SP100 (SP100 nuclear antigen) - Rat Genome Database

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Gene: SP100 (SP100 nuclear antigen) Homo sapiens
Analyze
Symbol: SP100
Name: SP100 nuclear antigen
RGD ID: 1348100
HGNC Page HGNC:11206
Description: Enables several functions, including DNA-binding transcription factor activity, RNA polymerase II-specific; chromo shadow domain binding activity; and protein homodimerization activity. Involved in several processes, including innate immune response; regulation of DNA-templated transcription; and regulation of signal transduction. Located in Mre11 complex; cytoplasm; and nuclear lumen.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: DKFZp686E07254; FLJ00340; FLJ34579; lysp100b; nuclear autoantigen Sp-100; nuclear dot-associated Sp100 protein; SP100-HMG nuclear autoantigen; speckled 100 kDa
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: HMGB1P37  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382230,416,201 - 230,545,606 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2230,415,942 - 230,545,606 (+)EnsemblGRCh38hg38GRCh38
GRCh372231,280,916 - 231,410,321 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362230,989,115 - 231,118,561 (+)NCBINCBI36Build 36hg18NCBI36
Build 342231,106,485 - 231,206,745NCBI
Celera2225,057,025 - 225,186,692 (+)NCBICelera
Cytogenetic Map2q37.1NCBI
HuRef2223,121,005 - 223,250,289 (+)NCBIHuRef
CHM1_12231,286,764 - 231,416,096 (+)NCBICHM1_1
T2T-CHM13v2.02230,899,281 - 231,028,667 (+)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
(-)-alpha-phellandrene  (EXP)
(-)-demecolcine  (EXP)
(-)-epigallocatechin 3-gallate  (EXP)
1,2-dichloroethane  (ISO)
17beta-estradiol  (EXP,ISO)
2,3',4,4',5-Pentachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
2,4-dibromophenyl 2,4,5-tribromophenyl ether  (EXP)
2-palmitoylglycerol  (EXP)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
3-methylcholanthrene  (ISO)
4,4'-sulfonyldiphenol  (ISO)
4-hydroxynon-2-enal  (ISO)
acetamide  (ISO)
all-trans-retinoic acid  (EXP)
alpha-phellandrene  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
benzo[a]pyrene  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (EXP,ISO)
caffeine  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
chloroprene  (ISO)
chromium(6+)  (ISO)
cisplatin  (EXP)
clofibrate  (ISO)
cobalt dichloride  (EXP)
copper(II) sulfate  (EXP)
coumarin  (EXP)
cyclosporin A  (EXP)
deoxynivalenol  (ISO)
dexamethasone  (EXP)
Dibutyl phosphate  (EXP)
dimethylarsinic acid  (ISO)
dioxygen  (ISO)
diquat  (ISO)
doxorubicin  (EXP)
elemental selenium  (EXP)
entinostat  (EXP)
folic acid  (ISO)
geraniol  (EXP)
gold atom  (EXP)
gold(0)  (EXP)
GSK-J4  (EXP)
indometacin  (EXP)
ivermectin  (EXP)
lead diacetate  (ISO)
lipopolysaccharide  (EXP)
manganese atom  (EXP)
manganese(0)  (EXP)
manganese(II) chloride  (EXP)
methamphetamine  (ISO)
methyl methanesulfonate  (EXP)
methylarsonic acid  (ISO)
N-ethyl-N-nitrosourea  (ISO)
nickel atom  (EXP)
nickel dichloride  (EXP)
ozone  (ISO)
paracetamol  (EXP,ISO)
pentachlorophenol  (ISO)
perfluorohexanesulfonic acid  (ISO)
potassium chromate  (EXP)
propanal  (EXP)
quercetin  (EXP)
resveratrol  (EXP)
ruxolitinib  (EXP)
selenium atom  (EXP)
silicon dioxide  (EXP)
silver atom  (ISO)
silver(0)  (ISO)
sodium arsenate  (ISO)
sodium arsenite  (EXP,ISO)
tert-butyl hydroperoxide  (ISO)
tetrachloromethane  (ISO)
thioacetamide  (ISO)
titanium dioxide  (ISO)
trichloroethene  (ISO)
triclosan  (EXP)
triptonide  (ISO)
valproic acid  (EXP)
vincristine  (EXP)
vitamin E  (EXP)
vorinostat  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
chromosome, telomeric region  (HDA)
cytoplasm  (IDA,IEA)
Mre11 complex  (IDA)
nuclear body  (IDA,IEA)
nuclear periphery  (IDA)
nucleolus  (IDA,IMP)
nucleoplasm  (IDA,TAS)
nucleus  (IBA,IDA,IEA)
PML body  (IDA,IEA)

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:2258622   PMID:8695863   PMID:8810287   PMID:9230084   PMID:9412458   PMID:9636146   PMID:9636147   PMID:9973607   PMID:10212234   PMID:10766566   PMID:10921892   PMID:11112690  
PMID:11313457   PMID:11574059   PMID:11716541   PMID:11792325   PMID:11909962   PMID:12470659   PMID:12477932   PMID:14647468   PMID:14702039   PMID:15017387   PMID:15247905   PMID:15489334  
PMID:15592518   PMID:15608651   PMID:15767676   PMID:15882967   PMID:16177824   PMID:16189514   PMID:16344560   PMID:16415175   PMID:16524884   PMID:16873258   PMID:17000644   PMID:17081983  
PMID:17245429   PMID:17332504   PMID:17491593   PMID:18029348   PMID:18538659   PMID:18691969   PMID:19135898   PMID:19274049   PMID:19279115   PMID:20130140   PMID:20211142   PMID:20379614  
PMID:20512085   PMID:20805487   PMID:20936779   PMID:21044950   PMID:21172801   PMID:21274506   PMID:21383994   PMID:21471311   PMID:21516116   PMID:21734036   PMID:21779164   PMID:21873635  
PMID:21880768   PMID:21988832   PMID:22086178   PMID:22278248   PMID:22419217   PMID:22544055   PMID:22658674   PMID:22863883   PMID:22878415   PMID:22939629   PMID:23221561   PMID:23485562  
PMID:23830076   PMID:23867815   PMID:24089549   PMID:24194542   PMID:24623443   PMID:24637324   PMID:24740910   PMID:24981860   PMID:25027693   PMID:25416956   PMID:25593309   PMID:25693804  
PMID:25910212   PMID:26057166   PMID:26491169   PMID:26496610   PMID:27107012   PMID:27107014   PMID:27129259   PMID:27211601   PMID:28439026   PMID:28514442   PMID:28620180   PMID:28680062  
PMID:28750047   PMID:28968443   PMID:29180619   PMID:29509190   PMID:29852174   PMID:30021884   PMID:30060604   PMID:30260704   PMID:30854688   PMID:31180531   PMID:31515488   PMID:31753913  
PMID:31839598   PMID:32001251   PMID:32296183   PMID:32513696   PMID:32814053   PMID:33961781   PMID:34349018   PMID:34795231   PMID:35235311   PMID:35353002   PMID:35575683   PMID:36129980  
PMID:36217029   PMID:36526897   PMID:37689310   PMID:38118002   PMID:38334954   PMID:38943005   PMID:39358380  


Genomics

Comparative Map Data
SP100
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382230,416,201 - 230,545,606 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2230,415,942 - 230,545,606 (+)EnsemblGRCh38hg38GRCh38
GRCh372231,280,916 - 231,410,321 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362230,989,115 - 231,118,561 (+)NCBINCBI36Build 36hg18NCBI36
Build 342231,106,485 - 231,206,745NCBI
Celera2225,057,025 - 225,186,692 (+)NCBICelera
Cytogenetic Map2q37.1NCBI
HuRef2223,121,005 - 223,250,289 (+)NCBIHuRef
CHM1_12231,286,764 - 231,416,096 (+)NCBICHM1_1
T2T-CHM13v2.02230,899,281 - 231,028,667 (+)NCBIT2T-CHM13v2.0
Sp100
