LSP1 (lymphocyte specific protein 1) - Rat Genome Database

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Gene: LSP1 (lymphocyte specific protein 1) Homo sapiens
Analyze
Symbol: LSP1
Name: lymphocyte specific protein 1
RGD ID: 1314573
HGNC Page HGNC:6707
Description: Predicted to enable actin binding activity. Predicted to be involved in cellular defense response. Predicted to act upstream of or within cellular response to interleukin-7; chemotaxis; and defense response. Located in extracellular exosome and membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: 47 kDa actin binding protein; 47 kDa actin-binding protein; 52 kDa phosphoprotein; F-actin binding and cytoskeleton associated protein; leufactin (leukocyte F-actin binding protein); leukocyte-specific protein 1; lymphocyte-specific antigen WP34; lymphocyte-specific protein 1; lymphocyte-specific protein pp52; pp52; WP34
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: LSP1P1   LSP1P2   LSP1P4   LSP1P5  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38111,853,084 - 1,892,263 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl111,850,904 - 1,892,267 (+)EnsemblGRCh38hg38GRCh38
GRCh37111,874,314 - 1,913,493 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36111,830,776 - 1,870,069 (+)NCBINCBI36Build 36hg18NCBI36
Build 34111,830,882 - 1,870,068NCBI
Celera11333 - 5,385 (+)NCBICelera
Celera111,911,965 - 1,943,689 (+)NCBICelera
Cytogenetic Map11p15.5NCBI
HuRef111,665,106 - 1,704,058 (+)NCBIHuRef
CHM1_1111,873,026 - 1,912,407 (+)NCBICHM1_1
T2T-CHM13v2.0111,938,882 - 1,978,157 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP,ISO)
17beta-estradiol 3-benzoate  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (ISO)
4-amino-2,6-dinitrotoluene  (ISO)
4-hydroxyphenyl retinamide  (ISO)
4-tert-Octylphenol  (ISO)
6-propyl-2-thiouracil  (ISO)
acetamide  (ISO)
acrylamide  (ISO)
aflatoxin B1  (EXP,ISO)
Aflatoxin B2 alpha  (EXP)
all-trans-retinoic acid  (EXP,ISO)
amphetamine  (ISO)
arsane  (EXP)
arsenic atom  (EXP)
arsenous acid  (EXP)
atrazine  (ISO)
benzo[a]pyrene  (EXP)
benzo[e]pyrene  (EXP)
Benzo[k]fluoranthene  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (EXP,ISO)
butanal  (EXP)
calcitriol  (EXP)
cantharidin  (ISO)
carbon nanotube  (ISO)
carmustine  (ISO)
chlordecone  (ISO)
chloroprene  (ISO)
choline  (ISO)
cisplatin  (EXP)
clofibrate  (ISO)
cocaine  (ISO)
copper(II) sulfate  (EXP)
Cuprizon  (ISO)
cyclosporin A  (EXP)
decabromodiphenyl ether  (ISO)
deoxynivalenol  (EXP,ISO)
dexamethasone  (EXP)
diarsenic trioxide  (EXP)
diazinon  (EXP,ISO)
dieldrin  (ISO)
diethylstilbestrol  (ISO)
dioxygen  (ISO)
diuron  (ISO)
doxorubicin  (ISO)
elemental selenium  (EXP)
fenvalerate  (ISO)
folic acid  (ISO)
formaldehyde  (ISO)
fulvestrant  (EXP)
genistein  (ISO)
gentamycin  (ISO)
glycidol  (ISO)
L-methionine  (ISO)
methamphetamine  (ISO)
methapyrilene  (EXP)
methotrexate  (EXP,ISO)
methylmercury chloride  (ISO)
N-nitrosodiethylamine  (ISO)
nickel dichloride  (ISO)
nickel sulfate  (EXP)
niclosamide  (EXP)
ozone  (EXP,ISO)
p-tert-Amylphenol  (ISO)
paracetamol  (ISO)
perfluorooctane-1-sulfonic acid  (EXP)
piperonyl butoxide  (ISO)
pirinixic acid  (ISO)
potassium chromate  (EXP)
selenium atom  (EXP)
silicon dioxide  (EXP,ISO)
silver atom  (ISO)
silver(0)  (ISO)
succimer  (ISO)
sulforaphane  (EXP)
tamibarotene  (EXP)
testosterone  (ISO)
thioacetamide  (ISO)
tioguanine  (ISO)
trichloroethene  (ISO)
triclosan  (EXP)
triptonide  (ISO)
tris(2-butoxyethyl) phosphate  (EXP)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)
zearalenone  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:2174784   PMID:2295815   PMID:2674678   PMID:7561054   PMID:7706408   PMID:8125298   PMID:8274738   PMID:8468046   PMID:8838798   PMID:8995217   PMID:9890705   PMID:10233704  
PMID:10925289   PMID:11746662   PMID:12477932   PMID:12972289   PMID:14702039   PMID:15090600   PMID:15188402   PMID:15489334   PMID:17296787   PMID:17481585   PMID:17529967   PMID:17827388  
PMID:17997823   PMID:18029348   PMID:18437204   PMID:18973230   PMID:19094228   PMID:19232126   PMID:19656774   PMID:19700666   PMID:19718030   PMID:19789366   PMID:19843670   PMID:19856316  
PMID:19913121   PMID:19946888   PMID:20054709   PMID:20095854   PMID:20145138   PMID:20237496   PMID:20417875   PMID:20453838   PMID:20458337   PMID:20554749   PMID:20605201   PMID:20628086  
PMID:21127985   PMID:21297633   PMID:22454379   PMID:23119100   PMID:23128233   PMID:23182705   PMID:23535729   PMID:23824909   PMID:23936387   PMID:24162774   PMID:24163127   PMID:24681604  
PMID:24867235   PMID:25342443   PMID:25640309   PMID:26191300   PMID:26554018   PMID:26641092   PMID:27165221   PMID:27590509   PMID:28514442   PMID:29080679   PMID:29410425   PMID:30009671  
PMID:30397336   PMID:32279313   PMID:32738313   PMID:32770294   PMID:33961781   PMID:34691030   PMID:35156780   PMID:36397430   PMID:37928435   PMID:38254711   PMID:38511641  


Genomics

Comparative Map Data
LSP1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38111,853,084 - 1,892,263 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl111,850,904 - 1,892,267 (+)EnsemblGRCh38hg38GRCh38
GRCh37111,874,314 - 1,913,493 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36111,830,776 - 1,870,069 (+)NCBINCBI36Build 36hg18NCBI36
Build 34111,830,882 - 1,870,068NCBI
Celera11333 - 5,385 (+)NCBICelera
Celera111,911,965 - 1,943,689 (+)NCBICelera
Cytogenetic Map11p15.5NCBI
HuRef111,665,106 - 1,704,058 (+)NCBIHuRef
CHM1_1111,873,026 - 1,912,407 (+)NCBICHM1_1
T2T-CHM13v2.0111,938,882 - 1,978,157 (+)NCBIT2T-CHM13v2.0
Lsp1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm397142,014,583 - 142,048,605 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl7142,014,546 - 142,048,604 (+)EnsemblGRCm39 Ensembl
GRCm387142,458,223 - 142,494,868 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl7142,460,809 - 142,494,867 (+)EnsemblGRCm38mm10GRCm38
MGSCv377149,646,775 - 149,680,504 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv367142,281,233 - 142,303,989 (+)NCBIMGSCv36mm8
Celera7142,216,990 - 142,250,583 (+)NCBICelera
Cytogenetic Map7F5NCBI
cM Map787.93NCBI
Lsp1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81207,044,157 - 207,077,891 (+)NCBIGRCr8
mRatBN7.21197,614,677 - 197,648,414 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1197,614,687 - 197,648,416 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1205,987,391 - 206,021,123 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01213,073,261 - 213,106,982 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01205,747,412 - 205,781,135 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01215,628,750 - 215,662,505 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1215,628,785 - 215,662,504 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01222,524,134 - 222,557,295 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41202,707,305 - 202,741,026 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11202,867,020 - 202,901,488 (+)NCBI
Celera1195,233,475 - 195,265,776 (+)NCBICelera
Cytogenetic Map1q41NCBI
Lsp1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495542213,664,129 - 13,700,126 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495542213,664,594 - 13,697,682 (+)NCBIChiLan1.0ChiLan1.0
LSP1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v294,275,003 - 4,316,280 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1113,485,759 - 3,527,683 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0111,889,625 - 1,931,192 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1111,921,905 - 1,963,192 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl111,921,905 - 1,963,192 (+)Ensemblpanpan1.1panPan2
LSP1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11846,087,886 - 46,127,307 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1846,087,922 - 46,127,263 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1844,698,103 - 44,737,407 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01846,769,276 - 46,808,582 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1846,769,308 - 46,808,582 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11846,229,553 - 46,255,843 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01845,796,936 - 45,836,174 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01846,543,073 - 46,582,385 (+)NCBIUU_Cfam_GSD_1.0
Lsp1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244049471,497,865 - 1,532,878 (+)NCBIHiC_Itri_2
SpeTri2.0NW_004936816752,021 - 786,998 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
LSP1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl21,262,079 - 1,295,887 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.121,261,957 - 1,295,891 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
LSP1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.111,672,916 - 1,713,160 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl11,672,695 - 1,715,502 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603898,869,425 - 98,909,619 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Lsp1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462476714,747,861 - 14,779,941 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in LSP1
