
Chr15:45444684 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3286A>G (p.Met1096Val) single nucleotide variant Inborn genetic diseases [RCV003374202] Chr15:45152378 [GRCh38]
Chr15:45444576 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.2343C>T (p.Ala781=) single nucleotide variant not provided [RCV003393764] Chr15:45147453 [GRCh38]
Chr15:45439651 [GRCh37]
Chr15:15q21.1
likely benign
NM_175940.3(DUOX1):c.1397A>G (p.Glu466Gly) single nucleotide variant Inborn genetic diseases [RCV003374478] Chr15:45140902 [GRCh38]
Chr15:45433100 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.4621C>T (p.Arg1541Trp) single nucleotide variant Inborn genetic diseases [RCV003354660] Chr15:45164866 [GRCh38]
Chr15:45457064 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.2070C>A (p.Asn690Lys) single nucleotide variant Inborn genetic diseases [RCV003366676] Chr15:45144169 [GRCh38]
Chr15:45436367 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3524+15_3524+26del deletion not provided [RCV003875078] Chr15:45153494..45153505 [GRCh38]
Chr15:45445692..45445703 [GRCh37]
Chr15:15q21.1
likely benign
NM_175940.3(DUOX1):c.4561G>C (p.Gly1521Arg) single nucleotide variant not provided [RCV003393770] Chr15:45164806 [GRCh38]
Chr15:45457004 [GRCh37]
Chr15:15q21.1
likely benign
NM_175940.3(DUOX1):c.615T>C (p.Phe205=) single nucleotide variant not provided [RCV003393762] Chr15:45135593 [GRCh38]
Chr15:45427791 [GRCh37]
Chr15:15q21.1
likely benign
NM_175940.3(DUOX1):c.4547G>A (p.Gly1516Glu) single nucleotide variant not provided [RCV003393769] Chr15:45164792 [GRCh38]
Chr15:45456990 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.1264A>T (p.Ser422Cys) single nucleotide variant not provided [RCV003393763] Chr15:45139474 [GRCh38]
Chr15:45431672 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.4271G>A (p.Arg1424Gln) single nucleotide variant not provided [RCV003393766] Chr15:45163554 [GRCh38]
Chr15:45455752 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.4442G>A (p.Arg1481Gln) single nucleotide variant not provided [RCV003393768] Chr15:45163827 [GRCh38]
Chr15:45456025 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.3929G>T (p.Cys1310Phe) single nucleotide variant not provided [RCV003393765] Chr15:45161810 [GRCh38]
Chr15:45454008 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.579C>G (p.Ser193=) single nucleotide variant not provided [RCV003393760] Chr15:45135557 [GRCh38]
Chr15:45427755 [GRCh37]
Chr15:15q21.1
benign
NM_175940.3(DUOX1):c.3789C>A (p.Asp1263Glu) single nucleotide variant DUOX1-related condition [RCV003412213] Chr15:45160923 [GRCh38]
Chr15:45453121 [GRCh37]
Chr15:15q21.1
uncertain significance
Single allele deletion not provided [RCV003448697] Chr15:41321409..51718601 [GRCh37]
Chr15:15q15.1-21.2
pathogenic
NM_175940.3(DUOX1):c.4392G>T (p.Arg1464Ser) single nucleotide variant not provided [RCV003393767] Chr15:45163675 [GRCh38]
Chr15:45455873 [GRCh37]
Chr15:15q21.1
uncertain significance
NM_175940.3(DUOX1):c.580A>G (p.Arg194Gly) single nucleotide variant not provided [RCV003393761] Chr15:45135558 [GRCh38]
Chr15:45427756 [GRCh37]
Chr15:15q21.1
likely benign
NM_175940.3(DUOX1):c.1524A>G (p.Leu508=) single nucleotide variant not provided [RCV003390482] Chr15:45141029 [GRCh38]
Chr15:45433227 [GRCh37]
Chr15:15q21.1
likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4822
Count of miRNA genes:1163
Interacting mature miRNAs:1518
Transcripts:ENST00000321429, ENST00000389037, ENST00000557893, ENST00000558322, ENST00000558446, ENST00000558744, ENST00000558991, ENST00000559219, ENST00000559221, ENST00000559716, ENST00000561166, ENST00000561220
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
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.

