TMEM50B (transmembrane protein 50B) - Rat Genome Database

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Gene: TMEM50B (transmembrane protein 50B) Homo sapiens
Analyze
Symbol: TMEM50B
Name: transmembrane protein 50B
RGD ID: 1316828
HGNC Page HGNC
Description: Predicted to be involved in late endosome to vacuole transport via multivesicular body sorting pathway. Localizes to endoplasmic reticulum; INTERACTS WITH 2,2',4,4'-Tetrabromodiphenyl ether; 3-isobutyl-1-methyl-7H-xanthine; acrolein.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: C21orf4; chromosome 21 open reading frame 4; DKFZp686C2482; FLJ26146; HCV p7-trans-regulated protein 3; HCV p7-transregulated protein 3; HCVP7TP3
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2133,432,485 - 33,479,974 (-)EnsemblGRCh38hg38GRCh38
GRCh382133,432,486 - 33,480,004 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372134,804,793 - 34,852,281 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362133,743,318 - 33,774,151 (-)NCBINCBI36hg18NCBI36
Build 342133,726,662 - 33,774,120NCBI
Celera2120,011,535 - 20,051,915 (-)NCBI
Cytogenetic Map21q22.11NCBI
HuRef2120,273,351 - 20,330,637 (-)NCBIHuRef
CHM1_12134,367,161 - 34,415,001 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

Additional References at PubMed
PMID:8889548   PMID:10077530   PMID:10830953   PMID:11256614   PMID:12477932   PMID:12975309   PMID:15489334   PMID:16344560   PMID:16780588   PMID:17567994   PMID:21873635   PMID:23128233  
PMID:25201988   PMID:29117863   PMID:29509190   PMID:32296183   PMID:33001583  


Genomics

Comparative Map Data
TMEM50B
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2133,432,485 - 33,479,974 (-)EnsemblGRCh38hg38GRCh38
GRCh382133,432,486 - 33,480,004 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372134,804,793 - 34,852,281 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362133,743,318 - 33,774,151 (-)NCBINCBI36hg18NCBI36
Build 342133,726,662 - 33,774,120NCBI
Celera2120,011,535 - 20,051,915 (-)NCBI
Cytogenetic Map21q22.11NCBI
HuRef2120,273,351 - 20,330,637 (-)NCBIHuRef
CHM1_12134,367,161 - 34,415,001 (-)NCBICHM1_1
Tmem50b
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391691,371,390 - 91,394,568 (-)NCBIGRCm39mm39
GRCm39 Ensembl1691,371,391 - 91,394,688 (-)Ensembl
GRCm381691,574,508 - 91,597,680 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1691,574,503 - 91,597,800 (-)EnsemblGRCm38mm10GRCm38
MGSCv371691,574,753 - 91,597,925 (-)NCBIGRCm37mm9NCBIm37
MGSCv361691,463,367 - 91,486,539 (-)NCBImm8
Celera1692,651,244 - 92,674,477 (-)NCBICelera
Cytogenetic Map16C3.3NCBI
Tmem50b
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21130,804,835 - 30,837,675 (-)NCBI
Rnor_6.0 Ensembl1131,719,443 - 31,752,243 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01131,719,441 - 31,752,276 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01135,327,975 - 35,361,018 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41131,533,823 - 31,566,625 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11131,572,882 - 31,605,683 (-)NCBI
Celera1130,472,297 - 30,505,079 (-)NCBICelera
Cytogenetic Map11q11NCBI
Tmem50b
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540732,874,905 - 32,916,036 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495540732,876,380 - 32,916,036 (-)NCBIChiLan1.0ChiLan1.0
TMEM50B
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.12133,163,876 - 33,219,556 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2133,163,876 - 33,219,556 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v02119,789,799 - 19,847,335 (-)NCBIMhudiblu_PPA_v0panPan3
TMEM50B
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13128,061,730 - 28,117,485 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3128,059,668 - 28,115,211 (-)NCBI
ROS_Cfam_1.03128,266,679 - 28,322,494 (-)NCBI
UMICH_Zoey_3.13128,133,780 - 28,189,375 (-)NCBI
UNSW_CanFamBas_1.03128,146,996 - 28,203,005 (-)NCBI
UU_Cfam_GSD_1.03128,647,598 - 28,703,167 (-)NCBI
Tmem50b
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440497128,594,313 - 28,641,933 (-)NCBI
SpeTri2.0NW_0049365008,825,956 - 8,873,510 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TMEM50B
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl13197,046,679 - 197,093,251 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.113197,048,285 - 197,093,308 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
TMEM50B
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1258,701,542 - 58,730,311 (+)NCBI
ChlSab1.1 Ensembl258,701,557 - 58,733,139 (+)Ensembl
Tmem50b
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474521,649,759 - 21,704,734 (-)NCBI

Position Markers
RH93313  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,823,032 - 34,823,151UniSTSGRCh37
Build 362133,744,902 - 33,745,021RGDNCBI36
Celera2120,013,119 - 20,013,238RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,291,594 - 20,291,713UniSTS
GeneMap99-GB4 RH Map21155.56UniSTS
RH80707  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,804,809 - 34,805,056UniSTSGRCh37
Build 362133,726,679 - 33,726,926RGDNCBI36
Celera2119,994,896 - 19,995,143RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,273,367 - 20,273,614UniSTS
GeneMap99-GB4 RH Map21150.53UniSTS
RH118439  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,827,933 - 34,828,263UniSTSGRCh37
Build 362133,749,803 - 33,750,133RGDNCBI36
Celera2120,018,020 - 20,018,350RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,296,495 - 20,296,825UniSTS
TNG Radiation Hybrid Map2111503.0UniSTS
D21S1733E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,821,469 - 34,821,624UniSTSGRCh37
Build 362133,743,339 - 33,743,494RGDNCBI36
Celera2120,011,556 - 20,011,711RGD
Cytogenetic Map21q22.11UniSTS
HuRef1948,942,020 - 48,942,171UniSTS
HuRef2120,290,029 - 20,290,184UniSTS
SHGC-106201  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,832,158 - 34,832,453UniSTSGRCh37
Build 362133,754,028 - 33,754,323RGDNCBI36
Celera2120,022,245 - 20,022,540RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,300,720 - 20,301,015UniSTS
TNG Radiation Hybrid Map2111503.0UniSTS
SHGC-170109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,849,289 - 34,849,633UniSTSGRCh37
Build 362133,771,159 - 33,771,503RGDNCBI36
Celera2120,048,923 - 20,049,267RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,327,610 - 20,327,954UniSTS
TNG Radiation Hybrid Map2111532.0UniSTS
SHGC-170293  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,845,131 - 34,845,411UniSTSGRCh37
Build 362133,767,001 - 33,767,281RGDNCBI36
Celera2120,035,218 - 20,035,498RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,313,562 - 20,313,842UniSTS
TNG Radiation Hybrid Map2111519.0UniSTS
SHGC-87557  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,804,924 - 34,805,075UniSTSGRCh37
Build 362133,726,794 - 33,726,945RGDNCBI36
Celera2119,995,011 - 19,995,162RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,273,482 - 20,273,633UniSTS
TNG Radiation Hybrid Map2111492.0UniSTS
GeneMap99-GB4 RH Map21154.3UniSTS
ECD05142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,822,847 - 34,823,591UniSTSGRCh37
Build 362133,744,717 - 33,745,461RGDNCBI36
Celera2120,012,934 - 20,013,678RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,291,409 - 20,292,153UniSTS
ECD06298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,850,820 - 34,851,532UniSTSGRCh37
Build 362133,772,690 - 33,773,402RGDNCBI36
Celera2120,050,454 - 20,051,166RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,329,141 - 20,329,853UniSTS
ECD06569  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,851,575 - 34,852,280UniSTSGRCh37
Build 362133,773,445 - 33,774,150RGDNCBI36
Celera2120,051,209 - 20,051,914RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,329,896 - 20,330,601UniSTS
ECD08740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,832,417 - 34,833,064UniSTSGRCh37
Build 362133,754,287 - 33,754,934RGDNCBI36
Celera2120,022,504 - 20,023,151RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,300,979 - 20,301,626UniSTS
ECD11066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,821,259 - 34,821,842UniSTSGRCh37
Build 362133,743,129 - 33,743,712RGDNCBI36
Celera2120,011,346 - 20,011,929RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,289,819 - 20,290,402UniSTS
ECD11245  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,821,933 - 34,822,511UniSTSGRCh37
Build 362133,743,803 - 33,744,381RGDNCBI36
Celera2120,012,020 - 20,012,598RGD
Cytogenetic Map21q22.11UniSTS
ECD11462  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,831,099 - 34,831,670UniSTSGRCh37
Build 362133,752,969 - 33,753,540RGDNCBI36
Celera2120,021,186 - 20,021,757RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,299,660 - 20,300,231UniSTS
ECD11566  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,827,829 - 34,828,397UniSTSGRCh37
Build 362133,749,699 - 33,750,267RGDNCBI36
Celera2120,017,916 - 20,018,484RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,296,391 - 20,296,959UniSTS
ECD12613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,840,389 - 34,840,928UniSTSGRCh37
Build 362133,762,259 - 33,762,798RGDNCBI36
Celera2120,030,476 - 20,031,015RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,308,810 - 20,309,351UniSTS
ECD13777  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,833,130 - 34,833,639UniSTSGRCh37
Build 362133,755,000 - 33,755,509RGDNCBI36
Celera2120,023,217 - 20,023,726RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,301,692 - 20,302,201UniSTS