25 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11p15.5-15.4(chr11:196966-3377077)x3 copy number gain See cases [RCV000050947] Chr11:196966..3377077 [GRCh38]
Chr11:196966..3398307 [GRCh37]
Chr11:186966..3354883 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:196966-4435344)x3 copy number gain See cases [RCV000050927] Chr11:196966..4435344 [GRCh38]
Chr11:196966..4456574 [GRCh37]
Chr11:186966..4413150 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5(chr11:758848-1998025)x1 copy number loss See cases [RCV000052645] Chr11:758848..1998025 [GRCh38]
Chr11:758848..2019255 [GRCh37]
Chr11:748848..1975831 [NCBI36]
Chr11:11p15.5		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:218365-3377077)x3 copy number gain See cases [RCV000053614] Chr11:218365..3377077 [GRCh38]
Chr11:218365..3398307 [GRCh37]
Chr11:208365..3354883 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5-13(chr11:202758-31726224)x3 copy number gain See cases [RCV000053613] Chr11:202758..31726224 [GRCh38]
Chr11:202758..31747772 [GRCh37]
Chr11:192758..31704348 [NCBI36]
Chr11:11p15.5-13		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:196966-3624139)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053592]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053592]|See cases [RCV000053592] Chr11:196966..3624139 [GRCh38]
Chr11:196966..3645369 [GRCh37]
Chr11:186966..3601945 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
NM_001242932.1(LSP1):c.361G>A (p.Gly121Ser) single nucleotide variant Malignant melanoma [RCV000069285] Chr11:1866835 [GRCh38]
Chr11:1888065 [GRCh37]
Chr11:1844641 [NCBI36]
Chr11:11p15.5		 not provided
NM_001242932.1(LSP1):c.437+2940C>A single nucleotide variant Lung cancer [RCV000109900] Chr11:1869851 [GRCh38]
Chr11:1891081 [GRCh37]
Chr11:11p15.5		 uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:10701-5080415)x2 copy number gain See cases [RCV001310286] Chr11:10701..5080415 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5-15.1(chr11:446754-18904742)x3 copy number gain See cases [RCV000133997] Chr11:446754..18904742 [GRCh38]
Chr11:446754..18926289 [GRCh37]
Chr11:436754..18882865 [NCBI36]
Chr11:11p15.5-15.1		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:1537379-3360769)x3 copy number gain See cases [RCV000136847] Chr11:1537379..3360769 [GRCh38]
Chr11:1558609..3381999 [GRCh37]
Chr11:1515185..3338575 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:61793-10727969)x3 copy number gain See cases [RCV000139987] Chr11:61793..10727969 [GRCh38]
Chr11:61793..10749516 [GRCh37]
Chr11:51793..10706092 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:1132899-3213923)x1 copy number loss See cases [RCV000142464] Chr11:1132899..3213923 [GRCh38]
Chr11:1126807..3235153 [GRCh37]
Chr11:1116807..3191729 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:196855-5321874)x3 copy number gain See cases [RCV000142890] Chr11:196855..5321874 [GRCh38]
Chr11:196855..5343104 [GRCh37]
Chr11:186855..5299680 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5(chr11:196855-2116185)x3 copy number gain See cases [RCV000142923] Chr11:196855..2116185 [GRCh38]
Chr11:196855..2137415 [GRCh37]
Chr11:186855..2093991 [NCBI36]
Chr11:11p15.5		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:193187-5291338)x3 copy number gain See cases [RCV000446036] Chr11:193187..5291338 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5(chr11:1621232-2228572) copy number gain Beckwith-Wiedemann syndrome [RCV002280763] Chr11:1621232..2228572 [GRCh37]
Chr11:11p15.5		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-6644927)x3 copy number gain See cases [RCV000449417] Chr11:230615..6644927 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5-12(chr11:230615-37698540)x3 copy number gain See cases [RCV000511561] Chr11:230615..37698540 [GRCh37]
Chr11:11p15.5-12		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-15.3(chr11:193146-12643136) copy number gain Silver-Russell syndrome 1 [RCV000767567] Chr11:193146..12643136 [GRCh37]
Chr11:11p15.5-15.3		 pathogenic
GRCh37/hg19 11p15.5-14.3(chr11:230615-25584362)x3 copy number gain See cases [RCV000512225] Chr11:230615..25584362 [GRCh37]
Chr11:11p15.5-14.3		 pathogenic
GRCh37/hg19 11p15.5-13(chr11:230615-31995219)x3 copy number gain See cases [RCV000512477] Chr11:230615..31995219 [GRCh37]
Chr11:11p15.5-13		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-9704511)x3 copy number gain not provided [RCV000683369] Chr11:230615..9704511 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5-15.1(chr11:230615-17099213)x3 copy number gain not provided [RCV000683372] Chr11:230615..17099213 [GRCh37]
Chr11:11p15.5-15.1		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
NC_000011.9:g.(?_532616)_(2906985_?)dup duplication Neuronal ceroid lipofuscinosis [RCV001032557] Chr11:532616..2906985 [GRCh37]
Chr11:11p15.5-15.4		 uncertain significance
GRCh37/hg19 11p15.5-13(chr11:235934-33826995)x3 copy number gain not provided [RCV001006372] Chr11:235934..33826995 [GRCh37]
Chr11:11p15.5-13		 pathogenic
NC_000011.9:g.(?_1774733)_(2019125_?)dup duplication Neuronal ceroid lipofuscinosis [RCV003107551] Chr11:1774733..2019125 [GRCh37]
Chr11:11p15.5		 uncertain significance
NC_000011.9:g.(?_612625)_(2193840_?)dup duplication Immunodeficiency 39 [RCV001033372] Chr11:612625..2193840 [GRCh37]
Chr11:11p15.5		 uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:230615-4851537)x3 copy number gain See cases [RCV001263059] Chr11:230615..4851537 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:210300-8664358)x3 copy number gain Silver-Russell syndrome 1 [RCV001263222] Chr11:210300..8664358 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NC_000011.9:g.(?_612625)_(2193840_?)dup duplication Autosomal recessive DOPA responsive dystonia [RCV001301561]|Immunodeficiency 39 [RCV001033372] Chr11:612625..2193840 [GRCh37]
Chr11:11p15.5		 uncertain significance
NC_000011.9:g.(?_298501)_(4113028_?)dup duplication Early infantile epileptic encephalopathy with suppression bursts [RCV001316682] Chr11:298501..4113028 [GRCh37]
Chr11:11p15.5-15.4		 uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:230615-5525355)x3 copy number gain not provided [RCV001825269] Chr11:230615..5525355 [GRCh37]
Chr11:11p15.5-15.4		 not provided
GRCh37/hg19 11p15.5(chr11:1719815-2321109)x3 copy number gain not provided [RCV001827983] Chr11:1719815..2321109 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NC_000011.9:g.(?_1278740)_(2906719_?)dup duplication Autosomal recessive DOPA responsive dystonia [RCV003113999] Chr11:1278740..2906719 [GRCh37]
Chr11:11p15.5-15.4		 uncertain significance
NC_000011.9:g.(?_721044)_(3988932_?)dup duplication not provided [RCV003113442] Chr11:721044..3988932 [GRCh37]
Chr11:11p15.5-15.4		 uncertain significance
GRCh37/hg19 11p15.5-14.2(chr11:230615-26881146)x3 copy number gain See cases [RCV002286351] Chr11:230615..26881146 [GRCh37]
Chr11:11p15.5-14.2		 pathogenic
NC_000011.10:g.(499700_4999400)_(5279346_5279697)del deletion Thalassemia, gamma-delta-beta [RCV000015529] Chr11:4999400..5279346 [GRCh38]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230616-8250724)x3 copy number gain not provided [RCV002472435] Chr11:230616..8250724 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5(chr11:461373-2157956)x4 copy number gain not provided [RCV002473945] Chr11:461373..2157956 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_002339.3(LSP1):c.40G>A (p.Glu14Lys) single nucleotide variant Inborn genetic diseases [RCV002802763] Chr11:1853184 [GRCh38]
Chr11:1874414 [GRCh37]
Chr11:11p15.5		 uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:192764-3362853)x3 copy number gain not provided [RCV003484828] Chr11:192764..3362853 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NM_001395380.1(PRR33):c.15T>C (p.Ala5=) single nucleotide variant not provided [RCV003424763] Chr11:1890570 [GRCh38]
Chr11:1911800 [GRCh37]
Chr11:11p15.5		 likely benign
NM_002339.3(LSP1):c.654C>A (p.Ser218=) single nucleotide variant not provided [RCV003424762] Chr11:1884518 [GRCh38]
Chr11:1905748 [GRCh37]
Chr11:11p15.5		 likely benign
GRCh37/hg19 11p15.5-15.4(chr11:230615-8821443)x3 copy number gain Russell-Silver syndrome [RCV003444025] Chr11:230615..8821443 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NM_001395380.1(PRR33):c.1412G>A (p.Arg471His) single nucleotide variant not provided [RCV003885712] Chr11:1889173 [GRCh38]
Chr11:1910403 [GRCh37]
Chr11:11p15.5		 benign
GRCh37/hg19 11p15.5(chr11:1436158-2321134)x3 copy number gain not provided [RCV001259591] Chr11:1436158..2321134 [GRCh37]
Chr11:11p15.5		 pathogenic
GRCh37/hg19 11p15.5(chr11:1690968-2277648)x3 copy number gain See cases [RCV000512345] Chr11:1690968..2277648 [GRCh37]
Chr11:11p15.5		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:5479
Count of miRNA genes:976
Interacting mature miRNAs:1226
Transcripts:ENST00000311604, ENST00000381775, ENST00000405957, ENST00000406638, ENST00000417766, ENST00000418975, ENST00000421485, ENST00000429923, ENST00000432093, ENST00000446808, ENST00000451814, ENST00000457279, ENST00000464670, ENST00000472974, ENST00000484895, ENST00000485341
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.