Markers in Region
DUOX1_9771  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371545,457,156 - 45,457,791UniSTSGRCh37
Build 361543,244,448 - 43,245,083RGDNCBI36
Celera1522,348,440 - 22,349,075RGD
HuRef1522,281,365 - 22,282,000UniSTS
D15S222  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371545,445,630 - 45,445,836UniSTSGRCh37
Build 361543,232,922 - 43,233,128RGDNCBI36
Celera1522,336,925 - 22,337,117RGD
HuRef1522,269,850 - 22,270,042UniSTS
AFM189xg5  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371545,445,601 - 45,445,831UniSTSGRCh37
Build 361543,232,893 - 43,233,123RGDNCBI36
Celera1522,336,896 - 22,337,112RGD
Cytogenetic Map15q15.3UniSTS
HuRef1522,269,821 - 22,270,037UniSTS
Whitehead-RH Map15120.4UniSTS
Whitehead-YAC Contig Map15 UniSTS
NCBI RH Map15187.0UniSTS
IB532  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371545,440,905 - 45,441,126UniSTSGRCh37
Build 361543,228,197 - 43,228,418RGDNCBI36
Celera1522,332,201 - 22,332,422RGD
Cytogenetic Map15q15.3UniSTS
HuRef1522,265,124 - 22,265,345UniSTS
GeneMap99-GB4 RH Map15160.64UniSTS
Whitehead-RH Map15131.1UniSTS
NCBI RH Map15169.1UniSTS
D15S1477  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map4q32-q35UniSTS
Cytogenetic Map5q11UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map2q31UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q11.21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map1q31.3UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map3p25-p24UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map3p12UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map6p21.1-p12.2UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map14q11.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p22.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map15q21-q23UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map11q12UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map20p11.22-p11.1UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map17qUniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map6p24.2UniSTS
D16S325  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map10q11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map3q13.32UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map2p13-p12UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map8q21.13UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map9p24.1-p23UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map10pter-q25.3UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map1p36.3-p34.3UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19q13.4UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
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Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
D1S1425  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map2p23-p22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic Map2p11.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map3q11.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map15q11-q12UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map4q31.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map10p15-p14UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6q16UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic MapXq21.1UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 275 12 892 81 7 6 1410 7 129 31 392 1324 82 9 796
Low 2044 1936 479 199 889 113 1977 1175 2843 235 1010 187 91 1109 1184 4 1
Below cutoff 109 1037 346 334 1036 337 966 1009 749 149 56 99 2 1 86 808 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_017434 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_175940 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011521681 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011521682 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047432690 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047432691 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047432692 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047432693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378218 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378221 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488970 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC051619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC091117 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF213465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF230495 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK075268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128591 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK172859 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290372 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL137592 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC114628 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC114938 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB852814 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471082 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF584410 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KC877542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MN115831 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000321429   ⟹   ENSP00000317997