ECD14684  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,837,222 - 34,837,710UniSTSGRCh37
Build 362133,759,092 - 33,759,580RGDNCBI36
Celera2120,027,309 - 20,027,797RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,305,637 - 20,306,126UniSTS
ECD15778  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,841,019 - 34,841,481UniSTSGRCh37
Build 362133,762,889 - 33,763,351RGDNCBI36
Celera2120,031,106 - 20,031,568RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,309,442 - 20,309,904UniSTS
ECD15857  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,837,723 - 34,838,183UniSTSGRCh37
Build 362133,759,593 - 33,760,053RGDNCBI36
Celera2120,027,810 - 20,028,270RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,306,139 - 20,306,599UniSTS
ECD17196  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,806,115 - 34,806,524UniSTSGRCh37
Build 362133,727,985 - 33,728,394RGDNCBI36
Celera2119,996,202 - 19,996,611RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,274,673 - 20,275,082UniSTS
ECD19228  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,824,270 - 34,824,599UniSTSGRCh37
Build 362133,746,140 - 33,746,469RGDNCBI36
Celera2120,014,357 - 20,014,686RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,292,832 - 20,293,161UniSTS
ECD19364  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,839,135 - 34,839,459UniSTSGRCh37
Build 362133,761,005 - 33,761,329RGDNCBI36
Celera2120,029,222 - 20,029,546RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,307,551 - 20,307,875UniSTS
ECD19675  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,852,428 - 34,852,741UniSTSGRCh37
Build 362133,774,298 - 33,774,611RGDNCBI36
Celera2120,052,062 - 20,052,375RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,330,749 - 20,331,062UniSTS
ECD19966  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,835,009 - 34,835,311UniSTSGRCh37
Build 362133,756,879 - 33,757,181RGDNCBI36
Celera2120,025,096 - 20,025,398RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,303,572 - 20,303,874UniSTS
ECD21880  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,828,673 - 34,828,909UniSTSGRCh37
Build 362133,750,543 - 33,750,779RGDNCBI36
Celera2120,018,760 - 20,018,996RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,297,235 - 20,297,471UniSTS
ECD23595  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,849,605 - 34,849,789UniSTSGRCh37
Build 362133,771,475 - 33,771,659RGDNCBI36
Celera2120,049,239 - 20,049,423RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,327,926 - 20,328,110UniSTS
REN85232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,804,858 - 34,805,082UniSTSGRCh37
Build 362133,726,728 - 33,726,952RGDNCBI36
Celera2119,994,945 - 19,995,169RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,273,416 - 20,273,640UniSTS
REN85233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,805,026 - 34,805,270UniSTSGRCh37
Build 362133,726,896 - 33,727,140RGDNCBI36
Celera2119,995,113 - 19,995,357RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,273,584 - 20,273,828UniSTS
REN85234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,805,106 - 34,805,349UniSTSGRCh37
Build 362133,726,976 - 33,727,219RGDNCBI36
Celera2119,995,193 - 19,995,436RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,273,664 - 20,273,907UniSTS
REN85235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,805,495 - 34,805,726UniSTSGRCh37
Build 362133,727,365 - 33,727,596RGDNCBI36
Celera2119,995,582 - 19,995,813RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,274,053 - 20,274,284UniSTS
REN85236  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371180,398,342 - 180,398,608UniSTSGRCh37
GRCh372134,805,720 - 34,805,959UniSTSGRCh37
Build 361178,664,965 - 178,665,231RGDNCBI36
Celera1153,505,222 - 153,505,490RGD
Celera2119,995,807 - 19,996,046UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map21q22.11UniSTS
HuRef313,505,675 - 13,505,927UniSTS
HuRef2120,274,278 - 20,274,517UniSTS
REN85237  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,805,955 - 34,806,205UniSTSGRCh37
Build 362133,727,825 - 33,728,075RGDNCBI36
Celera2119,996,042 - 19,996,292RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,274,513 - 20,274,763UniSTS
REN85238  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,806,183 - 34,806,443UniSTSGRCh37
Build 362133,728,053 - 33,728,313RGDNCBI36
Celera2119,996,270 - 19,996,530RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,274,741 - 20,275,001UniSTS
REN85239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,806,301 - 34,806,529UniSTSGRCh37
Build 362133,728,171 - 33,728,399RGDNCBI36
Celera2119,996,388 - 19,996,616RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,274,859 - 20,275,087UniSTS
REN85298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,821,034 - 34,821,281UniSTSGRCh37
Build 362133,742,904 - 33,743,151RGDNCBI36
Celera2120,011,121 - 20,011,368RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,289,594 - 20,289,841UniSTS
REN85299  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,821,233 - 34,821,494UniSTSGRCh37
Build 362133,743,103 - 33,743,364RGDNCBI36
Celera2120,011,320 - 20,011,581RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,289,793 - 20,290,054UniSTS
REN85300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,821,471 - 34,821,705UniSTSGRCh37
Build 362133,743,341 - 33,743,575RGDNCBI36
Celera2120,011,558 - 20,011,792RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,290,031 - 20,290,265UniSTS
REN85301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,821,682 - 34,821,932UniSTSGRCh37
Build 362133,743,552 - 33,743,802RGDNCBI36
Celera2120,011,769 - 20,012,019RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,290,242 - 20,290,492UniSTS
REN85302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,821,926 - 34,822,167UniSTSGRCh37
Build 362133,743,796 - 33,744,037RGDNCBI36
Celera2120,012,013 - 20,012,254RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,290,486 - 20,290,727UniSTS
REN85303  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,822,070 - 34,822,316UniSTSGRCh37
Build 362133,743,940 - 33,744,186RGDNCBI36
Celera2120,012,157 - 20,012,403RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,290,630 - 20,290,876UniSTS
REN85304  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,822,287 - 34,822,514UniSTSGRCh37
Build 362133,744,157 - 33,744,384RGDNCBI36
Celera2120,012,374 - 20,012,601RGD
Cytogenetic Map21q22.11UniSTS
REN85305  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,822,420 - 34,822,652UniSTSGRCh37
Build 362133,744,290 - 33,744,522RGDNCBI36
Celera2120,012,507 - 20,012,739RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,290,980 - 20,291,214UniSTS
REN85306  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,822,521 - 34,822,746UniSTSGRCh37
Build 362133,744,391 - 33,744,616RGDNCBI36
Celera2120,012,608 - 20,012,833RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,291,083 - 20,291,308UniSTS
REN85307  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,822,798 - 34,823,055UniSTSGRCh37
Build 362133,744,668 - 33,744,925RGDNCBI36
Celera2120,012,885 - 20,013,142RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,291,360 - 20,291,617UniSTS
REN85308  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,823,042 - 34,823,311UniSTSGRCh37
Build 362133,744,912 - 33,745,181RGDNCBI36
Celera2120,013,129 - 20,013,398RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,291,604 - 20,291,873UniSTS
REN85309  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,823,290 - 34,823,542UniSTSGRCh37
Build 362133,745,160 - 33,745,412RGDNCBI36
Celera2120,013,377 - 20,013,629RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,291,852 - 20,292,104UniSTS
REN85310  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,823,522 - 34,823,785UniSTSGRCh37
Build 362133,745,392 - 33,745,655RGDNCBI36
Celera2120,013,609 - 20,013,872RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,292,084 - 20,292,347UniSTS
REN85311  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,823,783 - 34,824,038UniSTSGRCh37
Build 362133,745,653 - 33,745,908RGDNCBI36
Celera2120,013,870 - 20,014,125RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,292,345 - 20,292,600UniSTS
REN85312  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,824,015 - 34,824,264UniSTSGRCh37
Build 362133,745,885 - 33,746,134RGDNCBI36
Celera2120,014,102 - 20,014,351RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,292,577 - 20,292,826UniSTS
REN85313  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,824,258 - 34,824,511UniSTSGRCh37
Build 362133,746,128 - 33,746,381RGDNCBI36
Celera2120,014,345 - 20,014,598RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,292,820 - 20,293,073UniSTS
REN85314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,824,470 - 34,824,715UniSTSGRCh37
Build 362133,746,340 - 33,746,585RGDNCBI36
Celera2120,014,557 - 20,014,802RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,293,032 - 20,293,277UniSTS
REN85315  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,824,697 - 34,824,952UniSTSGRCh37
Build 362133,746,567 - 33,746,822RGDNCBI36
Celera2120,014,784 - 20,015,039RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,293,259 - 20,293,514UniSTS
REN85316  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,824,927 - 34,825,174UniSTSGRCh37
Build 362133,746,797 - 33,747,044RGDNCBI36
Celera2120,015,014 - 20,015,261RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,293,489 - 20,293,736UniSTS
REN85317  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,825,129 - 34,825,353UniSTSGRCh37