Markers in Region
D11S3146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,874,155 - 1,874,264UniSTSGRCh37
Build 36111,830,731 - 1,830,840RGDNCBI36
Celera111,911,920 - 1,912,029RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,665,061 - 1,665,170UniSTS
ECD00178  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,889,618 - 1,890,545UniSTSGRCh37
Build 36111,846,194 - 1,847,121RGDNCBI36
Celera111,927,419 - 1,928,346RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,680,356 - 1,681,283UniSTS
ECD00201  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,910,398 - 1,911,322UniSTSGRCh37
Build 36111,866,974 - 1,867,898RGDNCBI36
Celera112,290 - 3,214RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,700,962 - 1,701,886UniSTS
ECD00575  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,905,599 - 1,906,498UniSTSGRCh37
Build 36111,862,175 - 1,863,074RGDNCBI36
Celera111,943,477 - 1,944,376RGD
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,696,480 - 1,697,379UniSTS
ECD00620  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,888,650 - 1,889,547UniSTSGRCh37
Build 36111,845,226 - 1,846,123RGDNCBI36
Celera111,926,451 - 1,927,348RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,679,388 - 1,680,285UniSTS
ECD00664  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,908,517 - 1,909,412UniSTSGRCh37
Build 36111,865,093 - 1,865,988RGDNCBI36
Celera11409 - 1,304RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,699,081 - 1,699,976UniSTS
ECD00704  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,900,612 - 1,901,505UniSTSGRCh37
Build 36111,857,188 - 1,858,081RGDNCBI36
Celera111,938,490 - 1,939,383RGD
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,691,493 - 1,692,386UniSTS
ECD00814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,901,641 - 1,902,530UniSTSGRCh37
Build 36111,858,217 - 1,859,106RGDNCBI36
Celera111,939,519 - 1,940,408RGD
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,692,522 - 1,693,411UniSTS
ECD00905  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,883,703 - 1,884,588UniSTSGRCh37
Build 36111,840,279 - 1,841,164RGDNCBI36
Celera111,921,523 - 1,922,389RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,674,460 - 1,675,326UniSTS
ECD01070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,903,623 - 1,904,502UniSTSGRCh37
Build 36111,860,199 - 1,861,078RGDNCBI36
Celera111,941,501 - 1,942,380RGD
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,694,504 - 1,695,383UniSTS
ECD01112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,906,596 - 1,907,473UniSTSGRCh37
Build 36111,863,172 - 1,864,049RGDNCBI36
Celera111,944,474 - 1,945,352RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,697,477 - 1,698,037UniSTS
ECD01140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,904,592 - 1,905,468UniSTSGRCh37
Build 36111,861,168 - 1,862,044RGDNCBI36
Celera111,942,470 - 1,943,346RGD
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,695,473 - 1,696,349UniSTS
ECD01405  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,909,463 - 1,910,329UniSTSGRCh37
Build 36111,866,039 - 1,866,905RGDNCBI36
Celera111,355 - 2,221RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,700,027 - 1,700,893UniSTS
ECD01896  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,887,689 - 1,888,538UniSTSGRCh37
Build 36111,844,265 - 1,845,114RGDNCBI36
Celera111,925,490 - 1,926,339RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,678,427 - 1,679,276UniSTS
ECD01951  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,877,931 - 1,878,778UniSTSGRCh37
Build 36111,834,507 - 1,835,354RGDNCBI36
Celera111,915,696 - 1,916,543RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,668,837 - 1,669,684UniSTS
ECD01978  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,877,060 - 1,877,906UniSTSGRCh37
Build 36111,833,636 - 1,834,482RGDNCBI36
Celera111,914,825 - 1,915,671RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,667,966 - 1,668,812UniSTS
ECD02009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,899,434 - 1,900,279UniSTSGRCh37
Build 36111,856,010 - 1,856,855RGDNCBI36
Celera111,937,312 - 1,938,157RGD
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,690,315 - 1,691,160UniSTS
ECD02134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,891,581 - 1,892,421UniSTSGRCh37
Build 36111,848,157 - 1,848,997RGDNCBI36
Celera111,929,383 - 1,930,223RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,682,320 - 1,683,160UniSTS
ECD02686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,875,330 - 1,876,151UniSTSGRCh37
Build 36111,831,906 - 1,832,727RGDNCBI36
Celera111,913,095 - 1,913,916RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,666,236 - 1,667,057UniSTS
ECD02788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,872,719 - 1,873,536UniSTSGRCh37
Build 36111,829,295 - 1,830,112RGDNCBI36
Celera111,910,484 - 1,911,301RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,663,625 - 1,664,442UniSTS
ECD02789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,886,830 - 1,887,647UniSTSGRCh37
Build 36111,843,406 - 1,844,223RGDNCBI36
Celera111,924,631 - 1,925,448RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,677,568 - 1,678,385UniSTS
ECD02855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,885,881 - 1,886,696UniSTSGRCh37
Build 36111,842,457 - 1,843,272RGDNCBI36
Celera111,923,682 - 1,924,497RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,676,619 - 1,677,434UniSTS
ECD02987  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,876,205 - 1,877,015UniSTSGRCh37
Build 36111,832,781 - 1,833,591RGDNCBI36
Celera111,913,970 - 1,914,780RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,667,111 - 1,667,921UniSTS
ECD03584  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,874,463 - 1,875,253UniSTSGRCh37
Build 36111,831,039 - 1,831,829RGDNCBI36
Celera111,912,228 - 1,913,018RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,665,369 - 1,666,159UniSTS
ECD03685  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,898,621 - 1,899,408UniSTSGRCh37
Build 36111,855,197 - 1,855,984RGDNCBI36
Celera111,936,499 - 1,937,286RGD
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,689,502 - 1,690,289UniSTS
ECD03960  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,896,864 - 1,897,643UniSTSGRCh37
Build 36111,853,440 - 1,854,219RGDNCBI36
Celera111,934,742 - 1,935,521RGD
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,687,679 - 1,688,458UniSTS
ECD04127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,911,373 - 1,912,147UniSTSGRCh37
Build 36111,867,949 - 1,868,723RGDNCBI36
Celera113,265 - 4,039RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,701,937 - 1,702,711UniSTS
ECD04219  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,902,687 - 1,903,458UniSTSGRCh37
Build 36111,859,263 - 1,860,034RGDNCBI36
Celera111,940,565 - 1,941,336RGD
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,693,568 - 1,694,339UniSTS
ECD06537  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,873,626 - 1,874,332UniSTSGRCh37
Build 36111,830,202 - 1,830,908RGDNCBI36
Celera111,911,391 - 1,912,097RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,664,532 - 1,665,238UniSTS
ECD07638  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,880,101 - 1,880,777UniSTSGRCh37
Build 36111,836,677 - 1,837,353RGDNCBI36
Celera111,917,866 - 1,918,542RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,671,007 - 1,671,683UniSTS
ECD09663  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,913,224 - 1,913,847UniSTSGRCh37
Build 36111,869,800 - 1,870,423RGDNCBI36
Celera115,116 - 5,739RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,703,789 - 1,704,412UniSTS
ECD10242  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,896,037 - 1,896,644UniSTSGRCh37
GRCh37291,846,964 - 91,847,570UniSTSGRCh37
Build 36291,210,691 - 91,211,297RGDNCBI36
Celera111,933,915 - 1,934,522RGD
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,686,852 - 1,687,459UniSTS
ECD10394  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,912,597 - 1,913,200UniSTSGRCh37
Build 36111,869,173 - 1,869,776RGDNCBI36
Celera114,489 - 5,092RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,703,161 - 1,703,765UniSTS
ECD11955  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,895,443 - 1,896,000UniSTSGRCh37
GRCh37111,895,523 - 1,896,000UniSTSGRCh37
Build 36111,852,019 - 1,852,576RGDNCBI36
Celera111,933,320 - 1,933,878RGD
Celera111,933,400 - 1,933,878UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,686,257 - 1,686,815UniSTS
HuRef111,686,337 - 1,686,815UniSTS
ECD12207  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,880,802 - 1,881,352UniSTSGRCh37
GRCh37111,880,802 - 1,881,351UniSTSGRCh37
Build 36111,837,378 - 1,837,928RGDNCBI36
Celera111,918,567 - 1,919,117RGD
Celera111,918,567 - 1,919,116UniSTS
Cytogenetic Map11p15.5UniSTS
HuRef111,671,708 - 1,672,257UniSTS
HuRef111,671,708 - 1,672,258UniSTS
ECD14063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,879,545 - 1,880,047UniSTSGRCh37
Build 36111,836,121 - 1,836,623RGDNCBI36
Celera111,917,310 - 1,917,812RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,670,451 - 1,670,953UniSTS
ECD15393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,884,803 - 1,885,274UniSTSGRCh37
Build 36111,841,379 - 1,841,850RGDNCBI36
Celera111,922,604 - 1,923,075RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,675,541 - 1,676,012UniSTS
ECD17290  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,890,740 - 1,891,145UniSTSGRCh37
Build 36111,847,316 - 1,847,721RGDNCBI36
Celera111,928,541 - 1,928,947RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,681,478 - 1,681,884UniSTS
ECD18397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,894,339 - 1,894,700UniSTSGRCh37
Build 36111,850,915 - 1,851,276RGDNCBI36
Celera111,932,141 - 1,932,502RGD
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,685,078 - 1,685,439UniSTS
ECD24199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,885,457 - 1,885,610UniSTSGRCh37
Build 36111,842,033 - 1,842,186RGDNCBI36
Celera111,923,258 - 1,923,411RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,676,195 - 1,676,348UniSTS
REN115971  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,872,631 - 1,872,900UniSTSGRCh37
Build 36111,829,207 - 1,829,476RGDNCBI36
Celera111,910,396 - 1,910,665RGD
HuRef111,663,537 - 1,663,806UniSTS