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39185,577,683 - 85,637,719 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl185,577,709 - 85,637,719 (+)EnsemblGRCm39 Ensembl
GRCm38185,649,948 - 85,709,998 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl185,649,988 - 85,709,998 (+)EnsemblGRCm38mm10GRCm38
MGSCv37187,546,625 - 87,606,023 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36187,481,185 - 87,532,732 (+)NCBIMGSCv36mm8
Celera188,624,849 - 88,674,129 (+)NCBICelera
Cytogenetic Map1C5NCBI
cM Map143.6NCBI
Sp100
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8993,758,975 - 93,825,068 (+)NCBIGRCr8
mRatBN7.2986,310,990 - 86,377,036 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl986,311,032 - 86,377,034 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx994,728,134 - 94,794,889 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0999,856,630 - 99,923,388 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0998,237,941 - 98,304,055 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0992,675,103 - 92,718,489 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl992,681,078 - 92,717,929 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0992,405,689 - 92,449,075 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.0990,732,749 - 90,750,820 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4984,374,288 - 84,409,976 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1984,557,706 - 84,593,391 (+)NCBI
Celera983,734,331 - 83,769,903 (+)NCBICelera
Cytogenetic Map9q35NCBI
Sp100
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554534,773,030 - 4,853,814 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554534,774,739 - 4,856,238 (-)NCBIChiLan1.0ChiLan1.0
SP100
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v213133,045,138 - 133,177,230 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12B133,062,928 - 133,192,182 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02B117,673,152 - 117,799,911 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12B236,474,298 - 236,601,277 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2B236,496,446 - 236,601,096 (+)Ensemblpanpan1.1panPan2
SP100
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12542,538,428 - 42,635,825 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2542,538,571 - 42,635,649 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2543,163,525 - 43,261,071 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02542,794,971 - 42,892,656 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2542,795,086 - 42,892,647 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12542,724,896 - 42,822,209 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02542,566,980 - 42,664,684 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02542,722,157 - 42,819,867 (+)NCBIUU_Cfam_GSD_1.0
Sp100
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405303184,708,642 - 184,803,432 (+)NCBIHiC_Itri_2
SpeTri2.0NW_0049365256,136,343 - 6,231,051 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
LOC100517129
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.115131,299,923 - 131,381,253 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.215145,104,815 - 145,137,478 (-)NCBISscrofa10.2Sscrofa10.2susScr3
SP100
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.110116,454,261 - 116,587,093 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl10116,459,050 - 116,590,215 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604082,883,256 - 83,027,176 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Sp100
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248433,983,040 - 4,061,930 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248433,982,920 - 4,058,081 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SP100
69 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 2q32.3-37.3(chr2:194898783-236473913)x3 copy number gain See cases [RCV000051119] Chr2:194898783..236473913 [GRCh38]
Chr2:195763507..237382556 [GRCh37]
Chr2:195471752..237047295 [NCBI36]
Chr2:2q32.3-37.3
pathogenic
GRCh38/hg38 2q36.1-37.3(chr2:223992431-242126245)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052972]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052972]|See cases [RCV000052972] Chr2:223992431..242126245 [GRCh38]
Chr2:224857148..243059659 [GRCh37]
Chr2:224565392..242717069 [NCBI36]
Chr2:2q36.1-37.3
pathogenic
GRCh38/hg38 2q37.1(chr2:230385715-230513525)x3 copy number gain See cases [RCV000134236] Chr2:230385715..230513525 [GRCh38]
Chr2:231250430..231378240 [GRCh37]
Chr2:230958674..231086484 [NCBI36]
Chr2:2q37.1
benign
GRCh38/hg38 2q36.3-37.3(chr2:226978129-236886599)x1 copy number loss See cases [RCV000052637] Chr2:226978129..236886599 [GRCh38]
Chr2:227842845..237795242 [GRCh37]
Chr2:227551089..237459981 [NCBI36]
Chr2:2q36.3-37.3
pathogenic
GRCh38/hg38 2q36.3-37.2(chr2:227343278-235339168)x1 copy number loss See cases [RCV000052638] Chr2:227343278..235339168 [GRCh38]
Chr2:228207994..236247812 [GRCh37]
Chr2:227916238..235912551 [NCBI36]
Chr2:2q36.3-37.2
pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:188818195-242065208)x3 copy number gain See cases [RCV000052958] Chr2:188818195..242065208 [GRCh38]
Chr2:189682921..243007359 [GRCh37]
Chr2:189391166..242656032 [NCBI36]
Chr2:2q32.2-37.3
pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3 copy number gain See cases [RCV000052959] Chr2:190310736..241892770 [GRCh38]
Chr2:191175462..242834921 [GRCh37]
Chr2:190883707..242483594 [NCBI36]
Chr2:2q32.2-37.3
pathogenic
GRCh38/hg38 2q32.3-37.3(chr2:193122313-241074980)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052960]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052960]|See cases [RCV000052960] Chr2:193122313..241074980 [GRCh38]
Chr2:193987039..242014395 [GRCh37]
Chr2:193695284..241663068 [NCBI36]
Chr2:2q32.3-37.3
pathogenic
GRCh38/hg38 2q36.3-37.3(chr2:227803148-242086301)x3 copy number gain See cases [RCV000052973] Chr2:227803148..242086301 [GRCh38]
Chr2:228667864..243028452 [GRCh37]
Chr2:228376108..242677125 [NCBI36]
Chr2:2q36.3-37.3
pathogenic
GRCh38/hg38 2q36.3-37.3(chr2:228723579-241404867)x3 copy number gain See cases [RCV000134169] Chr2:228723579..241404867 [GRCh38]
Chr2:229588295..242344282 [GRCh37]
Chr2:229296539..241992955 [NCBI36]
Chr2:2q36.3-37.3
pathogenic
GRCh37/hg19 2q36.3-37.1(chr2:230411764-232019784)x1 copy number loss not specified [RCV000515677] Chr2:230411764..232019784 [GRCh37]
Chr2:2q36.3-37.1
uncertain significance
GRCh38/hg38 2q34-37.3(chr2:210579676-242126245)x3 copy number gain See cases [RCV000135934] Chr2:210579676..242126245 [GRCh38]
Chr2:211444400..243059659 [GRCh37]
Chr2:211152645..242717069 [NCBI36]
Chr2:2q34-37.3
pathogenic