Build 362133,746,999 - 33,747,223RGDNCBI36
Celera2120,015,216 - 20,015,440RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,293,691 - 20,293,915UniSTS
REN85318  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,825,224 - 34,825,468UniSTSGRCh37
Build 362133,747,094 - 33,747,338RGDNCBI36
Celera2120,015,311 - 20,015,555RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,293,786 - 20,294,030UniSTS
REN85319  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,825,713 - 34,825,939UniSTSGRCh37
Build 362133,747,583 - 33,747,809RGDNCBI36
Celera2120,015,800 - 20,016,026RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,294,275 - 20,294,501UniSTS
REN85320  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,825,914 - 34,826,138UniSTSGRCh37
Build 362133,747,784 - 33,748,008RGDNCBI36
Celera2120,016,001 - 20,016,225RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,294,476 - 20,294,700UniSTS
REN85321  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,826,102 - 34,826,327UniSTSGRCh37
Build 362133,747,972 - 33,748,197RGDNCBI36
Celera2120,016,189 - 20,016,414RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,294,664 - 20,294,889UniSTS
REN85322  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,826,312 - 34,826,565UniSTSGRCh37
Build 362133,748,182 - 33,748,435RGDNCBI36
Celera2120,016,399 - 20,016,652RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,294,874 - 20,295,127UniSTS
REN85323  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,826,467 - 34,826,711UniSTSGRCh37
Build 362133,748,337 - 33,748,581RGDNCBI36
Celera2120,016,554 - 20,016,798RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,295,029 - 20,295,273UniSTS
REN85324  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,826,905 - 34,827,159UniSTSGRCh37
Build 362133,748,775 - 33,749,029RGDNCBI36
Celera2120,016,992 - 20,017,246RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,295,467 - 20,295,721UniSTS
REN85325  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,827,146 - 34,827,397UniSTSGRCh37
Build 362133,749,016 - 33,749,267RGDNCBI36
Celera2120,017,233 - 20,017,484RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,295,708 - 20,295,959UniSTS
REN85326  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,827,388 - 34,827,645UniSTSGRCh37
Build 362133,749,258 - 33,749,515RGDNCBI36
Celera2120,017,475 - 20,017,732RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,295,950 - 20,296,207UniSTS
REN85327  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,827,633 - 34,827,880UniSTSGRCh37
Build 362133,749,503 - 33,749,750RGDNCBI36
Celera2120,017,720 - 20,017,967RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,296,195 - 20,296,442UniSTS
REN85328  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,827,867 - 34,828,139UniSTSGRCh37
Build 362133,749,737 - 33,750,009RGDNCBI36
Celera2120,017,954 - 20,018,226RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,296,429 - 20,296,701UniSTS
REN85329  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,828,130 - 34,828,377UniSTSGRCh37
Build 362133,750,000 - 33,750,247RGDNCBI36
Celera2120,018,217 - 20,018,464RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,296,692 - 20,296,939UniSTS
REN85330  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,828,348 - 34,828,597UniSTSGRCh37
Build 362133,750,218 - 33,750,467RGDNCBI36
Celera2120,018,435 - 20,018,684RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,296,910 - 20,297,159UniSTS
REN85331  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,828,666 - 34,828,890UniSTSGRCh37
Build 362133,750,536 - 33,750,760RGDNCBI36
Celera2120,018,753 - 20,018,977RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,297,228 - 20,297,452UniSTS
REN85332  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,828,880 - 34,829,106UniSTSGRCh37
Build 362133,750,750 - 33,750,976RGDNCBI36
Celera2120,018,967 - 20,019,193RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,297,442 - 20,297,668UniSTS
REN85333  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,829,056 - 34,829,294UniSTSGRCh37
Build 362133,750,926 - 33,751,164RGDNCBI36
Celera2120,019,143 - 20,019,381RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,297,618 - 20,297,856UniSTS
REN85334  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,829,502 - 34,829,746UniSTSGRCh37
Build 362133,751,372 - 33,751,616RGDNCBI36
Celera2120,019,589 - 20,019,833RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,298,064 - 20,298,308UniSTS
REN85335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,829,821 - 34,830,047UniSTSGRCh37
Build 362133,751,691 - 33,751,917RGDNCBI36
Celera2120,019,908 - 20,020,134RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,298,383 - 20,298,608UniSTS
REN85336  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,830,031 - 34,830,265UniSTSGRCh37
Build 362133,751,901 - 33,752,135RGDNCBI36
Celera2120,020,118 - 20,020,352RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,298,592 - 20,298,826UniSTS
REN85337  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,830,253 - 34,830,492UniSTSGRCh37
Build 362133,752,123 - 33,752,362RGDNCBI36
Celera2120,020,340 - 20,020,579RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,298,814 - 20,299,053UniSTS
REN85338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,830,284 - 34,830,544UniSTSGRCh37
Build 362133,752,154 - 33,752,414RGDNCBI36
Celera2120,020,371 - 20,020,631RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,298,845 - 20,299,105UniSTS
REN85339  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,830,824 - 34,831,050UniSTSGRCh37
Build 362133,752,694 - 33,752,920RGDNCBI36
Celera2120,020,911 - 20,021,137RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,299,385 - 20,299,611UniSTS
REN85340  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,831,027 - 34,831,286UniSTSGRCh37
Build 362133,752,897 - 33,753,156RGDNCBI36
Celera2120,021,114 - 20,021,373RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,299,588 - 20,299,847UniSTS
REN85341  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,831,198 - 34,831,453UniSTSGRCh37
Build 362133,753,068 - 33,753,323RGDNCBI36
Celera2120,021,285 - 20,021,540RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,299,759 - 20,300,014UniSTS
REN85342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,831,452 - 34,831,698UniSTSGRCh37
Build 362133,753,322 - 33,753,568RGDNCBI36
Celera2120,021,539 - 20,021,785RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,300,013 - 20,300,259UniSTS
REN85343  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,831,629 - 34,831,898UniSTSGRCh37
Build 362133,753,499 - 33,753,768RGDNCBI36
Celera2120,021,716 - 20,021,985RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,300,190 - 20,300,459UniSTS
REN85344  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,831,879 - 34,832,136UniSTSGRCh37
Build 362133,753,749 - 33,754,006RGDNCBI36
Celera2120,021,966 - 20,022,223RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,300,440 - 20,300,698UniSTS
REN85345  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,832,132 - 34,832,356UniSTSGRCh37
Build 362133,754,002 - 33,754,226RGDNCBI36
Celera2120,022,219 - 20,022,443RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,300,694 - 20,300,918UniSTS
REN85346  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,832,338 - 34,832,570UniSTSGRCh37
Build 362133,754,208 - 33,754,440RGDNCBI36
Celera2120,022,425 - 20,022,657RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,300,900 - 20,301,132UniSTS
REN85347  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,832,546 - 34,832,794UniSTSGRCh37
Build 362133,754,416 - 33,754,664RGDNCBI36
Celera2120,022,633 - 20,022,881RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,301,108 - 20,301,356UniSTS
REN85348  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,832,771 - 34,833,019UniSTSGRCh37
Build 362133,754,641 - 33,754,889RGDNCBI36
Celera2120,022,858 - 20,023,106RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,301,333 - 20,301,581UniSTS
REN85349  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,832,993 - 34,833,254UniSTSGRCh37
Build 362133,754,863 - 33,755,124RGDNCBI36
Celera2120,023,080 - 20,023,341RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,301,555 - 20,301,816UniSTS
REN85350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,833,249 - 34,833,480UniSTSGRCh37
Build 362133,755,119 - 33,755,350RGDNCBI36
Celera2120,023,336 - 20,023,567RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,301,811 - 20,302,042UniSTS
REN85351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,833,425 - 34,833,670UniSTSGRCh37
Build 362133,755,295 - 33,755,540RGDNCBI36
Celera2120,023,512 - 20,023,757RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,301,987 - 20,302,232UniSTS
REN85352  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,833,644 - 34,833,897UniSTSGRCh37
Build 362133,755,514 - 33,755,767RGDNCBI36
Celera2120,023,731 - 20,023,984RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,302,206 - 20,302,459UniSTS
REN85353  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,833,877 - 34,834,113UniSTSGRCh37
Build 362133,755,747 - 33,755,983RGDNCBI36
Celera2120,023,964 - 20,024,200RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,302,439 - 20,302,675UniSTS
REN85354  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,834,073 - 34,834,331UniSTSGRCh37
Build 362133,755,943 - 33,756,201RGDNCBI36
Celera2120,024,160 - 20,024,418RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,302,635 - 20,302,894UniSTS