REN115972  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,872,908 - 1,873,150UniSTSGRCh37
Build 36111,829,484 - 1,829,726RGDNCBI36
Celera111,910,673 - 1,910,915RGD
HuRef111,663,814 - 1,664,056UniSTS
REN115973  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,873,146 - 1,873,388UniSTSGRCh37
Build 36111,829,722 - 1,829,964RGDNCBI36
Celera111,910,911 - 1,911,153RGD
HuRef111,664,052 - 1,664,294UniSTS
REN115974  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,873,399 - 1,873,625UniSTSGRCh37
Build 36111,829,975 - 1,830,201RGDNCBI36
Celera111,911,164 - 1,911,390RGD
HuRef111,664,305 - 1,664,531UniSTS
REN115975  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,873,626 - 1,873,860UniSTSGRCh37
Build 36111,830,202 - 1,830,436RGDNCBI36
Celera111,911,391 - 1,911,625RGD
HuRef111,664,532 - 1,664,766UniSTS
REN115976  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,873,890 - 1,874,135UniSTSGRCh37
Build 36111,830,466 - 1,830,711RGDNCBI36
Celera111,911,655 - 1,911,900RGD
HuRef111,664,796 - 1,665,041UniSTS
REN115977  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,874,114 - 1,874,339UniSTSGRCh37
Build 36111,830,690 - 1,830,915RGDNCBI36
Celera111,911,879 - 1,912,104RGD
HuRef111,665,020 - 1,665,245UniSTS
REN115978  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,874,321 - 1,874,560UniSTSGRCh37
Build 36111,830,897 - 1,831,136RGDNCBI36
Celera111,912,086 - 1,912,325RGD
HuRef111,665,227 - 1,665,466UniSTS
REN115979  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,874,545 - 1,874,794UniSTSGRCh37
Build 36111,831,121 - 1,831,370RGDNCBI36
Celera111,912,310 - 1,912,559RGD
HuRef111,665,451 - 1,665,700UniSTS
REN115980  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,874,772 - 1,875,042UniSTSGRCh37
Build 36111,831,348 - 1,831,618RGDNCBI36
Celera111,912,537 - 1,912,807RGD
HuRef111,665,678 - 1,665,948UniSTS
REN115981  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,875,026 - 1,875,253UniSTSGRCh37
Build 36111,831,602 - 1,831,829RGDNCBI36
Celera111,912,791 - 1,913,018RGD
HuRef111,665,932 - 1,666,159UniSTS
REN115982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,875,284 - 1,875,521UniSTSGRCh37
Build 36111,831,860 - 1,832,097RGDNCBI36
Celera111,913,049 - 1,913,286RGD
HuRef111,666,190 - 1,666,427UniSTS
REN115983  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,875,535 - 1,875,771UniSTSGRCh37
Build 36111,832,111 - 1,832,347RGDNCBI36
Celera111,913,300 - 1,913,536RGD
HuRef111,666,441 - 1,666,677UniSTS
REN115984  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,875,775 - 1,876,036UniSTSGRCh37
Build 36111,832,351 - 1,832,612RGDNCBI36
Celera111,913,540 - 1,913,801RGD
HuRef111,666,681 - 1,666,942UniSTS
REN115985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,876,049 - 1,876,314UniSTSGRCh37
Build 36111,832,625 - 1,832,890RGDNCBI36
Celera111,913,814 - 1,914,079RGD
HuRef111,666,955 - 1,667,220UniSTS
REN115986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,876,412 - 1,876,653UniSTSGRCh37
Build 36111,832,988 - 1,833,229RGDNCBI36
Celera111,914,177 - 1,914,418RGD
HuRef111,667,318 - 1,667,559UniSTS
REN115987  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,876,639 - 1,876,863UniSTSGRCh37
Build 36111,833,215 - 1,833,439RGDNCBI36
Celera111,914,404 - 1,914,628RGD
HuRef111,667,545 - 1,667,769UniSTS
REN115988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,876,841 - 1,877,108UniSTSGRCh37
Build 36111,833,417 - 1,833,684RGDNCBI36
Celera111,914,606 - 1,914,873RGD
HuRef111,667,747 - 1,668,014UniSTS
REN115989  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,877,085 - 1,877,353UniSTSGRCh37
Build 36111,833,661 - 1,833,929RGDNCBI36
Celera111,914,850 - 1,915,118RGD
HuRef111,667,991 - 1,668,259UniSTS
REN115990  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,877,330 - 1,877,571UniSTSGRCh37
Build 36111,833,906 - 1,834,147RGDNCBI36
Celera111,915,095 - 1,915,336RGD
HuRef111,668,236 - 1,668,477UniSTS
REN115991  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,877,550 - 1,877,805UniSTSGRCh37
Build 36111,834,126 - 1,834,381RGDNCBI36
Celera111,915,315 - 1,915,570RGD
HuRef111,668,456 - 1,668,711UniSTS
REN115992  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,877,787 - 1,878,059UniSTSGRCh37
Build 36111,834,363 - 1,834,635RGDNCBI36
Celera111,915,552 - 1,915,824RGD
HuRef111,668,693 - 1,668,965UniSTS
REN115993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,878,099 - 1,878,326UniSTSGRCh37
Build 36111,834,675 - 1,834,902RGDNCBI36
Celera111,915,864 - 1,916,091RGD
HuRef111,669,005 - 1,669,232UniSTS
REN115994  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,878,407 - 1,878,651UniSTSGRCh37
Build 36111,834,983 - 1,835,227RGDNCBI36
Celera111,916,172 - 1,916,416RGD
HuRef111,669,313 - 1,669,557UniSTS
REN115995  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,878,665 - 1,878,894UniSTSGRCh37
Build 36111,835,241 - 1,835,470RGDNCBI36
Celera111,916,430 - 1,916,659RGD
HuRef111,669,571 - 1,669,800UniSTS
REN115996  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,878,933 - 1,879,190UniSTSGRCh37
Build 36111,835,509 - 1,835,766RGDNCBI36
Celera111,916,698 - 1,916,955RGD
HuRef111,669,839 - 1,670,096UniSTS
REN115997  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,879,300 - 1,879,534UniSTSGRCh37
Build 36111,835,876 - 1,836,110RGDNCBI36
Celera111,917,065 - 1,917,299RGD
HuRef111,670,206 - 1,670,440UniSTS
REN115998  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,879,524 - 1,879,760UniSTSGRCh37
Build 36111,836,100 - 1,836,336RGDNCBI36
Celera111,917,289 - 1,917,525RGD
HuRef111,670,430 - 1,670,666UniSTS
REN115999  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,879,769 - 1,879,993UniSTSGRCh37
Build 36111,836,345 - 1,836,569RGDNCBI36
Celera111,917,534 - 1,917,758RGD
HuRef111,670,675 - 1,670,899UniSTS
REN116000  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,879,971 - 1,880,205UniSTSGRCh37
Build 36111,836,547 - 1,836,781RGDNCBI36
Celera111,917,736 - 1,917,970RGD
HuRef111,670,877 - 1,671,111UniSTS
REN116001  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,880,193 - 1,880,448UniSTSGRCh37
Build 36111,836,769 - 1,837,024RGDNCBI36
Celera111,917,958 - 1,918,213RGD
HuRef111,671,099 - 1,671,354UniSTS
REN116002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,880,426 - 1,880,679UniSTSGRCh37
Build 36111,837,002 - 1,837,255RGDNCBI36
Celera111,918,191 - 1,918,444RGD
HuRef111,671,332 - 1,671,585UniSTS
REN116003  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,880,658 - 1,880,886UniSTSGRCh37
Build 36111,837,234 - 1,837,462RGDNCBI36
Celera111,918,423 - 1,918,651RGD
HuRef111,671,564 - 1,671,792UniSTS
REN116004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,880,863 - 1,881,112UniSTSGRCh37
Build 36111,837,439 - 1,837,688RGDNCBI36
Celera111,918,628 - 1,918,877RGD
HuRef111,671,769 - 1,672,018UniSTS
REN116005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,881,111 - 1,881,349UniSTSGRCh37
Build 36111,837,687 - 1,837,925RGDNCBI36
Celera111,918,876 - 1,919,114RGD
HuRef111,672,017 - 1,672,255UniSTS
REN116006  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,881,346 - 1,881,585UniSTSGRCh37
Build 36111,837,922 - 1,838,161RGDNCBI36
Celera111,919,111 - 1,919,362RGD
HuRef111,672,252 - 1,672,503UniSTS
REN116007  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,881,562 - 1,881,801UniSTSGRCh37
Build 36111,838,138 - 1,838,377RGDNCBI36
Celera111,919,339 - 1,919,578RGD
HuRef111,672,480 - 1,672,719UniSTS
REN116008  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,881,800 - 1,882,065UniSTSGRCh37
Build 36111,838,376 - 1,838,641RGDNCBI36
Celera111,919,577 - 1,919,842RGD
HuRef111,672,718 - 1,672,983UniSTS
REN116009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,882,070 - 1,882,308UniSTSGRCh37
Build 36111,838,646 - 1,838,884RGDNCBI36
Celera111,919,847 - 1,920,101RGD
HuRef111,672,988 - 1,673,242UniSTS
REN116010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,882,316 - 1,882,542UniSTSGRCh37
Build 36111,838,892 - 1,839,118RGDNCBI36
Celera111,920,109 - 1,920,335RGD
HuRef111,673,250 - 1,673,476UniSTS
REN116011  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,882,596 - 1,882,852UniSTSGRCh37
Build 36111,839,172 - 1,839,428RGDNCBI36
HuRef111,673,530 - 1,673,823UniSTS
HuRef111,673,530 - 1,673,786UniSTS
REN116012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,883,308 - 1,883,534UniSTSGRCh37
Build 36111,839,884 - 1,840,110RGDNCBI36
Celera111,921,128 - 1,921,354RGD
HuRef111,674,066 - 1,674,291UniSTS
REN116013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,883,537 - 1,883,761UniSTSGRCh37
Build 36111,840,113 - 1,840,337RGDNCBI36
Celera111,921,357 - 1,921,581RGD
HuRef111,674,294 - 1,674,518UniSTS
REN116014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,883,738 - 1,883,995UniSTSGRCh37
Build 36111,840,314 - 1,840,571RGDNCBI36
Celera111,921,558 - 1,921,815RGD
HuRef111,674,495 - 1,674,752UniSTS
REN116015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,883,972 - 1,884,226UniSTSGRCh37
Build 36111,840,548 - 1,840,802RGDNCBI36
Celera111,921,792 - 1,922,027RGD
HuRef111,674,729 - 1,674,964UniSTS
REN116016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,884,257 - 1,884,489UniSTSGRCh37
Build 36111,840,833 - 1,841,065RGDNCBI36
Celera111,922,058 - 1,922,290RGD
HuRef111,674,995 - 1,675,227UniSTS
REN116017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,884,491 - 1,884,724UniSTSGRCh37
Build 36111,841,067 - 1,841,300RGDNCBI36
Celera111,922,292 - 1,922,525RGD
HuRef111,675,229 - 1,675,462UniSTS
REN116018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,884,704 - 1,884,953UniSTSGRCh37
Build 36111,841,280 - 1,841,529RGDNCBI36
Celera111,922,505 - 1,922,754RGD
HuRef111,675,442 - 1,675,691UniSTS
REN116019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,885,043 - 1,885,267UniSTSGRCh37
Build 36111,841,619 - 1,841,843RGDNCBI36
Celera111,922,844 - 1,923,068RGD
HuRef111,675,781 - 1,676,005UniSTS
REN116020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,885,243 - 1,885,477UniSTSGRCh37
Build 36111,841,819 - 1,842,053RGDNCBI36
Celera111,923,044 - 1,923,278RGD
HuRef111,675,981 - 1,676,215UniSTS
REN116021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,885,509 - 1,885,775UniSTSGRCh37
Build 36111,842,085 - 1,842,351RGDNCBI36
Celera111,923,310 - 1,923,576RGD
HuRef111,676,247 - 1,676,513UniSTS
REN116022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,885,900 - 1,886,170UniSTSGRCh37