GRCh38/hg38 2q36.3-37.2(chr2:228014149-234976424)x3 copy number gain See cases [RCV000136967] Chr2:228014149..234976424 [GRCh38]
Chr2:228878865..235885068 [GRCh37]
Chr2:228587109..235549807 [NCBI36]
Chr2:2q36.3-37.2
pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:189436149-241841232)x3 copy number gain See cases [RCV000142307] Chr2:189436149..241841232 [GRCh38]
Chr2:190300875..242783384 [GRCh37]
Chr2:190009120..242432057 [NCBI36]
Chr2:2q32.2-37.3
pathogenic
GRCh38/hg38 2q35-37.3(chr2:218101759-242126245)x3 copy number gain See cases [RCV000143216] Chr2:218101759..242126245 [GRCh38]
Chr2:218966482..243059659 [GRCh37]
Chr2:218674727..242717069 [NCBI36]
Chr2:2q35-37.3
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2q36.1-37.1(chr2:223378640-232061074)x1 copy number loss See cases [RCV000448773] Chr2:223378640..232061074 [GRCh37]
Chr2:2q36.1-37.1
likely pathogenic
GRCh37/hg19 2q35-37.3(chr2:219966808-237815985)x3 copy number gain See cases [RCV000448049] Chr2:219966808..237815985 [GRCh37]
Chr2:2q35-37.3
pathogenic
GRCh37/hg19 2q36.1-37.3(chr2:222077224-239394441)x3 copy number gain See cases [RCV000511816] Chr2:222077224..239394441 [GRCh37]
Chr2:2q36.1-37.3
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
NM_001080391.2(SP100):c.2116G>A (p.Glu706Lys) single nucleotide variant not specified [RCV004297688] Chr2:230539288 [GRCh38]
Chr2:231404003 [GRCh37]
Chr2:2q37.1
uncertain significance
GRCh37/hg19 2q36.3-37.1(chr2:230491213-231404389)x1 copy number loss See cases [RCV000511869] Chr2:230491213..231404389 [GRCh37]
Chr2:2q36.3-37.1
likely pathogenic
GRCh37/hg19 2q34-37.3(chr2:213518431-242783384)x3 copy number gain See cases [RCV000512009] Chr2:213518431..242783384 [GRCh37]
Chr2:2q34-37.3
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
NM_001080391.2(SP100):c.2576A>T (p.Gln859Leu) single nucleotide variant not specified [RCV004302451] Chr2:230542864 [GRCh38]
Chr2:231407579 [GRCh37]
Chr2:2q37.1
uncertain significance
GRCh37/hg19 2q35-37.3(chr2:219225872-242016876)x3 copy number gain not provided [RCV000682170] Chr2:219225872..242016876 [GRCh37]
Chr2:2q35-37.3
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2q36.3-37.1(chr2:228966709-231528909)x1 copy number loss not provided [RCV000740932] Chr2:228966709..231528909 [GRCh37]
Chr2:2q36.3-37.1
pathogenic
NM_001080391.2(SP100):c.1008C>T (p.Asp336=) single nucleotide variant not provided [RCV000951244] Chr2:230462469 [GRCh38]
Chr2:231327184 [GRCh37]
Chr2:2q37.1
benign
GRCh37/hg19 2q34-37.3(chr2:210779657-239879183)x3 copy number gain See cases [RCV000790568] Chr2:210779657..239879183 [GRCh37]
Chr2:2q34-37.3
pathogenic
NM_001080391.2(SP100):c.875G>A (p.Arg292Gln) single nucleotide variant not provided [RCV000961033] Chr2:230461316 [GRCh38]
Chr2:231326031 [GRCh37]
Chr2:2q37.1
likely benign
GRCh37/hg19 2q31.2-37.3(chr2:178397959-243007457)x3 copy number gain See cases [RCV001263052] Chr2:178397959..243007457 [GRCh37]
Chr2:2q31.2-37.3
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373) copy number gain Mosaic trisomy 2 [RCV002280628] Chr2:1..243199373 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2q36.3-37.1(chr2:228807574-235475892) copy number loss not specified [RCV002053291] Chr2:228807574..235475892 [GRCh37]
Chr2:2q36.3-37.1
pathogenic
NC_000002.11:g.(?_231033840)_(234978657_?)dup duplication Joubert syndrome 22 [RCV001877690]|Perlman syndrome [RCV001877689] Chr2:231033840..234978657 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.490G>A (p.Glu164Lys) single nucleotide variant not specified [RCV004299331] Chr2:230446869 [GRCh38]
Chr2:231311584 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.596C>T (p.Pro199Leu) single nucleotide variant not specified [RCV004143321] Chr2:230449570 [GRCh38]
Chr2:231314285 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.209A>C (p.Lys70Thr) single nucleotide variant not specified [RCV004156699] Chr2:230443038 [GRCh38]
Chr2:231307753 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1124G>A (p.Arg375Gln) single nucleotide variant not specified [RCV004215518] Chr2:230464133 [GRCh38]
Chr2:231328848 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1625A>G (p.Lys542Arg) single nucleotide variant not specified [RCV004126910] Chr2:230494440 [GRCh38]
Chr2:231359155 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.590C>A (p.Thr197Lys) single nucleotide variant not specified [RCV004173841] Chr2:230449564 [GRCh38]
Chr2:231314279 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1087A>G (p.Asn363Asp) single nucleotide variant not specified [RCV004355000] Chr2:230464096 [GRCh38]
Chr2:231328811 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2626G>A (p.Glu876Lys) single nucleotide variant not specified [RCV004341072] Chr2:230542914 [GRCh38]
Chr2:231407629 [GRCh37]
Chr2:2q37.1
uncertain significance
GRCh37/hg19 2q35-37.3(chr2:218376403-242783384)x3 copy number gain not provided [RCV003484087] Chr2:218376403..242783384 [GRCh37]
Chr2:2q35-37.3
pathogenic
NM_001080391.2(SP100):c.1190A>G (p.Lys397Arg) single nucleotide variant not specified [RCV004670682] Chr2:230466349 [GRCh38]
Chr2:231331064 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2107A>G (p.Asn703Asp) single nucleotide variant not specified [RCV004670683] Chr2:230539279 [GRCh38]
Chr2:231403994 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.478G>C (p.Glu160Gln) single nucleotide variant not specified [RCV004864930] Chr2:230446857 [GRCh38]
Chr2:231311572 [GRCh37]
Chr2:2q37.1
uncertain significance
GRCh37/hg19 2q36.3-37.3(chr2:230814690-242783384)x3 copy number gain not provided [RCV001007519] Chr2:230814690..242783384 [GRCh37]
Chr2:2q36.3-37.3
pathogenic
NM_001080391.2(SP100):c.2486G>A (p.Arg829Gln) single nucleotide variant not specified [RCV004310669] Chr2:230541974 [GRCh38]
Chr2:231406689 [GRCh37]
Chr2:2q37.1
likely benign
NM_001080391.2(SP100):c.2282dup (p.His761fs) duplication Hereditary breast ovarian cancer syndrome [RCV001374502] Chr2:230540946..230540947 [GRCh38]
Chr2:231405661..231405662 [GRCh37]
Chr2:2q37.1
uncertain significance
GRCh37/hg19 2q35-37.3(chr2:219606537-239217703) copy number loss not specified [RCV002053285] Chr2:219606537..239217703 [GRCh37]
Chr2:2q35-37.3
pathogenic
GRCh37/hg19 2q36.1-37.1(chr2:223378640-232061074) copy number loss not specified [RCV002053287] Chr2:223378640..232061074 [GRCh37]
Chr2:2q36.1-37.1
pathogenic
GRCh37/hg19 2q36.3-37.1(chr2:229968217-231883182) copy number loss not specified [RCV002053293] Chr2:229968217..231883182 [GRCh37]
Chr2:2q36.3-37.1
pathogenic
NM_001080391.2(SP100):c.938C>A (p.Ala313Glu) single nucleotide variant not specified [RCV004330676] Chr2:230461379 [GRCh38]