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1545,129,933 - 45,165,576 (+)Ensembl
RefSeq Acc Id: ENST00000389037   ⟹   ENSP00000373689
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1545,129,994 - 45,165,574 (+)Ensembl
RefSeq Acc Id: ENST00000557893
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1545,147,955 - 45,153,239 (+)Ensembl
RefSeq Acc Id: ENST00000558322   ⟹   ENSP00000454121
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1545,130,018 - 45,133,934 (+)Ensembl
RefSeq Acc Id: ENST00000558446
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1545,150,300 - 45,151,881 (+)Ensembl
RefSeq Acc Id: ENST00000558744
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1545,153,788 - 45,155,851 (+)Ensembl
RefSeq Acc Id: ENST00000558991
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1545,138,646 - 45,141,039 (+)Ensembl
RefSeq Acc Id: ENST00000559219
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1545,147,546 - 45,148,558 (+)Ensembl
RefSeq Acc Id: ENST00000559221
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1545,152,500 - 45,155,535 (+)Ensembl
RefSeq Acc Id: ENST00000559716
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1545,151,829 - 45,160,990 (+)Ensembl
RefSeq Acc Id: ENST00000561166   ⟹   ENSP00000454065
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1545,138,818 - 45,165,573 (+)Ensembl
RefSeq Acc Id: ENST00000561220   ⟹   ENSP00000452623
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1545,130,038 - 45,164,966 (+)Ensembl
RefSeq Acc Id: ENST00000682390   ⟹   ENSP00000508006
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1545,161,820 - 45,165,574 (+)Ensembl
RefSeq Acc Id: NM_017434   ⟹   NP_059130
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381545,129,994 - 45,165,574 (+)NCBI
GRCh371545,422,192 - 45,457,776 (+)NCBI
Build 361543,209,484 - 43,245,066 (+)NCBI Archive
HuRef1522,246,405 - 22,281,985 (+)NCBI
CHM1_11545,540,525 - 45,576,454 (+)NCBI
T2T-CHM13v2.01542,938,016 - 42,973,584 (+)NCBI
Sequence:
RefSeq Acc Id: NM_175940   ⟹   NP_787954
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381545,129,994 - 45,165,574 (+)NCBI
GRCh371545,422,192 - 45,457,776 (+)NCBI
Build 361543,209,484 - 43,245,066 (+)NCBI Archive
HuRef1522,246,405 - 22,281,985 (+)NCBI
CHM1_11545,540,525 - 45,576,454 (+)NCBI
T2T-CHM13v2.01542,938,016 - 42,973,584 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011521681   ⟹   XP_011519983
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381545,129,994 - 45,165,574 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011521682   ⟹   XP_011519984
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381545,139,072 - 45,165,574 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047432690   ⟹   XP_047288646
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381545,129,994 - 45,165,574 (+)NCBI
RefSeq Acc Id: XM_047432691   ⟹   XP_047288647
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381545,129,994 - 45,165,574 (+)NCBI
RefSeq Acc Id: XM_047432692   ⟹   XP_047288648
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381545,130,136 - 45,165,574 (+)NCBI
RefSeq Acc Id: XM_047432693   ⟹   XP_047288649
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381545,130,136 - 45,165,574 (+)NCBI
RefSeq Acc Id: XM_054378216   ⟹   XP_054234191
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01542,938,016 - 42,973,584 (+)NCBI
RefSeq Acc Id: XM_054378217   ⟹   XP_054234192
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01542,938,158 - 42,973,584 (+)NCBI
RefSeq Acc Id: XM_054378218   ⟹   XP_054234193
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01542,938,158 - 42,973,584 (+)NCBI
RefSeq Acc Id: XM_054378219   ⟹   XP_054234194
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01542,938,016 - 42,973,584 (+)NCBI
RefSeq Acc Id: XM_054378220   ⟹   XP_054234195
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01542,947,098 - 42,973,584 (+)NCBI
RefSeq Acc Id: XM_054378221   ⟹   XP_054234196
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01542,938,155 - 42,963,930 (+)NCBI
RefSeq Acc Id: XR_008488970
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01542,938,152 - 42,955,532 (+)NCBI
Protein Sequences
Protein RefSeqs NP_059130 (Get FASTA)   NCBI Sequence Viewer  
  NP_787954 (Get FASTA)   NCBI Sequence Viewer  