Build 36111,842,476 - 1,842,746RGDNCBI36
Celera111,923,701 - 1,923,971RGD
HuRef111,676,638 - 1,676,908UniSTS
REN116023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,886,161 - 1,886,386UniSTSGRCh37
Build 36111,842,737 - 1,842,962RGDNCBI36
Celera111,923,962 - 1,924,187RGD
HuRef111,676,899 - 1,677,124UniSTS
REN116024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,886,362 - 1,886,602UniSTSGRCh37
Build 36111,842,938 - 1,843,178RGDNCBI36
Celera111,924,163 - 1,924,403RGD
HuRef111,677,100 - 1,677,340UniSTS
REN116025  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,886,584 - 1,886,852UniSTSGRCh37
Build 36111,843,160 - 1,843,428RGDNCBI36
Celera111,924,385 - 1,924,653RGD
HuRef111,677,322 - 1,677,590UniSTS
REN116026  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,886,832 - 1,887,094UniSTSGRCh37
Build 36111,843,408 - 1,843,670RGDNCBI36
Celera111,924,633 - 1,924,895RGD
HuRef111,677,570 - 1,677,832UniSTS
REN116027  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,887,074 - 1,887,330UniSTSGRCh37
Build 36111,843,650 - 1,843,906RGDNCBI36
Celera111,924,875 - 1,925,131RGD
HuRef111,677,812 - 1,678,068UniSTS
REN116028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,887,352 - 1,887,589UniSTSGRCh37
Build 36111,843,928 - 1,844,165RGDNCBI36
Celera111,925,153 - 1,925,390RGD
HuRef111,678,090 - 1,678,327UniSTS
REN116029  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,887,619 - 1,887,853UniSTSGRCh37
Build 36111,844,195 - 1,844,429RGDNCBI36
Celera111,925,420 - 1,925,654RGD
HuRef111,678,357 - 1,678,591UniSTS
REN116030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,887,937 - 1,888,174UniSTSGRCh37
Build 36111,844,513 - 1,844,750RGDNCBI36
Celera111,925,738 - 1,925,975RGD
HuRef111,678,675 - 1,678,912UniSTS
REN116031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,888,154 - 1,888,422UniSTSGRCh37
Build 36111,844,730 - 1,844,998RGDNCBI36
Celera111,925,955 - 1,926,223RGD
HuRef111,678,892 - 1,679,160UniSTS
REN116032  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,888,399 - 1,888,655UniSTSGRCh37
Build 36111,844,975 - 1,845,231RGDNCBI36
Celera111,926,200 - 1,926,456RGD
HuRef111,679,137 - 1,679,393UniSTS
REN116033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,888,634 - 1,888,885UniSTSGRCh37
Build 36111,845,210 - 1,845,461RGDNCBI36
Celera111,926,435 - 1,926,686RGD
HuRef111,679,372 - 1,679,623UniSTS
REN116034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,888,912 - 1,889,136UniSTSGRCh37
Build 36111,845,488 - 1,845,712RGDNCBI36
Celera111,926,713 - 1,926,937RGD
HuRef111,679,650 - 1,679,874UniSTS
REN116035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,889,113 - 1,889,345UniSTSGRCh37
Build 36111,845,689 - 1,845,921RGDNCBI36
Celera111,926,914 - 1,927,146RGD
HuRef111,679,851 - 1,680,083UniSTS
REN116036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,889,416 - 1,889,640UniSTSGRCh37
Build 36111,845,992 - 1,846,216RGDNCBI36
Celera111,927,217 - 1,927,441RGD
HuRef111,680,154 - 1,680,378UniSTS
REN116037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,889,619 - 1,889,888UniSTSGRCh37
Build 36111,846,195 - 1,846,464RGDNCBI36
Celera111,927,420 - 1,927,689RGD
HuRef111,680,357 - 1,680,626UniSTS
REN116038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,889,909 - 1,890,147UniSTSGRCh37
Build 36111,846,485 - 1,846,723RGDNCBI36
Celera111,927,710 - 1,927,948RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,680,647 - 1,680,885UniSTS
REN116039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,890,240 - 1,890,471UniSTSGRCh37
Build 36111,846,816 - 1,847,047RGDNCBI36
Celera111,928,041 - 1,928,272RGD
HuRef111,680,978 - 1,681,209UniSTS
REN116040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,890,522 - 1,890,756UniSTSGRCh37
Build 36111,847,098 - 1,847,332RGDNCBI36
Celera111,928,323 - 1,928,557RGD
HuRef111,681,260 - 1,681,494UniSTS
REN116041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,890,865 - 1,891,117UniSTSGRCh37
Build 36111,847,441 - 1,847,693RGDNCBI36
Celera111,928,666 - 1,928,919RGD
HuRef111,681,603 - 1,681,856UniSTS
REN116042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,891,104 - 1,891,358UniSTSGRCh37
Build 36111,847,680 - 1,847,934RGDNCBI36
Celera111,928,906 - 1,929,160RGD
HuRef111,681,843 - 1,682,097UniSTS
REN116043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,891,352 - 1,891,605UniSTSGRCh37
Build 36111,847,928 - 1,848,181RGDNCBI36
Celera111,929,154 - 1,929,407RGD
HuRef111,682,091 - 1,682,344UniSTS
REN116044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,891,583 - 1,891,839UniSTSGRCh37
Build 36111,848,159 - 1,848,415RGDNCBI36
Celera111,929,385 - 1,929,641RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,682,322 - 1,682,578UniSTS
REN116045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,891,959 - 1,892,209UniSTSGRCh37
Build 36111,848,535 - 1,848,785RGDNCBI36
Celera111,929,761 - 1,930,011RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,682,698 - 1,682,948UniSTS
REN116046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,892,190 - 1,892,420UniSTSGRCh37
Build 36111,848,766 - 1,848,996RGDNCBI36
Celera111,929,992 - 1,930,222RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,682,929 - 1,683,159UniSTS
REN116047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,892,397 - 1,892,640UniSTSGRCh37
Build 36111,848,973 - 1,849,216RGDNCBI36
Celera111,930,199 - 1,930,442RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,683,136 - 1,683,379UniSTS
REN116048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,892,618 - 1,892,866UniSTSGRCh37
Build 36111,849,194 - 1,849,442RGDNCBI36
Celera111,930,420 - 1,930,668RGD
HuRef111,683,357 - 1,683,605UniSTS
REN116049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,893,217 - 1,893,483UniSTSGRCh37
Build 36111,849,793 - 1,850,059RGDNCBI36
Celera111,931,019 - 1,931,285RGD
HuRef111,683,956 - 1,684,222UniSTS
REN116051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,893,923 - 1,894,186UniSTSGRCh37
GRCh37111,893,735 - 1,894,186UniSTSGRCh37
Build 36111,850,311 - 1,850,762RGDNCBI36
Celera111,931,537 - 1,931,988RGD
Celera111,931,725 - 1,931,988UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,684,474 - 1,684,925UniSTS
HuRef111,684,662 - 1,684,925UniSTS
REN116052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,894,166 - 1,894,398UniSTSGRCh37
Build 36111,850,742 - 1,850,974RGDNCBI36
Celera111,931,968 - 1,932,200RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,684,905 - 1,685,137UniSTS
REN116053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,894,377 - 1,894,618UniSTSGRCh37
Build 36111,850,953 - 1,851,194RGDNCBI36
Celera111,932,179 - 1,932,420RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,685,116 - 1,685,357UniSTS
REN116054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,894,594 - 1,894,833UniSTSGRCh37
Build 36111,851,170 - 1,851,409RGDNCBI36
Celera111,932,396 - 1,932,639RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,685,333 - 1,685,576UniSTS
REN116055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,894,812 - 1,895,040UniSTSGRCh37
Build 36111,851,388 - 1,851,616RGDNCBI36
Celera111,932,618 - 1,932,846RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,685,555 - 1,685,783UniSTS
REN116056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,895,586 - 1,895,824UniSTSGRCh37
Build 36111,852,162 - 1,852,400RGDNCBI36
Celera111,933,463 - 1,933,701RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,686,400 - 1,686,638UniSTS
REN116061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,897,383 - 1,897,640UniSTSGRCh37
Build 36111,853,959 - 1,854,216RGDNCBI36
Celera111,935,261 - 1,935,518RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,688,198 - 1,688,455UniSTS
REN116062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,897,627 - 1,897,858UniSTSGRCh37
Build 36111,854,203 - 1,854,434RGDNCBI36
Celera111,935,505 - 1,935,736RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,688,442 - 1,688,673UniSTS
REN116063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,897,840 - 1,898,095UniSTSGRCh37
Build 36111,854,416 - 1,854,671RGDNCBI36
Celera111,935,718 - 1,935,973RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,688,655 - 1,688,910UniSTS
REN116064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,898,454 - 1,898,710UniSTSGRCh37
GRCh37291,844,889 - 91,845,145UniSTSGRCh37
Build 36291,208,616 - 91,208,872RGDNCBI36
Celera111,936,332 - 1,936,588RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,689,335 - 1,689,591UniSTS
REN116065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,898,726 - 1,898,953UniSTSGRCh37
Build 36111,855,302 - 1,855,529RGDNCBI36
Celera111,936,604 - 1,936,831RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,689,607 - 1,689,834UniSTS
REN116067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,899,158 - 1,899,410UniSTSGRCh37
Build 36111,855,734 - 1,855,986RGDNCBI36
Celera111,937,036 - 1,937,288RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,690,039 - 1,690,291UniSTS
REN116068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,899,400 - 1,899,649UniSTSGRCh37
Build 36111,855,976 - 1,856,225RGDNCBI36
Celera111,937,278 - 1,937,527RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,690,281 - 1,690,530UniSTS
REN116069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,899,628 - 1,899,860UniSTSGRCh37
Build 36111,856,204 - 1,856,436RGDNCBI36
Celera111,937,506 - 1,937,738RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,690,509 - 1,690,741UniSTS
REN116070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,899,931 - 1,900,195UniSTSGRCh37
Build 36111,856,507 - 1,856,771RGDNCBI36
Celera111,937,809 - 1,938,073RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,690,812 - 1,691,076UniSTS
REN116071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,900,583 - 1,900,815UniSTSGRCh37
Build 36111,857,159 - 1,857,391RGDNCBI36
Celera111,938,461 - 1,938,693RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,691,464 - 1,691,696UniSTS
REN116072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,900,795 - 1,901,033UniSTSGRCh37
Build 36111,857,371 - 1,857,609RGDNCBI36
Celera111,938,673 - 1,938,911RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,691,676 - 1,691,914UniSTS
REN116073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,901,027 - 1,901,260UniSTSGRCh37
Build 36111,857,603 - 1,857,836RGDNCBI36