Chr2:231326094 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1892A>G (p.Gln631Arg) single nucleotide variant not specified [RCV004290918] Chr2:230506324 [GRCh38]
Chr2:231371039 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1545G>C (p.Met515Ile) single nucleotide variant not specified [RCV004139045] Chr2:230473439 [GRCh38]
Chr2:231338154 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.744C>G (p.Cys248Trp) single nucleotide variant not specified [RCV004149346] Chr2:230450179 [GRCh38]
Chr2:231314894 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1627G>A (p.Val543Ile) single nucleotide variant not specified [RCV004076529] Chr2:230494442 [GRCh38]
Chr2:231359157 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2162C>G (p.Pro721Arg) single nucleotide variant not specified [RCV004247287] Chr2:230539334 [GRCh38]
Chr2:231404049 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1979G>A (p.Arg660His) single nucleotide variant not specified [RCV004221270] Chr2:230506411 [GRCh38]
Chr2:231371126 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2087A>T (p.Asp696Val) single nucleotide variant not specified [RCV004107348] Chr2:230511159 [GRCh38]
Chr2:231375874 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.424A>G (p.Lys142Glu) single nucleotide variant not specified [RCV004120600] Chr2:230444331 [GRCh38]
Chr2:231309046 [GRCh37]
Chr2:2q37.1
likely benign
NM_001080391.2(SP100):c.14G>T (p.Gly5Val) single nucleotide variant not specified [RCV004241968] Chr2:230416310 [GRCh38]
Chr2:231281025 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1984G>A (p.Gly662Ser) single nucleotide variant not specified [RCV004263178] Chr2:230506416 [GRCh38]
Chr2:231371131 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.527C>T (p.Thr176Ile) single nucleotide variant not specified [RCV004268107] Chr2:230449091 [GRCh38]
Chr2:231313806 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2396C>A (p.Pro799Gln) single nucleotide variant not specified [RCV004267449] Chr2:230541365 [GRCh38]
Chr2:231406080 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2227A>G (p.Ile743Val) single nucleotide variant not specified [RCV004280029] Chr2:230540892 [GRCh38]
Chr2:231405607 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1388A>C (p.Glu463Ala) single nucleotide variant not specified [RCV004360355] Chr2:230470057 [GRCh38]
Chr2:231334772 [GRCh37]
Chr2:2q37.1
uncertain significance
Single allele duplication not provided [RCV003448672] Chr2:230077026..243049549 [GRCh37]
Chr2:2q36.3-37.3
pathogenic
GRCh37/hg19 2q36.2-37.3(chr2:225995545-237594511)x3 copy number gain not provided [RCV003484091] Chr2:225995545..237594511 [GRCh37]
Chr2:2q36.2-37.3
pathogenic
GRCh37/hg19 2q35-37.3(chr2:216815496-242782258)x3 copy number gain See cases [RCV004442836] Chr2:216815496..242782258 [GRCh37]
Chr2:2q35-37.3
pathogenic
NM_001080391.2(SP100):c.2647A>C (p.Met883Leu) single nucleotide variant not specified [RCV004457697] Chr2:230542935 [GRCh38]
Chr2:231407650 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.382G>A (p.Asp128Asn) single nucleotide variant not specified [RCV004457699] Chr2:230444289 [GRCh38]
Chr2:231309004 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1390C>A (p.Leu464Ile) single nucleotide variant not specified [RCV004457687] Chr2:230470059 [GRCh38]
Chr2:231334774 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1552A>G (p.Met518Val) single nucleotide variant not specified [RCV004457689] Chr2:230474399 [GRCh38]
Chr2:231339114 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1948G>A (p.Gly650Arg) single nucleotide variant not specified [RCV004457692] Chr2:230506380 [GRCh38]
Chr2:231371095 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.545G>A (p.Arg182Gln) single nucleotide variant not specified [RCV004457701] Chr2:230449109 [GRCh38]
Chr2:231313824 [GRCh37]
Chr2:2q37.1
likely benign
NM_001080391.2(SP100):c.998G>A (p.Gly333Glu) single nucleotide variant not specified [RCV004457705] Chr2:230462459 [GRCh38]
Chr2:231327174 [GRCh37]
Chr2:2q37.1
likely benign
NM_001080391.2(SP100):c.1475T>A (p.Met492Lys) single nucleotide variant not specified [RCV004457688] Chr2:230473369 [GRCh38]
Chr2:231338084 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1246G>A (p.Ala416Thr) single nucleotide variant not specified [RCV004457685] Chr2:230467170 [GRCh38]
Chr2:231331885 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1346G>T (p.Arg449Leu) single nucleotide variant not specified [RCV004457686] Chr2:230470015 [GRCh38]
Chr2:231334730 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2396C>T (p.Pro799Leu) single nucleotide variant not specified [RCV004457693] Chr2:230541365 [GRCh38]
Chr2:231406080 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2478G>A (p.Met826Ile) single nucleotide variant not specified [RCV004457695] Chr2:230541966 [GRCh38]
Chr2:231406681 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2581C>G (p.Gln861Glu) single nucleotide variant not specified [RCV004457696] Chr2:230542869 [GRCh38]
Chr2:231407584 [GRCh37]
Chr2:2q37.1
likely benign
NM_001080391.2(SP100):c.284C>G (p.Ser95Cys) single nucleotide variant not specified [RCV004457698] Chr2:230444191 [GRCh38]
Chr2:231308906 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.476A>G (p.Glu159Gly) single nucleotide variant not specified [RCV004457700] Chr2:230446855 [GRCh38]
Chr2:231311570 [GRCh37]
Chr2:2q37.1
likely benign
NM_001080391.2(SP100):c.937G>C (p.Ala313Pro) single nucleotide variant not specified [RCV004457704] Chr2:230461378 [GRCh38]
Chr2:231326093 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1241C>T (p.Ala414Val) single nucleotide variant not specified [RCV004457684] Chr2:230467165 [GRCh38]
Chr2:231331880 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.162C>A (p.Phe54Leu) single nucleotide variant not specified [RCV004457691] Chr2:230442991 [GRCh38]
Chr2:231307706 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2471A>C (p.Glu824Ala) single nucleotide variant not specified [RCV004457694] Chr2:230541959 [GRCh38]
Chr2:231406674 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.895G>A (p.Glu299Lys) single nucleotide variant not specified [RCV004457702] Chr2:230461336 [GRCh38]
Chr2:231326051 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1208A>G (p.Asp403Gly) single nucleotide variant not specified [RCV004670680] Chr2:230467132 [GRCh38]
Chr2:231331847 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2174A>T (p.His725Leu) single nucleotide variant not specified [RCV004670684] Chr2:230539346 [GRCh38]
Chr2:231404061 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.901C>A (p.Pro301Thr) single nucleotide variant not specified [RCV004670681] Chr2:230461342 [GRCh38]