REN85355  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,834,322 - 34,834,577UniSTSGRCh37
Build 362133,756,192 - 33,756,447RGDNCBI36
Celera2120,024,409 - 20,024,664RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,302,885 - 20,303,140UniSTS
REN85356  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,834,568 - 34,834,841UniSTSGRCh37
Build 362133,756,438 - 33,756,711RGDNCBI36
Celera2120,024,655 - 20,024,928RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,303,131 - 20,303,404UniSTS
REN85357  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,834,747 - 34,835,018UniSTSGRCh37
Build 362133,756,617 - 33,756,888RGDNCBI36
Celera2120,024,834 - 20,025,105RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,303,310 - 20,303,581UniSTS
REN85358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,835,010 - 34,835,249UniSTSGRCh37
Build 362133,756,880 - 33,757,119RGDNCBI36
Celera2120,025,097 - 20,025,336RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,303,573 - 20,303,812UniSTS
REN85359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,835,098 - 34,835,322UniSTSGRCh37
Build 362133,756,968 - 33,757,192RGDNCBI36
Celera2120,025,185 - 20,025,409RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,303,661 - 20,303,885UniSTS
REN85360  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,835,665 - 34,835,901UniSTSGRCh37
Build 362133,757,535 - 33,757,771RGDNCBI36
Celera2120,025,752 - 20,025,988RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,304,228 - 20,304,464UniSTS
REN85361  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,835,878 - 34,836,109UniSTSGRCh37
Build 362133,757,748 - 33,757,979RGDNCBI36
Celera2120,025,965 - 20,026,196RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,304,441 - 20,304,672UniSTS
REN85362  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,836,097 - 34,836,338UniSTSGRCh37
Build 362133,757,967 - 33,758,208RGDNCBI36
Celera2120,026,184 - 20,026,425RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,304,660 - 20,304,901UniSTS
REN85363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,836,319 - 34,836,575UniSTSGRCh37
Build 362133,758,189 - 33,758,445RGDNCBI36
Celera2120,026,406 - 20,026,662RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,304,882 - 20,305,139UniSTS
REN85364  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,836,427 - 34,836,663UniSTSGRCh37
Build 362133,758,297 - 33,758,533RGDNCBI36
Celera2120,026,514 - 20,026,750RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,304,990 - 20,305,227UniSTS
REN85365  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,836,736 - 34,836,977UniSTSGRCh37
Build 362133,758,606 - 33,758,847RGDNCBI36
Celera2120,026,823 - 20,027,064RGD
Cytogenetic Map21q22.11UniSTS
REN85366  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,836,983 - 34,837,221UniSTSGRCh37
Build 362133,758,853 - 33,759,091RGDNCBI36
Celera2120,027,070 - 20,027,308RGD
Cytogenetic Map21q22.11UniSTS
REN85367  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,837,218 - 34,837,457UniSTSGRCh37
Build 362133,759,088 - 33,759,327RGDNCBI36
Celera2120,027,305 - 20,027,544RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,305,633 - 20,305,873UniSTS
REN85368  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,837,438 - 34,837,677UniSTSGRCh37
Build 362133,759,308 - 33,759,547RGDNCBI36
Celera2120,027,525 - 20,027,764RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,305,854 - 20,306,093UniSTS
REN85369  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,837,667 - 34,837,924UniSTSGRCh37
Build 362133,759,537 - 33,759,794RGDNCBI36
Celera2120,027,754 - 20,028,011RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,306,083 - 20,306,340UniSTS
REN85370  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,837,897 - 34,838,169UniSTSGRCh37
Build 362133,759,767 - 33,760,039RGDNCBI36
Celera2120,027,984 - 20,028,256RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,306,313 - 20,306,585UniSTS
REN85371  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,838,097 - 34,838,342UniSTSGRCh37
Build 362133,759,967 - 33,760,212RGDNCBI36
Celera2120,028,184 - 20,028,429RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,306,513 - 20,306,758UniSTS
REN85372  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,838,319 - 34,838,557UniSTSGRCh37
Build 362133,760,189 - 33,760,427RGDNCBI36
Celera2120,028,406 - 20,028,644RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,306,735 - 20,306,973UniSTS
REN85373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,838,534 - 34,838,785UniSTSGRCh37
Build 362133,760,404 - 33,760,655RGDNCBI36
Celera2120,028,621 - 20,028,872RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,306,950 - 20,307,201UniSTS
REN85374  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,838,762 - 34,839,005UniSTSGRCh37
Build 362133,760,632 - 33,760,875RGDNCBI36
Celera2120,028,849 - 20,029,092RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,307,178 - 20,307,421UniSTS
REN85375  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,838,998 - 34,839,263UniSTSGRCh37
Build 362133,760,868 - 33,761,133RGDNCBI36
Celera2120,029,085 - 20,029,350RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,307,414 - 20,307,679UniSTS
REN85376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,839,240 - 34,839,486UniSTSGRCh37
Build 362133,761,110 - 33,761,356RGDNCBI36
Celera2120,029,327 - 20,029,573RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,307,656 - 20,307,902UniSTS
REN85377  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,839,438 - 34,839,683UniSTSGRCh37
Build 362133,761,308 - 33,761,553RGDNCBI36
Celera2120,029,525 - 20,029,770RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,307,854 - 20,308,099UniSTS
REN85378  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,839,696 - 34,839,931UniSTSGRCh37
Build 362133,761,566 - 33,761,801RGDNCBI36
Celera2120,029,783 - 20,030,018RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,308,112 - 20,308,347UniSTS
REN85379  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,840,060 - 34,840,298UniSTSGRCh37
Build 362133,761,930 - 33,762,168RGDNCBI36
Celera2120,030,147 - 20,030,385RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,308,476 - 20,308,714UniSTS
REN85380  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,840,275 - 34,840,541UniSTSGRCh37
Build 362133,762,145 - 33,762,411RGDNCBI36
Celera2120,030,362 - 20,030,628RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,308,691 - 20,308,963UniSTS
REN85381  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,840,518 - 34,840,787UniSTSGRCh37
Build 362133,762,388 - 33,762,657RGDNCBI36
Celera2120,030,605 - 20,030,874RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,308,940 - 20,309,210UniSTS
REN85382  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,840,764 - 34,841,021UniSTSGRCh37
Build 362133,762,634 - 33,762,891RGDNCBI36
Celera2120,030,851 - 20,031,108RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,309,187 - 20,309,444UniSTS
REN85383  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,840,998 - 34,841,250UniSTSGRCh37
Build 362133,762,868 - 33,763,120RGDNCBI36
Celera2120,031,085 - 20,031,337RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,309,421 - 20,309,673UniSTS
REN85384  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,841,225 - 34,841,481UniSTSGRCh37
Build 362133,763,095 - 33,763,351RGDNCBI36
Celera2120,031,312 - 20,031,568RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,309,648 - 20,309,904UniSTS
REN85385  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,841,563 - 34,841,821UniSTSGRCh37
Build 362133,763,433 - 33,763,691RGDNCBI36
Celera2120,031,650 - 20,031,908RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,309,986 - 20,310,244UniSTS
REN85386  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,841,801 - 34,842,048UniSTSGRCh37
Build 362133,763,671 - 33,763,918RGDNCBI36
Celera2120,031,888 - 20,032,135RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,310,224 - 20,310,471UniSTS
REN85387  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,842,029 - 34,842,279UniSTSGRCh37
Build 362133,763,899 - 33,764,149RGDNCBI36
Celera2120,032,116 - 20,032,366RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,310,452 - 20,310,702UniSTS
REN85388  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,842,256 - 34,842,504UniSTSGRCh37
Build 362133,764,126 - 33,764,374RGDNCBI36
Celera2120,032,343 - 20,032,591RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,310,679 - 20,310,926UniSTS
REN85389  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,843,044 - 34,843,270UniSTSGRCh37
Build 362133,764,914 - 33,765,140RGDNCBI36
Celera2120,033,131 - 20,033,357RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,311,472 - 20,311,698UniSTS
REN85390  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,843,247 - 34,843,502UniSTSGRCh37
Build 362133,765,117 - 33,765,372RGDNCBI36
Celera2120,033,334 - 20,033,589RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,311,675 - 20,311,930UniSTS
REN85391  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,843,500 - 34,843,762UniSTSGRCh37
Build 362133,765,370 - 33,765,632RGDNCBI36
Celera2120,033,587 - 20,033,849RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,311,928 - 20,312,189UniSTS
REN85392  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,843,730 - 34,843,960UniSTSGRCh37
Build 362133,765,600 - 33,765,830RGDNCBI36
Celera2120,033,817 - 20,034,047RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,312,157 - 20,312,387UniSTS