Celera111,938,905 - 1,939,138RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,691,908 - 1,692,141UniSTS
REN116074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,901,259 - 1,901,504UniSTSGRCh37
Build 36111,857,835 - 1,858,080RGDNCBI36
Celera111,939,137 - 1,939,382RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,692,140 - 1,692,385UniSTS
REN116075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,901,548 - 1,901,799UniSTSGRCh37
Build 36111,858,124 - 1,858,375RGDNCBI36
Celera111,939,426 - 1,939,677RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,692,429 - 1,692,680UniSTS
REN116076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,901,778 - 1,902,047UniSTSGRCh37
Build 36111,858,354 - 1,858,623RGDNCBI36
Celera111,939,656 - 1,939,925RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,692,659 - 1,692,928UniSTS
REN116079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,902,484 - 1,902,708UniSTSGRCh37
Build 36111,859,060 - 1,859,284RGDNCBI36
Celera111,940,362 - 1,940,586RGD
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,693,365 - 1,693,589UniSTS
REN116080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,903,009 - 1,903,233UniSTSGRCh37
Build 36111,859,585 - 1,859,809RGDNCBI36
Celera111,940,887 - 1,941,111RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,693,890 - 1,694,114UniSTS
REN116081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,903,210 - 1,903,462UniSTSGRCh37
Build 36111,859,786 - 1,860,038RGDNCBI36
Celera111,941,088 - 1,941,340RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,694,091 - 1,694,343UniSTS
REN116082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,903,528 - 1,903,772UniSTSGRCh37
Build 36111,860,104 - 1,860,348RGDNCBI36
Celera111,941,406 - 1,941,650RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,694,409 - 1,694,653UniSTS
REN116083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,903,936 - 1,904,177UniSTSGRCh37
Build 36111,860,512 - 1,860,753RGDNCBI36
Celera111,941,814 - 1,942,055RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,694,817 - 1,695,058UniSTS
REN116084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,904,164 - 1,904,406UniSTSGRCh37
Build 36111,860,740 - 1,860,982RGDNCBI36
Celera111,942,042 - 1,942,284RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,695,045 - 1,695,287UniSTS
REN116085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,904,384 - 1,904,622UniSTSGRCh37
Build 36111,860,960 - 1,861,198RGDNCBI36
Celera111,942,262 - 1,942,500RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,695,265 - 1,695,503UniSTS
REN116086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,904,601 - 1,904,857UniSTSGRCh37
Build 36111,861,177 - 1,861,433RGDNCBI36
Celera111,942,479 - 1,942,735RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,695,482 - 1,695,738UniSTS
REN116087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,904,847 - 1,905,088UniSTSGRCh37
Build 36111,861,423 - 1,861,664RGDNCBI36
Celera111,942,725 - 1,942,966RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,695,728 - 1,695,969UniSTS
REN116088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,905,065 - 1,905,312UniSTSGRCh37
Build 36111,861,641 - 1,861,888RGDNCBI36
Celera111,942,943 - 1,943,190RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,695,946 - 1,696,193UniSTS
REN116089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,905,296 - 1,905,553UniSTSGRCh37
Build 36111,861,872 - 1,862,129RGDNCBI36
Celera111,943,174 - 1,943,431RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,696,177 - 1,696,434UniSTS
REN116090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,905,531 - 1,905,786UniSTSGRCh37
Build 36111,862,107 - 1,862,362RGDNCBI36
Celera111,943,409 - 1,943,664RGD
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,696,412 - 1,696,667UniSTS
REN116091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,905,773 - 1,906,002UniSTSGRCh37
Build 36111,862,349 - 1,862,578RGDNCBI36
Celera111,943,651 - 1,943,880RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,696,654 - 1,696,883UniSTS
REN116092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,905,988 - 1,906,243UniSTSGRCh37
GRCh37111,905,988 - 1,907,220UniSTSGRCh37
Build 36111,862,564 - 1,862,819RGDNCBI36
Celera111,943,866 - 1,945,098UniSTS
Celera111,943,866 - 1,944,121RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,696,869 - 1,697,124UniSTS
REN116093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,906,221 - 1,906,480UniSTSGRCh37
Build 36111,862,797 - 1,863,056RGDNCBI36
Celera111,944,099 - 1,944,358RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,697,102 - 1,697,361UniSTS
REN116094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,906,458 - 1,906,717UniSTSGRCh37
Build 36111,863,034 - 1,863,293RGDNCBI36
Celera111,944,336 - 1,944,595RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,697,339 - 1,697,598UniSTS
REN116095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,906,694 - 1,906,933UniSTSGRCh37
Build 36111,863,270 - 1,863,509RGDNCBI36
Celera111,944,572 - 1,944,811RGD
REN116096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,906,954 - 1,907,182UniSTSGRCh37
Build 36111,863,530 - 1,863,758RGDNCBI36
Celera111,944,832 - 1,945,060RGD
REN116097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,907,159 - 1,907,384UniSTSGRCh37
Build 36111,863,735 - 1,863,960RGDNCBI36
Celera111,945,037 - 1,945,263RGD
REN116098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,907,361 - 1,907,608UniSTSGRCh37
Build 36111,863,937 - 1,864,184RGDNCBI36
Celera111,945,240 - 1,945,487RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,697,925 - 1,698,172UniSTS
REN116100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,907,800 - 1,908,040UniSTSGRCh37
Build 36111,864,376 - 1,864,616RGDNCBI36
Cytogenetic Map2p11.1UniSTS
HuRef111,698,364 - 1,698,604UniSTS
REN116102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,908,601 - 1,908,841UniSTSGRCh37
Build 36111,865,177 - 1,865,417RGDNCBI36
Celera11493 - 733RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,699,165 - 1,699,405UniSTS
REN116103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,908,821 - 1,909,059UniSTSGRCh37
Build 36111,865,397 - 1,865,635RGDNCBI36
Celera11713 - 951RGD
HuRef111,699,385 - 1,699,623UniSTS
REN116104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,909,040 - 1,909,266UniSTSGRCh37
Build 36111,865,616 - 1,865,842RGDNCBI36
Celera11932 - 1,158RGD
HuRef111,699,604 - 1,699,830UniSTS
REN116105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,909,247 - 1,909,476UniSTSGRCh37
Build 36111,865,823 - 1,866,052RGDNCBI36
Celera111,139 - 1,368RGD
HuRef111,699,811 - 1,700,040UniSTS
REN116106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,909,453 - 1,909,690UniSTSGRCh37
Build 36111,866,029 - 1,866,266RGDNCBI36
Celera111,345 - 1,582RGD
HuRef111,700,017 - 1,700,254UniSTS
REN116107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,909,668 - 1,909,910UniSTSGRCh37
Build 36111,866,244 - 1,866,486RGDNCBI36
Celera111,560 - 1,802RGD
HuRef111,700,232 - 1,700,474UniSTS
REN116108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,909,888 - 1,910,146UniSTSGRCh37
Build 36111,866,464 - 1,866,722RGDNCBI36
Celera111,780 - 2,038RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,700,452 - 1,700,710UniSTS
REN116109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,910,125 - 1,910,380UniSTSGRCh37
Build 36111,866,701 - 1,866,956RGDNCBI36
Celera112,017 - 2,272RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,700,689 - 1,700,944UniSTS
REN116110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,910,398 - 1,910,627UniSTSGRCh37
Build 36111,866,974 - 1,867,203RGDNCBI36
Celera112,290 - 2,519RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,700,962 - 1,701,191UniSTS
REN116111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,910,776 - 1,911,023UniSTSGRCh37
Build 36111,867,352 - 1,867,599RGDNCBI36
Celera112,668 - 2,915RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,701,340 - 1,701,587UniSTS
REN116112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,911,025 - 1,911,249UniSTSGRCh37
Build 36111,867,601 - 1,867,825RGDNCBI36
Celera112,917 - 3,141RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,701,589 - 1,701,813UniSTS
REN116113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,911,368 - 1,911,595UniSTSGRCh37
Build 36111,867,944 - 1,868,171RGDNCBI36
Celera113,260 - 3,487RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,701,932 - 1,702,159UniSTS
REN116114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,911,653 - 1,911,887UniSTSGRCh37
Build 36111,868,229 - 1,868,463RGDNCBI36
Celera113,545 - 3,779RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,702,217 - 1,702,451UniSTS
REN116115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,911,876 - 1,912,131UniSTSGRCh37
Build 36111,868,452 - 1,868,707RGDNCBI36
Celera113,768 - 4,023RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,702,440 - 1,702,695UniSTS
REN116116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,912,126 - 1,912,387UniSTSGRCh37
Build 36111,868,702 - 1,868,963RGDNCBI36
Celera114,018 - 4,279RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,702,690 - 1,702,951UniSTS
REN116117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,912,363 - 1,912,621UniSTSGRCh37
Build 36111,868,939 - 1,869,197RGDNCBI36
Celera114,255 - 4,513RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,702,927 - 1,703,185UniSTS
REN116118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,912,645 - 1,912,869UniSTSGRCh37
Build 36111,869,221 - 1,869,445RGDNCBI36
Celera114,537 - 4,761RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,703,209 - 1,703,433UniSTS
REN116119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,912,848 - 1,913,109UniSTSGRCh37
Build 36111,869,424 - 1,869,685RGDNCBI36
Celera114,740 - 5,001RGD
Cytogenetic Map11p15.5UniSTS
REN116120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,913,087 - 1,913,337UniSTSGRCh37
Build 36111,869,663 - 1,869,913RGDNCBI36
Celera114,979 - 5,229RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,703,652 - 1,703,902UniSTS
REN116121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,913,317 - 1,913,557UniSTSGRCh37
Build 36111,869,893 - 1,870,133RGDNCBI36
Celera115,209 - 5,449RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,703,882 - 1,704,122UniSTS
REN116122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,913,539 - 1,913,763UniSTSGRCh37