  XP_011519983 (Get FASTA)   NCBI Sequence Viewer  
  XP_011519984 (Get FASTA)   NCBI Sequence Viewer  
  XP_047288646 (Get FASTA)   NCBI Sequence Viewer  
  XP_047288647 (Get FASTA)   NCBI Sequence Viewer  
  XP_047288648 (Get FASTA)   NCBI Sequence Viewer  
  XP_047288649 (Get FASTA)   NCBI Sequence Viewer  
  XP_054234191 (Get FASTA)   NCBI Sequence Viewer  
  XP_054234192 (Get FASTA)   NCBI Sequence Viewer  
  XP_054234193 (Get FASTA)   NCBI Sequence Viewer  
  XP_054234194 (Get FASTA)   NCBI Sequence Viewer  
  XP_054234195 (Get FASTA)   NCBI Sequence Viewer  
  XP_054234196 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF71295 (Get FASTA)   NCBI Sequence Viewer  
  AAF73921 (Get FASTA)   NCBI Sequence Viewer  
  AAI14629 (Get FASTA)   NCBI Sequence Viewer  
  AAI14939 (Get FASTA)   NCBI Sequence Viewer  
  BAD18816 (Get FASTA)   NCBI Sequence Viewer  
  BAF83061 (Get FASTA)   NCBI Sequence Viewer  
  CAB70831 (Get FASTA)   NCBI Sequence Viewer  
  CCQ43907 (Get FASTA)   NCBI Sequence Viewer  
  EAW77295 (Get FASTA)   NCBI Sequence Viewer  
  EAW77296 (Get FASTA)   NCBI Sequence Viewer  
  EAW77297 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000317997
  ENSP00000317997.4
  ENSP00000373689
  ENSP00000373689.3
  ENSP00000452623.1
  ENSP00000454065
  ENSP00000454065.1
  ENSP00000454121.1
  ENSP00000508006.1
GenBank Protein Q9NRD9 (Get FASTA)   NCBI Sequence Viewer  
  QFU28536 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_059130   ⟸   NM_017434
- Peptide Label: precursor
- UniProtKB: Q6ZR09 (UniProtKB/Swiss-Prot),   Q6ZMB3 (UniProtKB/Swiss-Prot),   Q14C94 (UniProtKB/Swiss-Prot),   A6NH28 (UniProtKB/Swiss-Prot),   Q9NZC1 (UniProtKB/Swiss-Prot),   Q9NRD9 (UniProtKB/Swiss-Prot),   A8K2V7 (UniProtKB/TrEMBL),   Q14C85 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_787954   ⟸   NM_175940
- Peptide Label: precursor
- UniProtKB: Q6ZR09 (UniProtKB/Swiss-Prot),   Q6ZMB3 (UniProtKB/Swiss-Prot),   Q14C94 (UniProtKB/Swiss-Prot),   A6NH28 (UniProtKB/Swiss-Prot),   Q9NZC1 (UniProtKB/Swiss-Prot),   Q9NRD9 (UniProtKB/Swiss-Prot),   A8K2V7 (UniProtKB/TrEMBL),   Q14C85 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011519983   ⟸   XM_011521681
- Peptide Label: isoform X2
- UniProtKB: A8K2V7 (UniProtKB/TrEMBL),   Q14C85 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011519984   ⟸   XM_011521682
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: ENSP00000454121   ⟸   ENST00000558322
RefSeq Acc Id: ENSP00000373689   ⟸   ENST00000389037
RefSeq Acc Id: ENSP00000317997   ⟸   ENST00000321429
RefSeq Acc Id: ENSP00000454065   ⟸   ENST00000561166
RefSeq Acc Id: ENSP00000452623   ⟸   ENST00000561220
RefSeq Acc Id: ENSP00000508006   ⟸   ENST00000682390
RefSeq Acc Id: XP_047288646   ⟸   XM_047432690
- Peptide Label: isoform X1
- UniProtKB: Q9NRD9 (UniProtKB/Swiss-Prot),   Q6ZR09 (UniProtKB/Swiss-Prot),   Q6ZMB3 (UniProtKB/Swiss-Prot),   Q14C94 (UniProtKB/Swiss-Prot),   A6NH28 (UniProtKB/Swiss-Prot),   Q9NZC1 (UniProtKB/Swiss-Prot),   A8K2V7 (UniProtKB/TrEMBL),   Q14C85 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047288647   ⟸   XM_047432691
- Peptide Label: isoform X1
- UniProtKB: Q9NRD9 (UniProtKB/Swiss-Prot),   Q6ZR09 (UniProtKB/Swiss-Prot),   Q6ZMB3 (UniProtKB/Swiss-Prot),   Q14C94 (UniProtKB/Swiss-Prot),   A6NH28 (UniProtKB/Swiss-Prot),   Q9NZC1 (UniProtKB/Swiss-Prot),   A8K2V7 (UniProtKB/TrEMBL),   Q14C85 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047288649   ⟸   XM_047432693
- Peptide Label: isoform X1
- UniProtKB: Q9NRD9 (UniProtKB/Swiss-Prot),   Q6ZR09 (UniProtKB/Swiss-Prot),   Q6ZMB3 (UniProtKB/Swiss-Prot),   Q14C94 (UniProtKB/Swiss-Prot),   A6NH28 (UniProtKB/Swiss-Prot),   Q9NZC1 (UniProtKB/Swiss-Prot),   A8K2V7 (UniProtKB/TrEMBL),   Q14C85 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047288648   ⟸   XM_047432692
- Peptide Label: isoform X1
- UniProtKB: Q9NRD9 (UniProtKB/Swiss-Prot),   Q6ZR09 (UniProtKB/Swiss-Prot),   Q6ZMB3 (UniProtKB/Swiss-Prot),   Q14C94 (UniProtKB/Swiss-Prot),   A6NH28 (UniProtKB/Swiss-Prot),   Q9NZC1 (UniProtKB/Swiss-Prot),   A8K2V7 (UniProtKB/TrEMBL),   Q14C85 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054234191   ⟸   XM_054378216
- Peptide Label: isoform X1
- UniProtKB: A8K2V7 (UniProtKB/TrEMBL),   Q14C85 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054234194   ⟸   XM_054378219
- Peptide Label: isoform X2
- UniProtKB: A8K2V7 (UniProtKB/TrEMBL),   Q14C85 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054234196   ⟸   XM_054378221
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054234193   ⟸   XM_054378218
- Peptide Label: isoform X1
- UniProtKB: A8K2V7 (UniProtKB/TrEMBL),   Q14C85 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054234192   ⟸   XM_054378217
- Peptide Label: isoform X1