REN85393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,843,840 - 34,844,064UniSTSGRCh37
Build 362133,765,710 - 33,765,934RGDNCBI36
Celera2120,033,927 - 20,034,151RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,312,267 - 20,312,491UniSTS
REN85394  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,844,650 - 34,844,911UniSTSGRCh37
Build 362133,766,520 - 33,766,781RGDNCBI36
Celera2120,034,737 - 20,034,998RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,313,081 - 20,313,342UniSTS
REN85395  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,844,785 - 34,845,047UniSTSGRCh37
Build 362133,766,655 - 33,766,917RGDNCBI36
Celera2120,034,872 - 20,035,134RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,313,216 - 20,313,478UniSTS
REN85396  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,845,023 - 34,845,278UniSTSGRCh37
Build 362133,766,893 - 33,767,148RGDNCBI36
Celera2120,035,110 - 20,035,365RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,313,454 - 20,313,709UniSTS
REN85397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,845,128 - 34,845,353UniSTSGRCh37
Build 362133,766,998 - 33,767,223RGDNCBI36
Celera2120,035,215 - 20,035,440RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,313,559 - 20,313,784UniSTS
REN85398  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,845,330 - 34,845,555UniSTSGRCh37
Build 362133,767,200 - 33,767,425RGDNCBI36
Celera2120,035,417 - 20,035,642RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,313,761 - 20,313,986UniSTS
REN85399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,845,393 - 34,845,642UniSTSGRCh37
Build 362133,767,263 - 33,767,512RGDNCBI36
Celera2120,035,480 - 20,035,729RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,313,824 - 20,314,073UniSTS
REN85400  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,845,621 - 34,845,848UniSTSGRCh37
Build 362133,767,491 - 33,767,718RGDNCBI36
Celera2120,035,708 - 20,035,935RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,314,052 - 20,314,278UniSTS
REN85401  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,845,782 - 34,846,006UniSTSGRCh37
Build 362133,767,652 - 33,767,876RGDNCBI36
Celera2120,035,869 - 20,036,093RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,314,212 - 20,314,438UniSTS
REN85402  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,845,973 - 34,846,214UniSTSGRCh37
Build 362133,767,843 - 33,768,084RGDNCBI36
Celera2120,036,060 - 20,036,301RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,314,405 - 20,314,646UniSTS
REN85403  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,846,211 - 34,846,448UniSTSGRCh37
Build 362133,768,081 - 33,768,318RGDNCBI36
Celera2120,036,298 - 20,036,535RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,314,643 - 20,314,880UniSTS
REN85404  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,846,387 - 34,846,654UniSTSGRCh37
Build 362133,768,257 - 33,768,524RGDNCBI36
Celera2120,036,474 - 20,036,741RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,314,819 - 20,315,086UniSTS
REN85405  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,846,718 - 34,846,944UniSTSGRCh37
Build 362133,768,588 - 33,768,814RGDNCBI36
Celera2120,036,805 - 20,037,031RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,315,150 - 20,315,376UniSTS
REN85406  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,847,155 - 34,847,381UniSTSGRCh37
Build 362133,769,025 - 33,769,251RGDNCBI36
Celera2120,046,789 - 20,047,015RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,325,122 - 20,325,630UniSTS
REN85407  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,847,529 - 34,847,770UniSTSGRCh37
Build 362133,769,399 - 33,769,640RGDNCBI36
Celera2120,047,163 - 20,047,404RGD
Cytogenetic Map21q22.11UniSTS
REN85408  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,848,043 - 34,848,276UniSTSGRCh37
Build 362133,769,913 - 33,770,146RGDNCBI36
Celera2120,047,677 - 20,047,910RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,326,364 - 20,326,597UniSTS
REN85409  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,848,272 - 34,848,531UniSTSGRCh37
Build 362133,770,142 - 33,770,401RGDNCBI36
Celera2120,047,906 - 20,048,165RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,326,593 - 20,326,852UniSTS
REN85410  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,848,285 - 34,848,532UniSTSGRCh37
Build 362133,770,155 - 33,770,402RGDNCBI36
Celera2120,047,919 - 20,048,166RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,326,606 - 20,326,853UniSTS
REN85411  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,849,161 - 34,849,403UniSTSGRCh37
Build 362133,771,031 - 33,771,273RGDNCBI36
Celera2120,048,795 - 20,049,037RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,327,482 - 20,327,724UniSTS
REN85412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,849,301 - 34,849,561UniSTSGRCh37
Build 362133,771,171 - 33,771,431RGDNCBI36
Celera2120,048,935 - 20,049,195RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,327,622 - 20,327,882UniSTS
REN85413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,849,538 - 34,849,787UniSTSGRCh37
Build 362133,771,408 - 33,771,657RGDNCBI36
Celera2120,049,172 - 20,049,421RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,327,859 - 20,328,108UniSTS
REN85414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,849,779 - 34,850,025UniSTSGRCh37
Build 362133,771,649 - 33,771,895RGDNCBI36
Celera2120,049,413 - 20,049,659RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,328,100 - 20,328,346UniSTS
REN85415  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,850,524 - 34,850,757UniSTSGRCh37
Build 362133,772,394 - 33,772,627RGDNCBI36
Celera2120,050,158 - 20,050,391RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,328,845 - 20,329,078UniSTS
REN85416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,850,734 - 34,850,973UniSTSGRCh37
Build 362133,772,604 - 33,772,843RGDNCBI36
Celera2120,050,368 - 20,050,607RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,329,055 - 20,329,294UniSTS
REN85417  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,850,955 - 34,851,210UniSTSGRCh37
Build 362133,772,825 - 33,773,080RGDNCBI36
Celera2120,050,589 - 20,050,844RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,329,276 - 20,329,531UniSTS
REN85418  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,851,197 - 34,851,446UniSTSGRCh37
Build 362133,773,067 - 33,773,316RGDNCBI36
Celera2120,050,831 - 20,051,080RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,329,518 - 20,329,767UniSTS
REN85419  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,851,423 - 34,851,669UniSTSGRCh37
Build 362133,773,293 - 33,773,539RGDNCBI36
Celera2120,051,057 - 20,051,303RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,329,744 - 20,329,990UniSTS
REN85420  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,851,634 - 34,851,863UniSTSGRCh37
Build 362133,773,504 - 33,773,733RGDNCBI36
Celera2120,051,268 - 20,051,497RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,329,955 - 20,330,184UniSTS
REN85421  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,851,845 - 34,852,080UniSTSGRCh37
Build 362133,773,715 - 33,773,950RGDNCBI36
Celera2120,051,479 - 20,051,714RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,330,166 - 20,330,401UniSTS
REN85422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,852,272 - 34,852,537UniSTSGRCh37
Build 362133,774,142 - 33,774,407RGDNCBI36
Celera2120,051,906 - 20,052,171RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,330,593 - 20,330,858UniSTS
REN85423  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,852,517 - 34,852,785UniSTSGRCh37
Build 362133,774,387 - 33,774,655RGDNCBI36
Celera2120,052,151 - 20,052,419RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,330,838 - 20,331,106UniSTS
REN85424  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,852,768 - 34,853,011UniSTSGRCh37
Build 362133,774,638 - 33,774,881RGDNCBI36
Celera2120,052,402 - 20,052,645RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,331,089 - 20,331,331UniSTS
REN85425  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,852,988 - 34,853,214UniSTSGRCh37
Build 362133,774,858 - 33,775,084RGDNCBI36
Celera2120,052,622 - 20,052,848RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,331,308 - 20,331,534UniSTS
REN85426  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,853,190 - 34,853,454UniSTSGRCh37
Build 362133,775,060 - 33,775,324RGDNCBI36
Celera2120,052,824 - 20,053,088RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,331,510 - 20,331,774UniSTS
REN85427  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,853,430 - 34,853,663UniSTSGRCh37
Build 362133,775,300 - 33,775,533RGDNCBI36
Celera2120,053,064 - 20,053,297RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,331,750 - 20,331,983UniSTS
REN85428  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,853,622 - 34,853,871UniSTSGRCh37
Build 362133,775,492 - 33,775,741RGDNCBI36
Celera2120,053,256 - 20,053,505RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,331,942 - 20,332,191UniSTS
REN85429  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,853,848 - 34,854,112UniSTSGRCh37
Build 362133,775,718 - 33,775,982RGDNCBI36
Celera2120,053,482 - 20,053,746RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,332,168 - 20,332,432UniSTS
stSG607163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,805,567 - 34,806,871UniSTSGRCh37
Build 362133,727,437 - 33,728,741RGDNCBI36
Celera2119,995,654 - 19,996,958RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,274,125 - 20,275,429UniSTS