Build 36111,870,115 - 1,870,339RGDNCBI36
Celera115,431 - 5,655RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,704,104 - 1,704,328UniSTS
STS-W73739  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,913,107 - 1,913,316UniSTSGRCh37
Build 36111,869,683 - 1,869,892RGDNCBI36
Celera114,999 - 5,208RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,703,672 - 1,703,881UniSTS
GeneMap99-GB4 RH Map117.14UniSTS
NCBI RH Map118.6UniSTS
stSG548524  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,873,058 - 1,874,639UniSTSGRCh37
Build 36111,829,634 - 1,831,215RGDNCBI36
Celera111,910,823 - 1,912,404RGD
HuRef111,663,964 - 1,665,545UniSTS
stSG548525  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,874,620 - 1,876,151UniSTSGRCh37
Build 36111,831,196 - 1,832,727RGDNCBI36
Celera111,912,385 - 1,913,916RGD
HuRef111,665,526 - 1,667,057UniSTS
stSG548526  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,876,132 - 1,877,611UniSTSGRCh37
Build 36111,832,708 - 1,834,187RGDNCBI36
Celera111,913,897 - 1,915,376RGD
HuRef111,667,038 - 1,668,517UniSTS
stSG548527  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,877,598 - 1,878,864UniSTSGRCh37
Build 36111,834,174 - 1,835,440RGDNCBI36
Celera111,915,363 - 1,916,629RGD
HuRef111,668,504 - 1,669,770UniSTS
stSG548528  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,878,855 - 1,880,522UniSTSGRCh37
Build 36111,835,431 - 1,837,098RGDNCBI36
Celera111,916,620 - 1,918,287RGD
HuRef111,669,761 - 1,671,428UniSTS
stSG548530  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,881,793 - 1,883,510UniSTSGRCh37
Build 36111,838,369 - 1,840,086RGDNCBI36
Celera111,919,570 - 1,921,330RGD
HuRef111,672,711 - 1,674,267UniSTS
stSG548531  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,883,491 - 1,883,742UniSTSGRCh37
Build 36111,840,067 - 1,840,318RGDNCBI36
Celera111,921,311 - 1,921,562RGD
HuRef111,674,248 - 1,674,499UniSTS
stSG548532  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,883,750 - 1,885,223UniSTSGRCh37
Build 36111,840,326 - 1,841,799RGDNCBI36
Celera111,921,570 - 1,923,024RGD
HuRef111,674,507 - 1,675,961UniSTS
stSG548533  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,885,204 - 1,886,849UniSTSGRCh37
Build 36111,841,780 - 1,843,425RGDNCBI36
Celera111,923,005 - 1,924,650RGD
HuRef111,675,942 - 1,677,587UniSTS
stSG548534  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,886,832 - 1,888,352UniSTSGRCh37
Build 36111,843,408 - 1,844,928RGDNCBI36
Celera111,924,633 - 1,926,153RGD
HuRef111,677,570 - 1,679,090UniSTS
stSG548536  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,889,820 - 1,891,145UniSTSGRCh37
Build 36111,846,396 - 1,847,721RGDNCBI36
Celera111,927,621 - 1,928,947RGD
HuRef111,680,558 - 1,681,884UniSTS
stSG548537  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,891,126 - 1,892,409UniSTSGRCh37
Build 36111,847,702 - 1,848,985RGDNCBI36
Celera111,928,928 - 1,930,211RGD
HuRef111,681,865 - 1,683,148UniSTS
stSG548541  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,896,572 - 1,898,247UniSTSGRCh37
Build 36111,853,148 - 1,854,823RGDNCBI36
Celera111,934,450 - 1,936,125RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,687,387 - 1,689,062UniSTS
stSG548542  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,898,228 - 1,899,828UniSTSGRCh37
Build 36111,854,804 - 1,856,404RGDNCBI36
Celera111,936,106 - 1,937,706RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,689,043 - 1,690,709UniSTS
stSG548543  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,899,818 - 1,901,255UniSTSGRCh37
Build 36111,856,394 - 1,857,831RGDNCBI36
Celera111,937,696 - 1,939,133RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,690,699 - 1,692,136UniSTS
stSG548544  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,901,236 - 1,902,503UniSTSGRCh37
GRCh37111,901,236 - 1,902,380UniSTSGRCh37
Build 36111,857,812 - 1,858,956RGDNCBI36
Celera111,939,114 - 1,940,258RGD
Celera111,939,114 - 1,940,381UniSTS
Cytogenetic Map2p11.1UniSTS
HuRef111,692,117 - 1,693,261UniSTS
HuRef111,692,117 - 1,693,384UniSTS
stSG548545  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,902,492 - 1,903,878UniSTSGRCh37
Build 36111,859,068 - 1,860,454RGDNCBI36
Celera111,940,370 - 1,941,756RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,693,373 - 1,694,759UniSTS
stSG548546  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,903,859 - 1,905,298UniSTSGRCh37
Build 36111,860,435 - 1,861,874RGDNCBI36
Celera111,941,737 - 1,943,176RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,694,740 - 1,696,179UniSTS
stSG548547  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,905,279 - 1,906,708UniSTSGRCh37
Build 36111,861,855 - 1,863,284RGDNCBI36
Celera111,943,157 - 1,944,586RGD
Cytogenetic Map2p11.1UniSTS
HuRef111,696,160 - 1,697,589UniSTS
stSG548548  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,906,689 - 1,908,272UniSTSGRCh37
Build 36111,863,265 - 1,864,848RGDNCBI36
HuRef111,697,570 - 1,698,836UniSTS
stSG548550  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,908,433 - 1,909,998UniSTSGRCh37
Build 36111,865,009 - 1,866,574RGDNCBI36
Celera11325 - 1,890RGD
HuRef111,698,997 - 1,700,562UniSTS
stSG548551  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,909,979 - 1,911,727UniSTSGRCh37
Build 36111,866,555 - 1,868,303RGDNCBI36
Celera111,871 - 3,619RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,700,543 - 1,702,291UniSTS
stSG548552  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,911,708 - 1,913,243UniSTSGRCh37
Build 36111,868,284 - 1,869,819RGDNCBI36
Celera113,600 - 5,135RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,702,272 - 1,703,808UniSTS
LSP1_2796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37111,912,957 - 1,913,486UniSTSGRCh37
Build 36111,869,533 - 1,870,062RGDNCBI36
Celera114,849 - 5,378RGD
HuRef111,703,522 - 1,704,051UniSTS
REN116077  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map11p15.5UniSTS
REN116078  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map11p15.5UniSTS


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 1423 1776 744 215 1848 72 2914 756 641 147 528 1045 144 1034 1717 1
Low 896 1209 955 392 70 372 1190 1400 1824 211 826 372 25 1 170 1070 1 1
Below cutoff 45 1 14 9 19 12 113 17 1229 51 52 82 3 1 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_011509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001013253 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001013254 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001013255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001242932 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001289005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002339 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC051649 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF043107 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF043349 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI817126 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056576 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK092071 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093859 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129684 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK222733 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292033 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001785 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BE043985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ893037 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ893821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471158 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR541728 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR541754 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S58726 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S67783 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X55188 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000311604   ⟹   ENSP00000308383
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,853,084 - 1,892,263 (+)Ensembl
RefSeq Acc Id: ENST00000381775   ⟹   ENSP00000371194
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,865,165 - 1,892,263 (+)Ensembl
RefSeq Acc Id: ENST00000405957   ⟹   ENSP00000383932
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,868,673 - 1,892,263 (+)Ensembl
RefSeq Acc Id: ENST00000406638   ⟹   ENSP00000384022
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,870,244 - 1,892,263 (+)Ensembl
RefSeq Acc Id: ENST00000417766   ⟹   ENSP00000416363
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,870,886 - 1,886,866 (+)Ensembl
RefSeq Acc Id: ENST00000418975   ⟹   ENSP00000403460
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,870,244 - 1,881,552 (+)Ensembl
RefSeq Acc Id: ENST00000421485   ⟹   ENSP00000411191
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,863,246 - 1,883,428 (+)Ensembl
RefSeq Acc Id: ENST00000429923   ⟹   ENSP00000400999
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,870,150 - 1,884,009 (+)Ensembl
RefSeq Acc Id: ENST00000432093   ⟹   ENSP00000412405
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,876,477 - 1,886,866 (+)Ensembl
RefSeq Acc Id: ENST00000446808   ⟹   ENSP00000402543
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,864,172 - 1,883,997 (+)Ensembl
RefSeq Acc Id: ENST00000451814   ⟹   ENSP00000414106
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,869,144 - 1,883,442 (+)Ensembl
RefSeq Acc Id: ENST00000457279   ⟹   ENSP00000400346
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,869,642 - 1,886,866 (+)Ensembl
RefSeq Acc Id: ENST00000464670
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,886,732 - 1,887,345 (+)Ensembl
RefSeq Acc Id: ENST00000472974
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,871,352 - 1,887,576 (+)Ensembl
RefSeq Acc Id: ENST00000484895
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,884,388 - 1,887,502 (+)Ensembl
RefSeq Acc Id: ENST00000485341
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,880,677 - 1,892,267 (+)Ensembl
RefSeq Acc Id: ENST00000612798   ⟹   ENSP00000484140
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,870,252 - 1,892,263 (+)Ensembl
RefSeq Acc Id: ENST00000676039   ⟹   ENSP00000502383
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl111,850,904 - 1,853,197 (+)Ensembl
RefSeq Acc Id: NM_001013253   ⟹   NP_001013271