Chr2:231326057 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2470G>A (p.Glu824Lys) single nucleotide variant not specified [RCV004868445] Chr2:230541958 [GRCh38]
Chr2:231406673 [GRCh37]
Chr2:2q37.1
likely benign
NM_001080391.2(SP100):c.967A>G (p.Ile323Val) single nucleotide variant not specified [RCV004868446] Chr2:230461408 [GRCh38]
Chr2:231326123 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2270G>A (p.Ser757Asn) single nucleotide variant not specified [RCV004868447] Chr2:230540935 [GRCh38]
Chr2:231405650 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2441G>T (p.Trp814Leu) single nucleotide variant not specified [RCV004868448] Chr2:230541929 [GRCh38]
Chr2:231406644 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.598C>T (p.Pro200Ser) single nucleotide variant not specified [RCV004868449] Chr2:230449572 [GRCh38]
Chr2:231314287 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.2459C>G (p.Thr820Arg) single nucleotide variant not specified [RCV004868450] Chr2:230541947 [GRCh38]
Chr2:231406662 [GRCh37]
Chr2:2q37.1
likely benign
NM_001080391.2(SP100):c.2278G>A (p.Gly760Ser) single nucleotide variant not specified [RCV004868451] Chr2:230540943 [GRCh38]
Chr2:231405658 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.532G>A (p.Glu178Lys) single nucleotide variant not specified [RCV004868452] Chr2:230449096 [GRCh38]
Chr2:231313811 [GRCh37]
Chr2:2q37.1
uncertain significance
NM_001080391.2(SP100):c.1558G>A (p.Val520Ile) single nucleotide variant not specified [RCV004868453] Chr2:230474405 [GRCh38]
Chr2:231339120 [GRCh37]
Chr2:2q37.1
likely benign
NM_001080391.2(SP100):c.2557T>C (p.Phe853Leu) single nucleotide variant not specified [RCV004864929] Chr2:230542845 [GRCh38]
Chr2:231407560 [GRCh37]
Chr2:2q37.1
uncertain significance
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:2939
Count of miRNA genes:1141
Interacting mature miRNAs:1405
Transcripts:ENST00000264052, ENST00000340126, ENST00000341950, ENST00000409112, ENST00000409341, ENST00000409824, ENST00000409897, ENST00000413284, ENST00000427101, ENST00000431952, ENST00000432979, ENST00000452345, ENST00000459786, ENST00000462751, ENST00000466710, ENST00000470940, ENST00000488180, ENST00000492546, ENST00000494508, ENST00000494901
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407162772GWAS811748_HFEV/FVC ratio, response to bronchodilator QTL GWAS811748 (human)0.000001FEV/FVC ratio, response to bronchodilatorforced expiratory volume to forced vital capacity ratio (CMO:0000241)2230447662230447663Human
597145557GWAS1241631_HCOVID-19 QTL GWAS1241631 (human)4e-11COVID-192230432618230432619Human
2289332BW376_HBody weight QTL 376 (human)1.870.00168Body fat amountabdominal2213765566239765566Human
407259198GWAS908174_Hgenomic measurement QTL GWAS908174 (human)0.0000009genomic measurement2230545139230545140Human
597245875GWAS1341949_Hsex hormone-binding globulin measurement QTL GWAS1341949 (human)3e-09sex hormone-binding globulin measurement2230423167230423168Human
597096189GWAS1192263_Hsex hormone-binding globulin measurement QTL GWAS1192263 (human)2e-11sex hormone-binding globulin measurement2230421788230421789Human
597020281GWAS1116355_Hforced expiratory volume, response to bronchodilator QTL GWAS1116355 (human)0.000002forced expiratory volume, response to bronchodilatorforced expiratory volume (CMO:0000254)2230447662230447663Human
597099003GWAS1195077_Hmonocyte count QTL GWAS1195077 (human)3e-10monocyte quantity (VT:0000223)blood monocyte count (CMO:0000032)2230473441230473442Human
407254330GWAS903306_Hgenomic measurement QTL GWAS903306 (human)2e-11genomic measurement2230545139230545140Human
597096921GWAS1192995_Hsex hormone-binding globulin measurement QTL GWAS1192995 (human)3e-13sex hormone-binding globulin measurement2230421788230421789Human
407162267GWAS811243_HFEV/FVC ratio, response to bronchodilator QTL GWAS811243 (human)0.0000006FEV/FVC ratio, response to bronchodilatorforced expiratory volume to forced vital capacity ratio (CMO:0000241)2230468771230468772Human
597020282GWAS1116356_Hforced expiratory volume, response to bronchodilator QTL GWAS1116356 (human)0.000002forced expiratory volume, response to bronchodilatorforced expiratory volume (CMO:0000254)2230468771230468772Human

Markers in Region
RH70945  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372231,280,887 - 231,281,097UniSTSGRCh37
Build 362230,989,131 - 230,989,341RGDNCBI36
Celera2225,057,041 - 225,057,251RGD
Cytogenetic Map2q37.1UniSTS
HuRef2223,121,021 - 223,121,231UniSTS
GeneMap99-GB4 RH Map2711.41UniSTS
NCBI RH Map21877.6UniSTS
RH93607  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372231,334,197 - 231,334,323UniSTSGRCh37
Build 362231,042,441 - 231,042,567RGDNCBI36
Celera2225,110,369 - 225,110,495RGD
Cytogenetic Map2q37.1UniSTS
HuRef2223,173,924 - 223,174,050UniSTS
GeneMap99-GB4 RH Map2714.84UniSTS
SHGC-144697  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372231,310,791 - 231,311,139UniSTSGRCh37
Build 362231,019,035 - 231,019,383RGDNCBI36
Celera2225,086,960 - 225,087,308RGD
Cytogenetic Map2q37.1UniSTS
HuRef2223,150,857 - 223,151,205UniSTS
TNG Radiation Hybrid Map2128460.0UniSTS
D2S2641  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372231,334,835 - 231,334,958UniSTSGRCh37
Build 362231,043,079 - 231,043,202RGDNCBI36
Celera2225,111,007 - 225,111,130RGD
Cytogenetic Map2q37.1UniSTS
HuRef2223,174,562 - 223,174,685UniSTS
GeneMap99-GB4 RH Map2713.52UniSTS
Whitehead-RH Map21057.2UniSTS
Whitehead-YAC Contig Map2 UniSTS
NCBI RH Map21877.6UniSTS
WIAF-2192  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372231,330,508 - 231,330,607UniSTSGRCh37
Build 362231,038,752 - 231,038,851RGDNCBI36
Celera2225,106,673 - 225,106,772RGD
Cytogenetic Map2q37.1UniSTS
HuRef2223,170,227 - 223,170,326UniSTS
GeneMap99-GB4 RH Map2713.52UniSTS
PMC56901P1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372231,379,275 - 231,379,888UniSTSGRCh37
Build 362231,087,519 - 231,088,132RGDNCBI36
Celera2225,155,648 - 225,156,261RGD
Cytogenetic Map2q35UniSTS
Cytogenetic Map2q37.1UniSTS
HuRef2223,219,240 - 223,219,853UniSTS
PMC56901P2  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372231,375,422 - 231,375,951UniSTSGRCh37
Build 362231,083,666 - 231,084,195RGDNCBI36
Celera2225,151,796 - 225,152,325RGD
Cytogenetic Map2q37.1UniSTS
HuRef2223,215,390 - 223,215,919UniSTS
REN30944  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,626,332 - 132,626,581UniSTSGRCh37
GRCh372231,355,974 - 231,356,220UniSTSGRCh37
Build 362231,064,218 - 231,064,464RGDNCBI36
Celera6133,373,214 - 133,373,463UniSTS