stSG607176  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,821,259 - 34,822,315UniSTSGRCh37
Build 362133,743,129 - 33,744,185RGDNCBI36
Celera2120,011,346 - 20,012,402RGD
HuRef2120,289,819 - 20,290,875UniSTS
stSG607177  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,822,295 - 34,823,591UniSTSGRCh37
Build 362133,744,165 - 33,745,461RGDNCBI36
Celera2120,012,382 - 20,013,678RGD
HuRef2120,290,855 - 20,292,153UniSTS
stSG607178  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,823,571 - 34,824,599UniSTSGRCh37
Build 362133,745,441 - 33,746,469RGDNCBI36
Celera2120,013,658 - 20,014,686RGD
HuRef2120,292,133 - 20,293,161UniSTS
stSG607179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,824,581 - 34,826,070UniSTSGRCh37
Build 362133,746,451 - 33,747,940RGDNCBI36
Celera2120,014,668 - 20,016,157RGD
HuRef2120,293,143 - 20,294,632UniSTS
stSG607181  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,828,059 - 34,829,231UniSTSGRCh37
Build 362133,749,929 - 33,751,101RGDNCBI36
Celera2120,018,146 - 20,019,318RGD
HuRef2120,296,621 - 20,297,793UniSTS
stSG607182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,829,218 - 34,830,508UniSTSGRCh37
Build 362133,751,088 - 33,752,378RGDNCBI36
Celera2120,019,305 - 20,020,595RGD
HuRef2120,297,780 - 20,299,069UniSTS
stSG607183  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,830,489 - 34,831,576UniSTSGRCh37
Build 362133,752,359 - 33,753,446RGDNCBI36
Celera2120,020,576 - 20,021,663RGD
HuRef2120,299,050 - 20,300,137UniSTS
stSG607184  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,831,584 - 34,832,812UniSTSGRCh37
Build 362133,753,454 - 33,754,682RGDNCBI36
Celera2120,021,671 - 20,022,899RGD
HuRef2120,300,145 - 20,301,374UniSTS
stSG607185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,832,549 - 34,833,630UniSTSGRCh37
Build 362133,754,419 - 33,755,500RGDNCBI36
Celera2120,022,636 - 20,023,717RGD
HuRef2120,301,111 - 20,302,192UniSTS
stSG607186  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,833,609 - 34,834,731UniSTSGRCh37
Build 362133,755,479 - 33,756,601RGDNCBI36
Celera2120,023,696 - 20,024,818RGD
HuRef2120,302,171 - 20,303,294UniSTS
stSG607187  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,834,712 - 34,835,125UniSTSGRCh37
Build 362133,756,582 - 33,756,995RGDNCBI36
Celera2120,024,799 - 20,025,212RGD
HuRef2120,303,275 - 20,303,688UniSTS
stSG607188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,835,130 - 34,836,347UniSTSGRCh37
Build 362133,757,000 - 33,758,217RGDNCBI36
Celera2120,025,217 - 20,026,434RGD
HuRef2120,303,693 - 20,304,910UniSTS
stSG607189  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,836,340 - 34,837,742UniSTSGRCh37
Build 362133,758,210 - 33,759,612RGDNCBI36
Celera2120,026,427 - 20,027,829RGD
HuRef2120,304,903 - 20,306,158UniSTS
stSG607190  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,837,723 - 34,838,762UniSTSGRCh37
Build 362133,759,593 - 33,760,632RGDNCBI36
Celera2120,027,810 - 20,028,849RGD
HuRef2120,306,139 - 20,307,178UniSTS
stSG607191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,838,757 - 34,840,101UniSTSGRCh37
Build 362133,760,627 - 33,761,971RGDNCBI36
Celera2120,028,844 - 20,030,188RGD
HuRef2120,307,173 - 20,308,517UniSTS
stSG607192  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,840,389 - 34,841,438UniSTSGRCh37
Build 362133,762,259 - 33,763,308RGDNCBI36
Celera2120,030,476 - 20,031,525RGD
HuRef2120,308,810 - 20,309,861UniSTS
stSG607193  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,841,180 - 34,842,315UniSTSGRCh37
Build 362133,763,050 - 33,764,185RGDNCBI36
Celera2120,031,267 - 20,032,402RGD
HuRef2120,309,603 - 20,310,738UniSTS
stSG607194  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,842,295 - 34,843,274UniSTSGRCh37
Build 362133,764,165 - 33,765,144RGDNCBI36
Celera2120,032,382 - 20,033,361RGD
HuRef2120,310,718 - 20,311,702UniSTS
stSG607196  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,847,216 - 34,848,294UniSTSGRCh37
Build 362133,769,086 - 33,770,164RGDNCBI36
Celera2120,046,850 - 20,047,928RGD
HuRef2120,325,183 - 20,326,615UniSTS
stSG607197  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,848,274 - 34,849,685UniSTSGRCh37
Build 362133,770,144 - 33,771,555RGDNCBI36
Celera2120,047,908 - 20,049,319RGD
HuRef2120,326,595 - 20,328,006UniSTS
stSG607198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,849,759 - 34,850,847UniSTSGRCh37
Build 362133,771,629 - 33,772,717RGDNCBI36
Celera2120,049,393 - 20,050,481RGD
HuRef2120,328,080 - 20,329,168UniSTS
STS-AA031780  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372134,821,516 - 34,821,730UniSTSGRCh37
Build 362133,743,386 - 33,743,600RGDNCBI36
Celera2120,011,603 - 20,011,817RGD
Cytogenetic Map21q22.11UniSTS
HuRef2120,290,076 - 20,290,290UniSTS
GeneMap99-GB4 RH Map21149.49UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2734
Count of miRNA genes:974
Interacting mature miRNAs:1147
Transcripts:ENST00000420455, ENST00000432504, ENST00000441128, ENST00000442441, ENST00000459909, ENST00000468874, ENST00000470682, ENST00000474272, ENST00000484377, ENST00000542230
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


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 2428 2372 1649 554 1390 394 4317 2092 3633 401 1439 1585 174 1 1204 2767 3 2
Low 11 619 77 70 561 71 40 105 101 18 21 28 1 21 3
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_007570 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_006134 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_040016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011529746 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC207981 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF039906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF045606 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF086280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129657 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309977 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310701 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311870 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL355685 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000300 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000301 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000302 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP001717 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY358634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY820138 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000569 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF696480 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM152475 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB306801 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471079 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA286739 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ286229 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ656043 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000420455   ⟹   ENSP00000397773
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2133,432,485 - 33,479,943 (-)Ensembl
RefSeq Acc Id: ENST00000432504   ⟹   ENSP00000387622
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2133,465,378 - 33,479,289 (-)Ensembl
RefSeq Acc Id: ENST00000441128   ⟹   ENSP00000398859
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2133,450,521 - 33,468,926 (-)Ensembl
RefSeq Acc Id: ENST00000442441   ⟹   ENSP00000409942
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2133,450,547 - 33,479,936 (-)Ensembl
RefSeq Acc Id: ENST00000459909
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2133,468,420 - 33,479,948 (-)Ensembl
RefSeq Acc Id: ENST00000468874
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2133,436,884 - 33,449,189 (-)Ensembl
RefSeq Acc Id: ENST00000470682
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2133,432,798 - 33,449,410 (-)Ensembl
RefSeq Acc Id: ENST00000474272
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2133,465,018 - 33,467,135 (-)Ensembl
RefSeq Acc Id: ENST00000484377
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2133,432,485 - 33,448,964 (-)Ensembl
RefSeq Acc Id: ENST00000542230   ⟹   ENSP00000439768
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2133,449,141 - 33,479,974 (-)Ensembl
RefSeq Acc Id: NM_006134   ⟹   NP_006125
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,449,141 - 33,479,974 (-)NCBI
GRCh372134,804,793 - 34,852,316 (-)ENTREZGENE
Build 362133,743,318 - 33,774,151 (-)NCBI Archive
Celera2120,011,535 - 20,051,915 (-)RGD
HuRef2120,273,351 - 20,330,637 (-)ENTREZGENE
CHM1_12134,384,135 - 34,415,001 (-)NCBI
Sequence:
RefSeq Acc Id: NR_040016
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,432,486 - 33,479,974 (-)NCBI
GRCh372134,804,793 - 34,852,316 (-)ENTREZGENE
HuRef2120,273,351 - 20,330,637 (-)ENTREZGENE
CHM1_12134,367,161 - 34,415,001 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011529746   ⟹   XP_011528048
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,432,486 - 33,480,004 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_006125   ⟸   NM_006134
- UniProtKB: P56557 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011528048   ⟸   XM_011529746
- Peptide Label: isoform X1
- UniProtKB: P56557 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000439768   ⟸   ENST00000542230
RefSeq Acc Id: ENSP00000398859   ⟸   ENST00000441128
RefSeq Acc Id: ENSP00000409942   ⟸   ENST00000442441
RefSeq Acc Id: ENSP00000387622   ⟸   ENST00000432504