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38111,868,706 - 1,892,263 (+)NCBI
GRCh37111,874,200 - 1,913,493 (+)ENTREZGENE
Build 36111,846,479 - 1,870,069 (+)NCBI Archive
HuRef111,665,106 - 1,704,058 (+)ENTREZGENE
CHM1_1111,888,718 - 1,912,407 (+)NCBI
T2T-CHM13v2.0111,954,500 - 1,978,157 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001013254   ⟹   NP_001013272
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38111,870,869 - 1,892,263 (+)NCBI
GRCh37111,874,200 - 1,913,493 (+)ENTREZGENE
Build 36111,848,675 - 1,870,069 (+)NCBI Archive
HuRef111,665,106 - 1,704,058 (+)ENTREZGENE
CHM1_1111,890,915 - 1,912,407 (+)NCBI
T2T-CHM13v2.0111,956,664 - 1,978,157 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001013255   ⟹   NP_001013273
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38111,870,924 - 1,892,263 (+)NCBI
GRCh37111,874,200 - 1,913,493 (+)ENTREZGENE
Build 36111,848,730 - 1,870,069 (+)NCBI Archive
HuRef111,665,106 - 1,704,058 (+)ENTREZGENE
CHM1_1111,890,970 - 1,912,407 (+)NCBI
T2T-CHM13v2.0111,956,719 - 1,978,157 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001242932   ⟹   NP_001229861
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38111,865,165 - 1,892,263 (+)NCBI
GRCh37111,874,200 - 1,913,493 (+)NCBI
HuRef111,665,106 - 1,704,058 (+)NCBI
CHM1_1111,885,210 - 1,912,407 (+)NCBI
T2T-CHM13v2.0111,950,959 - 1,978,157 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001289005   ⟹   NP_001275934
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38111,870,244 - 1,892,263 (+)NCBI
HuRef111,665,106 - 1,704,058 (+)NCBI
CHM1_1111,890,298 - 1,912,407 (+)NCBI
T2T-CHM13v2.0111,956,039 - 1,978,157 (+)NCBI
Sequence:
RefSeq Acc Id: NM_002339   ⟹   NP_002330
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38111,853,084 - 1,892,263 (+)NCBI
GRCh37111,874,200 - 1,913,493 (+)ENTREZGENE
Build 36111,830,776 - 1,870,069 (+)NCBI Archive
HuRef111,665,106 - 1,704,058 (+)ENTREZGENE
CHM1_1111,873,026 - 1,912,407 (+)NCBI
T2T-CHM13v2.0111,938,882 - 1,978,157 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001013271 (Get FASTA)   NCBI Sequence Viewer  
  NP_001013272 (Get FASTA)   NCBI Sequence Viewer  
  NP_001013273 (Get FASTA)   NCBI Sequence Viewer  
  NP_001229861 (Get FASTA)   NCBI Sequence Viewer  
  NP_001275934 (Get FASTA)   NCBI Sequence Viewer  
  NP_002330 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB29545 (Get FASTA)   NCBI Sequence Viewer  
  AAB99825 (Get FASTA)   NCBI Sequence Viewer  
  AAC00495 (Get FASTA)   NCBI Sequence Viewer  
  AAD13906 (Get FASTA)   NCBI Sequence Viewer  
  AAH01785 (Get FASTA)   NCBI Sequence Viewer  
  BAC85216 (Get FASTA)   NCBI Sequence Viewer  
  BAD96453 (Get FASTA)   NCBI Sequence Viewer  
  BAF82968 (Get FASTA)   NCBI Sequence Viewer  
  BAF84722 (Get FASTA)   NCBI Sequence Viewer  
  BAG51753 (Get FASTA)   NCBI Sequence Viewer  
  BAG52478 (Get FASTA)   NCBI Sequence Viewer  
  CAA38971 (Get FASTA)   NCBI Sequence Viewer  
  CAG46529 (Get FASTA)   NCBI Sequence Viewer  
  CAG46554 (Get FASTA)   NCBI Sequence Viewer  
  EAX02470 (Get FASTA)   NCBI Sequence Viewer  
  EAX02471 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000308383
  ENSP00000308383.4
  ENSP00000371194
  ENSP00000371194.1
  ENSP00000383932
  ENSP00000383932.2
  ENSP00000384022
  ENSP00000384022.2
  ENSP00000400346.1
  ENSP00000400999.1
  ENSP00000402543.1
  ENSP00000403460.1
  ENSP00000411191.1
  ENSP00000412405.1
  ENSP00000414106.1
  ENSP00000416363.1
  ENSP00000484140
  ENSP00000484140.1
  ENSP00000500060.1
  ENSP00000500330.1
  ENSP00000500350.1
  ENSP00000500618.1
  ENSP00000500923.1
  ENSP00000502383.1
GenBank Protein P33241 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_002330   ⟸   NM_002339
- Peptide Label: isoform 1
- UniProtKB: Q6FHM3 (UniProtKB/Swiss-Prot),   Q53H48 (UniProtKB/Swiss-Prot),   Q16096 (UniProtKB/Swiss-Prot),   E9PFP3 (UniProtKB/Swiss-Prot),   E9PBV6 (UniProtKB/Swiss-Prot),   B3KRR6 (UniProtKB/Swiss-Prot),   B3KPP1 (UniProtKB/Swiss-Prot),   Q9BUY8 (UniProtKB/Swiss-Prot),   P33241 (UniProtKB/Swiss-Prot),   A8K2L4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001013271   ⟸   NM_001013253
- Peptide Label: isoform 2
- UniProtKB: A8K7L8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001013272   ⟸   NM_001013254
- Peptide Label: isoform 2
- UniProtKB: A8K7L8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001013273   ⟸   NM_001013255
- Peptide Label: isoform 2
- UniProtKB: A8K7L8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001229861   ⟸   NM_001242932
- Peptide Label: isoform 3
- UniProtKB: P33241 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001275934   ⟸   NM_001289005
- Peptide Label: isoform 2
- UniProtKB: A8K7L8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000414106   ⟸   ENST00000451814
RefSeq Acc Id: ENSP00000400999   ⟸   ENST00000429923
RefSeq Acc Id: ENSP00000484140   ⟸   ENST00000612798
RefSeq Acc Id: ENSP00000416363   ⟸   ENST00000417766
RefSeq Acc Id: ENSP00000400346   ⟸   ENST00000457279
RefSeq Acc Id: ENSP00000308383   ⟸   ENST00000311604
RefSeq Acc Id: ENSP00000403460   ⟸   ENST00000418975
RefSeq Acc Id: ENSP00000383932   ⟸   ENST00000405957
RefSeq Acc Id: ENSP00000384022   ⟸   ENST00000406638
RefSeq Acc Id: ENSP00000402543   ⟸   ENST00000446808
RefSeq Acc Id: ENSP00000412405   ⟸   ENST00000432093
RefSeq Acc Id: ENSP00000371194   ⟸   ENST00000381775
RefSeq Acc Id: ENSP00000411191   ⟸   ENST00000421485
RefSeq Acc Id: ENSP00000502383   ⟸   ENST00000676039

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P33241-F1-model_v2 AlphaFold P33241 1-339 view protein structure

Promoters
RGD ID:6789082
Promoter ID:HG_KWN:11939
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   K562,   Lymphoblastoid
Transcripts:NM_002339
Position:
Human AssemblyChrPosition (strand)Source
Build 36111,830,561 - 1,831,061 (+)MPROMDB
RGD ID:6789086
Promoter ID:HG_KWN:11940
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000315850
Position:
Human AssemblyChrPosition (strand)Source
Build 36111,840,376 - 1,841,252 (+)MPROMDB
RGD ID:6788417
Promoter ID:HG_KWN:11941
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000142925,   OTTHUMT00000315851
Position:
Human AssemblyChrPosition (strand)Source
Build 36111,841,519 - 1,842,019 (+)MPROMDB
RGD ID:6789080
Promoter ID:HG_KWN:11942
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:ENST00000381775
Position:
Human AssemblyChrPosition (strand)Source
Build 36111,842,554 - 1,843,054 (+)MPROMDB
RGD ID:6789081
Promoter ID:HG_KWN:11943
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   Lymphoblastoid
Transcripts:ENST00000381758,   NM_001013253,   NM_001013255,   OTTHUMT00000142912,   OTTHUMT00000142913,   OTTHUMT00000142914,   OTTHUMT00000142915,   OTTHUMT00000315852,   OTTHUMT00000320503
Position:
Human AssemblyChrPosition (strand)Source
Build 36111,845,801 - 1,849,187 (+)MPROMDB
RGD ID:7219293
Promoter ID:EPDNEW_H15393
Type:initiation region
Name:LSP1_1
Description:lymphocyte-specific protein 1
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
GRCh38111,853,084 - 1,853,144EPDNEW
RGD ID:6789083
Promoter ID:HG_KWN:11945
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000034044
Position:
Human AssemblyChrPosition (strand)Source
Build 36111,857,756 - 1,859,102 (+)MPROMDB
RGD ID:6789085
Promoter ID:HG_KWN:11946
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000142917
Position:
Human AssemblyChrPosition (strand)Source
Build 36111,861,476 - 1,862,502 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:6707 AgrOrtholog
COSMIC LSP1 COSMIC
Ensembl Genes ENSG00000130592 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000288199 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000311604 ENTREZGENE
  ENST00000311604.8 UniProtKB/Swiss-Prot
  ENST00000381775 ENTREZGENE
  ENST00000381775.5 UniProtKB/Swiss-Prot
  ENST00000405957 ENTREZGENE
  ENST00000405957.6 UniProtKB/Swiss-Prot
  ENST00000406638 ENTREZGENE
  ENST00000406638.6 UniProtKB/Swiss-Prot
  ENST00000417766.5 UniProtKB/TrEMBL
  ENST00000418975.1 UniProtKB/TrEMBL
  ENST00000421485.5 UniProtKB/TrEMBL
  ENST00000429923.5 UniProtKB/TrEMBL
  ENST00000432093.1 UniProtKB/TrEMBL
  ENST00000446808.5 UniProtKB/TrEMBL
  ENST00000451814.5 UniProtKB/TrEMBL
  ENST00000457279.5 UniProtKB/TrEMBL
  ENST00000612798 ENTREZGENE
  ENST00000612798.4 UniProtKB/Swiss-Prot
  ENST00000672349.1 UniProtKB/Swiss-Prot
  ENST00000672565.3 UniProtKB/Swiss-Prot
  ENST00000673051.1 UniProtKB/Swiss-Prot
  ENST00000673183.1 UniProtKB/Swiss-Prot
  ENST00000673397.1 UniProtKB/Swiss-Prot
  ENST00000676039.1 UniProtKB/TrEMBL
GTEx ENSG00000130592 GTEx
  ENSG00000288199 GTEx
HGNC ID HGNC:6707 ENTREZGENE
Human Proteome Map LSP1 Human Proteome Map
InterPro Caldesmon_LSP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Lymphspecific UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:4046 UniProtKB/Swiss-Prot
NCBI Gene 4046 ENTREZGENE
OMIM 153432 OMIM
PANTHER LYMPHOCYTE-SPECIFIC PROTEIN 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR18949 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Caldesmon UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA30472 PharmGKB
PRINTS LYMPHSPCIFIC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A6Q8PGR6_HUMAN UniProtKB/TrEMBL
  A8K2L4 ENTREZGENE, UniProtKB/TrEMBL
  A8K7L8 ENTREZGENE, UniProtKB/TrEMBL
  B3KPP1 ENTREZGENE
  B3KRR6 ENTREZGENE
  C9J9B9_HUMAN UniProtKB/TrEMBL
  C9JDV1_HUMAN UniProtKB/TrEMBL
  C9JKF7_HUMAN UniProtKB/TrEMBL
  C9JNQ1_HUMAN UniProtKB/TrEMBL
  C9JU59_HUMAN UniProtKB/TrEMBL
  E7EMG9_HUMAN UniProtKB/TrEMBL
  E9PBD8_HUMAN UniProtKB/TrEMBL
  E9PBV6 ENTREZGENE
  E9PFP3 ENTREZGENE
  LSP1_HUMAN UniProtKB/Swiss-Prot
  O43649_HUMAN UniProtKB/TrEMBL
  P33241 ENTREZGENE
  Q16003_HUMAN UniProtKB/TrEMBL
  Q16096 ENTREZGENE
  Q53H48 ENTREZGENE
  Q6FHM3 ENTREZGENE
  Q9BUY8 ENTREZGENE
  Q9UEV7_HUMAN UniProtKB/TrEMBL
  Q9UEV8_HUMAN UniProtKB/TrEMBL
UniProt Secondary B3KPP1 UniProtKB/Swiss-Prot
  B3KRR6 UniProtKB/Swiss-Prot
  E9PBV6 UniProtKB/Swiss-Prot
  E9PFP3 UniProtKB/Swiss-Prot
  Q16004 UniProtKB/TrEMBL
  Q16096 UniProtKB/Swiss-Prot
  Q53H48 UniProtKB/Swiss-Prot
  Q6FHM3 UniProtKB/Swiss-Prot
  Q9BUY8 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-05-15 LSP1  lymphocyte specific protein 1  LSP1  lymphocyte-specific protein 1  Symbol and/or name change 5135510 APPROVED