Celera2225,132,150 - 225,132,396RGD
Cytogenetic Map6q23.2UniSTS
Cytogenetic Map2q37.1UniSTS
HuRef6130,201,426 - 130,201,675UniSTS
HuRef5125,450,621 - 125,450,869UniSTS
D2S2624  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372231,326,089 - 231,326,196UniSTSGRCh37
Build 362231,034,333 - 231,034,440RGDNCBI36
Celera2225,102,254 - 225,102,361RGD
Cytogenetic Map2q37.1UniSTS
HuRef2223,165,808 - 223,165,915UniSTS
GeneMap99-GB4 RH Map2713.52UniSTS
Whitehead-RH Map21057.2UniSTS
Whitehead-YAC Contig Map2 UniSTS
NCBI RH Map21877.6UniSTS
SHGC-60177  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372231,334,119 - 231,334,220UniSTSGRCh37
Build 362231,042,363 - 231,042,464RGDNCBI36
Celera2225,110,291 - 225,110,392RGD
Cytogenetic Map2q37.1UniSTS
HuRef2223,173,846 - 223,173,947UniSTS
TNG Radiation Hybrid Map2128478.0UniSTS
RH68107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372231,334,201 - 231,334,343UniSTSGRCh37
Build 362231,042,445 - 231,042,587RGDNCBI36
Celera2225,110,373 - 225,110,515RGD
Cytogenetic Map2q37.1UniSTS
HuRef2223,173,928 - 223,174,070UniSTS
GeneMap99-GB4 RH Map2713.73UniSTS
GDB:335751  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map10q24.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map3q22.2UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map6p21.1-p12.2UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map13q12.13UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map4q24UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map10q24-q25UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map9q22.32UniSTS
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
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
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


Expression

RNA-SEQ Expression

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 4953 1726 2336 6 624 1951 465 2253 7306 6472 52 3729 1 852 1740 1602 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029842 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001080391 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001206701 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001206702 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001206703 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001206704 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003113 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA810108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC009949 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC010149 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF056322 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF076675 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF146342 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF255565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF378670 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI886092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK090565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091898 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK126529 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK160379 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293373 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW978040 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC011562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471063 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749288 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA442074 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA562355 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L79986 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L79987 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L79988 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L79989 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M60618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U36501 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X95472 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000264052   ⟹   ENSP00000264052
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,415,942 - 230,516,527 (+)Ensembl
Ensembl Acc Id: ENST00000340126   ⟹   ENSP00000343023
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,416,201 - 230,545,606 (+)Ensembl
Ensembl Acc Id: ENST00000409112   ⟹   ENSP00000386427
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,416,266 - 230,508,146 (+)Ensembl
Ensembl Acc Id: ENST00000409341   ⟹   ENSP00000386404
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,416,247 - 230,470,517 (+)Ensembl
Ensembl Acc Id: ENST00000409824   ⟹   ENSP00000387311
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,416,240 - 230,470,489 (+)Ensembl
Ensembl Acc Id: ENST00000409897   ⟹   ENSP00000386998
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,416,756 - 230,470,530 (+)Ensembl
Ensembl Acc Id: ENST00000413284   ⟹   ENSP00000400277
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,462,435 - 230,470,103 (+)Ensembl
Ensembl Acc Id: ENST00000427101   ⟹   ENSP00000399389
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,416,156 - 230,470,534 (+)Ensembl
Ensembl Acc Id: ENST00000431952   ⟹   ENSP00000393679
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,504,262 - 230,544,090 (+)Ensembl
Ensembl Acc Id: ENST00000432979   ⟹   ENSP00000391616
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,416,221 - 230,449,380 (+)Ensembl
Ensembl Acc Id: ENST00000452345   ⟹   ENSP00000416563
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,462,467 - 230,494,460 (+)Ensembl
Ensembl Acc Id: ENST00000459786
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,504,217 - 230,506,766 (+)Ensembl
Ensembl Acc Id: ENST00000462751
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,463,618 - 230,467,147 (+)Ensembl
Ensembl Acc Id: ENST00000466710
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,449,569 - 230,462,629 (+)Ensembl
Ensembl Acc Id: ENST00000470940
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,449,375 - 230,461,328 (+)Ensembl
Ensembl Acc Id: ENST00000488180
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,537,642 - 230,544,090 (+)Ensembl
Ensembl Acc Id: ENST00000492546
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,473,117 - 230,498,522 (+)Ensembl
Ensembl Acc Id: ENST00000494508
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,468,832 - 230,470,360 (+)Ensembl
Ensembl Acc Id: ENST00000494901
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,508,146 - 230,543,122 (+)Ensembl
RefSeq Acc Id: NM_001080391   ⟹   NP_001073860
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382230,416,201 - 230,545,606 (+)NCBI