- UniProtKB: A8K2V7 (UniProtKB/TrEMBL),   Q14C85 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054234195   ⟸   XM_054378220
- Peptide Label: isoform X3
Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9NRD9-F1-model_v2 AlphaFold Q9NRD9 1-1551 view protein structure

Promoters
RGD ID:7229357
Promoter ID:EPDNEW_H20424
Type:initiation region
Name:DUOX1_3
Description:dual oxidase 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H20425  EPDNEW_H20428  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381545,129,470 - 45,129,530EPDNEW
RGD ID:7229361
Promoter ID:EPDNEW_H20425
Type:initiation region
Name:DUOX1_2
Description:dual oxidase 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H20424  EPDNEW_H20428  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381545,129,689 - 45,129,749EPDNEW
RGD ID:7229363
Promoter ID:EPDNEW_H20428
Type:multiple initiation site
Name:DUOX1_1
Description:dual oxidase 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H20424  EPDNEW_H20425  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381545,129,994 - 45,130,054EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:3062 AgrOrtholog
COSMIC DUOX1 COSMIC
Ensembl Genes ENSG00000137857 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000321429 ENTREZGENE
  ENST00000321429.8 UniProtKB/Swiss-Prot
  ENST00000389037 ENTREZGENE
  ENST00000389037.7 UniProtKB/Swiss-Prot
  ENST00000558322.5 UniProtKB/TrEMBL
  ENST00000561166 ENTREZGENE
  ENST00000561166.1 UniProtKB/Swiss-Prot
  ENST00000561220.6 UniProtKB/TrEMBL
  ENST00000682390.1 UniProtKB/TrEMBL
Gene3D-CATH 1.10.640.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.50.80 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF-hand UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Translation factors UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000137857 GTEx
HGNC ID HGNC:3062 ENTREZGENE
Human Proteome Map DUOX1 Human Proteome Map
InterPro Cyt_b245_heavy_chain UniProtKB/TrEMBL
  DUOX_peroxidase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF-hand-dom_pair UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_Hand_1_Ca_BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_hand_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FAD-bd_8 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FAD-bd_FR_type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Fe3_Rdtase_TM_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Fe_red_NAD-bd_6 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FNR_nucleotide-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Haem_peroxidase_animal UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Haem_peroxidase_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Haem_peroxidase_sf_animal UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Riboflavin_synthase-like_b-brl UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:53905 UniProtKB/Swiss-Prot
NCBI Gene 53905 ENTREZGENE
OMIM 606758 OMIM
PANTHER NADPH OXIDASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OXIDASE/PEROXIDASE UniProtKB/TrEMBL
  PEROXINECTIN A UniProtKB/TrEMBL
  PTHR11972:SF75 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam An_peroxidase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF-hand_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF-hand_7 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FAD_binding_8 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ferric_reduct UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NAD_binding_6 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA27516 PharmGKB
PRINTS ANPEROXIDASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GP91PHOX UniProtKB/TrEMBL
PROSITE EF_HAND_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_HAND_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FAD_FR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PEROXIDASE_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART EFh UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF47473 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF48113 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF52343 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF63380 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A5P9KEJ7_HUMAN UniProtKB/TrEMBL
  A0A804HKN9_HUMAN UniProtKB/TrEMBL
  A6NH28 ENTREZGENE
  A8K2V7 ENTREZGENE, UniProtKB/TrEMBL
  DUOX1_HUMAN UniProtKB/Swiss-Prot
  H0YK19_HUMAN UniProtKB/TrEMBL
  H0YNR5_HUMAN UniProtKB/TrEMBL
  L8ECP1_HUMAN UniProtKB/TrEMBL
  Q14C85 ENTREZGENE, UniProtKB/TrEMBL
  Q14C94 ENTREZGENE
  Q6ZMB3 ENTREZGENE
  Q6ZR09 ENTREZGENE
  Q9NRD9 ENTREZGENE
  Q9NZC1 ENTREZGENE
UniProt Secondary A6NH28 UniProtKB/Swiss-Prot
  Q14C94 UniProtKB/Swiss-Prot
  Q6ZMB3 UniProtKB/Swiss-Prot
  Q6ZR09 UniProtKB/Swiss-Prot
  Q9NZC1 UniProtKB/Swiss-Prot