RefSeq Acc Id: ENSP00000397773   ⟸   ENST00000420455

Promoters
RGD ID:13602678
Promoter ID:EPDNEW_H27524
Type:initiation region
Name:TMEM50B_2
Description:transmembrane protein 50B
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H27529  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382133,479,943 - 33,480,003EPDNEW
RGD ID:6799603
Promoter ID:HG_KWN:40657
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000140083
Position:
Human AssemblyChrPosition (strand)Source
Build 362133,773,356 - 33,774,462 (-)MPROMDB
RGD ID:6799343
Promoter ID:HG_KWN:40658
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000140081,   UC002YRS.1,   UC002YRT.1,   UC010GMB.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362133,773,836 - 33,774,336 (-)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000050445] Chr21:7749532..46670405 [GRCh38]
Chr21:15499847..48090317 [GRCh37]
Chr21:14421718..46914745 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh38/hg38 21q22.11(chr21:33437186-33767838)x3 copy number gain See cases [RCV000052797] Chr21:33437186..33767838 [GRCh38]
Chr21:34809493..35140142 [GRCh37]
Chr21:33731363..34062012 [NCBI36]
Chr21:21q22.11
uncertain significance
GRCh38/hg38 21q22.11(chr21:33465408-33806416)x1 copy number loss See cases [RCV000052806] Chr21:33465408..33806416 [GRCh38]
Chr21:34837715..35178720 [GRCh37]
Chr21:33759585..34100590 [NCBI36]
Chr21:21q22.11
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3 copy number gain See cases [RCV000053042] Chr21:7749532..46623792 [GRCh38]
Chr21:14595524..48043704 [GRCh37]
Chr21:13517395..46868132 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3 copy number gain See cases [RCV000053043] Chr21:7749532..46623792 [GRCh38]
Chr21:14629063..48043704 [GRCh37]
Chr21:13550934..46868132 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670546)x3 copy number gain See cases [RCV000053045] Chr21:7749532..46670546 [GRCh38]
Chr21:15499647..48090458 [GRCh37]
Chr21:14421518..46914886 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46661140)x3 copy number gain See cases [RCV000053065] Chr21:7749532..46661140 [GRCh38]
Chr21:15499647..48081052 [GRCh37]
Chr21:14421518..46905480 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46661140)x3 copy number gain See cases [RCV000053067] Chr21:7749532..46661140 [GRCh38]
Chr21:15499847..48081052 [GRCh37]
Chr21:14421718..46905480 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000053068] Chr21:7749532..46670405 [GRCh38]
Chr21:20655360..48090317 [GRCh37]
Chr21:19577231..46914745 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000053069] Chr21:7749532..46670405 [GRCh38]
Chr21:34423268..48090317 [GRCh37]
Chr21:33345138..46914745 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3 copy number gain See cases [RCV000053039] Chr21:7749532..46623792 [GRCh38]
Chr21:14524963..48043704 [GRCh37]
Chr21:13446834..46868132 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46653090)x3 copy number gain See cases [RCV000053040] Chr21:7749532..46653090 [GRCh38]
Chr21:14539679..48073002 [GRCh37]
Chr21:13461550..46897430 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
NM_006134.6(TMEM50B):c.338C>T (p.Ser113Phe) single nucleotide variant Malignant melanoma [RCV000072819] Chr21:33460448 [GRCh38]
Chr21:34832755 [GRCh37]
Chr21:33754625 [NCBI36]
Chr21:21q22.11
not provided
NM_005534.3(IFNGR2):c.879+19del deletion Interferon gamma receptor deficiency [RCV000030046] Chr21:33432890 [GRCh38]
Chr21:34805197 [GRCh37]
Chr21:21q22.11
uncertain significance
NM_005534.3(IFNGR2):c.1008G>A (p.Thr336=) single nucleotide variant Immunodeficiency 28 [RCV001087048]|not provided [RCV000097433] Chr21:33436956 [GRCh38]
Chr21:34809263 [GRCh37]
Chr21:21q22.11
likely benign|not provided
NM_005534.3(IFNGR2):c.721+173A>C single nucleotide variant not provided [RCV000097453] Chr21:33432509 [GRCh38]
Chr21:34804816 [GRCh37]
Chr21:21q22.11
not provided
NM_005534.3(IFNGR2):c.722-42C>T single nucleotide variant not provided [RCV000097455] Chr21:33432672 [GRCh38]
Chr21:34804979 [GRCh37]
Chr21:21q22.11
not provided
NM_005534.3(IFNGR2):c.722-91A>T single nucleotide variant not provided [RCV000097456] Chr21:33432623 [GRCh38]
Chr21:34804930 [GRCh37]
Chr21:21q22.11
not provided
NM_005534.3(IFNGR2):c.780G>T (p.Ser260=) single nucleotide variant not provided [RCV000097459] Chr21:33432772 [GRCh38]
Chr21:34805079 [GRCh37]
Chr21:21q22.11
not provided
NM_005534.3(IFNGR2):c.889G>A (p.Asp297Asn) single nucleotide variant Immunodeficiency 28 [RCV001052465]|not provided [RCV000097461] Chr21:33436837 [GRCh38]
Chr21:34809144 [GRCh37]
Chr21:21q22.11
uncertain significance|not provided
NM_005534.3(IFNGR2):c.984G>A (p.Lys328=) single nucleotide variant Immunodeficiency 28 [RCV001089246]|not provided [RCV000097462] Chr21:33436932 [GRCh38]
Chr21:34809239 [GRCh37]
Chr21:21q22.11
benign|not provided
NM_005534.3(IFNGR2):c.*352C>T single nucleotide variant not provided [RCV000097432] Chr21:33437314 [GRCh38]
Chr21:34809621 [GRCh37]
Chr21:21q22.11
not provided
NM_005534.3(IFNGR2):c.880-135_880-113dup duplication not provided [RCV000097460] Chr21:33436686..33436687 [GRCh38]
Chr21:34808993..34808994 [GRCh37]
Chr21:21q22.11
not provided
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-42971047)x3 copy number gain See cases [RCV000133676] Chr21:7749532..42971047 [GRCh38]
Chr21:15499847..44391157 [GRCh37]
Chr21:14421718..43264226 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46653084)x3 copy number gain See cases [RCV000134727] Chr21:7749532..46653084 [GRCh38]
Chr21:15485038..48072996 [GRCh37]
Chr21:14406909..46897424 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46649831)x3 copy number gain See cases [RCV000134509] Chr21:7749532..46649831 [GRCh38]
Chr21:14577835..48069743 [GRCh37]
Chr21:13499706..46894171 [NCBI36]
Chr21:21q11.2-22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670440)x3 copy number gain See cases [RCV000134119] Chr21:7749532..46670440 [GRCh38]
Chr21:15485038..48090352 [GRCh37]
Chr21:14406909..46914780 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21q22.11-22.3(chr21:7749532-46670346)x3 copy number gain See cases [RCV000135310] Chr21:7749532..46670346 [GRCh38]
Chr21:34111831..48090258 [GRCh37]
Chr21:33033702..46914686 [NCBI36]
Chr21:21q22.11-22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46664250)x3 copy number gain See cases [RCV000134836] Chr21:7749532..46664250 [GRCh38]
Chr21:15485038..48084162 [GRCh37]
Chr21:14406909..46908590 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670440)x3 copy number gain See cases [RCV000134842] Chr21:7749532..46670440 [GRCh38]
Chr21:15513244..48090352 [GRCh37]
Chr21:14435115..46914780 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46660999)x3 copy number gain See cases [RCV000135448] Chr21:7749532..46660999 [GRCh38]
Chr21:15499847..48080911 [GRCh37]
Chr21:14421718..46905339 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3 copy number gain See cases [RCV000137255] Chr21:7749532..46671060 [GRCh38]
Chr21:35319225..48090972 [GRCh37]
Chr21:34241095..46915400 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3 copy number gain See cases [RCV000137337] Chr21:7749532..46671060 [GRCh38]
Chr21:10697897..48090972 [GRCh37]
Chr21:1..46915400 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.13(chr21:7749532-37653653)x1 copy number loss See cases [RCV000138095] Chr21:7749532..37653653 [GRCh38]
Chr21:15451032..39025955 [GRCh37]
Chr21:14372903..37947825 [NCBI36]
Chr21:21p11.2-q22.13
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3 copy number gain See cases [RCV000138216] Chr21:7749532..46671060 [GRCh38]
Chr21:10944001..48090972 [GRCh37]
Chr21:9965872..46915400 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3 copy number gain See cases [RCV000138436] Chr21:7749532..46671060 [GRCh38]
Chr21:15451032..48090972 [GRCh37]
Chr21:14372903..46915400 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic|conflicting data from submitters
GRCh38/hg38 21q22.11(chr21:33361172-34048047)x1 copy number loss See cases [RCV000140099] Chr21:33361172..34048047 [GRCh38]
Chr21:34733478..35420347 [GRCh37]
Chr21:33655348..34342217 [NCBI36]
Chr21:21q22.11
likely pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46670346)x3 copy number gain See cases [RCV000140103] Chr21:7749532..46670346 [GRCh38]
Chr21:14577894..48090258 [GRCh37]
Chr21:13499765..46914686 [NCBI36]
Chr21:21q11.2-22.3
pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46698247)x3 copy number gain See cases [RCV000141346] Chr21:7749532..46698247 [GRCh38]
Chr21:14577835..48118159 [GRCh37]
Chr21:13499706..46942587 [NCBI36]
Chr21:21q11.2-22.3
pathogenic
GRCh38/hg38 21q21.3-22.3(chr21:7749532-46677460)x3 copy number gain See cases [RCV000141827] Chr21:7749532..46677460 [GRCh38]
Chr21:28285299..48097372 [GRCh37]
Chr21:27207170..46921800 [NCBI36]
Chr21:21q21.3-22.3
uncertain significance
GRCh37/hg19 21q21.3-22.12(chr21:29880468-36062331)x1 copy number loss See cases [RCV000141575] Chr21:29880468..36062331 [GRCh37]
Chr21:28802339..34984201 [NCBI36]
Chr21:21q21.3-22.12
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7817158-46670440)x1 copy number loss See cases [RCV000142427] Chr21:7817158..46670440 [GRCh38]
Chr21:15485038..48090352 [GRCh37]
Chr21:14406909..46914780 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46677460)x3 copy number gain See cases [RCV000143120] Chr21:7749532..46677460 [GRCh38]
Chr21:15006457..48097372 [GRCh37]
Chr21:13928328..46921800 [NCBI36]
Chr21:21q11.2-22.3
pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46677460)x3 copy number gain See cases [RCV000143376] Chr21:7749532..46677460 [GRCh38]
Chr21:15006458..48097372 [GRCh37]
Chr21:13928329..46921800 [NCBI36]
Chr21:21q11.2-22.3
pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46677460) copy number gain See cases [RCV000143160] Chr21:7749532..46677460 [GRCh38]
Chr21:14386013..48097372 [GRCh37]
Chr21:13307884..46921800 [NCBI36]
Chr21:21q11.2-22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000148131] Chr21:7749532..46670405 [GRCh38]
Chr21:15499847..48090317 [GRCh37]
Chr21:14421718..46914745 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15538655-48080926)x1 copy number loss See cases [RCV000239948] Chr21:15538655..48080926 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15410701-48090317)x3 copy number gain See cases [RCV000240397] Chr21:15410701..48090317 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q22.11(chr21:32578640-35060092)x1 copy number loss See cases [RCV000240540] Chr21:32578640..35060092 [GRCh37]
Chr21:21q22.11
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-43598570)x3 copy number gain See cases [RCV000446716] Chr21:15006457..43598570 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q21.3-22.13(chr21:29812033-39282854)x3 copy number gain See cases [RCV000448874] Chr21:29812033..39282854 [GRCh37]
Chr21:21q21.3-22.13
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:14771770-48080867)x3 copy number gain See cases [RCV000447884] Chr21:14771770..48080867 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-44827632)x3 copy number gain See cases [RCV000448199] Chr21:15006457..44827632 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15285841-48097372)x3 copy number gain See cases [RCV000447729] Chr21:15285841..48097372 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-48097372)x3 copy number gain See cases [RCV000447749] Chr21:15006457..48097372 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006458-48097372) copy number gain See cases [RCV000511589] Chr21:15006458..48097372 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
NM_005534.3(IFNGR2):c.978G>A (p.Pro326=) single nucleotide variant Immunodeficiency 28 [RCV000530249]|not provided [RCV001093463] Chr21:33436926 [GRCh38]
Chr21:34809233 [GRCh37]
Chr21:21q22.11
benign|likely benign
NC_000021.8:g.(?_34638751)_(34809289_?)dup duplication Immunodeficiency 28 [RCV000652134] Chr21:34638751..34809289 [GRCh37]
Chr21:21q22.11
uncertain significance
GRCh37/hg19 21q22.11-22.2(chr21:33980213-42542987)x3 copy number gain not provided [RCV000684166] Chr21:33980213..42542987 [GRCh37]
Chr21:21q22.11-22.2
pathogenic
GRCh37/hg19 21q22.11(chr21:34117564-34917877)x3 copy number gain not provided [RCV000684151] Chr21:34117564..34917877 [GRCh37]
Chr21:21q22.11
uncertain significance
NM_005534.3(IFNGR2):c.940G>A (p.Asp314Asn) single nucleotide variant Immunodeficiency 28 [RCV000706945] Chr21:33436888 [GRCh38]
Chr21:34809195 [GRCh37]
Chr21:21q22.11
uncertain significance
GRCh37/hg19 21q22.11(chr21:34281910-35748170)x1 copy number loss not provided [RCV000709834] Chr21:34281910..35748170 [GRCh37]
Chr21:21q22.11
not provided
NM_005534.3(IFNGR2):c.780G>A (p.Ser260=) single nucleotide variant Immunodeficiency 28 [RCV000690166] Chr21:33432772 [GRCh38]
Chr21:34805079 [GRCh37]
Chr21:21q22.11
uncertain significance
GRCh37/hg19 21p11.2-q22.3(chr21:10824040-48090629)x3 copy number gain not provided [RCV000741418] Chr21:10824040..48090629 [GRCh37]
Chr21:21p11.2-q22.3
pathogenic
GRCh37/hg19 21p11.2-q22.3(chr21:10827533-48100155)x3 copy number gain not provided [RCV000741419] Chr21:10827533..48100155 [GRCh37]
Chr21:21p11.2-q22.3
pathogenic
GRCh37/hg19 21q21.3-22.11(chr21:30214872-34896962)x3 copy number gain not provided [RCV000741530] Chr21:30214872..34896962 [GRCh37]
Chr21:21q21.3-22.11
pathogenic
GRCh37/hg19 21p11.2-q22.3(chr21:10699330-48117896)x3 copy number gain not provided [RCV000741413] Chr21:10699330..48117896 [GRCh37]
Chr21:21p11.2-q22.3
pathogenic
GRCh37/hg19 21p11.2-q22.3(chr21:10704198-48117896)x3 copy number gain not provided [RCV000741415] Chr21:10704198..48117896 [GRCh37]
Chr21:21p11.2-q22.3
pathogenic
NM_005534.4(IFNGR2):c.949T>C (p.Trp317Arg) single nucleotide variant Immunodeficiency 28 [RCV001041921] Chr21:33436897 [GRCh38]
Chr21:34809204 [GRCh37]
Chr21:21q22.11
uncertain significance
NM_005534.4(IFNGR2):c.879+4C>T single nucleotide variant Immunodeficiency 28 [RCV001041922] Chr21:33432875 [GRCh38]
Chr21:34805182 [GRCh37]
Chr21:21q22.11
uncertain significance
NM_005534.3(IFNGR2):c.771G>A (p.Ser257=) single nucleotide variant Immunodeficiency 28 [RCV000926543] Chr21:33432763 [GRCh38]
Chr21:34805070 [GRCh37]
Chr21:21q22.11
likely benign
GRCh37/hg19 21q22.11(chr21:32589903-35359935) copy number loss not provided [RCV000767744] Chr21:32589903..35359935 [GRCh37]
Chr21:21q22.11
pathogenic
NM_005534.3(IFNGR2):c.764C>T (p.Thr255Ile) single nucleotide variant Immunodeficiency 28 [RCV000794039] Chr21:33432756 [GRCh38]
Chr21:34805063 [GRCh37]
Chr21:21q22.11
uncertain significance
NC_000021.8:g.(?_34799171)_(34809289_?)dup duplication Immunodeficiency 28 [RCV000805294] Chr21:33426864..33436982 [GRCh38]
Chr21:34799171..34809289 [GRCh37]
Chr21:21q22.11
uncertain significance
NM_005534.3(IFNGR2):c.1007C>G (p.Thr336Arg) single nucleotide variant Immunodeficiency 28 [RCV000822322] Chr21:33436955 [GRCh38]
Chr21:34809262 [GRCh37]
Chr21:21q22.11
uncertain significance
NM_005534.3(IFNGR2):c.914C>T (p.Ala305Val) single nucleotide variant Immunodeficiency 28 [RCV000820162] Chr21:33436862 [GRCh38]
Chr21:34809169 [GRCh37]
Chr21:21q22.11
uncertain significance
GRCh37/hg19 21q11.2-22.3(chr21:15006457-48097372)x3 copy number gain not provided [RCV000846937] Chr21:15006457..48097372 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
NM_005534.3(IFNGR2):c.756C>T (p.Ser252=) single nucleotide variant Immunodeficiency 28 [RCV000889781] Chr21:33432748 [GRCh38]
Chr21:34805055 [GRCh37]
Chr21:21q22.11
likely benign
NM_005534.4(IFNGR2):c.945C>T (p.Asp315=) single nucleotide variant not provided [RCV001171962] Chr21:33436893 [GRCh38]
Chr21:34809200 [GRCh37]
Chr21:21q22.11
likely benign
GRCh37/hg19 21q22.11-22.12(chr21:33205064-36039022) copy number loss 21q22.11q22.12 microdeletion syndrome [RCV001093501] Chr21:33205064..36039022 [GRCh37]
Chr21:21q22.11-22.12
pathogenic
NM_005534.4(IFNGR2):c.1006A>G (p.Thr336Ala) single nucleotide variant Immunodeficiency 28 [RCV001044993] Chr21:33436954 [GRCh38]
Chr21:34809261 [GRCh37]
Chr21:21q22.11
uncertain significance
NM_005534.4(IFNGR2):c.977C>T (p.Pro326Leu) single nucleotide variant Immunodeficiency 28 [RCV001234430] Chr21:33436925 [GRCh38]
Chr21:34809232 [GRCh37]
Chr21:21q22.11
uncertain significance
GRCh37/hg19 21q22.11(chr21:34379096-35572731)x1 copy number loss not provided [RCV001259407] Chr21:34379096..35572731 [GRCh37]
Chr21:21q22.11
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:14629063-48090317)x3 copy number gain See cases [RCV001263025] Chr21:14629063..48090317 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
NC_000021.8:g.(?_32439271)_(37133458_?)dup duplication Parkinson disease 20, early-onset [RCV001338842] Chr21:32439271..37133458 [GRCh37]
Chr21:21q22.11-22.12
uncertain significance
NC_000021.8:g.(?_34799171)_(34809289_?)dup duplication Immunodeficiency 28 [RCV001323302] Chr21:34799171..34809289 [GRCh37]
Chr21:21q22.11
uncertain significance
NM_005534.4(IFNGR2):c.788C>T (p.Ala263Val) single nucleotide variant Immunodeficiency 28 [RCV001294654] Chr21:33432780 [GRCh38]
Chr21:34805087 [GRCh37]
Chr21:21q22.11
uncertain significance
NM_005534.4(IFNGR2):c.990AGA[1] (p.Glu331del) microsatellite Immunodeficiency 28 [RCV001350508] Chr21:33436937..33436939 [GRCh38]
Chr21:34809244..34809246 [GRCh37]
Chr21:21q22.11
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:1280 AgrOrtholog
COSMIC TMEM50B COSMIC
Ensembl Genes ENSG00000142188 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000263160 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000387622 UniProtKB/TrEMBL
  ENSP00000397773 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000398859 UniProtKB/TrEMBL
  ENSP00000409942 UniProtKB/TrEMBL
  ENSP00000439768 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000458900 UniProtKB/Swiss-Prot
  ENSP00000459785 UniProtKB/TrEMBL
  ENSP00000460121 UniProtKB/Swiss-Prot
  ENSP00000461292 UniProtKB/TrEMBL
  ENSP00000461339 UniProtKB/TrEMBL
Ensembl Transcript ENST00000420455 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000432504 UniProtKB/TrEMBL
  ENST00000441128 UniProtKB/TrEMBL
  ENST00000442441 UniProtKB/TrEMBL
  ENST00000542230 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000571778 UniProtKB/Swiss-Prot
  ENST00000572455 UniProtKB/TrEMBL
  ENST00000573374 UniProtKB/Swiss-Prot
  ENST00000573687 UniProtKB/TrEMBL
  ENST00000574612 UniProtKB/TrEMBL
GTEx ENSG00000142188 GTEx
  ENSG00000263160 GTEx
HGNC ID HGNC:1280 ENTREZGENE
Human Proteome Map TMEM50B Human Proteome Map
InterPro UPF0220 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:757 UniProtKB/Swiss-Prot
NCBI Gene 757 ENTREZGENE
OMIM 617894 OMIM
PANTHER PTHR13180 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam UPF0220 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA25835 PharmGKB
UniProt C9K0I4_HUMAN UniProtKB/TrEMBL
  F8WBF4_HUMAN UniProtKB/TrEMBL
  F8WDH1_HUMAN UniProtKB/TrEMBL
  P56557 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary B2R4L4 UniProtKB/Swiss-Prot
  D3DSF1 UniProtKB/Swiss-Prot
  O60537 UniProtKB/Swiss-Prot
  Q5PY47 UniProtKB/Swiss-Prot