GRCh372231,280,871 - 231,410,317 (+)ENTREZGENE
GRCh372231,280,871 - 231,410,317 (+)NCBI
Build 362230,989,115 - 231,118,561 (+)NCBI Archive
HuRef2223,121,005 - 223,250,289 (+)ENTREZGENE
CHM1_12231,286,764 - 231,416,096 (+)NCBI
T2T-CHM13v2.02230,899,281 - 231,028,667 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001206701   ⟹   NP_001193630
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382230,416,201 - 230,508,146 (+)NCBI
GRCh372231,280,871 - 231,410,317 (+)NCBI
HuRef2223,121,005 - 223,250,289 (+)ENTREZGENE
CHM1_12231,286,764 - 231,378,696 (+)NCBI
T2T-CHM13v2.02230,899,281 - 230,991,224 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001206702   ⟹   NP_001193631
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382230,416,201 - 230,470,530 (+)NCBI
GRCh372231,280,871 - 231,410,317 (+)NCBI
HuRef2223,121,005 - 223,250,289 (+)ENTREZGENE
CHM1_12231,286,764 - 231,340,769 (+)NCBI
T2T-CHM13v2.02230,899,281 - 230,953,608 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001206703   ⟹   NP_001193632
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382230,416,201 - 230,470,530 (+)NCBI
GRCh372231,280,871 - 231,410,317 (+)NCBI
HuRef2223,121,005 - 223,250,289 (+)ENTREZGENE
CHM1_12231,286,764 - 231,340,769 (+)NCBI
T2T-CHM13v2.02230,899,281 - 230,953,608 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001206704   ⟹   NP_001193633
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382230,416,756 - 230,470,530 (+)NCBI
GRCh372231,280,871 - 231,410,317 (+)NCBI
HuRef2223,121,005 - 223,250,289 (+)ENTREZGENE
CHM1_12231,287,364 - 231,340,769 (+)NCBI
T2T-CHM13v2.02230,899,836 - 230,953,608 (+)NCBI
Sequence:
RefSeq Acc Id: NM_003113   ⟹   NP_003104
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382230,416,201 - 230,516,527 (+)NCBI
GRCh372231,280,871 - 231,410,317 (+)ENTREZGENE
GRCh372231,280,871 - 231,410,317 (+)NCBI
Build 362230,989,115 - 231,089,486 (+)NCBI Archive
HuRef2223,121,005 - 223,250,289 (+)ENTREZGENE
CHM1_12231,286,764 - 231,387,085 (+)NCBI
T2T-CHM13v2.02230,899,281 - 230,999,587 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001073860 (Get FASTA)   NCBI Sequence Viewer  
  NP_001193630 (Get FASTA)   NCBI Sequence Viewer  
  NP_001193631 (Get FASTA)   NCBI Sequence Viewer  
  NP_001193632 (Get FASTA)   NCBI Sequence Viewer  
  NP_001193633 (Get FASTA)   NCBI Sequence Viewer  
  NP_003104 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA35537 (Get FASTA)   NCBI Sequence Viewer  
  AAC39790 (Get FASTA)   NCBI Sequence Viewer  
  AAC50743 (Get FASTA)   NCBI Sequence Viewer  
  AAF39781 (Get FASTA)   NCBI Sequence Viewer  
  AAF43098 (Get FASTA)   NCBI Sequence Viewer  
  AAH11562 (Get FASTA)   NCBI Sequence Viewer  
  AAK51202 (Get FASTA)   NCBI Sequence Viewer  
  AAK57703 (Get FASTA)   NCBI Sequence Viewer  
  AAL77438 (Get FASTA)   NCBI Sequence Viewer  
  AAL77439 (Get FASTA)   NCBI Sequence Viewer  
  AAL77440 (Get FASTA)   NCBI Sequence Viewer  
  AAL77441 (Get FASTA)   NCBI Sequence Viewer  
  AAX88870 (Get FASTA)   NCBI Sequence Viewer  
  AAY14879 (Get FASTA)   NCBI Sequence Viewer  
  BAD18722 (Get FASTA)   NCBI Sequence Viewer  
  BAG56886 (Get FASTA)   NCBI Sequence Viewer  
  BAG65081 (Get FASTA)   NCBI Sequence Viewer  
  CAA64744 (Get FASTA)   NCBI Sequence Viewer  
  CAH18143 (Get FASTA)   NCBI Sequence Viewer  
  EAW70927 (Get FASTA)   NCBI Sequence Viewer  
  EAW70928 (Get FASTA)   NCBI Sequence Viewer  
  EAW70929 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000264052
  ENSP00000264052.5
  ENSP00000343023
  ENSP00000343023.4
  ENSP00000386404
  ENSP00000386404.1
  ENSP00000386427
  ENSP00000386427.1
  ENSP00000386998
  ENSP00000386998.1
  ENSP00000399389
  ENSP00000399389.2
GenBank Protein P23497 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001073860   ⟸   NM_001080391
- Peptide Label: isoform 1
- UniProtKB: P23497 (UniProtKB/Swiss-Prot),   Q6ZMK3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_003104   ⟸   NM_003113
- Peptide Label: isoform 2
- UniProtKB: Q9NP33 (UniProtKB/Swiss-Prot),   Q96T95 (UniProtKB/Swiss-Prot),   Q96T24 (UniProtKB/Swiss-Prot),   Q96F70 (UniProtKB/Swiss-Prot),   Q8TE34 (UniProtKB/Swiss-Prot),   Q13343 (UniProtKB/Swiss-Prot),   O75450 (UniProtKB/Swiss-Prot),   F8WFE2 (UniProtKB/Swiss-Prot),   E9PH61 (UniProtKB/Swiss-Prot),   E7EUA7 (UniProtKB/Swiss-Prot),   B8ZZD8 (UniProtKB/Swiss-Prot),   B4DDX5 (UniProtKB/Swiss-Prot),   Q9UE32 (UniProtKB/Swiss-Prot),   P23497 (UniProtKB/Swiss-Prot),   Q53TD0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001193630   ⟸   NM_001206701
- Peptide Label: isoform 3
- UniProtKB: P23497 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001193631   ⟸   NM_001206702
- Peptide Label: isoform 4
- UniProtKB: E9PHV6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001193632   ⟸   NM_001206703
- Peptide Label: isoform 5
- UniProtKB: E9PHV6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001193633   ⟸   NM_001206704
- Peptide Label: isoform 6
- UniProtKB: E9PHV6 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000400277   ⟸   ENST00000413284
Ensembl Acc Id: ENSP00000416563   ⟸   ENST00000452345
Ensembl Acc Id: ENSP00000399389   ⟸   ENST00000427101
Ensembl Acc Id: ENSP00000393679   ⟸   ENST00000431952
Ensembl Acc Id: ENSP00000343023   ⟸   ENST00000340126
Ensembl Acc Id: ENSP00000391616   ⟸   ENST00000432979
Ensembl Acc Id: ENSP00000387311   ⟸   ENST00000409824
Ensembl Acc Id: ENSP00000386998   ⟸   ENST00000409897
Ensembl Acc Id: ENSP00000386404   ⟸   ENST00000409341
Ensembl Acc Id: ENSP00000386427   ⟸   ENST00000409112
Ensembl Acc Id: ENSP00000264052   ⟸   ENST00000264052
Protein Domains
HMG box   HSR   PHD-type   SAND

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P23497-F1-model_v2 AlphaFold P23497 1-879 view protein structure

Promoters
RGD ID:6863046
Promoter ID:EPDNEW_H4688
Type:initiation region
Name:SP100_1
Description:SP100 nuclear antigen
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382230,416,220 - 230,416,280EPDNEW
RGD ID:6811972
Promoter ID:HG_ACW:47783
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:SP100ANDHMG1L3.HAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 362230,984,551 - 230,985,051 (+)MPROMDB
RGD ID:6798227
Promoter ID:HG_KWN:37633
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000341950,   ENST00000409897,   NM_001080391,   OTTHUMT00000256914,   OTTHUMT00000332254,   UC002VQQ.1,   UC002VQR.1,   UC002VQS.2
Position:
Human AssemblyChrPosition (strand)Source
Build 362230,989,001 - 230,989,501 (+)MPROMDB
RGD ID:6851978
Promoter ID:EP73795
Type:multiple initiation site
Name:HS_SP100
Description:Nuclear antigen Sp100.
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 AssemblyChrPosition (strand)Source
Build 362230,989,179 - 230,989,239EPD
RGD ID:6798224
Promoter ID:HG_KWN:37634
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000332255,   OTTHUMT00000332256
Position:
Human AssemblyChrPosition (strand)Source
Build 362231,021,676 - 231,022,777 (+)MPROMDB
RGD ID:6798226
Promoter ID:HG_KWN:37635
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000332258
Position:
Human AssemblyChrPosition (strand)Source
Build 362231,034,101 - 231,034,601 (+)MPROMDB
RGD ID:6798228
Promoter ID:HG_KWN:37636
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000332260,   OTTHUMT00000332261
Position:
Human AssemblyChrPosition (strand)Source
Build 362231,034,511 - 231,035,412 (+)MPROMDB
RGD ID:6798225
Promoter ID:HG_KWN:37637
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000332257
Position:
Human AssemblyChrPosition (strand)Source
Build 362231,036,764 - 231,037,264 (+)MPROMDB
RGD ID:6798230
Promoter ID:HG_KWN:37638
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000332259
Position:
Human AssemblyChrPosition (strand)Source
Build 362231,040,621 - 231,041,121 (+)MPROMDB
RGD ID:6798231
Promoter ID:HG_KWN:37639
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   K562,   Lymphoblastoid
Transcripts:OTTHUMT00000332263
Position:
Human AssemblyChrPosition (strand)Source
Build 362231,045,096 - 231,046,527 (+)MPROMDB
RGD ID:6798229
Promoter ID:HG_KWN:37640
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000332262,   UC010FXP.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362231,077,221 - 231,077,721 (+)MPROMDB
RGD ID:6798222
Promoter ID:HG_KWN:37642
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000332251
Position:
Human AssemblyChrPosition (strand)Source
Build 362231,080,621 - 231,082,872 (+)MPROMDB
RGD ID:6798223
Promoter ID:HG_KWN:37644
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000332253
Position:
Human AssemblyChrPosition (strand)Source
Build 362231,110,561 - 231,112,267 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:11206 AgrOrtholog
COSMIC SP100 COSMIC
Ensembl Genes ENSG00000067066 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000264052 ENTREZGENE
  ENST00000264052.9 UniProtKB/Swiss-Prot
  ENST00000340126 ENTREZGENE
  ENST00000340126.9 UniProtKB/Swiss-Prot
  ENST00000409112 ENTREZGENE
  ENST00000409112.5 UniProtKB/Swiss-Prot
  ENST00000409341 ENTREZGENE
  ENST00000409341.5 UniProtKB/Swiss-Prot
  ENST00000409897 ENTREZGENE
  ENST00000409897.5 UniProtKB/Swiss-Prot
  ENST00000427101 ENTREZGENE
  ENST00000427101.6 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.30.10 UniProtKB/Swiss-Prot
  3.10.390.10 UniProtKB/Swiss-Prot
GTEx ENSG00000067066 GTEx
HGNC ID HGNC:11206 ENTREZGENE
Human Proteome Map SP100 Human Proteome Map
InterPro HMG_box_dom UniProtKB/Swiss-Prot
  HMG_box_dom_sf UniProtKB/Swiss-Prot
  HSR_dom UniProtKB/Swiss-Prot
  SAND-like_dom_sf UniProtKB/Swiss-Prot
  SAND_dom UniProtKB/Swiss-Prot
  Sp110/Sp140/Sp140L UniProtKB/Swiss-Prot
KEGG Report hsa:6672 UniProtKB/Swiss-Prot
NCBI Gene 6672 ENTREZGENE
OMIM 604585 OMIM
PANTHER NUCLEAR AUTOANTIGEN SP-100 UniProtKB/Swiss-Prot
  PTHR46386 UniProtKB/Swiss-Prot
Pfam HMG_box UniProtKB/Swiss-Prot
  HMG_box_2 UniProtKB/Swiss-Prot
  HSR UniProtKB/Swiss-Prot
  SAND UniProtKB/Swiss-Prot
PharmGKB PA36043 PharmGKB
PRINTS HIGHMOBLTY12 UniProtKB/Swiss-Prot
PROSITE HMG_BOX_2 UniProtKB/Swiss-Prot
  HSR UniProtKB/Swiss-Prot
  SAND UniProtKB/Swiss-Prot
SMART HMG UniProtKB/Swiss-Prot
  SAND UniProtKB/Swiss-Prot
Superfamily-SCOP SSF47095 UniProtKB/Swiss-Prot
  SSF63763 UniProtKB/Swiss-Prot
UniProt B4DDX5 ENTREZGENE
  B8ZZD8 ENTREZGENE
  C9JBL0_HUMAN UniProtKB/TrEMBL
  E7EUA7 ENTREZGENE
  E9PH61 ENTREZGENE
  E9PHV6 ENTREZGENE, UniProtKB/TrEMBL
  F8WFE2 ENTREZGENE
  H0Y4R8_HUMAN UniProtKB/TrEMBL
  H7C1G8_HUMAN UniProtKB/TrEMBL
  H7C4B4_HUMAN UniProtKB/TrEMBL
  O75450 ENTREZGENE
  P23497 ENTREZGENE
  Q13343 ENTREZGENE
  Q4ZG64_HUMAN UniProtKB/TrEMBL
  Q53TD0 ENTREZGENE, UniProtKB/TrEMBL
  Q6ZMK3 ENTREZGENE, UniProtKB/TrEMBL
  Q8TE34 ENTREZGENE
  Q96F70 ENTREZGENE
  Q96T24 ENTREZGENE
  Q96T95 ENTREZGENE
  Q9NP33 ENTREZGENE
  Q9P0W1_HUMAN UniProtKB/TrEMBL
  Q9UE32 ENTREZGENE
  SP100_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary B4DDX5 UniProtKB/Swiss-Prot
  B8ZZD8 UniProtKB/Swiss-Prot
  E7EUA7 UniProtKB/Swiss-Prot
  E9PH61 UniProtKB/Swiss-Prot
  F8WFE2 UniProtKB/Swiss-Prot
  O75450 UniProtKB/Swiss-Prot
  Q13343 UniProtKB/Swiss-Prot
  Q8TE34 UniProtKB/Swiss-Prot
  Q96F70 UniProtKB/Swiss-Prot
  Q96T24 UniProtKB/Swiss-Prot
  Q96T95 UniProtKB/Swiss-Prot
  Q9NP33 UniProtKB/Swiss-Prot
  Q9UE32 UniProtKB/Swiss-Prot